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Chapter 12 - Substitute Consent to Medical and Dental Treatment

Contributed by Nick O’Neill with input from Carmelle Peisah, current to 30 April 2021.

12.1 Introduction

The judges in the common law world have not developed a regime for substitute decision-making for medical and dental treatment. Rather they have asserted that there are circumstances in which adults unable to give a valid consent to their own treatment can be treated without consent and the treating doctor is absolved from liability for trespass to the person in the form of battery or false imprisonment, but not necessarily from negligence.

The lack of a sufficient answer in the common law has led to the development, in the Australian States and the Australian Capital Territory, of legislative regimes for substitute decision-making in relation to the medical and dental treatment of those unable to give a valid consent to their own treatment.(1)

These regimes are discussed in this chapter, but first it is useful to consider the state of the common law as it applies to fill in any gaps in these regimes, some of which are more comprehensive than others.

While in the period 2014-2016 the Northern Territory introduced most elements of a modern guardianship system, it introduced an incomplete legislative regime in relation to substitute consent to what is called in the Territory “health care action”. The elements of the scheme that have been introduced are set out in 12. 10, below. Consequently, the common law, insofar as it has been stated by judges, may need to be applied in the Northern Territory to fill in the gaps to a far greater extent than it needs to be applied elsewhere in Australia.

This chapter deals with the issue of consent to medical treatment by adults. Dealing comprehensively with the ethical and clinical aspects of consent by and for minors is beyond the scope of this chapter. However, we deal briefly with some of the issues relating to consent by minors as it pertains to the concept of capacity at 12.14, below.

As is apparent from Chapter 11, the starting point of the common law is that, subject to some exceptions, adults cannot be given medical treatment without their consent. McHugh J of the High Court of Australia pointed out in 1992 in Marion's Case:

It is the central thesis of the common law doctrine of trespass to the person that the voluntary choices and decisions of an adult person of sound mind concerning what is or is not done to his or her body must be respected and accepted, irrespective of what others, including doctors, may think is in the best interests of that particular person.(2)

In 1984, Goff LJ, as he then was, stated in the Divisional Court of Queen's Bench that there was a general exception to trespass to the person in the form of battery, and possibly also to assault and false imprisonment, embracing all physical contact which is generally acceptable in the ordinary conduct of daily life. He said:

In each case, the test must be whether the physical contact so persisted in has in the circumstances gone beyond generally acceptable standards of conduct; and the answer to that question will depend upon the facts of the particular case.(3)

In a 1986 case the English Court of Appeal said of this "rationalisation" by Goff LJ:
It provides a solution to the old problem of what legal rule allows a casualty surgeon to perform an urgent operation on an unconscious patient who is brought into hospital. The patient cannot consent, and there may be no next of kin available to do it for him. Hitherto it has been customary to say in such cases that consent is to be implied for what would otherwise be a battery on the unconscious body. It is better simply to say that the surgeon's action is acceptable in the ordinary conduct of everyday life, and not a battery.(4)

Notwithstanding the “rationalisation” involved in that case and in urgent circumstances, it is incumbent upon doctors and other health care professionals giving treatment of any kind, to take heed of the consequences of not meeting their professional, ethical and legal responsibilities with regards to consent, as we outline in Chapter 7.

12.2.1 Emergence of the principle of necessity

By 1990 Goff LJ had become Lord Goff of Chieveley and in the House of Lords in the case In re F, he made statements about how doctors could lawfully treat those incapable of giving a valid consent to their own treatment. He adapted from the law of agency the principle of necessity which upholds the actions of agents who are unable to get instructions from their principals but must act in an emergency provided they act in a way that in the judgment of a wise and prudent person is in the best interests of the principal. He indicated that doctors dealing with patients who were likely to be incapable only for a short period because, for example, they were unconscious or delirious and, with care and treatment, would soon regain capacity could treat such patients by doing no more than was reasonably required in their best interests.(5)

Lord Goff of Chieveley extended the principle of necessity to the effect that, if a person's incapacity was permanent or more or less so, their doctor could treat them by acting in their best interests and treating them in accordance with a responsible and competent body of relevant professional opinion. He noted that it was good practice to consult relatives and others who are concerned with the care of the person.(6)

It would be unwise to treat the principle of necessity, in either its adapted or extended form, as enabling a doctor to give treatment that is contrary to the known wishes of the person.(7)

It is unclear how far the extended principle of necessity articulated by Lord Goff of Chieveley can be relied upon in Australia. In Marion's Case the High Court did not accept that necessity extended to the sterilisation of a child.(8)

The wider implications of the In re F Case were not in issue in Marion's Case. Nevertheless, it would be safe to say that the general exception to actions for trespass to the person and the adapted principle of necessity would come the aid of a doctor or other health professional who acted in an emergency to give urgent treatment to an adult unable to give a valid consent to their own treatment, provided that such treatment was not negligently provided in the circumstances.

In 2002, after considering this line of authority and other cases, a Full Board of the then Guardianship and Administration Board of Western Australia noted, that under the doctrine of necessity where there was an urgent need for medical treatment, the common law allowed a doctor, as an agent of necessity, to carry out such treatment as was necessary to meet the emergency without the need to obtain the incapable person's consent.(9) This view was supported by a subsequent Full Board.(10)

12.2.2 The defence of justified intervention, detention and restraint

Another line of authority, arising from the 19th century law relating to mentally ill people, and applied in the 20th century in Australia may be able to be called in aid in relation to keeping people currently or permanently incapable of giving a valid consent to their own treatment, in order for them to be kept under observation after head injuries or drug overuse, where harm that will need medical treatment is strongly suspected and where mental health legislation does not apply.

In an action for trespass to the person in the form of false imprisonment and restraint, as well as assault and battery brought, by a man addicted to drinking and subject to fits of delirium tremens, against the doctor who came to his house at his wife's request and had another man attend the delirious man overnight, Bramwell B, using the language of 1862, stated that the doctor would have a defence if the delirious man was:

[A]t the time of the original restraint a dangerous lunatic in such a state that it was likely that he might do mischief to any one, the [doctor] was justified in putting a restraint on him, not merely at the moment of the original danger, but until there was reasonable grounds to believe that the danger was over... (11)

In a 1971 an action was taken in the High Court of Australia, in its original jurisdiction, for trespass to the person and false imprisonment by a man who was admitted to a psychiatric hospital in Victoria and kept there for about a week.(12) Walsh J applied the statement of Harvey J of the Supreme Court of New South Wales that whether detention (of a mentally ill person) was lawful or not depended on the extent to which the person submitted to it or on the overriding necessity for the protection of himself or others.(13) Walsh J considered that the evidence in the case fell short of establishing that there was a necessity to protect the man himself or others such as would justify the steps taken by the doctor. While the doctor thought it was right that the man should be admitted to a hospital, it was not shown that the doctor apprehended an immediate danger of injury to the man himself or to others, if he were not taken into custody immediately.(14)

12.3 The Australian legislative regimes for substitute decision-making in relation to medical and dental treatment for incapable people

The legislative regimes for substitute decision-making in relation to the medical and dental treatment of those unable to give a valid consent to their own treatment of the States and the Australian Capital Territory have many similarities, but the different drafting of their provisions causes many differences in the way they operate. Consequently, except for New South Wales and Tasmania, it has been necessary to describe them all separately. Nevertheless, some of the common ground between them is discussed at the end of this chapter. The decided cases in the various States, with exceptions, can be of assistance in elucidating the legislation in other States. These are dealt with at the end of the chapter.

Part 5 of the Guardianship Act 1987 (NSW) which came into force in August 1989 established a regime for substitute decision-making in relation to the medical and dental treatment of people 16 years and above who are incapable of giving a valid consent to their own treatment.(15) The regime operates without the need for the intervention of the Guardianship Tribunal or the Supreme Court.

Tasmania adopted essentially the same regime as Part 6 of its Guardianship and Administration Act 1995 (Tas) which commenced in September 1997. However, that Part applies to a person of any age, including minors, persons less than 18 years, whatever their age.(16)

The legislation in both States sets down the test for incapacity to consent to one's own medical or dental treatment and nominates who is an incapable person's substitute decision-maker for such treatment. The legislation defines medical treatment and divides it into five categories, treatment which is outside the regime and doesn't require consent, urgent treatment, minor, major (there is no distinction between major and minor treatments in Tasmania) and special treatment. The legislation provides for the consent arrangements in relation to those categories of treatment as well as setting out a number of other related matters.

12.4.1 Objects of the legislation

The New South Wales Act, but not the Tasmanian Act, sets out the objects of this Part of the Act as being to ensure that:
  1. people are not deprived of necessary medical or dental treatment merely because they lack the capacity to consent to the carrying out of such treatment, and
  2. any medical or dental treatment that is carried out on such people is carried out for the purpose of promoting and maintaining their health and well-being.(17)
The Tasmanian Act states that one of its general objects is "to make better provision for the authorization and approval of medical and dental treatment for persons with a disability who are incapable of giving informed consent to any such treatment".(18)

A person is incapable of giving a valid consent to their own medical or dental treatment if:

  1. they are incapable of understanding;
    1. the general nature of the treatment, or
    2. the effect of the treatment, or
  2. they are incapable of indicating whether or not they consent to the carrying out of the treatment.(19)
If a person is incapable of understanding the general nature of a particular treatment or the effect of that treatment, or they are unable to communicate their consent (which can be done by oral or other means) they are incapable of giving consent to it. In particular, a person must understand the nature and effect of treatment not on patients in general, but on themselves.

Some people lack insight into their medical condition. This can result in them being incapable of giving a valid consent, or refusal of consent, to their own treatment on the ground that they are incapable of understanding the effect, on them, of the proposed treatment. This was demonstrated in a 2002 appeal against a decision of the Tasmanian Guardianship and Administration Board in which Blow J of the Supreme Court of Tasmania noted that the appellant was capable of understanding the general nature of the proposed treatment. He recognised that schizophrenia was a disorder that he had suffered from in the past and understood that the drugs that were proposed for him were drugs for the treatment of schizophrenia. However, he was firmly of the belief that he did not suffer from schizophrenia and therefore did not need that treatment. Blow J was of the view that the legislative test was not about the effect of proposed treatment on patients in general but referred to a person's understanding as to the effect of the proposed treatment on them.(20)

Consequently, where a person understands the nature and effect of treatment by particular drugs in general terms in relation to patients in general, but does not have insight into their own condition and therefore opposed the use of such treatment in relation to them, they lack the capacity to give a valid consent to their own treatment.

A useful way of determining whether or not a person is capable of understanding the general nature or effect of a particular treatment or of indicating whether or not they consent to the carrying out of that treatment is to apply the approach proposed by a Dr Eastman, a forensic psychologist, and adopted by Thorpe J of the High Court of Justice and the Court of Appeal in England and by the Guardianship Tribunal of New South Wales.(21)

Thorpe J stated the test twice in his judgment, in slightly different ways. Put together, they clarify the meaning of the test. The test has three elements. To be capable of giving a valid consent to medical treatment, the person must be able to:
  1. take in (and comprehend) and retain the treatment information,
  2. believe that information, and
  3. weigh that information, balancing risks and needs (weigh it in the balance and arrive at a choice).(22)

The person must not only be able to take in the information, they must be able to understand it, to a reasonable degree. They must not only believe that information as true but also be able to hold it long enough in their memories to weigh up the benefits and risks and then make a choice as to whether to give or refuse consent to the proposed treatment. A person is entitled to be ambivalent about a decision whether or not to consent to a particular treatment, and to vacillate on the subject.(23) However, if they are not able to come to a decision at all, they will be considered not to have capacity to give consent - for that treatment at least.

In practice, it falls to the doctors to assess whether the person they are proposing the treatment for has the capacity to consent to or refuse treatment according to the test set out above. The starting point is that every adult is assumed to have capacity.(24) That legal presumption can be set aside by evidence to the contrary. Because of this approach, it follows that the test is not to be applied harshly so as to prevent elderly, frail or ill people from making decisions about their own treatment because they may be slow to comprehend or may need time to come to terms with new or unexpected developments. Similarly, those with whole of life or acquired disabilities are not to be prevented from making their own decisions. Incapacity has to arise from the existence of evidence showing it. Also, a refusal of consent to proposed treatment is not necessarily evidence of incapacity to consent to treatment.(25) However, while the matter has not been determined in Australia, Lord Donaldson MR has noted in England that, in relation to the refusal of treatment at least, capacity to decide has to be commensurate with the gravity of the decision the person made. The more serious the decision, the greater the capacity required.(26)

These issues and the process for assessing capacity to consent or refuse treatment are discussed in detail at the end of this chapter.(27)

12.4.3 Medical and dental treatment defined

In New South Wales and Tasmania, medical and dental treatment are defined together. They are medical treatment, including any medical or surgical procedure, operation or examination and any prophylactic, palliative or rehabilitative care, normally carried out by, or under, the supervision of a registered practitioner as well as dental treatment (including any dental procedure, operation or examination) normally carried out by or under the supervision of a registered practitioner. They can also include any other act declared in the regulations to be "treatment" as just defined. (28)

12.4.4 The types of medical treatment

12.4.4.1 Excluded treatments

The first group in both New South Wales and Tasmania are treatments that are excluded from the regime with the intention that they do not need consent. They are non-intrusive examinations made for diagnostic purposes including visual examinations of the mouth, throat, nasal cavity, eyes or ears. Also in the group are first-aid medical or dental treatments, and drugs for which a prescription is not required and which are normally self-administered when they are being used for the purpose, and in accordance with the dosage level, recommended in the manufacturer's instructions. Other treatments can be included in this group by being declared in the regulations, but none have been.(29)

These treatments have been excluded largely because they are of such a minor nature or are so linked to day to day living and only carried out when necessary that it was inappropriate for consent to them to have to be sought through the substitute decision-making regime. However, this exclusion was not intended to cut across, or in any way downplay, the importance of hospitals, aged care facilities, group homes or other places where care or treatment is provided to people who are incapable of giving a valid consent to their own treatment keeping accurate records of any form of medication or treatment given to a patient or resident or having protocols as to who may permit such treatments to be carried out.

12.4.4.2 Urgent treatments

These are treatments which the doctor or dentist carrying out or supervising the treatment considers to be treatment that is necessary, as a matter of urgency:
  1. to save the incapable person's life, or
  2. to prevent serious damage to the incapable person's health, or
  3. except in the case of special treatment, to prevent the incapable person from suffering or continuing to suffer significant pain or distress.(30)

These treatments may be carried out without consent when they are urgent. When they are not urgent they will be categorized as major or minor treatment and consent for them to be carried out will be required according to the category of treatment they fit, according to the statutory definition.

12.4.4.3 Special treatments

For New South Wales these are:
  1. any treatment that is intended, or is reasonably likely, to have the effect of rendering permanently infertile the person on whom it is carried out, or
  2. any new treatment that has not yet gained the support of a substantial number of medical practitioners or dentists specialising in the area of practice concerned (these are experimental treatments proposed to be given not within the ambit of a clinical trial and have a different test for consent from the other forms of special treatment referred to in (a) and (c)),(31) or
  3. any other kind of treatment declared by the regulations to be special treatment.

In New South Wales treatments declared by the regulations to be special treatments are:
  1. any treatment that involves the administration of a drug of addiction (other than in association with the treatment of cancer or palliative care of a terminally ill patient) over a period or periods totalling more than 10 days in any period of 30 days,
  2. any treatment that is carried out for the purpose of terminating pregnancy,
  3. any treatment in the nature of a vasectomy or tubal occlusion,
  4. any treatment that involves the use of an aversive stimulus, whether mechanical, chemical, physical or otherwise.(32)

In New South Wales there are some "prescribed special treatments" which are also found in the regulations. They are:
  1. any treatment that involves the administration to an incapable person of one or more restricted substances for the purpose of affecting the central nervous system of that person, but only if the dosage levels, combinations or the numbers of restricted substances used or the duration of the treatment are outside the accepted mode of treatment for such a person, and
  2. any treatment that involves the use of androgen reducing medication for the purpose of behavioural control.(33)
While Tasmania has not made the "prescribed special treatments" just referred to special treatments, most of the other treatments set out above have been made special treatments in that State. However, they are distributed differently between the Act and the Regulations.(34)

In both New South Wales and Tasmania, only the Guardianship Division of NCAT or Guardianship and Administration Board respectively may consent to special treatment.(35) However both tribunals, when giving consent to special treatment, may give the person's guardian, if there is one, authority to consent to the continuation of the treatment or further special treatment of a similar nature.(36)

In New South Wales before the Guardianship Tribunal may give consent as to the carrying out of special medical treatment, it must be satisfied as to certain matters. These matters are different depending on whether the treatment is special medical treatment or experimental medical treatment.(37)

As already noted, the Tasmanian Act provides that only the Guardianship and Administration Board may consent to such treatment. However, the test for all treatments that the Board may be called upon to consent to is that the Board is satisfied that the treatment is otherwise lawful and that it would be in the best interests of the person.(38)

12.4.4.4 Major treatment

The Tasmanian Act does not differentiate between major and minor treatment, but the New South Wales Act does.(39)

In New South Wales major medical is described in the Regulation as:
  1. any treatment that involves the administration of a long-acting injectable hormonal substance for the purpose of contraception or menstrual regulation,
  2. any treatment that involves the administration of a drug of addiction (but which is not special treatment as described under "Special treatment"),
  3. any treatment that involves the administration of a general anaesthetic or other sedation,(40); but not treatment involving:
    1. sedation used to facilitate the management of fractured or dislocated limbs, or
    2. sedation used to facilitate the insertion of an endoscope into a patient's body for diagnostic purposes unless the endoscope is inserted through a breach or incision in the skin or a mucous membrane
  4. any treatment used for the purpose of eliminating menstruation (as different from any treatment which is intended to or is likely to render a person permanently infertile - which is special medical treatment),(41)
  5. any treatment that involves the administration of a restricted substance for the purpose of affecting the central nervous system, but not a treatment:
    1. involving a substance that is intended to be used for analgesic, antipyretic, antiparkinsonian, anticonvulsant, antiemetic, antinauseant or antihistaminic purposes, or
    2. that is to be given only once, or
    3. that is a PRN treatment (that is, given when required, according to the patient's needs) that may be given not more than 3 times a month, or
    4. given for sedation in minor medical procedures,
  6. any treatment that involves a substantial risk to the patient (that is, a risk that amounts to more than a mere possibility) of:
    1. death, or
    2. brain damage, or
    3. paralysis, or
    4. permanent loss of function of any organ or limb, or
    5. permanent and disfiguring scarring, or
    6. exacerbation of the condition being treated, or
    7. an unusually prolonged period of recovery, or
    8. a detrimental change of personality, or
    9. a high level of pain or stress,
  7. any treatment involving testing for the human immuno-deficiency virus (HIV).(42)

It should be noted that this definition of major medical treatment specifically excludes certain treatments which are clearly significant medical procedures from a medical perspective. These are surgical procedures to treat fractured or dislocated limbs, or the insertion of an endoscope into a patient's body for diagnostic purposes through an orifice and not involving the insertion of the endoscope through a breach or incision in the skin or a mucous membrane.(43) These treatments were made minor medical treatments so that the question of consent for them could be dealt with under the arrangements for minor treatment.(44)

Major dental treatment is described as:
  1. any treatment involving the administration of a general anaesthetic or simple sedation,
  2. any treatment intended, or likely, to result in the removal of all teeth,
  3. any treatment likely to result in the patient's ability to chew food being significantly impaired for an indefinite or prolonged period.(45)

Note that most dental treatments are minor treatments and subject to the arrangements for substitute consent to minor treatment.

The substitute decision-maker for these forms of major medical or dental treatment is the incapable person's "person responsible". However, as substitute consent must be obtained before such treatment may be carried out, if the person responsible is not available, any application for substitute consent must be made to the Guardianship Division of NCAT.(46)

12.4.4.5 Minor treatment

Again in New South Wales, any medical or dental treatment that is not special or major treatment, or treatment not excluded from the substitute consent regime by the legislation, is minor treatment.(47) Most non-surgical medical treatments and some surgical treatments are in the category of minor medical treatment.

12.4.5 Who is the substitute decision-maker for medical and dental treatment?

As most medical and dental treatments fit into the categories of minor or major treatment, the substitute decision-maker for an incapable person in most cases will be their "person responsible".

It should be noted that while in most cases an incapable person's person responsible will also be their next of kin, being a person's next of kin has never given, and does not now give, the next of kin the right to act as substitute decision-maker for an incapable person.(48) The authority of a person responsible, or their equivalent in the other States and the Australian Capital Territory, arises from the legislation that empowers then, without having to be appointed or approved by a tribunal, to act as the incapable person's substitute decision-maker. A different approach is taken in the Northern Territory. See 12.10.

In both New South Wales and Tasmania you determine who is a person's person responsible by consulting the list or hierarchy of persons responsible. The list, in order of priority, is:
  1. the person's guardian, including enduring guardian;(49)
  2. the person's her spouse, including their de facto partner and, in New South Wales, their same sex partner;(50)
  3. the person having the care of the incapable person;(51)
  4. a close friend or relative of the incapable person.(52)
There are special provisions in both New South Wales and Tasmania in relation to those who are in the care of a Minister or a Director-General or are a ward of the State.(53) In Tasmania if a person is under the age of 18 years and they have no spouse, their parents take the place of the spouse in the order of priority for persons responsible.(54)

12.4.6 How the list or hierarchy operates

If there is a guardian, with power to consent to medical and dental treatment, then they are the person responsible and no one else may act as the person responsible. If there is no guardian, which is usually the case, the incapable person's spouse is their person responsible, unless they too are incapable: and so on down the list. If there is no one in any of the four stages of the hierarchy, then the incapable person has no person responsible. This happens occasionally, particularly if the person is living alone and has become isolated from their family or the community. In that case in both New South Wales and Tasmania, the Guardianship Tribunal or the Guardianship and Administration Board may act as the substitute decision-maker if an application is made to them. This matter is taken up again in 12.4.8.

In New South Wales, if a person who, in accordance with the hierarchy, is the person responsible for an incapable person declines in writing to act as person responsible, or if a doctor or another person qualified to give an expert opinion on their condition certifies in writing that that person is not capable of carrying out the functions of a person responsible, then the person next in the hierarchy becomes the person responsible for the incapable person.(55) Note that a person responsible, for example an elderly spouse, wishes to abdicate their role as person responsible, they cannot nominate their replacement. The position of person responsible is determined by operation of the hierarchy. However, any adult with the capacity to do so may appoint an enduring guardian and give them the function of consenting to medical and dental treatment. That enduring guardian will then become their person responsible.(56)

In both New South Wales and Tasmania requests to the person responsible for substitute consent to treatment are to be in writing. However if, because of the need to provide the treatment quickly, it is not practicable to make the request in writing, it may be made orally. There are specific legislatively stipulated arrangements in each State about when an oral request has to be confirmed in writing and when substitute consent must be given in writing or when it may be given orally.(57)

In New South Wales, while a doctor will be responsible for carrying out or supervising the carrying out of any medical treatment and a dentist will be similarly responsible for dental treatment, any person may request the person responsible for consent to the carrying out of medical or dental treatment on the incapable person. However, even if it is not in writing, the request must specify:
  1. why the person cannot give a valid consent to their own treatment,
  2. the particular condition they have that requires treatment,
  3. alternative courses of treatment that are available in relation to that condition,
  4. the general nature and effect of each of those courses of treatment,
  5. the nature and degree of the significant risks (if any) associated with each of those courses of treatment, and
  6. why the particular course of treatment is proposed.(58)
The person responsible is required to have regard to the information supplied and the views of the incapable person, if they have any. It is suggested that if the incapable person has made an advance directive that is relevant to their current circumstances, the person responsible must give effect to that advance directive. The person responsible should consent only to medical or dental treatment that will promote the health and well-being of the incapable person.(59) However, it should be noted that any consent given by a person responsible has no effect if the proposed treatment is to be carried out for any purpose other than that of promoting or maintaining the health and well-being of the incapable person.(60)

The Tasmanian provisions are similar but not identical. While the person responsible must take into account the wishes of the incapable person, if these can be ascertained, they are not bound by those wishes. Again, it is suggested that if the incapable person has made an advance directive that is relevant to their current circumstances, the person responsible must give effect to that advance directive. The person responsible must consider the nature and degree of any significant risks associated with the proposed treatment or any alternative treatments and the consequences if treatment is not carried out. The person responsible must also be satisfied that the person is incapable of giving consent, that the treatment is in the best interests of the incapable person and that it is to be carried out only to promote and maintain their health and well-being.(61)

It should be noted that in both New South Wales and Tasmania persons responsible, including tribunal appointed and enduring guardians, make their own decisions as to the treatment they will consent to on behalf of the incapable person according to the statutory criteria. Except where they have a relevant advance directive to give effect to, they do not make a substituted judgment as to what the incapable person would have consented to in the circumstances.

In Tasmania where it is proposed to carry out medical or dental treatment which is not special treatment on a person who is unable to give a valid consent to their own treatment and:
  1. they have no person responsible; and
  2. the treatment is necessary and is the form of treatment that will most successfully promote that person's health and well-being; and
  3. they not object to the carrying out of the treatment
the medical or dental treatment can be carried out on that person without consent.

However, in order for the treatment to be carried out lawfully, a medical practitioner or dentist who carries out or supervises the treatment being carried out without consent, must certify in the clinical records relating to the treatment that:
  1. the treatment is necessary and is the form of treatment that will most successfully promote that person's health and wellbeing; and
  2. the person does not object to the carrying out of the treatment.(62)
The regulations may specify medical or dental treatment that, while it would otherwise these criteria, may not be carried out without consent as required under other sections of the Act.(63) Such treatments have been specified in Guardianship and Administration Regulations 2007 (Tas). They are set out in 12.4.9 below.

Both the Guardianship Division of NCAT in New South Wales and the Guardianship and Administration Board of Tasmania have the jurisdiction to deal with applications for substitute consent to medical and dental treatment. They both operate as the default or "fall back" substitute decision-maker when there is no person responsible or they cannot be contacted. Where an application comes to NCAT in New South Wales and it becomes apparent that the incapable person probably needs a guardian, NCAT will request that an application for guardianship be lodged with it. If it appears to it that the incapable person will require on-going treatment and a series of consents as the treatment is varied or changed, it may give its consent to the first treatment and request that an application for guardianship be lodged to see if a guardian should be appointed as the on-going substitute decision-maker for incapable person.

As already noted, the Tasmanian Act does not differentiate between major and minor treatment, but the Regulations do set out a list of treatments that may not be carried out without consent. Consequently, if the incapable person does not have a person responsible, an application must be made to the Board by someone with a proper interest in the matter for consent to carry out the treatment. This applies to the following medical treatments:
  1. treatment that is continuing or ongoing and involves the administration of a restricted substance primarily to control the conduct of the person to whom it is given; or
  2. treatment that involves the administration of a drug of addiction other than in association with the treatment of cancer or palliative care of a terminally ill patient; or
  3. electro convulsive therapy (ECT); or
  4. treatment involving a substantial risk to the incapable person of
    1. death; or
    2. brain damage; or
    3. paralysis; or
    4. permanent loss of function of any organ or limb; or
    5. permanent and disfiguring scarring; or
    6. extreme pain or distress.(64)

Also included is dental treatment that is intended, or likely, to result in the removal of all or a substantial number of teeth.(65)

Where the medical or dental treatment proposed for a person who is unable to give a valid consent or refusal of consent to the treatment, but is objecting to receiving the treatment, the Board must deal with an application for consent to that treatment is proposed. We also suggest that circumstances may arise in which, although the person is not objecting to the treatment, it seems appropriate for the treating doctor or dentist to seek and obtain the consent of the Board before proceeding to carry out the treatment.

In New South Wales the Guardianship Division of NCAT is the default substitute decision-maker for major medical and dental treatment. It should not be applied to if the person responsible is available. In exceptional circumstances where, for example, the capacity or general ability of the person responsible is in real doubt or it is likely that decisions of the person responsible will be opposed by other family members or significant others, then it may be appropriate to apply to NCAT in the first place. These considerations may be relevant in a decision in Tasmania to seek consent for proposed treatment from the Board.

In New South Wales, NCAT can be the default substitute decision-maker for minor medical and dental treatment, if there is a particular reason for applying to it. Normally this will not be required because the New South Wales Act provides that, minor treatment may be carried out on an incapable person without consent if the incapable person has no person responsible or they cannot be contacted or are unable or unwilling to make a decision concerning the request for their consent. However, before giving the treatment, the doctor or dentist carrying it out must certify in writing in the incapable person's clinical record that:
  1. the treatment is necessary, and
  2. is the form of treatment that will most successfully promote the incapable person's health and well-being, and the incapable person does not object to the carrying out of the treatment.(66)

As will be dealt with in section 12.4.11, if the person responsible refuses consent to the treatment and the treating doctor considers that the treatment will promote and maintain the incapable person's health and well-being or the incapable person objects to the treatment, the Tribunal becomes the substitute decision-maker. As has already been noted, in both New South Wales and Tasmania, only the Guardianship Tribunal or the Guardianship and Administration Board respectively may consent to special treatment.(67)

Applications to the Guardianship Division of NCAT in New South Wales and the Guardianship and Administration Board of Tasmania for substitute consent to medical and dental treatment must be in writing.(68) In New South Wales, as is the case with requests to persons responsible for substitute consent, while a doctor will be responsible for carrying out or supervising the carrying out of any medical treatment and a dentist will be similarly responsible for dental treatment, any person may apply to NCAT for consent to the carrying out of medical or dental treatment on the incapable person.(69)

The application must provide NCAT with information about the same six matters a person responsible must be informed about. These are:
  1. why the person cannot give a valid consent to their own treatment,
  2. the particular condition they have that requires treatment,
  3. alternative courses of treatment that are available in relation to that condition,
  4. the general nature and effect of each of those courses of treatment,
  5. the nature and degree of the significant risks (if any) associated with each of those courses of treatment, and
  6. why the particular course of treatment is proposed.(70)
NCAT is required to conduct a hearing into the application. When considering the application, it must have regard to the information supplied in the application, the views of the incapable person, if they have any, and the views of their person responsible, if there is one, and the views of the person proposing the treatment.(71) NCAT must also consider the objects of Part 5 of the Act. Before NCAT may give its consent to the carrying out of the treatment, it must be satisfied that:
  1. it is appropriate that the treatment be carried out, and
  2. the treatment is the most appropriate form of treatment for promoting and maintaining the patient's health and well-being.(72)
Similarly, the Tasmanian Board is required to conduct a hearing into the application. As with persons responsible in Tasmania, the Board must take into account the wishes of the incapable person, if these can be ascertained. However, it is not bound by those wishes. The Board must consider the consequences if the treatment is not carried out. The Board must also be satisfied that the person is incapable of giving consent, that the treatment is otherwise lawful and that it is in the best interests of the incapable person.(73) Nevertheless, acknowledging those provisions, it is again suggested that if the incapable person has made an advance directive that is relevant to their current circumstances, the Board, as substitute decision-maker, must give effect to that advance directive.

Unlike the person responsible, the Board must consider whether the proposed treatment can be postponed on the ground that a better treatment may become available and whether the incapable person is likely to become capable of consenting to the treatment.(74) However, where the Board considers the treatment urgent, it may dispense with notice of the hearing and give its consent to the treatment being carried out immediately. This also dispenses with the usual requirement that the appeal period expires before the order consenting to the treatment comes into effect.(75)

As has already been noted, in both New South Wales and Tasmania, only NCAT or Guardianship and Administration Board respectively may consent to special treatment.(76) Also, when giving consent to special treatment, both tribunals may give the person's guardian, if there is one, authority to consent to the continuation of the treatment or further special treatment of a similar nature.(77) However, in Tasmania the tests for consent to special medical treatments are the same as for any other treatments, namely those that have just been set out. The question of treatment that will result in sterilization is dealt with in more detail in Chapter 15.

In New South Wales, the same information as for any other treatment must be provided to NCAT in the application, but the there is an extra element to the test that has to be satisfied before NCAT may give consent. NCAT must be satisfied that the treatment is not only the most appropriate form of treatment to promote and maintain the incapable person's health and well-being, but also that the treatment is necessary either to save the incapable person's life or to prevent serious damage to the their health.(78)

If the proposed treatment is experimental special medical treatment - no dental treatment has been declared to be "special dental treatment" - or is "prescribed special treatment", then the test is slightly different.(79) Not only must NCAT be satisfied that the treatment is the most appropriate form of treatment to promote and maintain the incapable person's health and well-being, but also that the treatment is the only or most appropriate way of treating the patient and is manifestly in the best interests of the incapable person. Also, if the National Health and Medical Research Council has prescribed guidelines that are relevant to the carrying out of that treatment - those guidelines have been or will be complied with as regards the incapable person.

12.4.11 Objections to treatment

The New South Wales Act has provisions dealing with objections to treatment. The Tasmanian legislation does not deal with this matter.

In New South Wales, while an incapable person cannot consent to medical or dental treatment, they can still "object" to it. A person is to be taken to object to the carrying out of treatment if they indicate, by whatever means, that they do not want the treatment or if they have previously indicated in similar circumstances that they do not want the treatment and have not subsequently indicated to the contrary.(80) If they do object to the treatment, any consent given by a person responsible, including a guardian, is of no effect. (81) However, NCAT may authorise a guardian of an incapable person to override their objection to certain treatments, but only if the Tribunal is satisfied that any such objection will be made because of the incapable person's lack of understanding of the nature of, or reason for, the treatment.(82)

Also, an objection by an incapable person to the carrying out of proposed medical or dental treatment can be disregarded if:
  1. the incapable person has minimal or no understanding of what the treatment entails, and
  2. the treatment will cause them no distress or, if it will cause them some distress, that distress is likely to be reasonably tolerable and only transitory.(83)

If the objection is one that NCAT must deal with, it accepts an application for consent to the proposed treatment and deals with it according to the criteria set down in the Act for consenting to treatment. NCAT takes evidence about the objection and determines whether or not to give consent to the proposed treatment overriding the incapable person's objection. If NCAT gives consent to the treatment in these circumstances, its consent allows the treatment to be carried out. NCAT's consent does not require the treatment to be carried out.

The case of LD shows how NCAT deals with objections to treatment by an incapable person. LD developed gangrene in her right foot after attempts to increase the blood flow there failed. Her treating doctors recommended that her right leg be amputated below the knee. The evidence showed that she was unable to understand the nature and effect of the treatment. Nevertheless, she indicated that she didn't want the treatment. Consent was given by her person responsible, a family member and then withdrawn in the light of her objection. Her treating doctors applied to the then Guardianship Tribunal for consent to the amputation overriding LD’s objection.

The Tribunal took evidence from LD, the applicant and other doctors and members of her family. After consideration of the evidence, the Tribunal was satisfied that LD could not give a valid consent to her own treatment, and that the proposed treatment, while not without its risks, was the most appropriate form of treatment to promote and maintain her health and well-being. The Tribunal, without resistance from her family, gave its consent to the carrying out of the proposed amputation, overriding LD’s objection.(84)

In 2001 the then Guardianship Tribunal refused to give consent to a blood transfusion for an 84 year old woman who was a Jehovah's Witness, but who was incapable of consenting to or refusing consent to her own treatment because of dementia. One reason was that she had refused a transfusion seven years previously and had not subsequently indicated to the contrary. Indeed she had maintained her objection to receiving blood products because of her religious convictions. Other considerations were that the proposed blood transfusion was palliative in nature and would have little effect on the progress of her underlying renal condition. In addition there was an alternative treatment, Erythropoietin, which was acceptable to Jehovah's Witnesses but which had not yet been tried.(85)

If the person responsible refuses consent to the treatment and the treating doctor considers that the treatment should be given because it will promote and maintain the incapable person's health and well-being and the failure to receive the treatment will be disadvantageous to the incapable person, the treating doctor may make an application to NCAT for consent to the carrying out of the treatment. NCAT then becomes the substitute decision-maker. It deals with the matter as it would any other application for consent to treatment except that it would ensure that it obtained and had particular regard to the views of the person responsible.(86)

The Guardianship and Administration Act 2000 (Qld) contains a similar provision which has been interpreted in a different manner by the Queensland Guardianship and Administration Tribunal (now QCAT).(87) However, QCAT does not have jurisdiction to deal directly with applications for consent to medical and dental treatment, except for forms of special medical treatment, while NCAT does have such a role, as has just been demonstrated. This absence of a for mechanism for giving appropriate consideration to the person's objection but yet being able to override it and give an effective consent to the proposed treatment in appropriate cases, which can be done in New South Wales, may have contributed to the interpretation given to the relevant provision in Queensland.

Substitute decision-makers, whether persons responsible NCAT, have a discretion as to whether or not to consent to what might appear from a medical perspective to be the most appropriate treatment for promoting and maintaining the health and well-being of the incapable person. This is because not only do they have to consider the information about the treatment, but also they are required to have regard to the views of the incapable person and the objects of Part 5 of the Guardianship Act 1987 (NSW).(88) As far back as 1994, the tribunal (then called by its first name, the Guardianship Board) noted, in an application relating to a Christian Scientist, that it was not required under Part 5 "to impose medication on a person contrary to religious beliefs that were deeply held for a long time prior to the person acquiring their incapacity".(89)

As has already been suggested a number of times in this chapter, if the incapable person has made an advance directive that is relevant to their current circumstances, and which has been put beyond doubt by McDougall J's decision in Hunter and New England Area Health Service v A,(90) the substitute decision-maker must give effect to that advance directive. However, it is conceded that considerable difficulties arise in cases involving Jehovah's Witnesses where the Witness the subject of the application has not got a current "blood card" - a form of advance directive carried by many Jehovah's Witnesses setting out that they do not wish to receive blood products and what substitute non-blood products they are willing to receive. NCAT has stated that:

[W]hilst it has an obligation to have regard to the views of the patient and to take them very seriously indeed, it was not bound by those views and could make a decision in relation to treatment which was contrary to the views of the patient if the Tribunal believed there were strong reasons for doing so.(91)

The matter in which NCAT made that statement, and other cases involving NCAT in either giving or refusing substitute consent to blood transfusions, are discussed at the end of this chapter at 12.13.

12.4.13 Special powers under the Mental Health Act 1996 (Tas) of persons responsible and the Guardianship and Administration Board

Under the Mental Health Act 1996 (Tas), if a person has a mental illness and meets certain other criteria, they may be admitted to an approved hospital as an involuntary patient.(92) Their person responsible may apply to a doctor for an order for their admission.(93) When in an approved hospital, a mentally ill person may be given medical treatment, although certain medical treatments are excluded, either with their consent or if the treatment has been authorised by or under the Guardianship and Administration Act 1995 (Tas).(94) If the mentally ill person is incapable of giving "informed consent" to their medical treatment and they have a person responsible, their person responsible, to the extent of their powers and according to the requirements of the Guardianship Administration Act 1995 (Tas), may give substitute consent to the proposed treatment.(95) However, if the mentally ill person has refused or failed to undergo the treatment, or is likely to refuse or fail to undergo it, the Board may make an order authorizing the giving of the medical treatment regardless of whether or not the mentally ill person has lost capacity to give a valid consent to their own treatment. The Board has to be satisfied that:
  1. the mentally ill person's mental illness that is amenable to the proposed medical treatment; and
  2. a doctor has recommended medical treatment for the illness but the person has refused or failed, or is likely to refuse or fail, to undergo the treatment; and
  3. the mentally ill person should be given the treatment in their own interests or for the protection of others.(96)

12.5 South Australia

Part 5 of the Guardianship and Administration Act 1993 (SA) came into force in March 1995. It provides most of the regime for substitute decision-making in relation to the medical and dental treatment of people 18 years and above who are incapable of giving a valid consent to their own treatment. Most of the rest of the regime is provided for in the Consent to Medical Treatment and Palliative Care Act 1995 (SA). As in the other States, the regime operates without the need for the intervention of the Guardianship Board or the Supreme Court.

Part 5 applies in relation to a person who, because of their mental incapacity, is incapable of giving effective consent to their own medical or dental treatment.(97) The South Australian Act defines "mental incapacity" to mean the inability of a person to look after their own health, safety or welfare or to manage their own affairs, as a result of:
  1. any damage to, or any illness, disorder, imperfect or delayed development, impairment or deterioration, of the brain or mind; or
  2. any physical illness or condition that renders the person unable to communicate their intentions or wishes in any manner whatsoever.(98)
While no test determining whether a person has mental incapacity has been adopted in South Australia, Thorpe J's test, which has been described earlier in this chapter and which has been adopted in England and by the Guardianship Tribunal of New South Wales, would be a useful tool to use in deciding that matter.(99)

12.5.2 Medical and dental treatment defined

Consistent with the trend in the other States, both medical and dental treatment are given broad definitions in South Australia. Medical treatment is defined to mean treatment or procedures administered or carried out by a medical practitioner or other health professional in the course of professional practice and includes the prescription or supply of drugs.(100) Dental treatment means treatment or procedures carried out by a dentist in the course of dental practice.(101)

12.5.3 The types of medical treatment

12.5.3.1 Emergency medical treatment.

In South Australia urgent or emergency medical treatment is provided for in the Consent to Medical Treatment and Palliative Care Act 1995 (SA).(102) Under that Act, a doctor may, lawfully, administer medical treatment to mentally incapacitated person if:
  1. they are incapable of consenting to the treatment; and
  2. the doctor who is to administer the treatment is of the opinion that the treatment is necessary to meet an imminent risk to life or health and
  3. that opinion is supported by the written opinion of another doctor who has personally examined the mentally incapacitated person; and
  4. if that person is 16 years of age or over and has not, to the best of the doctor's knowledge, refused to consent to the treatment.(103)

Fortunately, a supporting opinion is not necessary if, in the circumstances of the case, it is not practicable to obtain such an opinion.(104)

The administration of emergency medical treatment is further complicated if the mentally incapacitated person has appointed a medical agent, that is an attorney appointed under a medical power of attorney made under the provisions of the Consent to Medical Treatment and Palliative Care Act 1995 (SA). This is because, if the doctor proposing to administer the treatment is aware of that appointment and of the conditions and directions contained in that medical power of attorney and the medical agent is available to decide whether the medical treatment should be administered, then the medical treatment may not be administered without the agent's consent.(105) A similar difficulty arises if the mentally incapacitated person has a guardian whether an enduring guardian appointed by the now incapable person or a guardian appointed by the Guardianship Board. If such a guardian is available, the medical treatment may not be administered without their consent.(106)

These limitations on the immediate provision of emergency treatment to the mentally incapacitated person impose a duty on doctors to make inquiries that are reasonable in the circumstances, as to whether or not the person has a medical agent or guardian and if they have, to make reasonable efforts to obtain their consent to the treatment.

12.5.3.2 Prescribed treatments.

Termination of pregnancy and sterilisation are treatments prescribed in the Guardianship and Administration Act 1993 (SA) as treatments that may not be carried out without the consent of the Guardianship Board and only in accordance with the regulations.(107) However, no relevant regulations have been made, nor have any further medical treatments been prescribed in the regulations.(108)

The Guardianship Board cannot consent to a termination of pregnancy unless it is satisfied as to a number of matters. These are that:
  1. the carrying out of the termination would not constitute an offence under the Criminal Law Consolidation Act 1935 (SA); and
  2. there is no likelihood of the woman acquiring the capacity to give an effective consent within the period that is reasonably available for the safe carrying out of the termination, and
  3. the Board has no knowledge of any refusal on the part of the woman to consent to the termination, being a refusal that was made while capable of giving effective consent and that was communicated by her to a medical practitioner.(109)

Also, before consenting to the carrying out of a termination of pregnancy, the Board must put its mind to whether or not it is appropriate to allow such of the woman's parents whose whereabouts are reasonably ascertainable a reasonable opportunity to make submissions to the Board on the matter. However, the Board is not required to allow this opportunity if it is of the opinion that to do so would not be in the best interests of the mentally incapacitated person.(110)

Furthermore, the decision of the Board to give consent a termination of pregnancy cannot be carried out until the period for appeal against the decision has expired or, if an appeal has been instituted, until the appeal has been dismissed or withdrawn.(111) As the period in which an appeal may be lodged is 28 days, the carrying out of the procedure to terminate the incapable woman's pregnancy must be delayed for at least that time. Because pregnancies in women with decision-making disabilities are often not discovered until they are well advanced, obtaining consent under this provision must be a difficult matter raising serious medical and ethical questions at the time when the treatment can be carried out lawfully.

There are also detailed limitations on the Board's power to consent to sterilisation. These are dealt with in Chapter 15 dealing with sterilisation.

12.5.3.3 Treatments that are neither urgent nor prescribed

All medical treatments that are neither urgent nor prescribed and all dental treatments, no matter how significant or how minor in nature, require the consent of the "appropriate authority".

12.5.4 Who is the "appropriate authority" to act as substitute decision-maker for medical and dental treatment?

If a person with a mental incapacity cannot consent to their own treatment, consent must be sought from a substitute decision-maker, who can be:
  1. their medical agent appointed by them under a medical power of attorney;(112)
  2. their enduring guardian appointed by them under an enduring power of guardianship under an appointment that does not exclude the guardian from giving consent to medical and dental treatment;(113)
  3. a guardian appointed for them by the Guardianship Board under an order that does not exclude the guardian from giving consent to medical and dental treatment;(114)
  4. if there is no medical agent, guardian or enduring guardian, then the following specified relatives can provide consent to medical or dental treatment:
    1. a spouse, including a "putative" spouse;(115)
    2. a parent
    3. a brother or sister of or over 18 years;
    4. a daughter or son over 18 years
    5. a person who acts in loco parentis i.e. the person who provides the main ongoing day to day care and supervision of the person (not being the person who is going to provide the treatment).(116) :
  5. Where no one is available in the above categories to provide substitute consent, or where there is a dispute or conflict about the treatment, the Guardianship Board can provide consent to medical or dental treatment. This involves an application being made to, and a hearing conducted by, the Board. The application to the Board has to be made by:
    1. a relative of the mentally incapacitated person; or
    2. the doctor, dentist or other health professional proposing to give the treatment; or
    3. any other person who the Board is satisfied has a proper interest in the matter.(117)

12.5.5 How the list or hierarchy operates.

If a person has appointed a medical agent, they may or may not have been given the authority to deal with the particular kind of treatment for which consent is sought. If they have the authority, they will take precedence as the appropriate authority. If they do not have the authority, then if there is a guardian, they will be the appropriate authority provided their appointment is not limited so as to exclude the guardian from giving consent to medical and dental treatment. If not, then if there is an enduring guardian they will be the appropriate authority unless their appointment excludes them from giving consent to medical and dental treatment or the Guardianship Board revokes their appointment and appoints a guardian for the mentally incapacitated person under an order that does not exclude the guardian from giving consent to medical and dental treatment.(118)

If the mentally incapacitated person does not have either a medical agent or a guardian, then either a relative of the mentally incapacitated person or the Guardianship Board is the appropriate authority. The list of relatives does not operate as a hierarchy so that if there is a spouse they are the appropriate authority to the exclusion of other the other relatives. The practice in South Australia is for consent to be obtained from any relative in the list. However, it should be noted that those in the list are either married to or in a marriage like relationship with the mentally incapacitated person or are closely related by blood to them.

The Act allows for a choice between seeking substitute consent from the relatives or the Board. There will be situations in which it is more appropriate to go to the Board. Two examples show situations in which applying to the Board makes sense. The first is where the mentally incapacitated person or the substitute decision-maker is objecting to the treatment, and this puts the mentally incapacitated person's health or safety at risk. The second is where there is dispute or conflict about the treatment and all reasonable attempts to resolve the dispute have failed.

While the Guardianship and Administration Act 1993 (SA) does not provide any specific criteria for the "appropriate authority" substitute decision-makers to consider and apply when deciding whether or not to consent to medical or dental treatment to be carried out on a mentally incapacitated person, at least two of the principles of the Act are relevant. The first principle requires them to consider what, in their opinion, the wishes of the mentally incapacitated person would be in relation to the proposed treatment if they were able to make the decision.(119) However, they are required to do this only when there is reasonably ascertainable evidence upon which to base their opinion. The second principle requires them to seek the present wishes of the mentally incapacitated person about the proposed treatment and to give consideration to those wishes, unless it is not possible or reasonably practicable to do so.(120) While there is an obligation to give consideration to the wishes of the person while they were competent and also now when they are mentally incapacitated, the substitute decision-maker is not bound by those wishes and so can make a decision that is the least restrictive of the mentally incapacitated person's rights and personal autonomy as is consistent with their care and protection, consistent with the fourth principle of the Act.(121) However, it is suggested that if the mentally incapacitated person has made an advance directive that is relevant to their current circumstances, the "appropriate authority" as substitute decision-maker, must give effect to that advance directive.

Public Advocate of South Australia has also suggested that the substitute decision-maker should ask the treating doctor to explain the proposed treatment, whether there are any risks with it, what the alternative treatments are, if any, and what are the likely outcomes of the treatment and what are the likely consequences of not undertaking the treatment. The Public Advocate also notes that it is important to consider whether the treatment will be of benefit to the mentally incapacitated person and how it will affect their quality of life.(122) The Public Advocate's suggestions are consistent with the obligation imposed on any substitute decision-maker operating under the Act to apply certain principles.(123)

As already noted, consent of the Board must be obtained before prescribed medical treatment may be carried out on a mentally incapacitated person. Consent to other medical and all dental treatment may be sought from the Board either if there is no other appropriate authority to consider the matter or if there is no medical agent or guardian to act as the appropriate authority and an application is made to the Board rather than to the appropriate relative.

While there are no direct statutory criteria for the Board to apply in dealing with an application made to it, the Board conducts a hearing and applies the principles of the Act. These require it to consider what, in its opinion, the wishes of the mentally incapacitated person would be if there was reasonably ascertainable evidence upon which to base such an opinion. They also require the Board to seek and consider the current wishes of the mentally incapacitated person unless it is not possible or reasonably practicable to do so. The decision the Board made in relation to the treatment must be the one that is the least restrictive of the person's rights and personal autonomy that is consistent with their proper care and protection.(124)

12.5.8 Objections to treatment

The Guardianship and Administration Act 1993 (SA) does not deal with objections by the mentally incapacitated person to the proposed treatment directly, but again, the principles of the Act are relevant here.(125) As already noted, this is a situation in which it is appropriate to make an application to the Board for it, through its ability to take evidence from all relevant sources, the treating doctors, the mentally incapacitated person, their relatives and others, to consider that evidence, is in the best position to make the decision as to whether to consent to the proposed treatment or not. In doing so, the Board must give consideration to what the wishes of the mentally incapacitated person would be if they were not mentally incapacitated, and to their present wishes. The Board's decision in relation to the treatment must be the one that is the least restrictive of the mentally incapacitated person's rights and personal autonomy that is consistent with their proper care and protection.(126) It is suggested that the "appropriate authority" as substitute decision-maker, must give effect to any advance directive that is relevant to their current circumstances made by the mentally incapacitated person when still capable.

12.6 Victoria

On New Years Day 2000 a regime for substitute decision-making in relation to medical and dental treatment on behalf of adults incapable of giving a valid consent to their own treatment commenced on in Victoria.(127) While it is based in the New South Wales model and there are important similarities, there were also significant differences between the two regimes.

However, from 12 March 2018, when the Medical Treatment Planning and Decisions Act 2016 (Vic) came into force, Victoria adopted a different approach to consent to not only to medical and dental treatment but also a wide range of health treatments for those unable to make decisions about their own health treatment. The Victorian legislation is based on the idea of extending a person’s decision-making autonomy into the time or times in which they are unable to make their own decisions about the health treatment proposed for them by health practitioners and certain others. This is clear from the set of principles set out in the Act and in particular the principle that requires that anyone exercising a power or performing a function or duty under the Act must have regard to the fact that a person may exercise autonomy in relation to medical treatment or medical research procedures that may be administered to them. And that the person may exercise that autonomy by: •making decisions (namely, instructional directives in an Advanced Care Directive); and
  • setting out preferences and values (in values directives in an Advanced Care Directive); and
  • appointing a medical treatment decision maker; and
  • appointing a support person; and
  • making collaborative decisions with family or community.(128)
This autonomy may be exercised by a person following the procedures, set out in the Medical Treatment Planning and Decisions Act 2016 (Vic), by which a person may make an advance directive that gives binding instructions (instructional directives) or expressing their preferences and values (values directives) in relation to their future medical treatment (as widely defined). Such autonomy is also maintained by the person appointing, via the procedures set out in the Act ,another person to make medical treatment decisions on their behalf when they do not have decision-making capacity and also by providing that they may appoint another person to support them and represent their interests in making medical treatment decisions.

The processes for making these directives and appointments under the Act are dealt with in more detail in Chapter 13.5.1.

The Act amends the Mental Health Act 1988 (Vic) in relation to approval procedures for electroconvulsive treatment of adults who do not have capacity and repeals the Medical Treatment Act 1988 (Vic). It replaces that Act with a much more comprehensive scheme for dealing with the questions of who should make substitute decisions in relation to the medical treatment (as widely defined in 12. 6. 3 below), and the matters to be considered in the making of those decisions for a person.

12.6.1 Objects and principles of the legislation

In addition to providing for individuals to make advance care directives and appoint another person to make medical treatment decisions on their behalf when they do not have decision-making capacity and also to appoint another person to support them and represent their interests in making medical treatment decisions, the Medical Treatment Planning and Decisions Act 2016 (Vic) provides the regime for substitute consent to medical treatment for those who do not have decision-making capacity in relation to the medical treatment proposed for them. The Act sets out the obligations of health practitioners and any substitute decision-maker to give effect to any instructional directives and any values directives that are included in any advance care directive made by the person the medical treatment is being proposed for when that person lacks the decision-making capacity to make the decision about that treatment.(129) Even where the person has not made an advance care directive or it cannot be located, or a substitute medical treatment decision-maker cannot be found, the Act provides a process the health practitioner can follow in order to provide the proposed treatment to the person.(130)

Nevertheless, the Act makes it clear that a health practitioner cannot be compelled by either a statement in an advance care directive or a decision by a medical treatment decision maker to administer a particular form of medical treatment or medical research procedure.(131)
Nor can a health practitioner be required to administer a futile or non-beneficial medical treatment or medical research procedure to a person.(132) These two statements in the Act reflect the established common law.(133)

The principles of the Act , which are set out in s.7 are very relevant to the sensitivity with which the processes of the Act are to be carried out. The principles reflect one of the basic assumptions underlying the Act namely, that the person that the medical treatment in question is being proposed for may, despite doubts by at least some of those involved in the process, still have decision-making capacity to make the treatment decision. Or they may soon recover that capacity or may be able, now, to exercise that capacity with the assistance of the support person appointed by them.

The first three and the fifth principle are to the effect, that the person who is to receive the proposed medical treatment has the right to make informed decisions about that treatment (or medical research procedures, if they are being proposed). Further, the person to be treated should be given, in a sensitively communicated and clear and open manner, information about the treatment or the medical research procedure options, including comfort and palliative care. This is to be done to enable them to make informed decisions, which the principles state should be respected and given effect to. In addition they should be supported in the decision-making process so that they can make the decisions about the medical treatment (or medical research procedures) involved.(134)

The fourth principle applies when the person to be treated lacks the decision-making capacity for the medical treatment proposed. It relates to the fact that those who are involved in the treatment of the person, particularly those who propose the treatment and those who have been appointed to be or have become the medical treatment decision maker of the person to be treated by operation of the provisions of the Act . That principle notes that the person to be treated has the right to be shown respect for their culture, beliefs, values and personal characteristics and their
preferences, values and personal and social wellbeing should direct decisions about the medical treatment (or medical research procedures) that may be administered to them.(135) For the role of a support person see, 12.6.5.5, below.

The sixth principle six refers to the ‘right’ given in the Act to anyone who wishes to extend their autonomy to either make their own medical decisions or significantly influence the nature of those decisions that have to be made after they have lost their capacity to make their own medical treatment decisions.(136) This principle is reflected in the wording of other sections of the Act which are dealt with in 12.6.5.1 to 12.6.5.3 and summarised in 12.6.5.3.1, below.

The Medical Treatment Planning and Decisions Act 2016 (Vic) adopts the established common law and regularly legislated test for decision-making capacity, namely that a person has decision-making capacity to make a decision covered by the Act if the person is able to do the following—
  1. understand the information relevant to the decision and the effect of the decision,
  2. retain that information to the extent necessary to make the decision,
  3. use or weigh that information as part of the process of making the decision,
  4. communicate the decision and the person's views and needs as to the decision in some way, including by speech, gestures or other means.(137)
The Act makes it clear that an adult is presumed to have decision-making capacity unless there is evidence to the contrary. An adult is a person aged 18 years or older. However some children will have decision-making capacity for the medical treatment decisions relating to them.(138) As already noted at the commencement of this chapter, that matter is taken up in 12.14 below.

A person is taken to understand information relevant to a decision if they understand an explanation of the information given to them in a way that is appropriate to the their circumstances, whether by using modified language, visual aids or any other means.(139)

The Act states that when deciding whether or not a person has decision-making capacity, the person deciding that matter must have regard to the following—
  1. a person may have decision-making capacity to make some decisions and not others,
  2. if a person does not have decision-making capacity for a particular decision, it may be temporary and not permanent, and
  3. it should not be assumed that a person does not have decision-making capacity to make a decision—
    1. on the basis of the person's appearance; or
    2. because the person makes a decision that is, in the opinion of others, unwise. .(140)
Importantly, the Act notes that a person has decision-making capacity to make a decision if it is possible for the person to make a decision with practicable and appropriate support.(141) </>

12.6.3 Medical treatment defined

The Medical Treatment Planning and Decisions Act 2016 (Vic) increases the number of health professionals who are required, by legislation, to seek consent from the person they propose treatment for or from that person’s substitute decision-maker when that person lacks the capacity to make the decision for themselves. The Act does this by applying that obligation not only doctors and dentists, but also any other health practitioner registered anywhere in Australia under the provisions of the Health Practitioner Regulation National Law who seeks to provide medical treatment in Victoria. Also included in the list of those who must seek such consent are operational staff members of the Ambulance Service (142), and the holders of a non-emergency patient transport service licence or an employee or contractor of such a holder who provides such a service. (143) However the definition of medical treatment in the Act covers only certain categories of treatment; but covers all dental treatment.

The Act defines the term ‘medical treatment’ to mean certain treatments of a person by a health practitioner for the purposes of diagnosing a physical
or mental condition, preventing disease, restoring or replacing bodily function in the face of disease or injury or improving comfort and quality of life. Such treatments are:
  • treatment with physical or surgical therapy,
  • treatment for mental illness,
  • treatment with—
    1. prescription pharmaceuticals; or
    2. an approved medicinal cannabis product,(144)
  • dental treatment and
  • palliative care.
We suggest that because of that definition of medical treatment, in addition to medical practitioners (doctors) and dentists, nurse practitioners, when prescribing prescription pharmaceuticals for a person who does not have decision-making capacity to consent to the proposed treatment will need consent through an instructional directive in their advance care directive, if they have made one. Otherwise the consent will have to be sought from their medical treatment decision maker, either appointed by them or provided for in the Act ; see 12.6.5 and following below, including the summary at 12.6.5.3.1.

Because chiropractors, osteotherapists, and physiotherapists provide treatment with physical therapy to restore (or possibly replace) bodily function in the face of disease or injury or improving comfort and quality of life, we suggest that when they are proposing to treat a person who does not have decision-making capacity to consent to the proposed treatment they too would need to consent through the processes described in the last paragraph.

Note that there are special provisions in relation to palliative care. These are dealt with in 12.6.4.4.

12.6.4 The types of medical treatment

The legislative obligation to gain consent to “medical treatment” now covers a very wide range of possible treatments that may be proposed not only by doctors or dentists, but also by physiotherapists, nurse practitioners, practitioners of Chinese Medicine and podiatrists to name only some of the 15 health professions covered by the Medical Treatment Planning and Decisions Act 2016 (Vic).(145)As a result medical treatments are divided into two groups “routine treatment” and “significant treatment”.

Significant treatment is any medical treatment of a person that involves any of the following—
  1. a significant degree of bodily intrusion,
  2. a significant risk to the person,
  3. significant side effects, or
  4. significant distress to the person.(146)
Routine treatment is any medical treatment other than significant treatment.(147)

Certain kinds of treatment have special provisions relating to them. These are emergency treatment, special medical procedures, medical research procedures and palliative care. Emergency treatment is dealt with at 12.6.4.1, special medical procedures at 12.6.4.2, medical research procedures at 12. 6.4.3 and palliative care at 12.6.4.4.

12.6.4.1 Emergency treatment.

A health practitioner may administer medical treatment (other than electroconvulsive treatment) or a medical research procedure to a person without consent or authorisation (in relation to a medical research procedure) if they believe on reasonable grounds that the medical treatment or medical research procedure is necessary, as a matter of urgency to—
  1. save the person's life; or
  2. prevent serious damage to their health; or
  3. prevent them from suffering or continuing to suffer significant pain or distress.(148)
A health practitioner is not permitted to administer such treatment or a research procedure if they are aware that the person has refused the particular medical treatment or procedure. A person may refuse treatment or a procedure by way of an instructional directive, a legally valid and informed refusal of treatment by or under another form of informed consent.Nevertheless, if the circumstances set out above exist, a health practitioner is not required to search for an advance care directive that is not readily available to them.(149)

Note that medical research procedures are also dealt with in 12.6.4.3 below and in Chapter 16.3.3.

12.6.4.2 Special medical procedures.

In Victoria only VCAT may give consent to a special medical procedure for people who do not have the decision-making capacity to make the decision for themselves. VCAT may give such a consent only if it is satisfied that:
  1. the patient has not given an instructional directive (within the meaning of the Medical Treatment Planning and Decisions Act 2016) in relation to the special medical procedure; and
  2. the patient does not have decision-making capacity in relation to giving consent; and
  3. the patient is not likely to have decision-making capacity in relation to giving consent within a reasonable time; and
  4. the patient would consent to the carrying out of the special medical procedure if the patient had decision-making capacity in relation to giving consent (150) 1 the special medical procedure, the likely effects and consequences are consistent with the patient’s preferences or values(151) 1 the special medical procedure will promote the personal and social wellbeing of the patient(152)
The special medical procedures are:
  1. any procedure that is intended, or is reasonably likely, to have the effect of rendering permanently infertile the person on whom it is carried out; or
  2. a termination of pregnancy; or
  3. any removal of tissue for the purposes of transplantation to another person; or
  4. any other medical treatment that is prescribed to be a special medical procedure.(153)
It is convenient to deal here the special procedural and other requirements that must be complied with before VCAT may give its consent to the carrying out of a special procedure. First, applications for such consent may be made to VCAT only by the person's medical treatment decision-maker by a person who, in the opinion of VCAT, has a special interest in the affairs of the patient. (154) Who is a person's medical treatment decision-maker is described below at 12.6.5.

The person the subject of the application is a party to the proceedings.(155) Notice of the application must be given to them or to others on their behalf. VCAT must also give notice of the application and of the hearing to the Public Advocate and any other person whom VCAT considers has a special interest in the affairs of the patient. (156) VCAT must commence to hear the application within 30 days after receiving the application.(157)

Any person who VCAT reasonably believes the patient would want to be consulted regarding special medical procedures, are to be consulted before VCAT provides consent.(158)

Sterilising treatment for people who lack the decision-making capacity to make decisions about sterilising treatment is discussed further in Chapter 15.

12.6.4.3 Medical research procedures.

Medical research procedures are now dealt with under the Medical treatment Planning and Decisions Act 2016 (Vic). A medical research procedure is a procedure carried out for the purposes of medical research, including, as part of a clinical trial, the administration of pharmaceuticals, the use of equipment or a device or a prescribed medical research procedure.(159) However, activities such as non-intrusive physical examinations, observing a person’s activities or conducting a survey are not included in the definition, so do not require consent.(160)

While one of the purposes of the Act is to provide for a process for obtaining approval and consent for medical research procedures to be administered to a person who does not have decision-making capacity, another policy behind the Act is to ensure that the stated or inferred views of the person about the proposed medical research procedure are given effect to in most cases.(161)

The Act is structured so that a medical research practitioner must not administer a medical research procedure to a person who does not have decision-making capacity to make a medical treatment decision in relation to that procedure unless, the research project has been approved by the relevant human research ethics committee.(162)

In addition to that committee’s approval of the research project, consent for a particular person to be given the treatment (the procedure) must also be provided. This can be done in one of three ways, namely where the person:
  1. has consented, in an instructional directive, to the procedure being administered to them, or
  2. has not made an instructional directive, but their medical treatment decision maker has consented to the procedure being administered, or
  3. does not have a medical treatment decision maker; but the procedure is authorised by the processes set out in ss 79-81 of the Act being complied with.(163)
The first way of consent being provided is another manifestation of the policy of the Act of maintaining a person’s decision-making autonomy into the period or periods in which they lack decision-making capacity.(164)

The second way provides for a substitute medical treatment decision-maker appointed by the person for whom the medical research procedure is proposed to make the decision. However they have to be reasonably available and willing and able to make the decision. If they do not meet those criteria and VCAT has appointed a guardian with power to make medical treatment decisions on behalf of the person, and in the circumstances, they are reasonably available and willing and able to make the medical treatment decision, then they are the person's medical treatment decision maker.(165)

If the person has not appointed a medical treatment decision-maker and has no VCAT appointed guardian or neither of such appointees is reasonably available and willing and able to make the decision, then the first in the hierarchy of persons, set out in the footnote to this sentence, who is in a close and continuing relationship with the person to be treated and who, in the circumstances, is reasonably available and willing and able to make the medical treatment decision, is the person's medical treatment decision maker for the special medical procedure.(166)

Where there is no one to act as the person's medical treatment decision maker, then it is up to the medical research practitioner to decide whether or not to administer the proposed research procedure without consent. If the practitioner decides to do this, they must comply with all the requirements of ss 79-81 of the Act .(167)

12.6.4.4 Palliative care

The Medical Treatment Planning and Decisions Act 2016 (Vic) defines palliative care to include:
  1. the provision of reasonable medical treatment for the relief of pain, suffering and discomfort, and
  2. the reasonable provision of food and water.(168)
However that definition does not preclude other medical treatment, as defined in the Act , being included in the definition of “palliative care” as a result of decisions of the Supreme Court of Victoria or VCAT interpreting the meaning of that term in the Act . However it should be noted that in a 2003 Morris J of the Supreme Court of Victoria, on the application of the Public Advocate of Victoria, made a declaration that providing nutrition and hydration via a percutaneous endoscopic gastrostomy (a PEG tube) constituted medical treatment and not palliative care.(169)

These specific provisions in the Act apply in the context already noted at 12. 6. 1 above. The Act makes it clear that a health practitioner cannot be compelled by either a statement in an advance care directive or a decision by a medical treatment decision maker to administer a particular form of medical treatment or medical research procedure.(170)
Nor can a health practitioner be required to administer a futile or non-beneficial medical treatment or medical research procedure to a person.(171) Nevertheless, while health practitioners will exercise their professional expertise in decision-making in relation to palliative care, they must have regard to any preferences and values of the person they are treating. This is a clear policy of the Act restated in different contexts throughout the Act .

Significantly the normal medical treatment decision-making processes do not apply to palliative care.(172) Also an instructional directive about palliative care is not binding on the treating health practitioners. This is because the Act treats any statement in a patient’s advance care directive concerning palliative care into a values directive.(173) However treating health practitioners do not have carte blanche to treat palliative care patients as they see fit. This is because, in making a decision to administer treatment, the Act requires the treating health practitioners to have regard to any preferences and values of the patient, whether expressed by way of a values directives or otherwise; and to consult the patient’s medical treatment decision maker – if there is one.(174)

12.6.5 The processes for making medical treatment decisions for those currently unable to make such decisions for themselves

The processes for making medical treatment decisions for those currently unable to make such decisions for themselves in relation to emergency treatment, special medical procedures, medical research procedures and palliative care are dealt with above at 12.6.4.1, 12.6.4.2, 12.6.4.3 and 12.6.4.4 respectively. This section deals with the for making medical treatment decisions for “routine treatment” and “significant treatment”, as described in 12.6.4 above, that does not fit into those special categories already dealt with above.

The Medical Treatment Planning and Decisions Act 2016 (Vic) makes it clear that a person has the right to exercise autonomy about their medical treatment or medical research procedures that may be administered to them (175) In giving effect to this principle, the Act provides for people to make advance care directives in which they may include instructional directives and values directives; and in a separate document appoint (substitute) medical treatment decision makers. The instructional directives, which are binding in most situations, extend the decision-making power of the makers of advance care directives into the times in which they have not have capacity to make decisions about the medical treatment proposed for them. Their capacity to influence medical treatment decision-making in other ways is taken up in the following paragraphs.

This is why the Actprovides that when a health practitioner proposes to administer medical treatment to a person who does not have decision-making capacity to make the medical treatment decision, that health practitioner must, before giving the treatment, make efforts that are reasonable in the circumstances to find out whether the person has made an advance care directive or has appointed a
medical treatment decision maker or both. (176) It is unprofessional conduct on the part of a health practitioner to contravene this legislative provision.(177)

If the person to be treated has included, in their advance care directive, an instructional directive, which is an express statement of the person's medical treatment decision that deals with the proposed treatment, then that decision takes effect as if the person has consented to, or refused the commencement or continuation of, medical treatment, proposed for them by the treating health practitioner. The Act gives as an example of an instructional directive consenting to treatment, a statement that the person consents to a heart bypass operation in specified circumstances; and as an example an instructional directive refusing treatment, a statement that the person refuses cardiopulmonary resuscitation.(178)

While the treating health professional’s obligation is to give effect to the person’s instructional directive, there are a number of circumstances in which they may refuse to comply. One is that they are not required to administer directed medical treatment if they are of the opinion that that treatment is not clinically appropriate.(179). Another is if they believe on reasonable grounds, that circumstances have changed since the person gave the advance care directive in which the instructional directive is found, so that the practical effect of it would no longer be consistent with the person's preferences and values and also that
the delay that would be caused by an application to VCAT, for an order relating to changed conditions, would result in a significant deterioration of person's condition.(180)

Also, unless there is a statement to the contrary in the advance care directive of the person to be treated, the treating health professional may, instead of the medical treatment referred to in the person’s instructional directive, administer other medical treatment that is either of substantially the same kind as the treatment consented to in the instructional directive or only distinguishable on technical grounds not likely to be understood or appreciated by the person who gave the advance care directive.(181)

If an instructional directive covers the proposed treatment, it operates as either the consent to the treatment or the refusal to it either being commenced or continued; and the decision-making process in relation to the proposed treatment is complete.

However, another proviso applies in circumstances in which the person the treatment is proposed for is likely to recover their decision-making capacity to make the treatment decision in reasonable time. In those circumstances the treating health practitioner may only administer the medical treatment before the person recovers decision-making capacity if; the proposed treatment is in accordance with any relevant instructional directive; or has been consented to by the person's medical treatment decision maker, and the health practitioner reasonably believes that a further delay in carrying out the proposed treatment would result in a significant deterioration of the person's condition.(182)

12.6.5.2 If the person to be treated has, in their advance care directive, not made any or any relevant instructional directive but has included a values directive, it must be considered before the treatment decision is made.

A values directive is a statement of a person's preferences and values as the basis on which the person would like any medical treatment decisions to be made on their behalf. Such a directive may be, but is not limited to, a statement of medical treatment outcomes that the person regards as acceptable. The Act gives as an example of a values directive the statement: "If I am unable to recognise my family and friends, and cannot communicate, I do not want any medical treatment to prolong my life.".(183)

If the advance care directive of the person to be treated contains a values directive, but no relevant instructional directive, the Act places an obligation on the treating medical practitioner to refer any medical treatment decision to the person's medical treatment decision maker for a decision.(184) When considering what treatment (if any) to propose the medical practitioner must
consider any values directive in offering and administering medical treatment. It is unprofessional conduct on the part of any registered health practitioner to fail to do either of these things.(185) Also we suggest that it would be wise to ensure that the person's medical treatment decision maker has a copy of the values directive of the person to be treated.

While the person’s medical treatment decision maker has replaced the person as decision-maker about the treatment proposed, they are obliged to make the decision that
they reasonably believe is the decision that the person to be treated would have made if they had had decision-making capacity.In order to make that decision they must first consider any valid and relevant values directive. Next they must consider any other relevant preferences that the person has expressed and the circumstances in which those preferences were expressed. If the medical treatment decision maker is unable to identify any relevant preferences by considering the person’s values directive or by preferences expressed in other circumstances, they must give consideration to the person's values, whether expressed other than by way of a values directive, or inferred from the person's life.

When a medical treatment decision maker, whether appointed by the person to be treated or VCAT (including the Public Guardian when acting as the guardian of the person to be treated) or becomes the person’s medical treatment decision maker by operation of the Act , is called upon by the treating health professional to make a particular medical treatment decision, they are authorised to access or collect information that is relevant to a medical treatment decision they have to make and is information that may lawfully be collected by the person to be treated.(186) Also ahealth practitioner is authorised to disclose health information about the person to be treated to the person's medical treatment decision maker.(187) In order to carry out their functions and duties as a medical treatment decision maker under the Act , the medical treatment decision maker may disclose that information.(188)

12.6.5.3 The hierarchy of medical treatment decision makers

The question of who is the medical treatment decision maker for the person to be treated arises when the person to be treated has either not made an advance care directive, or that directive does not contain any or any relevant instructional directive.

If the person to be treated has made a values directive and has appointed medical treatment decision maker, that medical treatment decision maker becomes responsible for making the treatment decision, if they are reasonably available and willing and able to make the medical treatment decision.(189) They do so according to the requirements set out in 12.6.5.2 above.

Note that a person may appoint their medical treatment decision maker when they make their advance care directive or at any other time that they have the decision-making capacity to make the appointment.(190) Appointing a person medical treatment decision maker is a separate and different process from making an advance care directive and such an appointment can be made without an advance care directive having been made first.

However, it will take some time for advance care directives made under the provisions of the Medical Treatment Planning and Decisions Act 2016 (Vic) to become the norm. Consequently, there will be many occasions when the person to be treated has neither made an advance care directive nor has not appointed a medical treatment decision maker.

In a limited number of cases VCAT will have appointed a guardian for the person to be treated with power to make medical treatment decisions on behalf of that person. That guardian will be the person's medical treatment decision maker if, in the circumstances, they are reasonably available and willing and able to make the medical treatment decision.(191)

If there is neither a medical treatment decision maker appointed by the person to be treated nor a guardian appointed by VCAT for them with the power to act as medical treatment decision maker, the person’s medical treatment decision maker of an adult (a person 18 years or above) will be the first of the following list of persons who is in a close and continuing relationship with the person and who, in the circumstances, is reasonably available and willing and able to make the medical treatment decision:
  1. the spouse or domestic partner of the person, (192)
  2. the primary carer of the person,(193)
  3. the first of the following and, if more than one person fits the description the oldest of those persons:
    1. an adult child of the person,
    2. a parent of the person,
    3. an adult sibling of the person.(194)

As has been suggested above, there are likely to be many cases in which the person to be treated has not made an advance care directive and thus no instructional or values directive and also has not appointed a medical treatment decision maker. Consequently those who become such a person’s medical treatment decision maker by operation of the Medical Treatment Planning and Decisions Act 2016 (Vic), whether they are the person’s guardian appointed by VCAT, and so including the Public Advocate (acting as the guardian of the person to be treated), or because of their familial or personal relationship with the person to be treated, they will have to make their decisions which the Act requires to be what they reasonably believe would have been the decision that the person to be treated if they had had decision-making capacity, from limited and not necessarily reliable sources of information about the person’s wishes.

These sources are first, expressions of preferences made in such circumstances that they should be taken seriously, and second, inferred from the life of the person to be treated.(195) If the preferences or values of the person to be treated can be discovered from the sources available to the medical treatment decision maker, then they have to consider:
  • the likely effects and consequencesof the proposed treatment and its likely effectiveness and whether those factors are consistent with the preferences or values of the person to be treated, and also,
  • whether there are any alternatives, including refusing medical treatment, that would be more consistent with the preferences or values of the person to be treated.(196)
However, if the medical treatment decision maker cannot ascertain or apply the preferences or values of the of the person to be treated, the medical treatment decision that they make must be a decision that promotes the personal and social wellbeing of the person to be treated, having regard to the need to respect their individuality. In this context, the medical treatment decision maker must consider:
  • the likely effects and consequences of the proposed treatment and its likely effectiveness and whether those factors promote the person's personal and social wellbeing, having regard to the need to respect the person's individuality, and also
  • whether there are any alternatives, including refusing medical treatment, that would better promote the person's personal and social wellbeing, having regard to the need to respect their individuality.(197)
In attending to these considerations, medical treatment decision makers must act in good faith and with due diligence.(198)

Inevitably there will be people for whom medical treatment is proposed, but for whom the treating health professional cannot find an advance care directive or any medical treatment decision maker either at all or anyone in the hierarchy set out above and summarised at 12.6.5.3.1 below who is reasonably available and willing and able to make the medical treatment decision.

In this situation, if the treatment is ‘routine’, the health practitioner may administer it without consent. If the proposed treatment is ‘significant’ treatment, the health practitioner may administer it only if the Public Advocate has consented to the treatment. In that situation the Public Advocate acts as medical treatment decision maker of last resort. The terms ‘routine’ and ‘significant’ are described at 12.6.4 above.
12.6.5.3.1 Roles of the Public Advocate in relation to medical treatment decision-making

The Public Advocate has a number of roles in relation to medical treatment decision-making. Although some of those roles have already been noted in 12.6.5.3 above, they are:
  1. As VCAT appointed guardian with power to make medical treatment decisions for the person under guardianship. In this role the Public Advocate has the same obligations as a medical treatment decision maker appointed by the person when they had decision-making capacity for medical decisions. See 12.6.5.3, above.
  2. When the Public Advocate acts as acts as medical treatment decision maker of last resort for ‘significant’ treatment as set out in 12.6.5.3, above.
When deciding whether to give or refuse consent to the medical treatment proposed by the treating health professional, the Public Advocate (or their delegate) usually will not have any information about the person to be treated and little or no opportunity to discover and apply their preferences. In these circumstances the medical treatment decision that the Public Advocate makes must be a decision that promotes the personal and social wellbeing of the person to be treated, having regard to the need to respect their individuality. In this context, the Public Advocate must consider, insofar as it is possible to do either at all or without significantly delaying the commencement or continuation of the treatment proposed:
  • the likely effects and consequences of the proposed treatment and its likely effectiveness and whether those factors promote the person's personal and social wellbeing, having regard to the need to respect the person's individuality, and also
  • whether there are any alternatives, including refusing medical treatment, that would better promote the person's personal and social wellbeing, having regard to the need to respect their individuality.(199)
In attending to these considerations, the Public Advocate must act in good faith and with due diligence.(200)
  1. In certain circumstances in which a medical treatment decision maker refuses treatment proposed for the person to be treated
If medical treatment decision maker refuses to consent to significant health treatment, and the health practitioner reasonably believes that the preferences and values of the person to be treated are not known or are unable to be known or inferred by that medical treatment decision maker, the health practitioner must notify the Public Advocate.(201)

If the Public Advocate is of the view that the refusal of treatment was not unreasonable in the circumstances, the Public Advocate must inform the health practitioner that no application about the matter will be made to VCAT. However, if the Public Advocate considers that the refusal was unreasonable, the Public Advocate must apply to VCAT within 14 days. VCAT has a discretion as to whether or not to make an order about the treatment and may make an order affirming, varying, setting aside or substituting the original decision for another decision concerning the proposed treatment.(202)
12.6.5.3.2 On request VCAT may give an advisory opinion to the medical treatment decision maker or the treating health practitioner

Either a person’s medical treatment decision maker
or the health practitioner treating them may apply to VCAT for directions or an advisory opinion on any matter or question relating to an advance care directive or the medical treatment of the person.VCAT has a discretion to give an advisory opinion or directions in relation to such an application. (203)
12.6.5.3.3 A summary of the sources of medical decision-making for those currently unable to make a decision about medical treatment proposed for them

When the person to be treated lacks the capacity to make a decision about the medical treatment proposed for them, the hierarchy of sources of decision-making is as follows:
  1. the relevant instructional directive in the advance care directive made by the person to be treated,
  2. the medical treatment decision maker appointed by the person to be treated, who in the circumstances is reasonably available and is willing and able to make the decision. They may make the decision after considering any relevant values directive, and any other matters they are required to consider by provisions in the Act .
  3. the guardian of the person to be treated appointed by VCAT and given power to make medical treatment decisions for that person, who in the circumstances is reasonably available and is willing and able to make the decision. They may make the decision after considering any relevant values directive, and any other matters they are required to consider by provisions in the Act .
  4. the first of the following list of persons who is in a close and continuing relationship with the person and who, in the circumstances, is reasonably available and willing and able to make the medical treatment decision. They may make the decision after considering any relevant values directive, and any other matters they are required to consider by provisions in the Act .
    1. the spouse or domestic partner of the person to be treated,
    2. the primary carer of the person to be treated,
    3. the first of the next list who meet the relationship and other criteria already set out ;
      1. an adult child of the person to be treated (if more than one, the oldest),
      2. a parent of the person to be treated, or
      3. an adult sibling of the person to be treated.(204)

12.6.5.4 Appointed medical treatment decision makers

Appointed medical treatment decision makers rank higher in the hierarchy of substitute decision-makers for medical treatment as broadly defined in the Medical Treatment Planning and Decisions Act 2016 (Vic) than those that become medical treatment decision makers by virtue of their relationship to the person to be treated. (205) Note that a person who was appointed an attorney for personal matters (including medical treatment matters) under an enduring power of attorney between 1 September 2015 and 12 March 2018 is deemed to be an appointed medical treatment decision maker under the Medical Treatment Planning and Decisions Act 2016 (Vic).(206)

As already noted in 12.6.5.3 above, a person may appoint their medical treatment decision maker when they make their advance care directive or at any other time that they have the decision-making capacity to make the appointment.(207) Appointing a person medical treatment decision maker is a separate and different process from making an advance care directive and such an appointment can be made without an advance care directive having been made first. Unlike in the case of support persons, only adults may appoint other adults as their medical treatment decision maker and may also have more than one medical treatment decision maker at a time.

An appointed medical treatment decision maker must accept their appointment in writing. This must be done by, on the same document as their appointment is signed by the appointor, signing that document which must include a statement of acceptance by each appointee to the effect that they:
  1. understand the obligations of an appointed medical treatment decision make; and
  2. undertake to act in accordance with any known preferences and values of the person making the appointment, and
  3. undertake to promote the personal and social wellbeing of the person appointing them, having regard to the need to respect that person's individuality, and
  4. have read and understood any advance care directive that the person has given before, or at the same time as, their appointment.(208)

Each signing must be witnessed by an adult who certifies that they witnessed the signing that they certify to.(209)

12.6.5.5 Support persons

The Medical Treatment Planning and Decisions Act 2016 (Vic) provides for the appointment of support persons whose role is to support the person who has appointed them to make, communicate and give effect to that person's medical treatment decisions.(210) Support persons may also represent the interests of the person in relation to their medical treatment, including when the person does not have decision-making capacity in relation to medical treatment decisions.(211)

Any person, including a child, may appoint another person, again including a child, as their support person as long as they have the decision-making capacity to make such an appointment. However they may have only one support person at any given time.(212) Also it is an offence to purport (pretend) to be a support person for another person when not currently appointed by them.(213)

The document by which a person appoints another person to be their support person must be signed by the appointor. Before the appointment can come into force the intended support person must sign the same document accepting that appointment and stating that they understand the role of support person. The signing of the document by the intended support person accepting that appointment must be witnessed and that action certified to by another person.(214)

A support person is authorised to access or collect health information that is relevant to a medical treatment decision to be made by the person who has appointed them and is information that may lawfully be collected by that person.(215) Also ahealth practitioner is authorised to disclose health information about the person who appointed the support person to their support person.(216) In order to carry out effectively their functions and duties as a support person under the Act , the support may disclose that information.(217)

12.7 Queensland

The Queensland regime for substitute decision-making in relation to medical and dental treatment on behalf of adults incapable of giving a valid consent to their own treatment commenced on 1 July 2000 with the commencement of the Guardianship and Administration Act 2000 (Qld). Most aspects of the regime are found in Chapter 5 of that Act, but the Powers of Attorney Act 1998 (Qld) sets out the responsibilities of attorneys for personal matters and its Chapter 4 deals with statutory health attorneys.

While substitute decision-makers for medical and dental treatment are called persons responsible in New South Wales, Victoria and Tasmania, in Queensland, if the incapable person has no guardian or attorney for health matters, their substitute decision-makers for medical and dental treatment are called statutory health attorneys. However, as will be seen, statutory health attorneys in Queensland have more functions than persons responsible in the other States.(218)

12.7.1 Objects of the legislation

The Guardianship and Administration Act 2000 (Qld) seeks to strike an appropriate balance between the right of an incapable adult, called an adult with impaired capacity in Queensland, to have autonomy in decision making the greatest possible degree and their right to adequate and appropriate support for decision-making.(219)

Chapter 6 seeks to strike a balance between ensuring that a person is not deprived of necessary health care only because they are an adult with impaired capacity while ensuring that the health care that they are given is necessary and appropriate to maintain or promote their health or wellbeing or is, in all the circumstances, health care that is in their best interests.(220)

The Queensland legislation reflects strongly the common law presumption that an adult has capacity to make their own decisions. It requires treating doctors and dentists to consider whether or not a person has capacity to make a particular decision about a particular health matter or special health matter.(221)

A person has impaired capacity for such a matter if they are:
  1. incapable of understanding the nature and effect of decisions about the matter; or
  2. cannot freely and voluntarily make decisions about the matter; or
  3. cannot communicate their decisions in some way.(222)

12.7.3 Health care defined

In Queensland the description of matters covered by the regime designed primarily to provide substitute decision-making for medical and dental treatment proposed for adults unable to give a valid consent to their own treatment is broader than elsewhere in Australia. The substitute decision-making relates to "matters relating to health care". Health care is described as, care or treatment of, or a service or a procedure for an adult:
  1. to diagnose, maintain, or treat the adult's physical or mental condition; and
  2. carried out by, or under the direction or supervision of, a health provider.(223)

Health care also includes withholding or withdrawal of a life-sustaining measure if the commencement or continuation of the measure would be inconsistent with good medical practice.(224)

The term "health provider" is defined to mean a person who provides health care, or special health care, in the practice of a profession or the ordinary course of business.(225) This definition covers doctors and dentists and other recognised health professionals including, psychologists, physiotherapists, optometrists, speech therapists and occupational therapists. While there has been no decided case on this as yet, because the definition of health provider includes those who provide health care in the ordinary course of business the term may include herbalists, particularly those qualified in Chinese medicine, counsellors and a range of others who run businesses offering to diagnose, maintain or treat physical or mental conditions.

All treatments that are not categorised as excluded or special health care are "health care".(226)

12.7.4 The types of health care

12.7.4.1 Excluded health care

As elsewhere in Australia, in Queensland a number of treatments are not included in the definition of health care with the intention that substitute consent in relation to them is not required. These treatments are:
  1. first aid treatment;
  2. non-intrusive examinations made for diagnostic purposes. For example a visual examination of an adult's mouth, throat, nasal cavity, eyes or ears; or
  3. the administration of a pharmaceutical drug which is normally self-administered and for which a prescription is not needed, provided the administration is for a recommended purpose and at a recommended dosage level.(227)

These types of health care have been excluded largely because they are of such a minor nature or are so linked to day to day living that they are carried out only when necessary that it is inappropriate for consent to them to have to be sought through the substitute decision-making regime. However, this exclusion is not intended to cut across, or in any way downplay, the importance of hospitals, aged care facilities or other places where personal care and health care is provided to adults with impaired capacity, keeping accurate records of any form of health care given to a patient or resident or having protocols as to who may permit such treatments to be carried out.

Health care, but not special health care, may be carried out on an adult without their consent if their health provider reasonably considers they have impaired capacity for the health matter concerned; and either:
  1. the health care should be carried out urgently to meet imminent risk to the adult's life or health; or
  2. the health care should be carried out urgently to prevent significant pain or distress to the adult

and it is not reasonably practicable to get consent from their attorney for health matters or their guardian for health matters (if they have one) or their statutory health attorney.(228)

However, health care to deal with imminent risk to the adult's life or health may not be carried without consent if the health provider knows that the adult has objected to the health care proposed in an advance health directive.(229)

Health care to prevent significant pain or distress to the adult may not be carried out without consent if the health provider knows that the adult objects to the health care. However, if the adult has minimal or no understanding of what the health care involves or why it is required, and the health care is likely to cause either no distress to the adult or temporary distress that is outweighed by the benefit of the health care to them, then the health care can be carried out.(230)

If the health care is carried out, the health provider must certify in the adult's clinical records as to the various things enabling it to be carried out because of this section.(231)

Proposed health care, that is not special health care but which is minor and uncontroversial, may be carried out without consent on an adult with impaired capacity if their health provider reasonably considers that:
  1. the adult cannot make a valid decision about the health matter concerned; and
  2. the health care that is necessary and is of the type that will best promote the adult's health and wellbeing.(232)

Also, the health provider must certify in the adult's clinical records as to the various things enabling the health care to be carried out.(233)

Nevertheless, such treatment cannot be carried out if the health provider knows (or could reasonably be expected to know) that the guardian or attorney for health matters of the adult with impaired capacity has made a decision about the health care in question or knows that there is a dispute among those who have a sufficient and continuing interest in the adult about the carrying out of the health care or about the capacity of the adult to make their own decision about the health care.(234)

Furthermore the health care cannot be carried out without consent if the health provider knows (or could reasonably be expected to know) that the adult objects to the health care.(235)

12.7.4.4 Special health care

Special health care has been defined as:
  1. removal of tissue from the adult while alive for donation to someone else;
  2. sterilisation of the adult;
  3. termination of a pregnancy of the adult;
  4. participation by the adult in special medical research or experimental health care;
  5. electroconvulsive therapy or psychosurgery for the adult;
  6. prescribed special health care of the adult.(236)

12.7.5 Who is the substitute decision-maker for health care?

The issue of consent to special health matters is dealt with below. For other health matters there is an order of priority starting with the any advance health directive made by the adult with impaired capacity. If they have given a direction that covers the particular health matter in an advance directive then the question of consent is decided according to the direction.(237) Advance health directives will become more common as time goes on, particularly for older people.

If the adult with impaired capacity has not made an advance health directive, the substitute decision-maker for the adult will be the first person who qualifies in the following list:
  1. any guardian for health matters appointed by the Queensland Civil and Administrative Tribunal (QCAT);
  2. any enduring attorney for health matters appointed by the adult;
  3. the first available and culturally appropriate statutory health attorney from the list below.(238)

The list of statutory health attorneys is as follows:
  1. a spouse of the adult if the relationship between the adult and the spouse is close and continuing;(239)
  2. an adult person who has the care of the adult and is not a paid carer for the adult;(240) 1 an adult person is a close friend or relation of the adult and is not a paid carer for the adult.(241)
If no-one in this list is readily available and culturally appropriate, the Public Guardian becomes the adult's statutory health attorney for the particular health matter.(242)

If there is a disagreement as to which of two or more people should be the statutory health attorney or how that power should be exercised, this can be referred to the Public Guardian for resolution by way of mediation.(243)

Even though they come down the list, in most cases the substitute decision-maker for the adult with impaired capacity will be their spouse, their unpaid carer or a close friend or relation. This responsibility comes to them not because they have been appointed the person's guardian for health matters by QCAT or their attorney for health matters by the now incapacitated person, but because of the operation of both the Powers of Attorney Act 1998 (Qld) and the Guardianship and Administration Act 2000 (Qld) which gives them the role of statutory health attorney.(244) They do not have to be appointed or approved by QCAT or the Supreme Court.

Anyone authorised to be a substitute decision-maker for the health matters under the Guardianship and Administration Act 2000 (Qld) to make substitute decisions in relation to health matters for an adult with impaired capacity must do so in accordance with both the general principles and the health care principle set out in that Act.(245)

The health care principle requires that substitute decision-makers make their decisions:
  1. in the way least restrictive of the adult's rights; and
  2. only if the decision is necessary and appropriate to maintain or promote the adult's health or wellbeing; or is, in all the circumstances, in the adult's best interests.
When making a health care decision, the substitute decision-maker, namely the guardian, the Public Guardian, QCAT or, in relation to special health care only, another entity, must, to the greatest extent practicable:
  1. seek the adult's views and wishes and take them into account; and
  2. take into account the information given by the adult's health provider.(246)

The health care principle states that it does not affect any right an adult has to refuse health care.(247)

12.7.6 Who is the substitute decision-maker for special health care?

As with other health matters, for special health matters there is an order of priority. It too starts with the any advance health directive made by the adult with impaired capacity. If they have given a direction in their advance directive that covers the particular special health matter then the question of consent is decided according to the direction.(248)

Because of the nature of the different kinds of special health care and the adults with impaired capacity for whom special health care is sought, it is unlikely that an adult whose capacity becomes impaired will have made an advance health directive which covers special health care. Consequently, it is more likely that a body authorised to act as the substitute decision-maker for special health care will be called upon to deal with the matter. Those bodies are QCAT and the Supreme Court.(249)

No substitute consent is needed for either health care excluded from the operation of Chapter 5 of the Guardianship and Administration Act 2000 (Qld) or for urgent health care, except under the limited circumstances set out above at 12.7.4.2.

Also, consent is not required for minor, uncontroversial health care, again except under the limited circumstances set out above at 12.7.4.3. Nevertheless, it is both ethically appropriate and useful in building rapport with the substitute decision-makers, family members or significant others of an adult with impaired capacity to seek consent for that health care from the appropriate substitute decision-maker whenever it is convenient to do so. If it is not possible to seek consent in advance of the treatment, it is wise to advise the substitute decision-maker of the more significant of such minor treatments that have been given, for example the administration of prescription antibiotics.

The Guardianship and Administration Act 2000 (Qld) creates an expectation on health providers to give to the guardian or attorney all the information necessary for them to exercise their power in relation to a health matter.(250) The Act also imposes a duty on health providers to give that information to the guardian or attorney unless the health provider has a reasonable excuse for not doing so.(251) The definition of "attorney" includes statutory health attorneys.(252) The definition of "guardian" includes the Public Guardian.(253)

The information which the health provider who is treating or has treated the adult with impaired capacity must give to the guardian or attorney includes information about the:
  1. nature of the adult's condition at the time of the treatment; and
  2. particular form of health care being, or that was, carried out; and
  3. reasons why the particular form of health care is being, or was, carried out; and
  4. alternative forms of health care available for the condition at the time of the treatment; and
  5. general nature and effect of each form of health care at the time of the treatment; and
  6. nature and extent of short-term, or long-term, significant risks associated with each form of health care; and
  7. for a health provider who is treating the adult - the reasons why it is proposed a particular form of health care should be carried out.(254)

12.7.8 The role of QCAAT in relation to special health care and health care

QCAT is substitute decision-maker in relation to:
  1. special health care for adults with impaired capacity for the special health matter, but not electroconvulsive therapy and psychosurgery;(255) and 1 consenting to the sterilisation of a child with an impairment.(256)

If QCAT consents to a form of special health care that needs to be continued, it may appoint a guardian for the adult and empower them to consent for the adult to continuation of the special health care or the carrying out on the adult of similar special health care. QCAT may also include in the appointment order a declaration, order, direction, recommendation, or advice about how the power is to be used.(257)

QCAT has other functions that can be useful in dealing with issues and problems arising in relation to health matters. These include:
  1. making declarations about the capacity of an adult, guardian or attorney;
  2. making declarations, orders or recommendations, or giving directions or advice, in relation to guardians and attorneys, enduring documents and related matters;(258)
  3. consenting to the withholding or withdrawal of a life-sustaining measure for adults with impaired capacity for the health matter concerned.(259)

QCAT's role in relation to consenting to specific treatments is limited to treatments categorised as special health care and treatments involving the consenting to the withholding or withdrawal of a life-sustaining measure for adults with impaired capacity for the health matter concerned.

12.7.9 Objections to health care

In Queensland objections to treatment by the adult with impaired capacity or by their guardian, attorney or statutory health attorney are dealt with in different ways.

12.7.9.1 Objections by the adult with impaired capacity

The Guardianship and Administration Act 2000 (Qld) states that generally substitute consent for a health matter or special health matter is ineffective if the health provider knows, or ought reasonably to know, the adult with impaired capacity objects to the health care.(260) However, the Act goes on to provide that the consent is effective, despite the objection:
  1. if the adult has minimal or no understanding of what the health care involves and why it is required, and
  2. the health care is likely to cause the adult either no distress or only temporary distress that is outweighed by the benefit of the proposed health care.(261)
As the Queensland Law Reform Commission's report upon which the Act is based shows, this provision was based on the New South Wales legislation which allows a person who cannot give a valid consent (or refusal) to their own medical or dental treatment to "object" nevertheless to the treatment.(262) However, while NCAT in New South Wales deals with these "objections" and decides whether or not to give its consent to the proposed treatment thereby overriding the objection of the incapable person, a different approach has been taken in Queensland.

In Re CJ, the then Queensland Guardianship and Administration Tribunal held that what is required before a person may object validly to health care "is not simply an ability to technically know what the procedure involves and what it is used for but an ability to understand the true nature and effect of a decision" in a health matter.(263) In that case a person with a more than 20 year history of paranoid schizophrenia was held to have no understanding of the nature and effect of the decisions she was making because she consistently stated that she did not have a mental illness and that she did not have a physical illness, namely diabetes. This satisfied the Tribunal that she had no understanding of the proposed health care or why it was required, because she refused to accept the fact that she had any illnesses.(264) The Tribunal was also satisfied that the proposed health care would cause either no distress or minimal distress because it involved medication being supplied by a tablet form and the monitoring of CJ's diabetes via testing for her sugar levels. In addition, the medication and monitoring of her sugar diabetes would provide benefits which far outweighed the minimal distress that the treatment would cause her.(265)

The way to deal with the objection in these circumstances is to make an application to QCAT for a declaration about the capacity of the adult and other orders, including appointing guardians and obtaining directions or advice from QCAT if appropriate.(266)

As already noted, QCAT does not have jurisdiction to deal directly with applications for consent to health care, except for forms of special health care, while NCAT in New South Wales does have such a role and can and does occasionally override the objections to treatment of incapable people. This absence of a formal mechanism for giving appropriate consideration to the person's objection but yet being able to override it and give an effective consent to the proposed health care in appropriate cases may have contributed to the interpretation given to the relevant provision in Queensland.(267) However, QCAT may give directions to guardians and attorneys, including statutory health attorneys.(268)

There are specific provisions in the Guardianship and Administration Act 2000 (QLD) dealing with the objections of an adult with impaired capacity to urgent health care and minor, uncontroversial health care.

If the objection by the adult with impaired capacity is to urgent health care that the adult's health provider reasonably considers should be carried out urgently to meet imminent risk to the adult's life, and the objection to the treatment is in the adult's advance directive, then the treatment may not be carried out without consent.(269) However, as a direction in an advance directive to withhold or withdraw a life-sustaining measure applies only in certain circumstances, despite the maker's wishes, it may still be legal for the treatment to be carried out.(270) Nevertheless the adult's health provider may withhold or withdraw a life-sustaining measure if that is consistent with good medical practice, the decision must be taken immediately and the adult does not object to the withholding or withdrawal.(271) In such circumstances, the treating doctors should only give the treatment if it is consistent with good medical practice to do so and the treatment is not excessively burdensome, intrusive or futile.

If the adult's health provider reasonably considers that certain health care should be carried out urgently to prevent significant pain or distress to the adult, but the adult objects to that treatment and it is not reasonably practicable to get consent from their guardian, attorney or statutory health attorney, then the treatment may be carried out if the adult has minimal or no understanding of what the health care involves or why it is required, and the health care is likely to cause either no distress to the adult or temporary distress that is outweighed by the benefit of the health care to them.(272)

It should be noted that when an adult makes an advance health directive, they can anticipate the possibility of them objecting to future health care and give a direction consenting to particular future health care being given in specified circumstances despite their objection at that future time.(273)

As already noted, minor, uncontroversial health care cannot be carried out without consent if the health provider knows (or could reasonably be expected to know) that the adult objects to the health care.(274) Substitute consent for the health care must be obtained.

Finally in relation to a person objecting to being given particular medical or dental treatment, the Guardianship and Administration Act 2000 (Qld) specifically provides that a health provider or any person acting under their direction or supervision may use the minimum force that is both necessary and reasonable to carry out health care authorised under the Act.(275)

The predecessor of QCAT, the Queensland Guardianship and Administration Tribunal has interpreted this provision to mean that only health providers or those acting under their direction or supervision may use force to carry out health care and that guardians, including the Public Guardian, or others acting under their direction or supervision cannot use force for this purpose.(276)

12.7.9.2 Objections in the form of disagreements between guardians or attorneys

The Guardianship and Administration Act 2000 (Qld) specifically addresses disagreements between guardians or attorneys, where more than one has been appointed, or between two or more eligible statutory health attorneys about health matters for an adult with impaired capacity. The Act provides for the Public Guardian to attempt mediation. If the disagreement cannot be resolved by mediation, the Public Guardian can make the decision about the health matter and then advise QCAT.(277)

If the guardian, appointed attorney or statutory health attorney either makes or refuses to make a decision about a health matter, and their action is contrary to the health care principle, the Public Guardian make the decision in relation to the health matter, in accordance with the health care principle.(278)

12.8 Western Australia

As from 15 February 2010, Western Australia has had comprehensive regime for substitute decision-making in relation to the medical and dental treatment of those unable to give a valid consent to their own treatment.(279) That regime imported the concept of "person responsible" from New South Wales and Tasmania and the hierarchy of persons responsible, called the "order of priority" in Western Australia, is similar to, but not identical with, the hierarchy in New South Wales. This matter is dealt with in 12.8.4 below.

However, the first question that arises when a person cannot give a valid consent to their own treatment is, do they have an advance health directive? If so the next question is whether that advance health directive, on a sensible reading of it, contains a treatment decision relevant to the treatment proposed for that person. If so, the treatment provided to that person must be decided according to that treatment decision.(280) If the person needs treatment urgently, it may not be practical to check on whether the person has an advance health directive.(281)

However, this new regime does not replace the parens patriae jurisdiction of the Supreme Court of WA as the Guardianship and Administration Act 1990 (WA) makes clear.(282).

12.8.1 Medical and dental treatment defined

The term "treatment" is defined as medical or surgical treatment, including both a life sustaining measure and palliative care. Treatment is also defined to mean dental treatment or other health care.(283) A treatment decision is defined to mean a decision to give or to refuse consent to the commencement or continuation of any treatment.(284)

It is suggested that this definition of treatment is consistent with the broad view of what is included in medical treatment taken by WASAT and its predecessor, the Guardianship and Administration Board. In the BTO Case, a Full Board of the Guardianship and Administration Board stated that it considered that the concept of treatment included not only medical or surgical procedures designed actively to treat a person's illness or condition, but also the provision of care in the form of oversight of a person's condition and medical advice as to by what measures it may best be managed, the prescription of courses of medication and the like.(285)

In the BTO Case, the Full Board then went on to include decisions about the provision and withdrawal artificial hydration and nutrition in medical treatment in the following terms:

Medical care, flowing from such oversight and medical advice, may also involve advice concerning the appropriateness of withdrawal of particular measures of treatment or care or the effect of not providing certain forms of treatment or care that may be available, including those by which a person is non-naturally hydrated or nourished, as well as the act of withdrawing such forms of medical treatment or care.(286)

Those matters are now covered by the term "palliative care" in the definition of treatment, as other aspects of palliative care also are.

The Full Board's broad view of the concept of treatment led it to suggest that whether certain actions or acts were "treatments" depended on the circumstances of each case and must be decided on a case by case basis.(287) In this regard the Full Board considered whether the use of physical and chemical restraints in a nursing home could constitute treatment under the section. The Full Board took the view that whether or not a particular form of physical or chemical restraint would fall within the definition of treatment would depend on the reasons for its use, the purposes to which it might be put and who prescribed its use.(288)

In ADP, WASAT saw the use of olanzapine in the circumstances of that case as both a chemical restraint and a treatment and appointed a guardian with authority to give consent to both treatment and the use of chemical and physical restraint.(289)

In SJ and MET, WASAT had to deal with a situation in which it was proposed that treatment to achieve "massive weight loss either through wiring her jaws or stomach stapling and feeding a liquid diet under medical supervision" on a woman with an intellectual impairment and behavioural problems. There were doubts about whether this treatment should be carried out on her and a "palliative care program" was suggested as an alternative treatment.(290) WASAT made a distinction between those actions relating to the proposed treatment that were physical and chemical restraints and those that were treatment. Its reasons for decision state:

While we accept that restraint of [MET] to facilitate her treatment may be in her best interests, given the evidence before us, we do not see it forming part of the treatment provided. The use of a 24 hour guard, the suggested use of restraints on the hands of the represented person, and medication to manage her behaviour used in the past are or would be attempts to control the voluntary movements of the represented person, albeit for the purposes of delivering health care which she needs and are therefore in our view restraints. It is not appropriate that such restraints be seen as an incident of treatment itself. In the case of the guard placed on the room of the represented person we conclude that this is clearly a restraint on her movement and not part of treatment.

The distinction between treatment and restraint to facilitate the delivery of that treatment is an important safeguard for [MET]. There is an obligation on the guardians, and those treating [her], to use the least restrictive possible means by which treatment may be delivered to her. Strategies to facilitate treatment may include the use of behaviour management programs, while she remains in hospital, or ...the use of medication to manage her distress and agitation.(291)

WASAT appointed MET's parents as her joint, limited guardians in order for the treatment restraining her and restricting her diet to be carried out.(292)

While WASAT considered that psychiatric treatment was treatment for the purposes of the Guardianship and Administration Act 1990 (WA), it was aware of the policy concerns about the appropriate relationship between that Act and the Mental Health Act 1996 (WA).(293) WASAT was also aware that it is sometimes difficult to determine whether the medications being administered to an incapable person constitute an attempt to modify their behaviour or whether they are treatments for a psychiatric condition.(294)

In relation to contraceptive treatment, the Full Board noted that an earlier Full Board:
had no hesitation in saying the definition of treatment in the Act was "broad enough to encompass" the proposed administration of contraception to a female person who did not have the capacity herself to consent to it.(295)

It may be implied from the Guardianship and Administration Act 1990 (WA) that sterilisation of a person is treatment for the purposes of the Act, but that a "person responsible" may not consent to that treatment.(296) Sterilisation is dealt with under Part 5, Division 3 of the Act. It is also dealt with in Chapter 15.

If a patient, that is a person who needs treatment, is unable to make reasonable judgments relating to any treatment proposed for them, their "person responsible" may make the treatment decision for them, subject to certain exceptions as to the nature of the treatment and other matters discussed below.

12.8.3 The types of treatment

The Guardianship and Administration Act 1990 (WA) does not differentiate between major and minor medical treatment for the purposes of substitute consent by a person responsible as the NSW legislation does. However, it provides specifically for urgently needed treatment and sterilisation treatment.

12.8.3.1 Urgent treatment

Urgent treatment includes both medical and dental treatment as well as any other treatment as defined in s 3 of the Act. It also includes those treatments described as medical treatments in 12.8.1 above that are urgently needed by a patient to:
  1. save their life;
  2. prevent serious damage to their health; or
  3. prevent them from suffering or continuing to suffer significant pain or distress.(297)

However, urgent treatment does not include sterilisation of the patient.(298)

If a patient, unable to make reasonable judgments about that treatment, needs urgent treatment and:
  1. it is not practicable for the health professional (299) who proposes to provide the treatment to determine whether the patient has an advance care directive containing a treatment decision inconsistent with providing the treatment, and
  2. it is not possible for them to obtain a treatment decision from the patient's tribunal appointed guardian, enduring guardian or person responsible,

the health professional may provide the treatment without first obtaining consent to do so from a substitute decision-maker.(300)

There are specific provisions relating to the provision of urgent treatment after an apparent attempted suicide by a patient.(301)

12.8.3.2 Sterilisation

The term "sterilisation" is not defined in the Guardianship and Administration Act 1990 (WA). However, that Act excludes sterilisation from the definition of urgent treatment, states that persons responsible cannot consent to sterilisation and contains specific provisions about the sterilisation of people under guardianship.(302) In relation to a person under guardianship, a guardian may consent to sterilisation only if a Full Tribunal of WASAT has first given its consent to the proposed procedure for sterilisation.(303) This matter is taken up in more detail in Chapter 15.6.4.

12.8.3.3 Treatment that is not urgent medical or dental treatment

If the proposed medical, dental or other treatment is not urgent or does not involve sterilisation of a person under guardianship, and the patient is unable to make reasonable judgments about that treatment, the treating doctor, dentist or other health professional must deal with the question of consent as set out in 12.8.4. (304)

12.8.4 Who is the substitute decision-maker for medical and dental treatment?

As already noted at 12.8, the first question that arises when a person cannot give a valid consent to their own treatment is, do they have an advance health directive? If do have an advance directive, the next question is whether that advance health directive on a sensible reading of it, contains a treatment decision relevant to the treatment proposed for that person. If so, the treatment provided to that person must be decided according to that treatment decision.(305)

If there is no relevant advance health directive, and the treatment is not urgent as described above at 12.8.3.1, the person who may consent to the proposed treatment as the substitute decision-maker is the first in order of priority of the following:
  1. an enduring guardian of the person needing the treatment who is authorised to make treatment decisions about the treatment, is reasonably available and is willing to make a decision to consent or to refuse consent to the treatment ;
  2. a guardian of the person needing the treatment, appointed by WASAT, and who is authorised to make treatment decisions about the treatment, is reasonably available and is willing to make a decision to consent or to refuse consent to the treatment;(306) ;
  3. the person's spouse or de facto partner who is of full legal capacity, has reached 18 years and is living with the person, who is also reasonably available and is willing to make a decision to consent or to refuse consent to the treatment;
  4. the person's nearest relative who maintains a close personal relationship with the person, has frequent personal contact with them and a genuine interest in their welfare, who is of full legal capacity, who has reached 18 years of age and who is also reasonably available and is willing to make a decision to consent or to refuse consent to the treatment and who is first in the following order of priority of relatives:
    1. their spouse or de facto partner who is not living at home with them,
    2. the person's child,
    3. the person's parent,
    4. a sibling of the person;
  5. the person’s primary provider of care and support, but who is not remunerated for providing that support and who also maintains a close personal relationship with the person, has frequent personal contact with them and a genuine interest in their welfare, who is of full legal capacity, who has reached 18 years of age and who is also reasonably available and is willing to make a decision to consent or to refuse consent to the treatment; and
  6. finally, a person who maintains a close personal relationship with the person, has frequent personal contact with them and a genuine interest in their welfare, who is of full legal capacity, who has reached 18 years of age and who is also reasonably available and is willing to make a decision to consent or to refuse consent to the treatment.(307)

Because of the reasonable availability requirement in particular, it is possible that different people will be the person responsible for an incapable person on different occasions when that person needs treatment.(308) Also while WASAT has the power to declare who is the person responsible of a patient, it has pointed out that it can do so only in relation to the treatment that is proposed for the patient at the time it makes the declaration.(309)In the same case, WASAT expressed the view that when declaring who was person responsible for a particular treatment decision, it could identify only a single person.(310)

It is the obligation of every person when acting as person responsible and making a treatment to act according to their opinion of the best interests of the person needing the treatment.(311)

12.9 Australian Capital Territory

The Australian Capital Territory's comprehensive regime for substitute decision-making in relation to the medical and dental treatment of those unable to give a valid consent to their own treatment came into operation 2 February 2009.(312)

12.9.1 Medical and dental treatment defined

In the Australian Capital Territory medical treatment is defined to include dental treatment and to include any medical procedure or treatment as well a series of procedures or a course of treatment.(313) It does not include prescribed medical procedures.(314) Consent to the carrying out of these procedures cannot be given under the substitute consent regime. This matter will be returned to in 12.9.3.2.

A person cannot give a valid consent to their own medical or dental treatment if they have impaired decision-making ability for giving consent to medical treatment.(315) Such impaired ability is defined as: a person's decision-making ability that is impaired because of a physical, mental, psychological or intellectual condition or state, whether or not the condition or state is a diagnosable illness.(316)

In the Australian Capital Territory substitute consent must be obtained for all treatments under the new legislative regime unless the treatment can be given in accordance with the Medical Treatment Act 2006 (ACT), is urgent or is a prescribed medical procedure. The latter two forms of treatment will be returned to below at 12.9.3.1 and 12.9.3.2 respectively. The Medical Treatment Act 2006 (ACT) is discussed further in 12.9.5.1 and in Chapter 13 at 13.4.4 and 13.5.4.

12.9.3.1 Urgent medical treatment

Urgent medical treatment is not defined in the Guardianship and Management of Property Act 1991 (ACT), but the substitute consent regime contained in it is stated not to affect "any common law right of a health professional to provide urgent medical treatment without consent". (317) The ACT Public Advocate suggests that treatment that is necessary to preserve the life of the patient or to prevent "serious morbidity" would be urgent medical treatment. (318) In New South Wales, as well as Tasmania, the statutory definition of urgent treatment is treatment that is necessary, as a matter of urgency to save the incapable person's life, or prevent serious damage to their health, or to prevent them from suffering or continuing to suffer significant pain or distress. (319) It is suggested that this broader definition could be adopted into the Australian Capital Territory and exercised in accordance with the experience of the ethical practices developed in those States as an appropriate way for doctors to decide whether treatment is urgent or not. It is also suggested that consideration be given to the concept of necessity. (320)

12.9.3.2 Prescribed treatments

The Guardianship and Management of Property Act 1991 (ACT) has prescribed a number of medical treatments and provided the process for obtaining consent to the carrying out of those treatments. The prescribed medical treatments are:
  1. abortion
  2. reproductive sterilisation
  3. hysterectomy
  4. medical procedures concerned with contraception
  5. removal of non-regenerative tissue for transplantation to the body of another living person
  6. treatment for mental illness, electroconvulsive therapy or psychiatric surgery.(321)

However, treatment for mental illness, including electroconvulsive therapy and psychiatric surgery, is dealt with under the Mental Health (Treatment and Care) Act 1994 (ACT).(322)

The process requires that first the Australian Capital Territory Civil and Administrative Tribunal (ACAT) appoints a guardian for the person unable to give a valid consent to their own treatment and then make a declaration that the person the subject of the guardianship order is "not competent to give a consent required for a prescribed medical procedure".(323)

The ACAT appointed guardian then applies to ACAT for an order consenting to the prescribed medical procedure proposed for the person under their guardianship. The guardian, the person under guardianship and any other person whom ACAT considers should have notice the hearing of an application are given notice of, and may attend, the hearing. After hearing the evidence, ACAT considers whether or not it should consent to a prescribed medical procedure for the person under guardianship if it is satisfied that:

  1. the procedure is otherwise lawful; and
  2. the person is not competent to give consent and is not likely to become competent in the foreseeable future; and
  3. the procedure would be in the person's best interests.(324)

12.9.4 Who is the substitute decision-maker for medical (and dental) treatment?

In most cases since 2 February 2009 the automatic substitute decision-maker for an adult person unable to give a valid consent to their own medical or dental treatment is, in order of precedence:

  1. the person's guardian appointed by the ACAT with authority to give consent to medical treatment,
  2. the person's enduring attorney with authority to give consent to medical treatment appointed either under the Powers of Attorney Act 2006 (ACT) or a law of a State or the Northern Territory that substantially corresponds with that Act,
  3. a health attorney for the person.(325)

The term health attorney is further defined in a "priority order" to mean a capable adult who is:

  1. the person's domestic partner who is in a close and continuing partnership with the person,(326)
  2. the person's carer,(327)
  3. a close relative or friend of the incapable person.(328)

Treating doctors and dentists are given a discretion to seek consent from the health attorney they believe is best able to represent the views of the now incapable person.(329) However, they must consider the health attorneys in priority order but may take into account any circumstance they believe, on reasonable grounds, is relevant, particularly how readily available a particular health attorney is. They need not consider a health attorney if they believe, on reasonable grounds, that that health attorney is not a suitable person to consent to medical treatment for the now incapable person. But they must make a record of the reasons for their belief.(330)

Another approach to the problem of unavailable or unsuitable health attorneys or where the person does not have a health attorney, is for the treating doctor to apply to the ACAT to appoint the Public Advocate as an emergency guardian for 10 days with authority to give consent to medical treatment on behalf of the now incapable person.(331)

If a doctor or dentist asks a health attorney to consent to medical treatment for a person, they must give the health attorney information about the following matters:
  1. the reasons why the person has impaired capacity for giving consent to treatment,
  2. their condition,
  3. the treatment for which consent is sought,
  4. any alternative treatment that is available,
  5. the nature and likely effect of the treatment for which consent is sought and any alternative treatment,
  6. the nature and degree of any significant risks involved with the treatment for which consent is sought and any alternative treatment,
  7. the likely effect of not providing the treatment,
  8. the decision-making principles,(332) and
  9. any other matter that the doctor or dentist believes, on reasonable grounds, is relevant to the provision of consent for the treatment.(333)

12.9.5 Objections to treatment

12.9.5.1 Objections by the incapable person

Objection to the proposed treatment by the incapable person is not addressed by the legislation. If the objection is in the form of a common law advance directive that is relevant to the person's current situation, it should be followed. If the now incapable person has made a health direction under the Medical Treatment (Health Directions) Act 2006 that is relevant to their current situation, it should be followed the extent possible under that Act. If their objection to the proposed treatment is known, but is not one of these, it must, nevertheless, be given effect to under the principles to be followed by (substitute) decision-makers under the Guardianship and Management of Property Act 1991 (ACT) unless, making the decision in accordance with those wishes is likely to significantly adversely affect the now incapable person's interests.(334)

12.9.5.2 Objections by health attorneys

Such objections may delay but not necessarily preclude the treatment from being given. If a doctor or dentist requests a health attorney to give consent to treatment and the health attorney refuses to give the consent, the doctor or dentist must refer the matter to the Public Advocate. If the Public Advocate considers the refusal reasonable, she must take no further action. Otherwise she must apply to the ACAT to be appointed as the guardian for the incapable person.(335)

12.9.5.3 Objections in the form of disagreements between health attorneys

If a doctor or dentist seeks substitute consent to treatment from the health attorney they believe is best able to represent the views of the incapable person, but they become aware that one or more of the other health attorneys for the person objects to the giving of consent, the doctor or dentist must refer the matter to the Public Advocate. The Public Advocate may then either:
  1. try to help the available health attorneys reach agreement about consent, or
  2. apply to the ACAT to be appointed as guardian for the incapable person, or
  3. do both.(336)

As already noted a doctor or dentist is not required to seek the views of other health attorneys for an incapable person before obtaining the consent of the health attorney that they believe, on reasonable grounds, is best able to represent the views of the incapable person.(337) Consequently, while they may avoid becoming aware of the objections of other health attorneys, if they do become aware of such an objection, they must refer the matter to the Public Guardian.

12.10 Northern Territory

The Advance Personal Planning Act (NT), which came into force on 17 March 2014, provides for anyone 18 years and above to make advance consent decisions about their future health care and to appoint decision makers to make substitute decisions for them concerning any health care not covered by any advance consent decisions they may have set out in the advance care plan they made under that Act.(338) We deal with the making of advance personal plans in Chapter 13.5.2 and with advance care decisions and advance care statements in Chapter 13.5.2.4.

In this Chapter we deal with that Act and its role in relation to consent to health care in some detail below. The term “health care” covers much more than medical or dental treatment; see 12.10.2, below.

However, it is likely that many people will not have made an advance personal plan covering health under the new Act or even if they have made such a plan, not made any advance care decisions or advance care statements in it, nor appointed a “decision maker” in it. As a consequence we need to look at how the Act deals with consent to health care where advance personal plans have been made and where they haven’t been made, or do not apply in the circumstances to hand.

We suggest that where a person has not made an advance care plan, or that the plan they have made does not apply to the circumstances that are to hand and other provisions of the Act do not apply, health care providers have to fall back on the common law that has developed in relation to consent to medical treatment and the ethical standards developed by the different health care professions in relation consent to medical treatment and the giving, refusing to give, and the withdrawal of medical treatment. These matters are taken up in 12.10.12, below.

The new legislative scheme in the Northern Territory does not provide a comprehensive regime for substitute consent to health care treatment of the kind that is provided for in, say, Victoria, or in the other States and the Australian Capital Territory, relation to medical and dental treatment. Except in relation to restricted health matters. It does not cover people who, because of intellectual disability, have never had the capacity to consent to their own medical treatment or other health care, or to appointment someone else to make those decisions for them. Nor does the Act cover people who lose decision-making capacity due to acquired brain injury, dementia or psychiatric condition who do not make advance personal plans under the Act before they lose the capacity to do so. Those with episodic mental illnesses will however be able to make their own advance personal plans when they are well and have what the Act calls “planning capacity”.(339)

Nevertheless, the Advance Personal Planning Act (NT) is an important step forward as it provides the processes by which adults in the Northern Territory may make advance consent decisions about future health care action and appoint their own (substitute) decision makers. It is important to appreciate that the Act also provides for the makers of advance personal plans to make advance care statements setting out their views, wishes and beliefs as a basis for their decision makers making decisions about a wide range of matters including care and welfare matters and financial matters.(340)

The Act itself is clear that it does not authorise a person to take health care action in relation to a person (give treatment) unable to give a valid consent to their own treatment because of impaired decision-making capacity in relation to that matter unless it would be lawful to take that health care action in relation to that person if they themselves gave a valid consent to the taking of the health care action.(341)

It is also clear from the Act that a person cannot make an advance consent decision, nor can a decision maker or guardian appointed under the Act or by the Northern Territory Civil and Administrative Tribunal (NTCAT) consent to health care action, that would be unlawful if it were undertaken. Also the Act states in terms that it; “does not permit the form of intentional killing of another called euthanasia or the assisting of a person to terminate his or her life”.(342)

12.10.1 The making of advance personal plans that cover health care matters either only or together with care and welfare matters (and financial matters)

In the Northern Territory, in order for an adult (those 18 years and older) to make an advance personal plan, they must have planning capacity in order to do so. The Advance Personal Planning Act (NT) provides that an adult has planning capacity if they:
  1. have decision-making capacity for making an advance personal plan; and
  2. do not have a guardian appointed for them by NTCAT.(343) See also 12.10.4, below.
An adult with decision-making capacity (for making an advance personal plan) may set out in their advance personal plan the future health care actions they want taken in relation to them when their decision-making capacity in relation to those matters becomes impaired so that they cannot make those decisions. Such a statement is called an advance consent decision.(344)

However the Act states that, a statement in an advance personal plan about health care action constitutes an advance consent decision if:
  1. it is an express statement of the maker's consent or refusal of consent for the health care action; or
  2. it would be reasonable to conclude from the statement that the maker would or would not want the health care action to be taken in the circumstances that exist at the time it is proposed to take the health care action.(345)
The scope of consent decisions about health care action, whether they be advance consent decisions made in an advance personal plan or made by a decision-maker, is set out in 12.10.3, below.

The maker of an advance personal plan may also appoint a decision maker to make decisions for them. The maker may also set out their views, wishes and beliefs as the basis on which their appointed decision maker (or anyone else) is to act if they make decisions for the maker. These are called advance care statements.(346) When making decisions under an advance personal plan, the decision maker must act in accordance with the decision-making principles set out in the Act.(347) Those decision-making principles set out and discussed in some detail in Chapter 9. 4. 6.

12.10.2 Health care and health and health care action (treatment) described

Health care is very broadly defined in the Act to mean health care of any kind that that is part of a health service defined in the s. 5 of the Health Practitioner Regulation National Law. Health care action means commencing, continuing, withholding or withdrawing health care for the adult.(348)

12.10.3 The scope of decisions about health care action

The scope of consent decisions about health care action, whether they be advance consent decisions made in an advance personal plan or made by a decision-maker, or a guardian appointed by NTCAT, is very wide. They may be made:
  1. in relation to health care to be provided in a particular instance or a course of health care to be provided over a period of time; and
  2. about one or more particular health care actions or generally about all health care action; and
  3. so as to apply;
    1. in all circumstances; or
    2. only in stated circumstances; or
    3. in all circumstances except in stated circumstances.(349)

The language of the Advance Personal Planning Act (NT) is not always consistent with the normal way of describing things, because so many different issues are being covered in the Act. So decision- making capacity for a matter when the matter is health care action means capacity to consent to the proposed (medical) treatment or treatment by another health professional. However, the test for that capacity in the Act is a restatement of the established common law test and consistent with the test used in the other States and Territories. The test is that a person has decision-making capacity for a matter if they have the capacity to:
  1. understand and retain information about the matter; and
  2. weigh the information in order to make a decision about the matter; and
  3. communicate that decision in some way.(350)
Also the Act restates the common law, namely a person 18 years or older is presumed to have decision-making capacity for a matter until the contrary is shown.(351) The Act notes that a person has impaired decision-making capacity for a matter if their decision-making capacity for that matter is impaired; but it points out that the cause of the impairment is immaterial.(352) The Act further notes that a person does not have impaired decision-making capacity for a matter only because of a range of matters that either do not, or may not necessarily, impair decision-making capacity.(353)

12.10.5.1 Where the patient has decision-making capacity for the proposed treatment (health care action)

If the patient has decision-making capacity for the proposed treatment (health care action), then the patient may give their own consent to that treatment; and that consent may be inconsistent with the advance consent decision in the patient’s advance personal plan.

12.10.5.2 Where the patient has impaired decision-making capacity for the proposed treatment (health care action) and has made a relevant advanced care decision in an advance personal plan; but has not appointed a decision maker

If the patient has impaired decision-making capacity for the proposed treatment (health care action) and the proposed treatment is consistent with the advance consent decision in the patient’s advance personal plan, then the health care provider may give or carry out the proposed treatment (health care action). The Act notes that when the health care provider does this, they will be taken for all purposes, to have taken the health care action with the consent of the patient. Also the advance consent decision relied on by the health care provider is treated as having effect as if it had been made as a current decision by the maker, with full legal capacity and fully informed, at the time the health care provider proposed that the health care action be carried out.(354)

Note that while the primary source of advance consent decisions is the advance personal plans made by patients when they had planning capacity, another source that will dwindle away over time is the directions in the now repealed Natural Death Act (NT). This is because the Advance Personal Planning Act (NT) provides that, when it came into force, an existing direction made under the now repealed Natural Death Act (NT), became an advance personal plan that contains an advance consent decision in accordance with its terms.(355) The now repealed Act provided that capable adults who desired not to be subjected to medical or surgical measures that would prolong or are intended to prolong life in the event of them suffering from a terminal illness could make a direction in a formal manner. The Act also specifically stated that it did not affect the rights of a capable person to refuse medical or surgical treatment.

Directions made under the Natural Death Act (NT) that are still in existence are also dealt with in Chapters 13.1, 13.4, 13. 4.2 and 13.5.2 and Chapter 14.4.4.

12.10.5.3 Where the patient has impaired decision-making capacity for the proposed treatment (health care action) and has made a relevant advanced care decision in an advance personal plan and has appointed a decision maker

If a decision maker has been appointed in the advance personal plan with authority in relation to health care matters, that decision maker will be able to exercise the authority given them in the plan by the maker, in relation to those matters for which the maker has impaired decision-making capacity.(356) If the plan contains an advance consent decision concerning health care action that needs to be given effect to, it is part of the decision maker’s role to seek out who can provide the health care action and give the relevant consent for it to be carried out.

In relation to emergency treatment. Where the issue of emergency treatment arises in circumstances in which the patient had made an advance consent decision to refuse the proposed treatment and NTCAT has not ordered that the advance care decision may be disregarded (or the health care provider does not know that such an order had been made), the health care provider should not commence or continue the treatment contrary to the patient’s advance consent decision. If the health provider commences or continues the treatment in contrary to the patient’s advance decision, they expose themselves to a charge of common assault at least. However, if the health care action is an operation as defined in the Emergency Medical Operations Act (NT), that Act applies. But that Act states that a doctor is not entitled to perform an operation under that Act where the circumstances outlined earlier in this paragraph apply. See 12. 10. 11. 1, below.

One of the many provisions of the Act that confirms the centrality of the policy that the wishes of the patient about health care action (treatment) proposed for them are to be complied with wherever possible is s. 41(1). It provides that an advance consent decision has effect for all purposes as if that advance decision had been made as a current decision by the adult at the time it was proposed that the health care action be carried out. And further, as if at that time, the patient had full legal capacity and was fully informed about the health care action, when in fact they were not because they lacked decision-making capacity for the proposed treatment.

However, same section of the Act also supplies the mechanism for dealing with advance consent decisions that are either seriously inappropriate in themselves or are seriously inappropriate for other reasons that may not have been appreciated by the patient when they made the advance consent decision. NTCAT may order that the advance consent decision be disregarded, but only if it is satisfied that:
  1. there is no reasonable possibility that the adult would have intended the advance consent decision to apply in the circumstances; or
  2. taking health care action in reliance on the advance consent decision,
    1. would cause the patient unacceptable pain and suffering; or
    2. would otherwise be so wholly unreasonable that it is justifiable to override the patient's wishes.(357)
We suggest that, unless NTCAT orders that the patient’s advance consent decision is to be disregarded, the patient’s advance consent decision is to take effect according to its terms, as no one else may make a decision about the health care action consented to by the person to be treated by operation of their advance consent decision.(358) Consequently, depending on the terms of the advance consent decision, the proposed health care would be commenced or continued if it had already been commenced or withheld if it had not been commenced, and withdrawn if it had already been commenced.

If the plan does not contain any (or any relevant) advance consent decision (or an advance consent decision that NTCAT has ordered to be disregarded), but contains advance care statements containing the maker’s views and wishes in relation to health care action, it is part of the role of the decision maker to give effect to those views and wishes insofar as they relate to the health care action under consideration. This is the effect of the decision-making principles set out in Advance Personal Planning Act (NT).(359) Those principles set out and discussed in some detail in Chapter 9. 4. 6.

Where the maker of an advance personal plan lacks decision-making capacity in relation to proposed health care action, the health care provider seeking consent in order to take the health care action must seek the consent of the decision maker to carry out the health care action.(360)

However, the Advance Personal Planning Act (NT) requires the decision maker to be both willing and able to make an informed consent decision about health care action proposed. In order to be willing and able to make that decision, the Act requires the decision maker to:
  1. have authority to make a consent decision about the health care action; and
  2. have unimpaired decision-making capacity for the health care action; and
  3. be reasonably available; and
  4. be willing to make the consent decision; and
  5. understand a decision maker's obligation to act in accordance with the decision-making principles set out in the Act; and
  6. have all the information they reasonably need to make a balanced decision about the health care action; and
  7. have had adequate time to consider that information; and
  8. understand the effect of making the consent decision; and
  9. be able to make the consent decision voluntarily and without undue influence from any person.(361)

In that situation, or where an adult person, who has not made an advance personal plan, lacks decision-making capacity in relation to proposed health care action, NTCAT may appoint a guardian for that person and give authority to the guardian to consent to the carrying out the health care on the person the subject of the guardianship order. However NTCAT may decide to make the treatment decision itself.(362)

12.10.7.1 Where NTCAT appoints a guardian

There will be a range of situations in which NTCAT will decide to appoint a guardian for a person and that guardian will need the authority to make decisions in relation to health care matters, including health care action in relation to the person they are appointed guardian for. In such a situation could be where NTCAT considered it appropriate to revoke an advance personal plan made by a person and appoint a guardian with powers in relation to health care.

If NTCAT appoints the Public Guardian as an adult person’s guardian, under a full, conditional or temporary order, and gives the Public Guardian authority to make informed consent decisions about health care action proposed for the person the subject of the guardianship order, the Public Guardian may carry out that role without further ado.

However, where NTCAT appoints a private person as the person’s guardian, the Advance Personal Planning Act (NT) requires the guardian to be both willing and able to make an informed consent decision about any health care action proposed by a health care provider. In order to be willing and able to make that decision, the Act requires the guardian to:
  1. have authority to make a consent decision about the health care action; and
  2. have unimpaired decision-making capacity for the health care action; and
  3. be reasonably available; and
  4. be willing to make the consent decision; and
  5. understand a guardian's obligation to act in accordance with sections 4, and 21 to 23 of the Guardianship Adults Act (NT); and
  6. have all the information they reasonably need to make a balanced decision about the health care action; and
  7. have had adequate time to consider that information; and
  8. understand the effect of making the consent decision; and
  9. be able to make the consent decision voluntarily and without undue influence from any person.(363)
If NTCAT has exercised its limited jurisdiction to terminate the appointment of a decision maker for health care matters, it may appoint a guardian for that person and give the guardian authority to consent to the carrying out the health care on the person the subject of the guardianship order. However, as noted in Chapter 10. 11. 8. 1, where a maker of an advance personal plan has appointed a decision maker in their plan, NTCAT may amend the plan so as to terminate the appointment of a person as a decision maker only if satisfied that doing so is the only practicable way to address the grounds for amendment of the plan.

However note that health care action for restricted health care is excluded from this process. This is because the relevant legislation specifically precludes both decision makers appointed under advance personal plans or guardians appointed by NTCAT from making consent decisions about health care action for restricted health care.(364) The question of who may consent to health care action for restricted health care is taken up at 12.10.8.2, below.

In relation to the decisions about health care or health care action in particular that a guardian appointed by NTCAT is authorised to make, the guardian must exercise that authority in accordance with the guardianship principles set out in the Guardianship of Adults Act (NT). The principles which are, or could be, relevant to health care action are:
  1. the guardian must exercise their authority in the way that they reasonably believe is in the best interests of the person the order is about (the patient);
  2. in determining what is in the patient's best interests, the guardian must: seek;
    1. to obtain the patient's current views and wishes, as far as it is practicable to do so; and
    2. to take into account all relevant considerations; and
    3. to weigh up the relevant considerations, giving each of them the weight that the decision maker reasonably believes is appropriate in the circumstances.
  3. in determining what is appropriate in the circumstances, the guardian must ensure that their authority is exercised in a way that;
    1. is the least restrictive of the adult's freedom of decision and action as is practicable; and
    2. provides the adult with as much support as is practicable to make the adult's own decisions.
  4. the relevant considerations include, but are not limited to, the following;
    1. the patient's current views and wishes and previously stated views and wishes;
    2. any views and wishes stated by an interested person for the patient;
    3. maintenance of the patient's freedom of decision and action to the greatest extent practicable;
    4. the ability of the patient to be as independent as is practicable;
    5. protection of the adult from harm, neglect, abuse and exploitation;
    6. the provision to the patient of appropriate care, including health care;
    7. promotion of the patient's happiness, enjoyment of life and wellbeing;
    8. the ability of the patient to achieve their maximum physical, social, emotional and intellectual potential;
    9. the ability of the patient to live in the general community and take part in community activities;
    10. maintenance of the patient's right to be treated with dignity and respect;
    11. the ability of the patient to maintain their preferred living environment and lifestyle;
    12. maintenance or creation of a support network for the patient;(365)
However, if the patient has made an advance care statement, the guardian must exercise their authority under the Act so as to give effect to the statement even if doing so is not in patient's best interests, unless:
  1. the patient, having capacity to do so, states that they do not want that statement to be given effect; or
  2. exercising substituted judgment;
    1. is impracticable or
    2. would be unlawful or
    3. would impose a burden on another person that is so unreasonably onerous that it is justifiable to override the patient's wishes;
    4. in the case of giving effect to an advance care statement – there is no reasonable possibility the patient would have intended the statement to apply in the circumstances;
    5. exercising substituted judgment would be so unreasonable that it is justifiable to override the adult's wishes.(366)
If, in reliance one or more of the matters set out above, the guardian does not exercise substituted judgment, they must keep a written record of having done so and the grounds on which the decision maker formed the required reasonable belief in relation to the matter.(367)

12.10.8.1 Health care action other than restricted health care action

NTCAT may make a consent decision about proposed health care action if:
  1. the patient has not made an advance consent decision about the proposed health care action; or
  2. NTCAT has made an order that the adult's advance consent decision be disregarded; and
  3. there is no available consenter (i. e. decision maker or adult guardian) who is willing and able to make a consent decision about the health care action.(368)
Note that if NTCAT makes a consent decision in relation to a course of health care action to be provided over a period of time, a later consent decision to withhold or withdraw the health care may be made only by NTCAT or by a decision maker or guardian authorised by NTCAT to make that decision.(369)

We suggest that in coming to its decision in relation to the proposed health care action, NTCAT would consider the views wishes and beliefs of the patient if the patient had made them known in an advance care statement in their advance personal plan, together with any other matters NCAT considered among the decision-making principles in the Advance Personal Planning Act (NT) and the relevant guardianship principles set out in the Guardianship of Adults Act (NT). For the relevant guardianship principles set out in the Guardianship of Adults Act (NT) see, 12. 10. 7, above.

12.10.8.2 Restricted health care action

Each of the following health care actions constitute restricted health care in the Northern Territory:
  1. sterilisation of an adult, that is, any procedure that is intended, or is reasonably likely, to have the effect of rendering the adult infertile, unless it occurs as a consequence of health care action that is taken primarily to treat an illness of or injury to the adult;
  2. termination of a pregnancy of an adult, unless it occurs as a consequence of health care action that is taken primarily to treat an illness of or injury to the adult;
  3. removal from an adult of non-regenerative tissue for transplantation to another person;
  4. health care provided for medical research purposes;
  5. new health care of a kind that is not yet accepted as evidence-based, best practice health care by a substantial number of health care providers specialising in the relevant area of health care;
  6. electroconvulsive therapy;
  7. health care prescribed by regulation to be restricted health care.(370)
We note that, in reality, it is very unlikely that an adult for whom a sterilising operation or a termination would be proposed under the provisions of the Advance Personal Planning Act (NT) would have the “planning capacity” to make an advance personal plan.(371) However, in relation to the removal of non-regenerative tissue, new health care or electroconvulsive therapy, the person proposed to be treated may well have made an advance personal plan with relevant advance consent decisions or advance care statements in it.

Consistent with the situation in the States and the Australian Capital Territory, neither decision makers appointed in advance personal plans nor guardians appointed by NTCAT may consent to health care action in relation to restricted health care.(372)

The final paragraph of the note to s. 23 of the Guardianship of Adults Act (NT) points out that, if health care action needs to be taken, and there is no advance consent decision and no guardian or decision maker with authority to make a consent decision, the guardian (without authority to make a consent decision) may apply to NTCAT under the Advance Personal Planning Act (NT) for NTCAT to make the consent decision.

NTCAT has jurisdiction to deal with matters under the Advance Personal Planning Act (NT). But that Act provides that both the affected adult person or “an interested person for the affected adult” may apply to NTCAT to exercise its jurisdiction to deal with matters under the Act. The list of interested persons includes not only a guardian but also a decision maker, a health care provider, the Public Guardian and any other person who has a genuine and sufficient interest in protecting the person's best interests, as well as others.(373)

NTCAT is required, when exercising jurisdiction under the Act, to act in accordance with the decision-making principles, set out in the Act, as if it were a decision maker. Those principles require NTCAT, in the event that the person has made an advance care statement about the matter (the restricted health care action proposed), to make its decision on the application so as to give effect to the statement in a way that NTCAT reasonably believes the maker of the statement would have given effect to it in the circumstances. If the person has not made a relevant advance care statement NTCAT must make its decision in the way that it reasonably believes the person would have in the circumstances.

Consistent with the policy of the Act of giving effect to decisions that the person would have made if they had the capacity to do so, NTCAT is required to make its decision in the way it reasonably believes the person would have done in the circumstances, even if the decision so made may not be in the person’s best interests.

If NTCAT is unable to form a reasonable belief about what the person would have done in the circumstances, it must make its decision in the way it reasonably believes is in the person's best interests. In doing that NTCAT must take into account all relevant considerations weighing up those considerations, giving each of them the weight that it reasonably believes is appropriate in the circumstances.

There is a non-exclusive list relevant considerations in the Act. The full list is set out below as follows:
  1. protection of the person from harm, neglect, abuse and exploitation;
  2. providing the person with appropriate care, including the taking of appropriate health care action;
  3. promotion of the adult's happiness, enjoyment of life and wellbeing;
  4. protecting the person's freedom of decision and action;
  5. the ability of the person to be as independent as is practicable;
  6. the ability of the person to achieve their maximum physical, social, emotional and intellectual potential;
  7. the ability of the person to live in the general community and take part in community activities;
  8. maintenance of the person's right to be treated with dignity and respect;
  9. the ability of the person to maintain their preferred living environment and lifestyle;
  10. maintenance or creation of a positive support network for the person;
  11. protection of the person's property and financial resources from loss, damage or misuse;
  12. protection of the person's right to confidentiality of information about him or her.(374)
The issue of sterilisation is taken up in more detail in Chapter 15; and in relation to the Northern Territory at 15.6.8 in particular.

Consistent with the policy of the Advance Personal Planning Act (NT) to render any advance consent decision about the proposed health care action made by the patient effective wherever possible, the Act provides that if a person has a right under another law of the Northern Territory to make a consent decision about health care action proposed for the patient, they may exercise that right only if:
  1. the patient has not made an advance consent decision about the proposed health care action, or NTCAT has ordered that the patient's advance consent decision be disregarded; and
  2. there is no decision maker appointed by the patient or a guardian appointed by NTCAT available who is willing and able to make a consent decision about the health care action in the exercise of their authority under the Act and
  3. where NTCAT has not made a consent decision about the health care action in the exercise of its jurisdiction under the Act.(375)
These are very strict limits on the ability of a person to make a consent decision about health care action proposed for the patient under another law. However, the Act goes on to state that this provision not affect any power under another law of the Northern Territory of a court, tribunal or statutory office holder to order that health care action be taken for an adult without the consent of the adult. We suggest that that means that the Mental Health Act (NT) and certain legislation relating to public health that would operate according to its terms and not be affected by the Advance Personal Planning Act (NT).

The substitute consent provisions of the Advance Personal Planning Act (NT) clearly reflect the fundamental policy of the Act, namely that the advance consent decisions of the patient made in their advance personal plan are to be given effect to unless disallowed by the Act or are ordered to be disregarded by NTCAT. Even then, or when the patient has expressed views, wishes or beliefs either in their plan or elsewhere these are to be given effect to or at least considered. We summarise the way that works out in the legislation, as follows:
  1. consent by the patient by way of an advance consent decision;
  2. by a decision maker appointed by the patient in their advance personal plan (but subject obligations to either act upon or consider the views, wishes and beliefs of the patient);
  3. by an adult guardian (subject to obligations similar to those of a decision maker);
  4. by NTCAT (we suggest subject to the kinds of obligations on a decision maker or guardian (appointed by NTCAT) where NTCAT has become the default consent authority); or
  5. by NTCAT when the proposed health care action is restricted health care action; or by a person with a right to do so under another law.

12.10.11 Emergency health care

As there are currently no provisions in Northern Territory legislation dealing generally with emergency/urgent and necessary health care, we suggest that any treatment not covered by the Emergency Medical Operations Act (NT) will be covered by the common law, which we deal with in 12.10.11.2, below.

12.10.11.1 Treatment under the Emergency Medical Operations Act (NT)

The Emergency Medical Operations Act (NT) deals only with surgical operations and the administration of an anaesthetic and blood transfusions. It provides that where a doctor is of the opinion that an adult (or a child) is in danger of dying or suffering a serious, permanent disability and the performance of the surgical operation or blood transfusion is desirable in order to prevent the death of the person or the disability occurring, then the doctor may perform the operation. However, if the patient has impaired decision-making capacity for the operation proposed, a doctor is not entitled to perform the operation unless they are of the opinion that it is not practicable to delay performing the operation to find out whether the patient has made an advance consent decision about the operation, or consent to carry out the operation can be obtained from a decision maker appointed by the patient in an advance personal plan of from a guardian appointed for the patient by NTCAT or from NTCAT itself or from another person who has a right under another law of the Territory to make a consent decision about the operation.

However note, if the patient has made an advance consent decision about the operation and that decision is to refuse the operation, the treating doctor may not perform that operation.

Where an operation is carried out in these circumstances the operation is deemed to have been carried out with the consent of the person authorised by law to give consent. The doctors carrying out the operation are protected against liability arising from the lack of consent but not from liability arising from performance of the operation.

12.10.11.2 Emergency/urgent and necessary health care at common law

Where there is an urgent need for health care, the common law, as set out in 12. 2 above, will apply in the absence of legislation. In New South Wales, as well as Victoria and Tasmania, the statutory definition of urgent treatment is treatment that is necessary, as a matter of urgency to save the incapable person's life, or prevent serious damage to their health, or to prevent them from suffering or continuing to suffer significant pain or distress.(376) This broad definition could be adopted by judicial decision in the Northern Territory and exercised in accordance with the experience of the ethical practices developed in those States that have provisions about urgent and necessary treatment in their legislation.

Another approach that has some currency in the Northern Territory is to carry out treatment that is urgent and necessary to save life or prevent serious damage to health on a person incapable of giving a valid consent to their own treatment under the extended principle of necessity referred to at the commencement of this chapter at 12.2.1.

The legislation covers the situation where a person has made an advance personal plan and appointed a decision maker with authority to make decisions in relation to health care action (treatment) for the maker when they lack decision-making capacity for the proposed treatment. The situation is also covered where the maker has included a relevant advance consent decision in their plan. It is also covered where NCAT appoints a guardian with authority to make consent decisions in relation to health care action proposed for the maker. Restricted health care action is also covered and so is emergency health care action.

What is not covered is health care action where the patient does not have a relevant advance personal plan, or a decision maker or guardian and the treatment is neither urgent and necessary nor restricted. Because of the very broad definition of health care in the Advance Personal Planning Act (NT), a great many proposed operations, procedures, treatments, courses of medication and so on that fit the definition and are appropriate to carry out on people unable to give a valid consent to the health care action on a non-urgent basis and are needed to restore those people to good health or to maintain them in good health.

As already noted at 12. 10. 8, NCAT can make decisions about health care action proposed by health providers. Also medical practitioners may make applications to NTCAT for urgent consent decisions in relation to their own patients. If the medical practitioner states in their application that they reasonably believe that a consent decision about the proposed health care action is urgently required, NTCAT must make the decision within 24 hours of receiving the decision or, if satisfied that a consent decision is not urgently required, adjourn the application to be dealt with as an ordinary application on for a consent decision in relation to health care action.

We also note that there is a special provision in the Advance Personal Planning Act (NT) (s 52) dealing with the situation where a health care provider, who is a registered as a health practitioner of a profession covered by the Health Practitioner Regulation National Law, takes health care action other than in reliance on consent given in accordance with an advance consent decision in the patient’s advance personal plan. That special provision renders the actions taken by the health care provider unprofessional conduct. However, that provision applies only where the health care provider ignores the patient’s advance consent decision and provides health care action (treatment) inconsistent with that decision.

It could be argued that “health care” and “health care action”, as defined in the Advance Personal Planning Act (NT) do not include non-intrusive examinations made for diagnostic purposes including visual examinations of the mouth, throat, nasal cavity, eyes or ears, first-aid medical or dental treatments, and drugs for which a prescription is not required and which are normally self-administered when they are being used for the purpose, and in accordance with the dosage level, recommended in the manufacturer's instructions. These forms of treatment are excluded from the definition of treatment in New South Wales and Tasmania so that substitute consent for them is not required.

In all the States and the Australian Capital Territory, there are automatic substitute decision-makers for medical and dental treatments, when a person has lost, either temporarily or permanently, their capacity to give a valid consent to their own treatment. They are sometimes called “persons responsible”. In Queensland they are called “statutory health attorneys”. In Victoria they are “medical treatment decision makers”.(377)

As there are no provisions in the Northern Territory setting out who can give substitute consent to proposed health care action for a person with decision-making incapacity in relation to that proposed health care action, except for the somewhat exceptional circumstances set out 12. 10. 5 to 12. 10. 11 above, we suggest that health care providers follow the best practice approaches developed in their professions, if they are registered in a health profession (or in their occupation if covered by the definition of health care provider in the Act). In particular, we suggest that they attempt to discover what the person with decision-making incapacity’s view of the proposed health care action was likely to be, based on their previous use of health services, if they had access to that information about that, and the opinions the person expressed about particular treatments or treatments in general when they had capacity. If that information can be provided, it should be considered along with the best interests of the person. The views of relatives, especially those who have responsibilities under customary law for the well-being of the person with the decision-making incapacity, should also be considered, but not so as to override the views or the best interests of the person with the decision-making incapacity.

While a substantial start on legislating for a comprehensive regime for substitute decision-making for those who cannot give a valid consent to some, most or all of the health care action proposed for them has been made, it is import that the process be completed soon. Otherwise people with decision-making disabilities will continue to miss out on receiving health care that they need because of concerns about consent

12.11 Common ground in the legislation and case law of the States

The greatest amount of common ground between the States in relation to substitute consent to medical treatment is found in relation to the test for incapacity to consent to medical or dental treatment and the definitions of medical and dental treatment. By contrast, in relation to objections to treatment, there is a marked contrast between the approach in New South Wales and the approach in Queensland

This test is the same in New South Wales, Tasmania and Victoria. In those States a person is incapable of giving a valid consent to their own medical or dental treatment if:
  1. they are incapable of understanding:
    1. the general nature of the treatment, or
    2. the effect of treatment.(378)

The three part common law test developed by Thorpe J in England which has been adopted in New South Wales is an effective way to assess whether or not a person has capacity to consent to their own treatment. For a person to be capable of giving a valid consent to their own treatment, they must be able to:
  1. take in (and comprehend) and retain the treatment information,
  2. believe that information, and
  3. weigh that information, balancing risks and needs. (weigh it in the balance and arrive at a choice).(379)

Put another way, while the legal standards that define capacity and competency vary in their language, operational definitions of the cognitive elements of capacity usually consist of a combination of the following abilities:
  1. To understand the specific situation, relevant facts or basic information about choices
  2. To evaluate [the] reasonable implications or consequences of making choices
  3. To use reasoned processes to weigh the risks and benefits of the choices
  4. To communicate relatively consistent or stable choices (i.e. make and communicate a stable decision).(380)

The fourth element of capacity, namely the ability to communicate a (consistent) decision is implied in Thorpe J's test, and is a stated requirement in the statutory tests in New South Wales, Tasmania and Victoria.

12.11.2 Definitions of medical and dental treatment

In New South Wales and Tasmania, medical and dental treatment are defined together. They are medical treatment, including any medical or surgical procedure, operation or examination and any prophylactic, palliative or rehabilitative care, normally carried out by, or under, the supervision of a registered practitioner as well as dental treatment (including any dental procedure, operation or examination) normally carried out by or under the supervision of a registered practitioner. They can also include any other act declared in the regulations to be "treatment" as just defined.(381)

In Victoria medical treatment is defined in the same way as in New South Wales and Tasmania while dental treatment is defined as dental treatment (including any dental procedure, operation or examination) normally carried out by or under the supervision of a registered practitioner.(382) In South Australia medical and dental treatment are defined in ways that are very similar to the definitions in the States already mentioned.(383)

In Queensland the role of the substitute decision-maker is broader than elsewhere in Australia. They make decisions relating to "matters relating to health care". Health care is described as, care or treatment of, or a service or a procedure for an adult:
  1. to diagnose, maintain, or treat the adult's physical or mental condition, and
  2. carried out by, or under the direction or supervision of, a health provider.(384)

Health care also includes withholding or withdrawal of a life-sustaining measure if the commencement or continuation of the measure would be inconsistent with good medical practice.(385) While this definition is very similar to the definition of medical and dental treatment in the other States, it applies to the health care provided by a much wider range of health care professional than just doctors and dentists.(386)

In 2005, the then Queensland Guardianship and Administration Tribunal relied on the England and Wales Court of Appeal’s broad view of the definition of medical treatment in the Mental Health Act 1983 (UK) to support its view that seclusion could be a medical treatment.(387) Giving the judgment of the Court of Appeal, Hale LJ noted that the House of Lords had held in Reid v Secretary of State for Scotland that medical treatment could include treatment which alleviated or prevented a deterioration of the symptoms of the disorder, even if the treatment would have no effect on the disorder itself and that similarly, in B v Croydon Health Authority, in the context of the force-feeding an anorexic woman, the Court of Appeal held that doing so was treatment for the mental disorder even if the treatment addressed only the symptoms of anorexia or was ancillary to trying to address the underlying disorder.(388) She then went on to point out that:

[S]ome psychotic patients deteriorate when over stimulated and when interaction with others becomes too intense. Seclusion can reduce their psychotic symptoms by reducing social stimulation. Some patients with persecutory delusions report feeling safer in seclusion.... It can also be said that, in a wider sense, seclusion aimed at addressing the risks to others presented by the behaviour of a patient in the manic phase of a bipolar affective disorder when the behaviour is itself the result of that disorder is treatment 'for' the disorder in the same way that force-feeding the anorexic patient was treatment for her disorder. While her behaviour was purely self-destructive, the consequences of allowing Mr S to persist in behaviour which was damaging to others would also have been damaging to him.

We take the view, therefore, that seclusion is certainly capable of being medical treatment...(389)

The Court of Appeal's decision was overturned by the House of Lords after the Queensland Tribunal had given its decision.(390) While Hale LJ's statement just quoted was not disapproved of by the House of Lords, it is respectfully suggested that, outside Queensland at least, seclusion may not be within the definition of medical treatment. As Lord Steyn pointed out in the House of Lords, the case concerned the use of seclusion in hospitals where mentally disordered patients were detained.(391) Lord Bingham was of the opinion the description of medical treatment in the Mental Health Act 1983 (UK) was wide enough “to cover the nursing and caring for a patient in seclusion, even though seclusion cannot properly form part of a treatment programme”.(392) Lord Hope stated that seclusion was not part of a patient's treatment. Its aim was to contain severely disturbed behaviour and the decision to resort to it was made by a nurse or a doctor and it is supervised by medical staff in the hospital. For that reason it fell well within the scope of the phrase "the medical treatment of patients suffering from mental disorder".(393)

Lord Scott reaffirmed the concerns of the other law lords when he stated:

It is accepted that the only legitimate purpose of placing an inmate in seclusion is the protection of others. Seclusion cannot be used as a punishment nor can it constitute medical treatment, at least in the narrow sense of that expression.(394)

Whether or not it is legitimate to use seclusion in a mental health facility is not the issue here. However, what is clear from the speeches (judgments) of all of the law lords in the case is that they did not consider seclusion to be medical treatment.

In Western Australia treatment is defined widely to mean any medical, surgical, dental or related treatment or care that may lawfully be provided to a patient with the patient's consent or the consent of any person authorised by law to consent on their behalf.(395)

In the Australian Capital Territory dental treatment is included in the definition of medical treatment.(396)

The broad view of what is included in medical and dental treatment, leaves open the question of whether or not particular treatments or aspects of treatment including oversight of the person's condition, medical advice about how that that condition could best be managed and the prescription of courses of medication are included. A group of Western Australian decisions show why those aspects of treatment are included in the definition.(397)The Victorian case Gardner; re BWV touches upon the criteria for determining whether or not an action or activity is medical treatment and explains why the provision of nutrition and hydration through artificial means is medical treatment.(398) The Western Australian case BTO includes the withdrawal of nutrition and hydration through artificial means in medical treatment.(399) Psychiatric treatment and contraceptive treatment have both been held to be included in medical treatment in Western Australia.(400)

Some Western Australian cases address the question of whether the giving of medications or the use of physical means to stop a person moving or walking is medical treatment or chemical or physical restraint.(401)

12.11.3 Objections

In New South Wales the cases involving proposals to treat Jehovah's Witnesses with blood products, and a case involving a Christian Scientist, show how the objection to treatment of the incapable person is dealt with.(402) This approach contrasts with the approach taken in Queensland where the legislative provision has been interpreted by the predecessor of QCAT, the Queensland Guardianship and Administration Tribunal.(403)

In 2018 the Supreme Court of Victoria used its parens patriae jurisdiction (powers) to override the objections of a young woman who had just turned 17, and her mother, both of whom were Jehovah’s Witnesses, to treatment proposed for the young woman involving the possibility of blood transfusions being used in relation to the imminent birth of her first child.(404) When the matter arose, D1 the 17 year old woman, was 38 weeks pregnant. She consented to induction of labour to take place very shortly at a hospital. She had also consented to a caesarian section, if that became necessary. However D1 was of very small stature, and the baby large, rendering likely the possibility of a caesarean section and need for transfusion associated with, and after, the delivery. The hospital sought her consent to the administration of blood or blood products during or after delivery, if this was necessary to prevent serious injury or to save her life. D1 refused such consent. (405)

The judge, Macaulay J, noted that because D1 was less than 18, she was a minor under law. As a Jehovah’s Witness, D1’s mother informed the hospital that, if asked, she would not provide consent to the administration of blood or blood products to D1.(406)

Given this situation, the hospital sought an urgent application to the Supreme Court for a declaration to authorise the hospital to administer to D1 blood or blood products as her treating doctors considered reasonably necessary to save her life or to prevent serious injury during the induction of labour, the labour itself, any caesarean section and related procedures, and the postnatal period .(407) The hospital sought the order under the Court’s parens patriae jurisdiction which, as Macaulay J noted, in relation to children, is directed to the protection of children who are not legally competent to look after themselves.(408)

D1 opposed the declaration. She did not want to receive blood or blood products because of her religious beliefs which, she said, should be respected as an assertion of her personal autonomy. (409)

Macaulay J noted the question of whether, in this case, the Court’s parens patriae jurisdiction was concerned only with the interests and well-being of D1 or whether it must also be concerned with the interests and well-being of her unborn baby, or of the baby when born.(410) However, because of the way he decided the case, he did not have to come to a conclusion on that question.

Having considered what he described as, various strands of medical and psychiatric evidence, Macaulay J went on to state that it was: “ difficult to be confident that D1’s presently expressed choices are the product of an independently formed, carefully considered and long-held adherence to the tenets of the Jehovah’s Witness faith”.(411)

Macaulay J then went on to consider the parens patriae jurisdiction, the Human Tissue Act 1982 (Vic) and the Mental Treatment Planning and Decisions Act 2016 (Victoria) before deciding whether he should make the declaration sought by the hospital. He went on to say:

The critical issue before the Court now is whether it considers that the expressed view of D1 and her mother D2 should be allowed to direct the hospital in its medical treatment should an emergency arise and her life is put at stake without a blood transfusion. In view of the potential for extremely grave consequences if D1’s choice were allowed to direct her treatment, I must consider her level of maturity and her understanding of what her best interests are, so as to determine if she is able to make such a choice about her medical treatment.

On the authorities, I should consider whether she has sufficient understanding and intelligence to enable her to understand fully what is proposed and the consequences of her decision. I should form a view about the extent to which her choice is a true reflection of who she really is, and what her beliefs really are, as opposed to the product of other forces. That should lead me to pay attention to the demonstrated conviction of the beliefs that she says are driving her decision, as best I can.(412)

Macaulay J was not satisfied D1 had sufficient understanding of the consequences of her choice. He was not convinced she has based her choice on a maturely formed and entrenched religious conviction. In particular, he was not convinced that overriding her expressed choice would so rob her of her essential self as to outweigh the loss she would suffer through losing her life or sustaining a catastrophic injury. Also, he did not consider that allowing her, in effect, to choose to die or only survive with serious injury is in her best interests taking into account a holistic view of her welfare (physical, spiritual and otherwise).(413)

Macaulay J, noting the undertaking by the hospital that all other strategies other than blood transfusion or blood products would be used first, went on to make the declarations sought, provided that the blood and/or blood products were administered if two registered medical practitioners considered that reasonably necessary in order (as a last resort) to to save her life or to prevent serious injury to D1.{[Ibid. [75], [77] and [78].}}

A number of aspects of this case make it especially noteworthy. Firstly, Macaulay J, albeit implicitly not explicitly, used both lack of capacity (that D1 lacked sufficient understanding of what was proposed and the consequences of her decision) and undue influence (he questioned the independence of D1’s decisions) as grounds for using the Court’s parens patriae jurisdiction. The question of undue influence, and the circumstances of this case are redolent of the landmark case, Re T [1992] EWCA Civ 18; [1993] Fam 95, from which the concept of independence of decision-making emerged as a necessary component of capacity.

Secondly, in deciding best interests which is often far more opaque in the Courts, Macaulay J explicitly articulated the need to weigh overriding D1’s expressed choice and as such robbing her of her essential self, against the loss she would suffer through losing her life or sustaining a catastrophic injury.

This is extremely valuable for health professionals increasingly confronted with such decisions clinically in a Western cultural setting that values autonomy highly. This often leads to subjective judgments of doctors about “the reasonableness” of such refusals, rather than assessments of whether the refusal is competently made (i.e. the patient had capacity). Frequently encountered situations in acute hospitals are situations where patients – with undiagnosed delirium impacting on capacity – refuse treatment, and this is accepted as a “reasonable” decision, without consideration of whether the person, as articulated above by Macaulay J, understands what is proposed and the consequences of the decision. This is the point, not whether the health care professional agrees with the patient or not.

12.12.1 What may affect capacity?

12.12.1.1 General medical conditions

A number of medical conditions may render a person unable to understand either the general nature or the effect of a particular treatment. Any chronic or acute perturbation of mental state may affect such understanding. Delirium, an impairment in attention and cognition caused by an underlying physical illness such as chest or urinary tract infection or drug toxicity, is frequently seen in the acute medical setting and it often impairs a person's capacity to consent to medical treatment. Because delirium is a transient disorder it is important that the person's capacity to consent to their own treatment is reassessed after the resolution of the delirium, if the proposed treatment can wait until that occurs.

Although executive impairment (i.e. impairment in frontal lobe functions) causing deficits in reasoning is generally associated with dementia, recent studies have suggested that patients with chronic diseases, such as hypertension, chronic obstructive pulmonary disease, and diabetes, may also have executive deficits independent of any co-occurring dementia or psychiatric condition.(414)

A range of medical conditions may also affect a person's ability to indicate whether or not they consent to the carrying out of treatment. A person may be unable to communicate whether or not they consent to the proposed treatment because they are unconscious, sedated, intubated, suffering the effects of a stroke or are otherwise either temporarily or permanently unable to communicate. It is important to appreciate that those suffering from strokes or other paralysing conditions may be able to communicate by means other than oral communication and where possible the consent process should be facilitated. For example, Stein and Wagner found that using a process of enhancing informed consent with a patient-selected "helper" during the informed consent process for persons with aphasia can improve the quality of the informed consent, while reserving final decision-making authority for the patient.(415)

12.12.1.2 Psychiatric conditions

Psychiatric disorders such as depression, schizophrenia, bipolar affective disorder (manic-depressive disorder) and schizoaffective disorder (a hybrid of schizophrenia and mood disorder) may be associated with cognitive dysfunction, poor insight or psychotic symptoms which interfere with medical decision-making capacity.(416)

In the case of schizophrenia, the strongest correlate or indicator of capacity, particularly understanding and appreciation of disclosed information, is performance on cognitive testing.(417) Specific psychotic symptoms may also impact on a person's capacity but only if they relate to the decision at hand. In the previously mentioned case of _Re C, a man with paranoid schizophrenia was held to meet the test for capacity to make a decision about whether or not to consent to the amputation of one of his legs because of gangrene, because his symptoms did not interfere with the decision at hand.(418)

Depression may affect capacity by virtue of either a passive or an active wish to die, or anergia (lack of energy) and amotivation (lack of motivation) with regards to decision making. Low self-esteem or apathy may render depressed patients at particular risk of "going along with" treatment suggestions regardless of their own views.(419) Some people with depression have psychotic symptoms such as delusions regarding their bodies. Severe Obsessive Compulsive Disorder may cause an indecisiveness that paralyses decision-making.

12.12.1.3 Dementia

Misunderstanding and faulty assumptions about the relationship between dementia and medical incapacity have led to poor practice in many health settings. Commonly, a diagnosis of dementia is equated with loss of capacity. A diagnosis of dementia does not preclude capacity to give consent to medical treatment. There are different causes of and different stages of dementia each with different effects on cognition. Furthermore, some decisions are simpler than others.

Notwithstanding this caution, there is increasing evidence to suggest that even patients with early dementia may have impairment of capacity to give medical consent. However, this depends on the type of dementia and associated cognitive deficits, and the complexity of the decision to be made. Moye and others found that some patients with mild-to-moderate dementia develop a clinically relevant impairment of their consent capacity within a year, particularly those who had initial problems with naming, logical memory and flexibility.(420) Similarly, in a two-year longitudinal study comparing healthy older adult subjects and mild Alzheimer's Disease patients, Huthwaite and others found that even at baseline, mild Alzheimer's Disease patients performed equivalently compared with controls on simple standards of evidencing a choice and making the reasonable choice, but significantly below controls on complex standards of appreciation, reasoning, and understanding. While the mild Alzheimer's Disease group did not show significant decline from baseline on any capacity standard at one year follow-up, at two-year follow-up the mild Alzheimer's Disease group showed significant declines from baseline on the complex consent abilities of appreciation, reasoning, and understanding.(421)

In the early stages of the disease the difficulties in understanding a treatment situation and choices probably relate to deficits in conceptualization and memory (e.g. semantic memory and verbal recall), while in the middle stages, declining capacity to identify the consequences of a treatment choice probably relates to executive dysfunction (loss of decision making and reasoning). In the advanced stages of the disease, receptive and expressive language deficits (aphasia and severe dysnomia) hamper ability to communicate simple treatment choices.(422)

These studies suggest the value of early assessment and regular monitoring of medical consent capacity even in patients with mild Alzheimer's Disease to ensure that it is adequate for each specific situation in which consent to treatment is sought.(423)

12.12.1.4 Intellectual disability

Intellectual disability is low general intellectual functioning as measured by IQ score associated with difficulties in adaptive behaviour (or handicap) manifesting before the age of 18.(424)There are many causes of intellectual disability including abnormalities of chromosomes or genes (e.g. Down syndrome, Fragile X syndrome), nutritional problems, problems with the pregnancy or birth, prematurity, exposure to infection (e.g. rubella) or drugs during pregnancy and developmental abnormalities such as autism. As with dementia, the extent to which intellectual disability hinders capacity to give medical and dental consent depends on the nature and severity of the intellectual disability and the complexity of the consent situation. This may vary within the same individual. For example, a person with an intellectual disability may be able to understand the nature and the effect of some treatments, because those matters are easy to understand or the treatment and its effect are familiar to the person. They may also be able to communicate clearly that they consent to or refuse to consent to the treatment. In relation to other treatments they may not be able to understand the treatment or its effects or they may not be able to come to a decision about it. In those situations, they will not be able to give a valid consent to the treatment.

Not surprisingly, performance of intellectually disabled people decreases with increasingly rigorous definitions of understanding nature and effect. Cea and Fisher found that most adults with mild intellectual disability and almost half with moderate disability were able to make and justify treatment choices and fully or partially understand treatment information while 50% with mild and 18% with moderate intellectual disability were able to appreciate partially the relevance of treatment choices to their situation and weigh the treatment risks against the benefits.(425) Looking at the comparative difficulty of different elements of the capacity task for 20 subjects with learning disability, Wong and others found that the risks of saying "no" were the most difficult to understand followed by the risks of the procedure, the voluntariness of the consent, the purpose of the procedure and the procedure itself.(426)

As mentioned previously with regards to people with communication difficulties (and indeed this applies also to people with mental illness), steps can be taken to facilitate decision-making with people with intellectual disability. For example, the decision-making task can be simplified by presenting the information about the decision in an uninterrupted form and then as constituent elements, and by limiting the verbal demands of the response by including recognition and non-verbal demonstration.(427)

12.12.1.5 Acquired brain injury

Acquired brain injury is damage to the brain after birth. It usually affects cognitive, physical, emotional, or independent functioning and can result from traumatic brain injury (i.e. accidents, falls, assaults etc.) and non-traumatic injury (i.e. poisoning, infection, brain tumours).

Again, the impact on capacity depends on the nature and severity of the person's deficit and the decision to be made. However, the nature of acquired brain injury is such that, unlike dementia which is a degenerative cognition, or intellectual disability which is usually a stable condition, there is potential for recovery in acquired brain injury. For example, in a six month longitudinal study of change in medical decision-making capacity in 24 subjects with moderate to severe traumatic brain injury, Marson and others found that patients showed substantial recovery of reasoning and partial recovery of appreciation and understanding consent abilities.(428)

12.12.2 The medical assessment of capacity

12.12.2.1 General assessment of capacity: myths and faulty assumptions

The assessment of capacity in clinical settings is often characterised by inconsistency, inaccuracy and subjective impressions.(429) Ganzini and others identified ten common myths clinicians hold about decision-making capacity:(430)
  1. decision-making capacity and competency are the same;
  2. lack of decision-making capacity can be presumed when patients go against medical advice;
  3. there is no need to assess decision-making capacity unless patients go against medical advice;
  4. decision-making capacity is an "all or nothing" phenomenon;
  5. cognitive impairment equals lack of decision-making capacity;
  6. lack of decision-making capacity is a permanent condition;
  7. patients who have not been given relevant and consistent information about their treatment lack decision-making capacity;
  8. all patients with certain psychiatric disorders lack decision-making capacity;
  9. patients who are involuntarily committed lack decision-making capacity; and
  10. only mental health experts can assess decision-making capacity.

A "functional" approach to capacity assessment which takes into account the individual's relevant abilities and the demands of the particular decision-making task is far preferable to the commonly used "status" approach which relies on the patient's diagnosis, age or legal status to make assumptions about capacity.(431) The functional approach invalidates the faulty assumption that all patients with dementia, schizophrenia or intellectual disability lack decision-making capacity.

Obtaining a valid consent from a patient is more than just signing a form or reading out a consent form and asking a patient if they understand what was read out to them. Even when they give some thought to the issue of capacity, health care professionals often make inaccurate and inconsistent determinations about a person's capacity to give a valid consent to their own treatment.(432) Practices that have been identified as problematic include capacity assessment based on bedside cognitive assessment at best or subjective impressions about capacity at worst. In a study of subjective estimates of cognitive impairment in older surgical patients, Davis and others have demonstrated that guessing at a patient's cognitive function commonly leads to error, resulting in procedures being undertaken without a valid consent having been obtained. Although staff found it easier to recognize extremes of cognitive functioning, when a patient's degree of cognitive impairment was intermediate, estimates were only slightly better than that expected by chance, resulting in patients undergoing procedures without their capacity to consent being properly assessed.(433)

The assumption that a patient with dementia still has capacity is often based on their acquiescence to treatment; while conversely, refusal of treatment is often equated with incapacity. A study of Massachusetts nursing homes showed that informed consent was not considered an issue and decision-making capacity was not being tested. The usual practice was for capacity to be presumed until a patient failed to acquiesce to treatment, and only at that point would the issue of capacity be fully addressed.(434)

12.12.3 General screening tools

There is widespread agreement among doctors that, while general screening tools such as the Mini Mental State Examination or the Abbreviated Mental Test provide a guide to the severity of cognitive impairment or dementia, and thus a context for the capacity assessment, they are inadequate to assess capacity to consent to medical treatment. Neither of them deals with the specific requirements for a valid consent. Nor does either of them test the crucial frontal lobe functions of judgment and reasoning upon which the task of medical decision-making relies. A patient may have intact language, memory, praxis (ability to perform coordinated movements or motor activities) and perceptual skills but still have impairment of capacity due to executive dysfunction. Ideally, a two-stage capacity assessment involving an assessment of global functioning first followed by an assessment of the specific medical decision making task is advised.(435)

12.12.4 Specific scales

The development of clinical assessment tools has been driven by the legal developments in this area, particularly in the Unites States. According to Appelbaum and Grisso,(436) the article that awakened modern interest in legal standards of competence to consent to treatment was by Roth and others, who despaired in attempting to identify a single operative legal standard and referred to this as the 'search for the holy grail'.(437) Over the last 30 years experts in the field have sought to develop clinically applicable tools incorporating various identified legal standards for defining capacity.

Some of the earlier instruments focused on assessing comprehension of presented information. Fitten and others used three written "vignettes" of increasingly complex hypothetical treatment situations followed by a structured interview to assess understanding of treatment decision-making in elderly nursing home patients.(438) Similarly, the Hopkins Competency Assessment Test is a brief instrument for evaluating competency to give consent to medical treatment or to write advance directives based on the patient's comprehension of a short essay outlining a doctor's assessment of medical decision-making capacity and the rights of patients to make durable (enduring) powers of attorney regarding future medical care.(439)

12.12.4.1 The four-abilities model

In a more inclusive approach, Grisso and others identified all four of the commonly applied legal standards in the USA courts for determining decision-making competence (the 'four-abilities model') vis: (440)(441)(442)(443)
  1. Ability to communicate a choice
  2. Ability to understand relevant information
  3. Ability to appreciate the situation and its likely consequences
  4. Ability to manipulate information rationally (or reason about it) in a manner that allows one to make comparison and weigh options.

Using three instruments to measure these abilities they found that different groups of patients were identified as impaired depending on the measure used. The proportion of patients identified as impaired increased when compound standards were used, i.e. when impairment was defined as poor performance on any of two or three measures.

What emerged from this work was the MacArthur Competence Assessment Tool-Treatment. This instrument assesses patients' competence to make treatment decisions by examining their capacities in four areas - understanding information relevant to their condition and the recommended treatment, reasoning about the potential risks and benefits of their choices, appreciating the nature of their situation and the consequences of their choices, and expressing a choice. A high degree of ease of use and inter-rater reliability (i.e. agreement between different raters) in both hospitalized, medically ill patients and patients with psychiatric disorders has been identified with this tool.(444)

12.12.4.2 Aid to Capacity Evaluation

In the attempt to create the "gold standard" of capacity assessment tools, a plethora of other instruments have been developed, most of which are based on the assessment of a composite of legal standards. The 'Aid to Capacity Evaluation' is a face to face semi-structured interview which has a high probability of identifying those incapable of giving consent.(445)

The Aid to Capacity Evaluation categorises patients into 'definitely incapable', 'probably incapable', 'probably capable' and 'definitely capable'. The clinical standards of the Aid to Capacity Evaluation include:
  1. able to understand medical problem
  2. able to understand proposed treatment
  3. able to understand alternative to proposed treatment
  4. able to understand option of refusing proposed treatment
  5. able to appreciate reasonably foreseeable consequences of accepting proposed treatment
  6. able to appreciate reasonably foreseeable consequences of refusing proposed treatment
  7. is the person's decision affecting by a) depression or b) delusion/psychosis

The Capacity to Consent to Treatment Instrument is a psychometric measure that tests capacity to consent to medical treatment using a series of four core capacity standards: S1 (evidencing/communicating choice), S3 (appreciating consequences), S4 (providing rational reasons), and S5 (understanding treatment situation), and one experimental standard [S2] (making the reasonable treatment choice).(446)

12.12.4.4 Health Care Capacity Decisional Aid

The Health Care Capacity Decisional Aid rates patient responses to a capacity assessment interview on a likert-like scale (from definitely able to definitely unable) in the following domains:(447)
  1. Ability to understand relevant information or health problem
  2. Ability to understand the various choices (one to four)
  3. Ability to appreciate consequences

12.12.4.5 Stewart and Biegler's specific questions

In a very practical way, Stewart and Biegler have suggested specific questions clinicians might ask patients to test comprehension, appreciation and reasoning, namely:
  1. Understanding/comprehension : Ask patient to recall and paraphrase information related to proposed treatment including risks and befits of treatment, alternative treatment and no treatment at all. (Retest later to check for stability.)
  2. Believing /appreciating : Tell me what you really believe is wrong with your health now? Do you believe that you need some kind of treatment? What is the treatment likely to do for you? Why do you think it will have that effect? What do you believe will happen if you are not treated? Why do you think the doctor has recommended this treatment for you?
  3. Weighing/reasoning: Tell me how you reached the decision to accept/reject treatment? What things were important to you in reaching the decision? How do you balance those things? (448)
  4. Choice: Have you decided whether to go along with your doctor's suggestion for treatment?

While the MacArthur Competence Assessment Tool-Treatment has been found to have the most empirical support, none of these tools or question sets provides the "gold standard" for capacity assessment. Although superior to a clinician's subjective rating of capacity, all instruments have limitations, ranging from lack of inter-rater reliability and lack of supporting psychometric data to lack of generalisability across contexts or ecological validity i.e. the difficulty extrapolating understanding of a hypothetical situation to the specific decision to be made.(449), (450). Given these limitations, the best use of such instruments is to standardize or structure capacity assessments so that the same questions are asked of all patients. This is particularly useful in research settings, but it is also useful for clinicians when making assessments as it ensures that they assess all the elements of decision-making and base their conclusions on comprehensive assessments rather than on subjective impressions.

12.12.5 The effect of the type of decision on capacity assessment

Two issues need to be taken into account in the assessment of medical decision-making. These are the risk of the procedure and complexity of the decision-making required. The assessment of capacity should be made with reference to the type of decision to be made. There is a spectrum or hierarchy of decisions from simple (e.g. having a blood test) to complex (e.g. carotid artery surgery) and accordingly, people may be capable of making simple decisions but not more complex ones. Freedom is maximized when a person is allowed to make the decisions they are capable of making.(451)

Further, when the risks are high, it is important that the criterion of competence is applied assiduously.(452) As stated previously, the courts have acknowledged that the more serious the decision, the greater the capacity required.(453) This is known as a "risk related standard" according to which the level of capacity to refuse a treatment may differ from that needed to consent to it. Frequently, the benefits of treatment are high and the risks low while the risks of refusal are high and the benefits low, suggesting that the level of capacity to refuse might be higher.(454)

This notion of "asymmetry" means that just because patient is competent to consent to treatment, it doesn't necessarily follow that he is also competent to refuse it. Consent to medical treatment requires a relatively lower level of capacity than the refusal of that same treatment.(455) This is extremely relevant to the area of end-of life decisions, which will be discussed in a later chapter.

12.12.6 Information, education and facilitation

One of the crucial elements of the health care capacity assessment is the presentation of the information about the health problems, treatments and choices available to the patient i.e. "the education step".(456) To be capable of making a decision people must be adequately informed. People can easily be mistaken to be incapable if education or information is not provided to them or it is given in such a way that it is incomprehensible. In order to maximize patient autonomy, barriers to communication (e.g. hearing and visual impairment, literacy or language differences) must be addressed if possible and communication facilitated by establishing rapport, tailoring and personalising information, giving sufficient time for assimilation of information and using visual aids which are readable.(457) Similarly, in patients with dementia, interventions aimed at maximising their understanding and reasoning by supporting naming, memory, and flexibility may help to optimise capacity.(458)

Such efforts can be fruitful even in patients who might otherwise be deemed incapable. For example, Palmer and Jeste found that an interactive dialogue between patient and investigator with repeated presentation of information is likely to aid understanding of disclosed information among patients with schizophrenia.(459)

Whether and how to treat now incapable people who for religious, cultural or ethical reasons either have refused to be or are known to oppose being given either certain medical treatments or any medical treatments are extremely difficult matters for treating doctors and other health professionals. This is because of the well-established common law right of capable people to refuse medical treatment, for any reason or no reason, and for their stated views, particularly those set out in advance directives, to be complied with if they lose capacity.

Doctors and other health professionals are faced with this difficulty most often with Jehovah's Witnesses and blood transfusions. However, it must be appreciated that while blood transfusions do save lives and assist in the recovery process in a number of situations, the giving of blood does involve risks and blood transfusions do not bring about miracle cures.

12.13.1 The medical approach to transfusion refusal

The right of competent adults to refuse blood transfusion is well respected. Fortunately, blood is not always needed and patients in relatively good health can tolerate a fair degree of anaemia. Transfusions carry risks, for example, transmission of viruses, prior disease and transfusion-associated immunosuppression. They also have benefits. There are alternatives to blood transfusions and the concept of "bloodless medicine" has been developed to deal with these very circumstances.

Bloodless medicine involves blood conservation approaches (i.e. in phlebotomy or taking blood) and the use of adjunctive (i.e. extra, or alternative) such as antifibrinolytics (stops clots breaking up), procoagulants (reduces haemeorrhage) or erythropoietin (increases red blood cell blood production) and blood substitutes.(460) Much has been written about pharmacological and surgical options to treat patients who refuse blood and studies have compared outcomes of open heart surgery and major, intermediate and minor gynaecological procedures in Jehovah's Witnesses compared with patients who accept the transfusion of blood products and found them comparable.(461)(462)

Rogers and Crookston have suggested the following guidelines on how to deal with the patient who refuses transfusion:
  1. Seek to understand the patient and develop good rapport, explore treatment possibilities, decide together on the course of action to be taken and also make contingency plans in advance
  2. Respect confidentiality
  3. Document carefully
  4. Access available resources to support the decision-making process including other professionals who have had experience in similar situations, ethics committees, risk management groups, or transfusion medicine specialists.(463)

In 2009, the decision of the Supreme Court of New South Wales in Hunter and New England Area Health Service v A made it clear that if an adult when capable had made an advance directive in an appointment of enduring guardianship directing the enduring guardian to refuse medical treatment, the person's treating doctors, and by implication the enduring guardian, are bound by that advance directive.(464) Nevertheless, considerable difficulties arise in cases involving Jehovah's Witnesses where the Witness the subject of the application has not got a current "blood card" - a form of advance directive carried by many Jehovah's Witnesses setting out that they do not wish to receive blood products and what substitute non-blood products they are willing to receive. The Guardianship Division of the New South Wales Civil and Administrative Tribunal (NCAT) has the power to give direct consent to proposed medical treatments. This is different from appointing a guardian to give such consent. It has said in relation to dealing with applications, usually by treating doctors, to consent to giving blood transfusions to Jehovah's Witnesses that:

[W]hilst it (now NCAT) has an obligation to have regards to the views of the patient and to take (those views) very seriously indeed, it was not bound by those views and could make a decision in relation to treatment which was contrary to the views of the patient if the Tribunal believed there were strong reasons for doing so. The Tribunal might well take a different view in cases where either the patient has a current and relevant “blood card” or other advance directive, or where the patient’s views have been clearly stated and proved to the Tribunal’s comfortable satisfaction.(465)

In the matter in which the Tribunal made that statement, the Tribunal refused to consent to a blood transfusion for a 19 year old woman who had toxic shock syndrome with multi-organ failure even though it was satisfied, from a medical treatment perspective, that the proposed blood transfusion was the most appropriate form of treatment for promoting and maintaining her health and well-being. The Tribunal took a number of things into account. The young woman had recently professed commitment to the key tenets of her religion including the obligation to abstain from blood transfusions, although she did not have a current blood card. Her parents, who were her persons responsible, wanted everything possible done for her medically and gave their consent to all proposed treatments except for blood transfusion. The Tribunal also considered the consequences of her having a blood transfusion. While it was unlikely that she would not be rejected by her church if she had a blood transfusion consented to on her behalf by others, this fact could lie heavily on her conscience and affect both her recovery and later health. Another factor was that the giving of a blood transfusion would not necessarily restore her health.(466) She was not given the blood transfusion for which consent was sought, but she recovered without it - probably as a result of the high quality of the other medical care provided to her.(467)

There have been other applications in which the Tribunal has followed the approach set out in this case, but in which the Tribunal has given consent to the proposed blood transfusion. In a 2004 case, the Tribunal decided to consent to an application for a blood transfusion to be given to AF, who was the only member of his family who was a Jehovah's Witness. The Tribunal accepted that he had signed an advance directive in the form of a "no transfusion card" or "blood card" in 2003 and may have signed others as well. However, there was no current card signed by him. Also, there was evidence that recently, when he had been asked, he had indicated that he wanted a blood transfusion. In addition, there was conflicting evidence about how closely he adhered to other tenets of the Jehovah's Witnesses and, evidence that he had already been given transfusion in the emergency setting.(468) Stewart has criticised the Tribunal's decision.(469)

There have been other cases in which the Guardianship Tribunal has either consented to or refused consent to blood transfusions.(470) Some of these are discussed earlier in this chapter under objections to medical treatment in New South Wales at 12.4.10. The question of advance directives and blood transfusions is discussed again in Chapter 13.6.4.4.

Many of the principles in relation to capacity set ot in this chapter relate equally to children as they do to adults. However, there are many grey areas in relation to young people because of the recognition that chronological age does not determine maturity with a number of arbitrary age-defined cut offs embedded within the legislation. For example, people under 18 are minors under Australian law, while most legislative substitute decision-making regimes in Australia relate to people 16 years and above. However, consent of the parent or guardian is generally considered necessary for medical treatment for young people under the age of 14.(471) It can therefore be assumed that young people under 14 do not have the capacity to give consent. However a child's age alone is an unreliable predictor of their competence to make decisions as the right of younger children to provide independent consent is proportionate to their competence. A young child may have capacity if they have sufficient intellectual and emotional maturity to make an informed decision. However as a general rule, the younger the person, the less likely it is that they will hold the relevant competency.

These concepts emerged from common law judgments, most notably, the test of “Gillick competence”, derived from the 1985 English case Gillick v West Norfolk and Wisbech Area Health Authority .(472) The Gillick Case involved a campaign against a health departmental circular advising doctors that the prescription of contraception was a matter for the doctor's discretion, and that they could be prescribed to children under sixteen without parental consent. Lord Scarman's test, generally considered to be the test of Gillick competence required that a child could consent if they fully understood the medical treatment proposed:
[I] would hold that as a matter of law the parental right to determine whether or not their minor child below the age of 16 will have medical treatment terminates if and when the child achieves sufficient understanding and intelligence to understand fully what is proposed.(473)

The issue of “termination” of parental right to consent has been debated since. In many cases, even if a child is competent to consent on their own behalf, a parent may still validly consent on their behalf.(474) If a health practitioner considers that a child is competent, it still may be appropriate and prudent to obtain both parental and patient consent. However, a child who is deemed Gillick competent i.e. has the capacity to consent, is generally entitled to confidentiality. This includes the right for the child’s health records to be kept confidential from their parents.(475) The young person’s right to privacy and confidentiality may be particularly important when there are risks of disclosing sensitive information to a parent, particularly regarding contraception and particularly in challenging family situations or family conflict, or with sensitive areas such as contraception and pregnancy. (476) Notwithstanding this, it must be borne in mind that these principles emerged from consent for contraception and while the legal issues still apply in other contexts (e.g. depression or anxiety), clinically the issues are different because of the intrinsic role parents play in the support and management of mental illness in minors.

The Gillick competence doctrine is part of Australian law. It is also common to refer to the ‘mature minor principle’. The doctrine was upheld in Marion’s Case discussed earlier in this chapter.(477) In that case, the High Court held that the authority of parents to consent to medical treatment for their children does not extend to treatment not in the child’s best interests. Also, the Court held that if medical treatment has sterilization as its principal objective, parents do not have the authority to consent on behalf of their child.

Another principle at stake here is that young people with intellectual disability are not automatically deemed incompetent to consent to treatment. As with any young person, the competence of a young person with an intellectual disability must be assessed on a case-by-case basis.(478)

While the Gillick Case introduced the concept of Gillick competence, the case came about because, in 1986, the Department of Health for England and Wales, which is responsible for the National Health Service (NHS), issued guidance to health-care professionals about the provision of contraceptive advice and treatment to young people under 16 years of age. This guidance led to Mrs Gillick seeking declarations in the High Court of Justice in England that no doctor or other professional person employed in the Health Services or otherwise may given any contraceptive and/or abortion advice and/or treatment to any child of the plaintiff below the age of 16 without the prior knowledge and/or consent of the said child's parent or guardian. Mrs Gillick failed in the High Court, succeeded in the Court of Appeal in getting the declarations she sought. However that decision was overruled by the House of Lords (now the Supreme Court of the United Kingdom). What came out of the decision of the House of Lords was guidance that became known as the Fraser Guidelines.(479) These are as follows:
[T]hat a doctor could give contraceptive advice and treatment to a young woman under the age of 16, without parental consent or knowledge if;
  1. she had sufficient maturity and intelligence to understand the nature and implications of the proposed treatment,
  2. she could not be persuaded to tell her parents or to allow her doctor to tell them,
  3. she was very likely to begin or continue having sexual intercourse with or without contraceptive treatment,
  4. her physical or mental health were likely to suffer unless she received the advice or treatment,
  5. the advice or treatment was in the young person’s best interests.

It should be noted however that the courts take the view that the extent of the parens patriae jurisdiction is “theoretically limitless” with the result that Supreme Courts have the power to override refusal of treatment by a Gillick competent minor and authorise that minor’s treating doctors to treat the minor in accordance with their clinical judgment.(480)

Probably because the concept of Gillick competence (the mature minor principle), there is no legislation specifying when a child may consent to medical treatment on their own behalf in any of the Australian States and Territories except South Australia.

However, in NSW the Minors (Property and Contracts) Act 1970 provides that the prior consent to medical or dental treatment by a parent or guardian of a person aged less than 16 or the prior consent by a minor aged 14 and above, will be treated as valid consent to the proposed treatment. (481) Kerridge and others state that this effectively means that children 14 years and older are presumed to be competent to give consent to their own medical and dental treatment. They go on to note that parents may also give consent to their children’s medical and dental treatment until they are 16. They note also that the presumption of competence by evidence to the contrary.

We suggest that the main purpose these provisions is to protect medical and dental practitioners from liability, as the relevant section states, in relation to a claim by the minor for assault or battery in respect of anything done in the course of any treatment that they may give to a child patient who is aged 14 years or above on the basis of that child’s consent to the treatment. However, if the claim was based on assault or battery that occurred during the course of the treatment that would still have been assault or battery if the child had in fact been 18 years or above and thus an adult, the child could still sue for the damages suffered. We suggest that the section is not intended to change the age at which competence to consent to medical or dental treatment can be presumed.

We also suggest that while it is good practice to involve children, particularly teenage children, in knowing and understanding the nature and effect of the medical and dental treatment that is proposed for them, it is still incumbent on doctors and dentists, as a matter of proper professional practice, to ensure that the child is Gillick competent before they rely on the consent that they give as the basis for carrying out the proposed treatment. We suggest that this is particularly the case where the treatment is risky, controversial, subject to significant, adverse side effects or likely to have irreversible consequences whether carried out successfully or unsuccessfully.(482)

It should also be noted that in NSW it is Part 5 of the Guardianship Act 1987 (NSW) which provides the arrangements for substitute consent to medical and dental treatment applies to persons aged 16 years and above who are incapable of giving (valid) consent to medical or dental treatment. (483)

In South Australia children 16 years and above may consent to their own medical, but not dental, treatment. The Consent to Medical Treatment and Palliative Care Act 1995 (SA) simply provides that:

A person of or over 16-years-of-age may make decisions about his or her own medical treatment as validly and effectively as an adult.(484)

This means that a child aged 16 or over has the capacity to refuse treatment as well as consent to it. It also means that the presumption of capacity to make such decisions applies to such children in the same way as it does to adults, so that the presumption of capacity may be rebutted by evidence that the child lacks capacity to make such decisions, whether particular decisions or medical treatment decisions generally.

The Act also provides that a child under 16 can validly consent to treatment if:
  1. the doctor who is to treat the child is of the opinion that the child capable of understanding the nature, consequences and risks of the treatment and that the treatment is in the best interest of the child’s health and well-being, and
  2. that opinion is supported by the written opinion of at least one other doctor who personally examines the child before the treatment is commenced. (485)
This is a statutory extension of Gillick competence to all children 16 years and above, provided they meet the statutory criteria for competence set out in the last paragraph.

In the other States and the two Territories, doctors, dentists and other health practitioners who need consent of the patient for the treatment they offer, should, as part of their professional practice, make an assessment of their competency to consent to the treatment they propose for all of their patients under the age of 18 years. Competency will depend on age, maturity, intelligence, education, level of independence, and ability to express their own wishes, as well as the gravity of the treatment proposed. As with adults, the “risk related standard” approach applies such that for more serious illness or more drastic, invasive or risky types of treatment, the medical practitioner will need to take special care to ensure that the young person possesses the required competence to consent to treatment. This is particularly the case for mental illness in minors.

As well, the principle of necessity applies to minors. (486)

In general, treatment may be performed without the consent of either the parent or the child if the health practitioner is of the opinion that the treatment is necessary, as a matter of urgency, in order to save the child or young person’s life. In practice, that means that emergency medical and first aid treatment may be provided without the consent of the minor or a parent or guardian.

If a health practitioner is unsure whether a minor is competent they should seek the opinion of a colleague, seek the consent of the minor’s parents or legal

Guardians and obtain legal or tribunal advice. Competency assessments should be documented and form part of the patient’s medical record.

Many minors aged 14 and above may have the capacity to consent to medical treatment depending on their level of maturity; their understanding of the proposed treatment and its consequences; and the severity of treatment. A health practitioner must make a case-by-case assessment of whether the young person has sufficient understanding and intelligence to enable him or her to fully understand what is proposed. A balance needs to be struck between promoting the autonomous rights of competent children – including their right to confidentiality - with the need to promote family relationships in support of the child.

12.15 Conclusion

Capacity reflects an interaction between the decision-maker and the demands of the decision-making task.(487) The legal definition of capacity to give consent to treatment is a broad one and usually encompasses an understanding of the nature and effect of the particular treatment and an ability to indicate consent. However, understanding the nature and effect of a treatment requires more than just parroting a description of treatment. The commonly adopted English common law test, Thorpe J's test, which is supported by current scientific literature in this area, suggests that capacity to give treatment consent is more complex and involves an ability to retain information about the treatment and appreciate or manipulate it, weighing up risks and alternatives.(488)

This higher order, medical conceptualization of capacity has been developed to ensure that false positive assessments of capacity do not occur and that we protect people from making decisions of which they are incapable. This of course creates a tension between the principles of beneficence and autonomy, the latter being the fundamental principle upon which much of the law is based. Setting too high a threshold for capacity will tend to offend against the principle of self-determination, while setting the standard too low potentially places people at risk of self-harm.(489)

Notes

1 : Guardianship Act 1987 (NSW) Pt 5; Guardianship and Administration Act 2000 (Qld) Ch 5 and Powers of Attorney Act 1998 (Qld) Chs 3 and 4; Guardianship and Administration Act 1993 (SA) Pt 5; Guardianship and Administration Act 1995 (Tas) Pt 6; Guardianship and Administration Act 2019 (Vic)Pt 6 and s 202; Guardianship and Management of Property Act 1991 (ACT) Pt 2A; Guardianship and Administration Act 1990 (WA) Pt 9C.

2 : Secretary, Department of Health and Community Services v. JWB and SMB (Marion’s Case)[1992] HCA 15, McHugh [3][1992] HCA 15; , 175 CLR 218, 309.

3 : Collins v Wilcock [1984] 3 ALL ER 374, 378

4 : In re F [1991] UKHL 1; (1990) 2 AC 1, 77. See also Re T [1992] EWCA Civ 18; [1993] Fam 95, 117 (Butler-Sloss LJ) and 117 (Staughton LJ).

5 : In re F [1991] UKHL 1; (1990) 2 AC 1, 77. See also Re T [1992] EWCA Civ 18; [1993] Fam 95, 117 (Butler-Sloss LJ) and 117 (Staughton LJ)

6 : Ibid. 78

7 : Ibid. 76. See also, Malette v Shulman (1990) 67 DLR (4th) 321.

8 : Secretary, Department of Health and Community Services v. JWB and SMB [1992] HCA 15, 175 CLR 218. See also, BCB [2002] WAGAB 1, [46], Re BCB, Application for Guardianship Order [2002] SR (NSW) 338.

9 : BCB [2002] WAGAB 1 [28], [2002] SR (WA) 338.

10 : BTO [2004] WAGAB 2 [20].

11 : Scott v Wakem [1862] EngR 200; (1862) 176 ER 147, 149.

12 : Watson v Marshall [1971] HCA 33, (1971) CLR 621.

13 : In re Hawke (1923) 40 WN (NSW) 58, 59.

14 : Watson v Marshall [1971] HCA 33 [7][1971] HCA 33; , (1971) 124 CLR 621.

15 : Guardianship Act 1989 (NSW) s 34.

16 : Guardianship and Administration Act 1995 (Tas) s 4.

17 : Guardianship Act 1989 (NSW) s 32.

18 : Guardianship and Administration Act 1995 (Tas) s 5.

19 : Guardianship Act 1989 (NSW) s 33(2) and Guardianship and Administration Act 1995 (Tas) s 36.

20 : C v Guardianship and Administration Board [2002] TASSC 29.

21 : In re C [1994] 1 All ER 819, 822 and 824; Re MB [1997] EWCA Civ 1361; Re B [EWHC 429 (Fam) [33]; Re NK (unreported Guardianship Tribunal NSW, C/28379, Matter Nos 2004/1672 and 2004/1673, 3 June 2004), 12. At the time of writing, Thorpe J’s test had not been considered by either the Guardianship and Administration Board or the Supreme Court of Tasmania.

22 : In re C [1994] 1 All ER 819, 822 and 824.

23 : Re B [2002] EWHC 429 (Fam) [34] and [35].

24 : Re MB [1997] 2 FCR 541, 553; Re B [2002] EWHC 429 (Fam) [28] and [100]. For a discussion of the presumption of capacity in the context of consent to medical treatment see, Skegg, PDG, Presuming competence to consent: could anything be sillier [2011] UQLawJl 11; (2011) 30(2) UQLJ 165.

25 : Lane v Candura 376 NE 2d 1232.

26 : Re T [1992] EWCA Civ 18; [1993] Fam 95, 113; Re MB [1997] EWCA Civ 1361 and Re B [2002] EWHC 429 (Fam) [31].

27 : See 12.11 and 12.12.

28 : Guardianship Act1989 (NSW) s 33(1) and Guardianship and Administration Act 1995 (Tas) s 3. The Victorian definition is almost identical. See, Guardianship and Administration Act2019 (Vic)s 3(1) for the definition of “medical treatment decision”, which under the Medical Treatment Planning and Decisions Act 2016 (Vic), is defined to mean “a decision to consent to or refuse the commencement or continuation of medical treatment or a medical research procedure”. As at 26-2-2016 no other kind of treatment has been declared under s 31(1)(g) of the Guardianship Act1989 (NSW) to be treatment for the purposes of Part 5 of the Act .

29 : Guardianship Act 1989 (NSW) s 33(1) and Guardianship and Administration Act 1995 (Tas) s 3.

30 : Guardianship Act 1989 (NSW) s 37(1) and Guardianship and Administration Act 1995 (Tas) s 4.

31 : Guardianship Act 1989 (NSW) s 33(1)

32 : Guardianship Regulation 2016 (NSW) reg 9. Note that palliative care and terminally ill were interpreted by the NSW Guardianship Tribunal in FAM [2007] NSWGT 13. The Tribunal noted, at [15], that palliative care “is generally understood to be provided to people of all ages who have a life limiting illness, with little or no prospect of a cure, for whom the primary treatment goal is quality of life”. It also noted that the common medical understanding of a terminal illness involved end stage illness when death was imminent or reasonably foreseeable and there was no cure or (realistic) possibility of remission, [19]-[20]. As FAM had advanced dementia which would inevitably lead to her death in the reasonably foreseeable future and there was no cure for dementia or possibility of recovery or remission, the Tribunal was satisfied that she was a terminally ill patient, [21].

33 : Ibid. reg 10.

34 : In Tasmania, new (experimental) treatments are not defined as special treatment, but termination of pregnancy and removal of non-regenerative tissue for the purposes of transplantation have been made special treatment the Act. See, Guardianship and Administration Act 1995 (Tas) s 3. The Guardianship and Administration Regulations 2007 (Tas) reg 6 includes aversive treatments as they are defined in New South Wales as special treatment, but not termination of pregnancy which is in the Tasmanian Act. While vasectomy or tubal occlusion are not specifically referred to in the legislation in Tasmania, they are considered special treatments as such treatments are usually intended to and, in any event, are reasonably likely to render a the person they are carried out on permanently infertile. Psychosurgery, including any neurological procedure carried out for the relief of the symptoms of Parkinson’s disease, is included as special treatment via the Guardianship and Administration Regulations 2007 (Tas) reg 6(a).

35 : Guardianship Act 1989 (NSW) s 36 and Guardianship and Administration Act 1995 (Tas) s 39.

36 : Guardianship Act 1989 (NSW) s 45A and Guardianship and Administration Act 1995 (Tas) ss 39(2) and 46.

37 : For special medical treatment see, Guardianship Act 1989 (NSW) ss 33(1) and 45(1) and (2). For experimental medical treatment see, ss 33(1) and 45(1) and (3) of the Act and Guardianship Regulation 2016 (NSW) reg 9. For a case in which NCAT gave consent to a “new” treatment as defined in s.33(1) see, EFC [2020] NSWCATGD 27.

38 : Guardianship and Administration Act 1995 (Tas) s 45.

39 : Guardianship Act 1989 (NSW) s 33(1) and Guardianship Regulation 2010 (NSW) reg 11.

40 : For an example of major medical treatment needed for a foreign national in NSW during the Covid-19 pandemic see, GMI [2020] NSWCATGD 6

41 : Guardianship Act 1989 (NSW) s 33(1).

42 : Guardianship Regulation 2005 (NSW) reg 10.

43 : Ibid. reg 10(c)(i) or (ii).

44 : See the next heading “Minor treatment” and the footnote under it.

45 : Ibid. reg 11.

46 : This follows from the fact that the doctors proposing to carryout major medical treatment are not absolved from obtaining substitute consent as they are for urgent treatment or absolved from obtaining substitute consent in certain circumstances as they are for minor treatment and the fact that applications for any kind of treatment may be made to the Guardianship Division of NCAT. See, Guardianship Act 1989 (NSW) ss 37 and 42.

47 : Guardianship Act 1989 (NSW) s 33A(4)(a) empowers the guardian to act only if they have been given the function of consenting to medical and dental treatment on behalf of the person under their guardianship. See also s 3(1) of the Act. While the Guardianship and Administration Act 1995 (Tas) does not deal with this matter specifically, it may be implied into the Act that only guardians (including enduring guardians) with the function of giving or refusing consent to medical treatment may act as persons responsible.

48 : In re T [1992] EWCA Civ 18; [1993] Fam 95, 103.

49 : Guardianship Act 1989 (NSW) ss 3(1) and 33A(4)(a) and Guardianship and Administration Act 1995 (Tas) ss 3 and 4.

50 : Guardianship Act 1989 (NSW) ss 3(1) and 33A(4)(b) and Guardianship and Administration Act 1995 (Tas) ss 3 and 4(1)(c)(ii) and 5(a).

51 : Guardianship Act 1989 (NSW) s 3D which sets out the circumstances in which the person has the care of the incapable person and s 33A(4)(c) and Guardianship and Administration Act 1995 (Tas) s 4(1)(c)(iii) and (3) and (4). Brain damaged adults will sometimes be looked after by their parents, and if those adults receive substantial as a result of their injuries, their parents may receive money for looking after them. In K v K [2000] NSWSC 1052 Young J suggested that s 3D of the NSW Act not be narrowly construed. Consequently, in that State parent carers in that situation are considered not precluded from being persons responsible.

52 : Guardianship Act 1989 (NSW) s 3E which sets out the meaning of “close friend or relative” and s 33A(4)(d) and Guardianship and Administration Act 1995 (Tas) s 4(1)(c)(iv) and 5(b) to (d).

53 : Guardianship Act 1989 (NSW) s 33A(2) and (3) and Guardianship and Administration Act 1995 (Tas) s 4(2).

54 : Guardianship and Administration Act 1995 (Tas) s 4(1).

55 : Guardianship Act 1989 (NSW) s 33A(5).

56 : For NSW see, Guardianship Act 1989 (NSW) ss 3(1) and 33A(4)(a) and Part 2 of the Act as to how to appoint an enduring guardian. For Tasmania see, Guardianship and Administration Act 1995 (Tas) ss 3 and 4 and Part 5 of the Act as to how to appoint an enduring guardian.

57 : Guardianship Regulation 2010 (NSW) regs 13 and 14 and Guardianship and Administration Regulations 2007 (Tas) reg 9.

58 : Guardianship Act 1989 (NSW) s 40(2).

59 : Ibid. ss 40(3) and 32.

60 : Ibid. s 46(2)(b).

61 : Guardianship and Administration Act 1995 (Tas) s 43.

62 : Ibid. s 41(1).

63 : Ibid. s 41(2).

64 : Guardianship and Administration Act 1995 (Tas) s 41(2) and Guardianship and Administration Regulations 2007 (Tas) reg 9

65 : Ibid

66 : Guardianship Act 1989 (NSW) s 37(2) and (3).

67 : Guardianship Act 1989 (NSW) s 36 and Guardianship and Administration Act 1995 (Tas) s 39.

68 : Guardianship and Administration Act 1995 (Tas) s 44. In NSW the legislation does not require this, but the Tribunal does. However, it provides an application form which is available on its website www.gt.nsw.gov.au/applications/medical-dental-consent-cfm. Also, if an application needs to be made urgently out of hours, the tribunal member on call will fill out the form as part of the information collecting process before the hearing.

69 : Guardianship Act 1989 (NSW) s 42(1). However, s 44(3) of the Act provides that the Tribunal is not required to consider an application if it is not satisfied that the applicant has sufficient interest in the health and well-being of the incapable person.

70 : Ibid. s 42(2).

71 : Ibid. s 44(2)

72 : Ibid. ss 44(1) and 45(1).

73 : Guardianship and Administration Act 1995 (Tas) s 45

74 : Ibid. s 45(2)(e)

75 : Ibid. ss 69(3) and 45(3) and (4). For an example of an application to the Guardianship and Administration Board of Tasmania for consent to medical treatment, see E.Q (Medical Consent) [2006] TASGAB 1.

76 : Guardianship Act 1989 (NSW) s 36 and Guardianship and Administration Act 1995 (Tas) s 39

77 : Guardianship Act 1989 (NSW) s 45A and Guardianship and Administration Act 1995 (Tas) ss 39(2) and 46.

78 : Guardianship Act 1989 (NSW) s 45(1) and (2).

79 : Prescribed special treatment is set out in Guardianship Regulation 2010 (NSW) reg 10

80 : Guardianship Act 1989 (NSW) s 33(3).

81 : Ibid. s 46(2).

82 : Ibid. s 46A. However, this authority will not always be given. See, Re LK (unreported, Guardianship Tribunal Matter Nos: 2004/1672, 2004/1673, 3 June 2004). For two cases in which NCAT gave the Public Guardian, as guardian of the person, the function of giving substitute decisions in relation to medical and dental treatment, including the authority to override the objections medical treatment by the person the subject of the guardianship order see, QCM [2015] NSWCATGD 38 (for both psychotic and physical health conditions) and SMD [2015] NSWCATGD 40 (objections to any medical or dental treatment). For a review of a guardianship order authorising a guardian to override a patient’s objections to medical treatment because of his anorexia nervosa complicated by obsessive compulsive features and the renewal of that order see, KSC [2013] NSWGT 20.

83 : Ibid. s 46(4).

84 : See, LD [2000] NSWGT 4. Sometimes an application is made for a guardianship order and consent to medical treatment. The Tribunal can the either make the medical treatment decision itself or appoint a guardian to do so. For an example see, Re SR (unreported, Guardianship Tribunal Matter Nos: 2000/5289, 2000/5326, 2000/5343, 26 September 2005). For an example of an application for consent to minor medical treatment (treatment to stabilise and repair a fractured femur) overriding an objection to minor medical treatment see PD [2004] NSWGT 4.

85 : See MA [2001] NSWGT 2.

86 : Guardianship Act 1989 (NSW) ss 42, 44 and 45(1).

87 : Re CJ [2006] QGAAT 11.

88 : Ibid. ss 40(3) and 44(2).

89 : Re RD (unreported, Guardianship Board, C/5887, Matter No. 94/1858, 22 June 1994).

90 : [2009] NSWSC 761.

91 : KN [1999] NSWGT 2. The Tribunal might well take a different view in cases where either the patient has a current and relevant “blood card” or other advance directive, or where the patient’s views have been clearly stated and proved to the Tribunal’s comfortable satisfaction.

92 : Mental Health Act 1996 (Tas) s 24. Mental illness is defined in s 4 of the Act

93 : Ibid. s 25. The term “person responsible” is defined in s 5 of the Mental Health Act 1996 (Tas) in the same terms as in s 4 of the Guardianship and Administration Act 1995 (Tas) (except for minor differences that are not relevant here).

94 : Mental Health Act 1996 (Tas) ss 31, 32 and 72G. The term “medical treatment” is not defined in the Act except to exclude certain treatments from the term.

95 : The term “informed consent” in defined in s 5AA of the Mental Health Act 1996 (Tas).

96 : Ibid. s 32(2).

97 : Guardianship and Administration Act 1993 (SA) s 58.

98 : Ibid. s 3.

99 : In re C [1994] 1 All ER 819, 822 and 824; Re MB [1997] EWCA Civ 1361; Re B [EWHC 429 (Fam) [33]; Re NK (unreported Guardianship Tribunal NSW, C/28379, Matter Nos 2004/1672 and 2004/1673, 3 June 2004), 12.

100 : Ibid.

101 : Ibid.

102 : Consent to Medical Treatment and Palliative Care Act 1995 (SA) s 13.

103 : Ibid. s 13(1).

104 : Ibid. s 13(2).

105 : Ibid. s 13(3).

106 : Ibid. s 13(4).

107 : Ibid. ss 3 and 61.

108 : Ibid. s 61 and Guardianship and Administration Regulation 1995 (SA).

109 : Guardianship and Administration Act 1993 (SA) s 61(3).

110 : Ibid. s 61(5).

111 : Ibid. s 61(6).

112 : Consent to Medical Treatment and Palliative Care Act 1995 (SA) ss 8(7) and (8) and 8.

113 : Consent to Medical Treatment and Palliative Care Act 1995 (SA) ss 8(7) and (8) and 8.

114 : Ibid. s 59(2)(a).

115 : Ibid. ss 3 and 59(2)(b)(i). A “putative” spouse is a person who has been cohabiting as a husband or wife of a member of the opposite sex currently for a continuous period of five years, or for periods amounting to at least five years in the last six years or has been cohabiting with a member of the opposite sex and they are the parents of a child who has been born. See, Family Relationships Act 1975 (SA) s 11.

116 : Guardianship and Administration Act 1993 (SA) s 3.

117 : Ibid. s 59(2)(b)(ii).

118 : Ibid. s 26.

119 : Ibid. s 5(a).

120 : Ibid. s 5(b).

121 : Ibid. s 5(d).

122 : The website for the Office of the Public Advocate in South Australia is: www.opa.sa.gov.au , then go to Consent.

123 : Guardianship and Administration Act 1993 (SA) s 5.

124 : Ibid.

125 : Ibid.

126 : Ibid.

127 : Guardianship and Administration (Amendment) Act 1999 (Vic).

128 : Medical Treatment Planning and Decisions Act 2016 (Vic) s 7(1)(f).

129 : Ibid. ss 60 and 61.

130 : Ibid. s 63.

131 : Ibid. s 8(1).

132 : Ibid. s 8(2).

133 : Issac Messiha (by his tutor Magdy Messiha) v South East Health [2004] NSWSC 1061.

134 : Ibid. s 7(1)(a), (b) and (e).

135 : Ibid. s 7(1)(e).

136 : Ibid. s 7(1)(f).

137 : Medical Treatment Planning and Decisions Act 2016 (Vic) s 4(1).

138 : Medical Treatment Planning and Decisions Act 2016 (Vic) s. 4(2).

139 : Ibid. s 4(3).

140 : Ibid. s 4(4)(a-c).

141 : _Ibid. s 4(4)(d).

142 : See Ambulance Services Act 1986 (Vic)

143 : See Non-Emergency Patient Services Act 2003 (Vic)

144 : See Access to Medicinal Cannabis Act 2016 (Vic)

145 : Ibid. ss 3(1) and 58.

146 : Ibid. ss 3(1).

147 : Ibid. ss 3(1).

148 : Medical Treatment Planning and Decisions Act 2016 (Vic) s 53(1).

149 : Ibid. s 53(2) and (3).

150 : Guardianship and Administration Act 2019 (Vic) s 145(1).

151 : Ibid s 145(2)(d).

152 : Ibid s 145(3).

153 : Ibid s 140.

154 : Ibid s 143(1).

155 : Ibid s 143(2).

156 : Ibid s 143(3).

157 : Ibid s 144.

158 : Ibid s 145(4).

159 : the Medical treatment Planning and Decisions Act 2016 (Vic), s 3(1).

160 : Ibid. s 3(1).

161 : Ibid. ss 1(d) and 3(1).

162 : Ibid. s 75(a).

163 : Ibid. s 75.

164 : Ibid. s 55(1).

165 : Ibid. s 55(2).

166 : (a) the spouse or domestic partner of the person; (b) the primary carer of the person; (c) the first of the following and, if more than one person fits the description in the subparagraph, the oldest of those persons—(i) an adult child of the person; (ii) a parent of the person;(iii) an adult sibling of the person. Ibid. s 55(3).

167 : Ibid. s 75(a)(iii).

168 : Ibid. s 3(1).

169 : .{{Gardner; re BWV Trust [2003] EWCA Civ 10.

170 : Ibid. s 8(1).

171 : Ibid. s 8(2).

172 : Ibid. s 57(1).

173 : Medical Treatment Planning and Decisions Act 2016 (Vic) s 12(3)(c)(iii).

174 : Ibid. s 54.

175 : Ibid. s 7(1)(a)(f).

176 : Ibid. s 50(1).

177 : Ibid. s 50(2). Note that the term “unprofessional conduct” has the same meaning as it has in the Health Practitioner Regulation National Law .

178 : Ibid. s 6(1).

179 : Ibid. s 60(1)(a)(ii).

180 : Ibid. ss 51 and 22(1)(c).

181 : Ibid. s 11.

182 : Ibid. s 59.

183 : Ibid. s 6(2).

184 : Ibid. s 61(1)(b).

185 : Ibid. s 61(2).

186 : Ibid. s 94(1).

187 : Ibid. s 94(2).

188 : Ibid. s 94(3). Note that the medical treatment decision maker is also authorised to disclose that information for the purpose of any proceeding under the Act , any report of a proceeding under the Act , or any other lawful purpose, see s 94(3)(b) and (c).

189 : Ibid. s 55(1).

190 : Ibid. s 26.

191 : Ibid. s 55(2).

192 : In this context ‘spouse’ means a person to whom the person to be treated is married and ‘domestic partner’ means a person who is in a registered relationship with the person to be treated, or an adult person to whom the person to be treated is not married but with whom the person is in a relationship as a couple where one or each of them provides personal or financial commitment and support of a domestic nature for the material benefit of the other, irrespective of their genders and whether or not they are living under the same roof. However, it doesnot include a person who provides domestic support and personal care to the person to be treated for fee or reward or on behalf of another person or an organisation (including a government, a government agency, a body corporate or a charitable or benevolent organisation). Ibid. s 3(1).

193 : In this context ‘primary carer’ of the person means an adult who is in a care relationship with the person to be treated, and has principal responsibility for the person's care. Ibid. s 3(1).

194 : Ibid. s 55(3).

195 : Ibid. s 61(20(b) and (c).

196 : Ibid. s 61(2)(d).

197 : Ibid. s 61(3)(a)and(b).

198 : Ibid. s 61(3)(c).

199 : Ibid. s 61(3)(a)and(b).

200 : Ibid. s 61(3)(c).

201 : Ibid. s 62.

202 : Ibid. s 67.

203 : Ibid. s 70.

204 : Ibid. s 55(1)-(3).

205 : Ibid. ss 3(2) and 55(1) and (3).

206 : Ibid. s 102(5).

207 : Ibid. s 26.

208 : Ibid. s 29(a) to (c).

209 : Ibid. s 29(d).

210 : Ibid. s 32(1).

211 : Ibid. s 32(2).

212 : Ibid. s 31.

213 : Ibid. s 41(2).

214 : Ibid. ss 33 and 34.

215 : Ibid. s 94(1).

216 : Ibid. s 94(2).

217 : Ibid. s 94(3). Note that the support person is also authorised to disclose that information for the purpose of any proceeding under the Act , any report of a proceeding under the Act , or any other lawful purpose, see s 94(3)(b) and (c).

218 : See 12.6.5 and 12.6.7.

219 : Guardianship and Administration Act 2000 (Qld) s 6.

220 : Ibid. s 61.

221 : The term “health matter” is described in Schedule 2 ss 4 and 5 and “special health matter” in Schedule 2 ss 6 to 10 of the Guardianship and Administration Act 2000 (Qld).

222 : Guardianship and Administration Act2000 (Qld) Schedule 4. For examples the test for capacity in action see, Re IM [2003] QGAAT 16, Re L [2005] QGAAT 13 and Re MHE [2006] QGAAT 9.

223 : Ibid. Schedule 2, s 5(1).

224 : Ibid, ss 5(2) and 5A. The Queensland law relating to care and treatment at the end of life is discussed in Chapter 14.

225 : Ibid. Schedule 4.

226 : Ibid. Schedule 2, ss 5 and 7.

227 : Ibid. Schedule 2, s 5(3).

228 : Ibid. s 63(1).

229 : Ibid. s 63(2).

230 : Ibid. s 63(3).

231 : Ibid. s 63(4).

232 : Ibid. s 64(1)(a) and (b).

233 : Ibid. s 64(3).

234 : Ibid. s 64(1)(c).

235 : Ibid. s 64(2).

236 : Ibid. Schedule 2, ss 7 to 10. There has been no special health care prescribed under Schedule 2, s 7.

237 : Ibid. s 66(2).

238 : Ibid. s 66(3) to (5).

239 : Acts Interpretation Act 1954 (Qld) ss 32DA and 36 define “spouse” to include a “de facto partner”. De facto partners can be of the opposite or the same sex. The criteria for determining whether or not people are de facto partners are set out in s 32DA(2) of that Act.

240 : Powers of Attorney Act 1998 (Qld) s 63(1)(b). A person has the care of an adult if they provide domestic services and support to the adult or arrange for the adult to be provided with domestic services and support. Note also that where an adult resides in an institution (for example, a hospital, aged care facility home, group home, boarding-house or hostel) and is cared for there, they are not to be regarded as being in the care of that institution but remain in the care of the person in whose care they were immediately before residing in the institution. See, Powers of Attorney Act 1998 (Qld) s 64(3) and (4). See also Re L [2005] QGAAT 9 in which the then Guardianship and Administration Tribunal held that the Director of Mental Health could not be recognised as a carer under Guardianship and Administration Act 2000 (Qld) s 63(4).

241 : Powers of Attorney Act 1998 (Qld) s 63(1). A close friend, of an adult with impaired capacity, means another person who has a close personal relationship with the adult with impaired capacity and a personal interest in their welfare. See, Guardianship and Administration Act 2000 (Qld), Schedule 4.

242 : Ibid. s 63(2).

243 : Guardianship and Administration Act 2000 (Qld) s 42.

244 : Powers of Attorney Act 1998 (Qld) ss 62 and 63 and Schedule 3 and Guardianship and Administration Act 2000 (Qld) s 66.

245 : Guardianship and Administration Act 2000 (Qld) Schedule 1.

246 : Ibid. Schedule 1, s 12. The adult's views and wishes may be expressed orally or in writing, in an advance health directive or in another way, including, by conduct.

247 : Ibid. s 12(4).

248 : Guardianship and Administration Act 2000 (Qld) s 65(2).

249 : The Tribunal’s authority comes from the Guardianship and Administration Act 2000 (Qld) s 65(4). The Supreme Court’s authority arises from its parens patriae jurisdiction and the operation of s 65(3) of the same Act.

250 : Guardianship and Administration Act 2000 (Qld) s 76(1)

251 : Ibid. s 76(2).

252 : The Powers of Attorney Act 1998 (Qld) s 6A provides that that Act and the Guardianship and Administration Act 2000 (Qld) are to be read together. The definition of “attorney” in the Powers of Attorney Act 1998 (Qld) includes statutory health attorneys, see Schedule 3. Consequently, they are attorneys for the purposes the Guardianship and Administration Act 2000 (Qld) s 76.

253 : The term “guardian” means a guardian appointed under the Guardianship and Administration Act 2000 (Qld). The Public Guardian is appointed under s 199 of that Act. See, Guardianship and Administration Act 2000 (Qld), Schedule 4.

254 : Guardianship and Administration Act 2000 (Qld) s 76(4).

255 : Ibid. ss 63-68 and 82(1)(g).

256 : Ibid. ss 80A – 80Q and 82(1)(h).

257 : Ibid. s 74.

258 : [1] Ibid. s 82(1)(a) and (d). S 82(3) specifically provides that in this section “attorney” includes both attorneys under enduring documents and statutory health attorneys.

259 : Ibid. s 82(f). This matter is dealt with in more detail in Chapter 16.4.3.

260 : Ibid. s 67(1).

261 : Ibid. s 67(2). Note that this provision does not apply to special health care involving removal of tissue for donation and participation in special medical research or experimental health care or approved clinical research. See s 67(3).

262 : Queensland Law Reform Commission, Report No 49, June 1996, 361-362. Guardianship Act 1987 (NSW) ss 33(3) and 46(1)(a). See 12.3.1.10.

263 : [2006] QGAAT 11, [35].

264 : Ibid. [38].

265 : Ibid. [42].

266 : See Re CJ [2006] QGAAT 11.

267 : So might the impact of the common law. See Re Bridges [2000] QSC 188, [2001] Qd R 574 and Re CJ [2006] QGAAT 11.

268 : Guardianship and Administration Act 2000 (Qld) s 82(1)(d).

269 : Ibid. s 63(1) and (2). The complexity of this matter is further discussed in Chapter 14.4.3.

270 : Powers of Attorney Act 1998 (Qld) s 36(2).

271 : Guardianship and Administration Act 2000 (Qld) s 63A.

272 : Guardianship and Administration Act 2000 (Qld) s 63(3). The question of the adult’s understanding of the proposed health care or why it was required would be determined according to the principles in Re CJ [2006] QGAAT 11.

273 : Guardianship and Administration Act 2000 (Qld) s 35(2).

274 : Ibid. s 64(2).

275 : Ibid. s 75.

276 : Re CJ [2006] QGAAT 11.

277 : Guardianship and Administration Act 2000 (Qld) s 42.

278 : Ibid. s 43.The health care principle is set out in the Guardianship and Administration Act 2000 (Qld), Schedule 1, s 12. It is outlined at above at 12.7.5.

279 : Parts 9C and 9D of the Guardianship and Administration Act 1990 (WA).

280 : Ibid. s 110ZJ(1).

281 : This and other matters are taken up in 12.8.3.1 below.

282 : Guardianship and Administration Act 1990 (WA) s 3A. This was an issue before s 3A was added to the Act. See BCB [2002] WAGAB 1, [46] and Re BCB, Application for Guardianship Order [2002] SR (NSW) 338. As to the parens patriae jurisdiction of the Supreme Court of WA see, Minister for Health V AS [2004] WASC 286

283 : Guardianship and Administration Act 1990 (WA) s 3.

284 : Ibid. s 3(1).

285 : BTO [2004] WAGAB 2 [39]. WASAT continued in that view, see ADP [2005] WASAT 131 [24] and AB [2005] WASAT 303 [50].

286 : BTO [2004] WAGAB 2 [39].

287 : Ibid. [36].

288 : Ibid. [36].

289 : ADP [2005] WASAT 131.

290 : SJ and MET [2006] WASAT 210 [16].

291 : Ibid. [36] and [37].

292 : Ibid. [39] and [40].

293 : MW [2005] WASAT 205 [55]. See also AB [2005] WASAT 303 [ 54]-[55].

294 : Ibid. [56].

295 : BTO [2004] WAGAB 2 [37] referring to Re MC; Review of Guardianship Order (unreported Full Board, 7 May 2004 (Mrs P Eldred, Deputy President, Dr A McCutcheon and Ms F Child, Members)) 7.

296 : Guardianship and Administration Act 1990 (WA) s 110ZD (7).

297 : Guardianship and Administration Act 1990 (WA) s 110ZH.

298 : Ibid.

299 : While the relevant health professional will usually be a doctor, the term “health professional” is very widely defined and includes, chiropractors, dentists, dental therapists or dental hygienists, dental prosthetists , medical radiation technologist, midwifes, nurses, occupational therapists, optometrists, osteopaths, pharmaceutical chemists, physiotherapists, podiatrists, psychologists and any other person who practises a discipline or profession in the health area that involves the application of a body of learning. See Civil Liability Act 2002 (WA) s 5PA.

300 : Guardianship and Administration Act 1990 (WA) s 110ZI (2).

301 : Ibid. s 110ZIA.

302 : Ibid. ss 110ZH, 110ZD(7) and 56-63.

303 : Ibid. ss 56A and 58(1). The term “Full Tribunal” is defined in s 3 of the Act.

304 : Ibid. s 110ZJ.

305 : Ibid. s 110ZJ(1).

306 : For a case involving the Public Advocate seeking authority to make medical treatment decisions for a person for whom she was already his guardian, see CB [2021] WASAT 67

307 : Ibid. s 110ZD. For a consideration of “close personal relationship” see, Public Advocate and F [2007] WASAT 14 and DMS [2008] WASAT 14.

308 : For a case in which WASAT considered there was not need to appoint a guardian because there were persons around capable of acting as “persons responsible” for the person the subject of the application see, CGH and NVF [2010] WASAT 76 [33].

309 : See s 110ZG of the Guardianship and Administration Act 1990 (WA) and AC and AM [2013] WASAT 95 [10].

310 : Ibid. [20].

311 : Ibid. s 110ZD(8).

312 : See, Guardianship and Administration of Property Amendment Act 2008 (ACT).

313 : Guardianship and Management of Property Act 1991 (ACT) s 32A.

314 : Ibid.

315 : Ibid.

316 : Ibid. s 5.

317 : Guardianship and Management of Property Act 1991 (ACT) s 32N.

318 : See Office of Public Advocate website, www.publicadvocate.act.gov.au.

319 : Guardianship Act 1989 (NSW) s 37(1) and in Tasmania see,Guardianship and Administration Act 1995(Tas) s 4.

320 : In re F (1990) 2 AC 11, 76. See also Northridge v Central Sydney Area Health Service [2000] NSWSC 1241 [19]-[20].

321 : Guardianship and Management of Property Act1991 (ACT), Dictionary. At the time of writing no other medical procedure had been prescribed in the Act or the Guardianship and Management of Property Regulation1991 (ACT).

322 : Ibid. s 70(1) note.

323 : Ibid. ss 7 and 69.

324 : Ibid. s 70. Other aspects of the procedure that has to be followed, the matters ACATl has to take into account when determining whether the proposed procedure is in the person’s best interests and the special requirements about non-regenerative tissue are set out in s 70.

325 : Ibid. ss 32A and 32B.

326 : Ibid. The Legislation Act 2001 (ACT) s 169 describes the term “domestic partner” as a reference to someone who lives with the person in a domestic partnership, and includes a reference to a spouse or civil partner of the person. As to who is a “civil partner”, see the Civil Partnerships Act2008 (ACT).

327 : Guardianship and Management of Property Act1991 (ACT) ss 32A, 32B(1)(b) and 23C. Consistent with the approach in NSW, a carer is a person who gives, or arranges for the giving of, care and support to the incapable person in a domestic context but does not receive remuneration or reward, but may receive the care’s pension, for giving, or arranging for the giving of, the care and support. However, if the protected person lives in a hospital, nursing home, group home, boarding-house, hostel or similar place, a person giving, or arranging for the giving of, care and assistance to the protected person at that place is not, only because of that fact, a carer for the protected person.

328 : The term “close relative or friend “ is defined in s 32A to mean the same as it means in NSW namely, a relative or someone else in a close personal relationship with the person who has frequent contact with the person and a personal interest in the person’s welfare but does not receive remuneration or reward for the contact.

329 : Guardianship and Management of Property Act 1991 (ACT) s 32D(2).

330 : Ibid. s 32F(2) and (3).

331 : Ibid. s 67.

332 : Ibid. s 4.

333 : Ibid. s 32G.

334 : Ibid. s 4(2)(a) and (b).

335 : Ibid. s 32H.

336 : Ibid. s 32I.

337 : Ibid. s 32I(4).

338 : Advance personal Planning Act (NT) s 8.

339 : Advance Personal Planning Act (NT) ss 4 and 8.

340 : Ibid. s 8.

341 : Ibid. s 51.

342 : Ibid. s 51(3).

343 : Ibid. s 4. Decision-making capacity is described in s 6. It is the established common law test set out in statutory form. S. 6 also describes “impaired decision-making capacity” and sets out a number of matters that are not related to impaired decision-making capacity.

344 : Ibid. s 8.

345 : Ibid. 39(2). Note that a statement that does not constitute an advance consent decision is an advance care statement, s 39(3).

346 : Ibid. s 8(1)(b).

347 : Ibid. s 22.

348 : Ibid. s 3.

349 : Ibid. s 38.

350 : Ibid. s 6. S. 6 also describes “impaired decision-making capacity” and sets out a number of matters that are not related to impaired decision-making capacity.

351 : Ibid. s6(2).

352 : Ibid. s 26(4).

353 : Ibid. s 6(5).

354 : Ibid. s 41(1).

355 : Ibid. s 92.

356 : Ibid. s 20.

357 : Ibid. s 41(2) and (3).

358 : Ibid. s 41(3).

359 : Ibid. s 22.

360 : Ibid. s 42(1).

361 : Ibid. s 43.

362 : Ibid. s 44.

363 : Ibid. s 43.

364 : Ibid. s 25.

365 : Guardianship of Adults Act (NT) s 4.

366 : the Advance Personal Planning Act (NT) s 41.

367 : Ibid. s 23.

368 : Ibid. s 44(1).

369 : Ibid. s 44(4).

370 : Guardianship of Adults Act (NT) s 25. Note that new health care and electroconvulsive therapy were prescribed as restricted health care by clause 3 of the Guardianship of Adults Regulations (NT).

371 : Ibid. s 4.

372 : Advance Personal Planning Act (NT) s 25 and Guardianship of Adults Act (NT) s 23(2).

373 : Advance Personal Planning Act (NT) s 3.

374 : Ibid. ss 22(6) and (7), and 57.

375 : Ibid. s 44(a).

376 : {See for example Medical Treatment Planning and Decisions Act 2016(Vic) s 53(1)(a) to (c).

377 : Medical Treatment Planning and Decisions Act 2016 (NSW) ss 3(1) and 55.

378 : Guardianship and Management of Property Act1991 (ACT) ss 5 and 32A.

379 : In re C [1994] 1 All ER 819, 822 and 824. The test articulated in this case was originally proposed by a forensic psychologist, Dr Eastman. For an example of the test in action in an application to medical treatment overriding a patient’s objection to medical treatment (treatment to stabilise and repair a broken femur) see, (Unreported, NSW Guardianship Tribunal, Matter No. 2004/6512, 26 Nov. 2004).

380 : For a case in which the evidence about a person’s capacity to consent to psychiatric treatment is thoroughly considered and the decision was based on a 4 limbed test that included the considerations stated in the 2 lists just set out see, In the matter of ER [1025] ACAT 73.

381 : Guardianship Act 1989 (NSW) s 33(1) and Guardianship and Administration Act 1995 (Tas) s 3.

382 : Guardianship and Administration Act 2019 (Vic) s 3(1), definition of “medical treatment decision”

383 : Guardianship and Administration Act 1993 (SA) s 3.

384 : Guardianship and Administration Act2000 (Qld) Schedule 2, s 5(1).

385 : Ibid. ss 5(2) and 5A.

386 : Ibid. Schedule 4.

387 : Munjaz v Mersey Care National Health Service Trust [2003] EWCA Civ 10.

388 : Reid v Secretary of State for Scotland [1998] UKHL 43; [1999] 2 AC 512 and B v Croydon Health Authority [1995] Fam 133.

389 : Munjaz v Mersey Care National Health Service Trust [2003] EWCA Civ 10, [42]-[45].

390 : Regina (Munjaz) v Mersey Care National Health Service Trust [2005] UKHL 58, [2006] 2 AC 148.

391 : Ibid. [39].

392 : Ibid. [19].

393 : Ibid. [67].

394 : Ibid. [103].

395 : Guardianship and Administration Act 1990 (WA) s 3(1).

396 : Guardianship and Management of Property Act 1991 (ACT) s 32A.

397 : BTO [2004] WAGAB 2 [39]. See also, ADP [2005 WASAT 131 [24] and AB [2005] WASAT 303 [50]. See 12. 7. 2.

398 : [2003] VSC 173, 7 VR 487 [75] – [78] and also [90] – [91].

399 : BTO [2004] WAGAB 2 [39]. See 12. 7. 2.

400 : MW [2005] WASAT 205 [55]. See also AB [2005] WASAT 303 [54]-[55]. BTO [2004] WAGAB 2 [37] referring to Re MC; Review of Guardianship Order (unreported Full Board, 7 May 2004 (Mrs P Eldred, Deputy President, Dr A MCCutcheon and Ms F Child, Members)) 7. See 12.7.2.

401 : BCB [2002] WAGAB 1, Re BCB; Application for a Guardianship Order [2002] SR (WA) 338.SJ and MET [2006] WASAT 210. See 12.7.2.

402 : See, LD [2000] NSWGT 4; MA [2001] NSWGT 2 ; FB [1994] NSWGB 2; KB [1999] NSWGT 2; PA [2004] NSWGT 1. See also FA [1994] NSWGB 1. See 12.3.1.10 and 12.12.1.

403 : Re CJ [2006] QGAAT 11. See 12.3.1.10.

404 : Mercy Hospitals Victoria v D1 & Anor [2018] VSC 519.

405 : Ibid. [1] and [2].

406 : Ibid. [2].

407 : Ibid. 3.

408 : Ibid.4.

409 : Ibid.5.

410 : Ibid. 6.

411 : Ibid. 44.

412 : Ibid. [73 and 74.

413 : Ibid. 76.

414 : Schillerstrom JE, Horton MS, Royall DR. (2005) “The impact of medical illness on executive function”, Psychosomatics (2005) 46(6):508-16.

415 : Stein J, Brady Wagner LC “Is informed consent a ‘yes or no’ response? Enhancing the shared decision-making process for persons with aphasia”. Top Stroke Rehabil. (2006)13(4):42-6.

416 : Cairns R, Maddock C, Buchanan A, David AS, Hayward P, Richardson G, Szmukler G, Hotopf M “Reliability of mental capacity assessments in psychiatric in-patients.” Br J Psychiatry. 2005 Oct;187:372-8.

417 : Palmer BW Jeste DV “Relationship of individual cognitive abilities to specific components of decisional capacity among middle-aged and older patients with schizophrenia.” Schizophr Bull. 2006 Jan;32(1):98-106

418 : In re C [1994] 1 All ER 819.

419 : BMA, op cit, (footnote 346) p 161.

420 : Moye J, Karel MJ, Gurrera RJ, Azar AR et al “Neuropsychological predictors of decision-making capacity over 9 months in mild-to-moderate dementia”, J Gen Intern Med 2006 21(1):78-83.

421 : Huthwaite JS, Martin RC, Griffith HR, Anderson B, Harrell LE, Marson DC. “Declining medical decision-making capacity in mild Alzheimer's Disease: a two-year longitudinal study”, Behav Sci Law. 2006 24(4):453-63.

422 : Marson DC,Chatterjee A, Ingram KK, Harrell LE, “Toward a neurologic model of competency: Cognitive predictors of capacity to consent in Alzheimer's disease using three different legal standards”, Neurology 1996; 46(3):666-72

423 : D.Moye J, Karel MJ, Gurrera RJ, Azar AR, “Neuropsychological predictors of decision-making capacity over 9 months in mild-to-moderate dementia”, J Gen Intern Med 2006 21(1):78-83.

424 : http://www.aihw.gov.au/publications/welfare/dpida/dpida-c00.html

425 : Cea CD, Fisher C.B. “Health care decision-making by adults with mental retardation.” Mental Retardation 2003; 41(2): 78-87.

426 : Wong J.G. Clare ICH, Holland A.J., Watson P.C., Gunn M. “The capacity of people with a “mental disability” to make a health care decision.” Psychological Medicine 2000, 30(2); 295-306.

427 : Ibid.

428 : Marson D.C., Dreer L.E., Krzywanski S., Huthwaite J.S., Devivo M.J., Novack TA. (2005) “Impairment and partial recovery of medical decision-making capacity in traumatic brain injury: a 6 month longitudinal study” Arch Phys Med Rehabi 2005 86(5) :889-95.

429 : Sullivan K. “Neuropsychological assessment of mental capacity.” Neuropsychology Review 2004; 14(3):131-142.

430 : Ganzini L, Volicer L, Nelson WA, Fox E, Derse AR, “Ten myths about decision-making capacity.” J Am Med Dir Assoc 2005 6(3 Suppl):S100-4.

431 : Wong J.G. Clare ICH, Holland A.J., Watson P.C., Gunn M. “The capacity of people with a ‘mental disability’ to make a health care decision.” Psychological Medicine 2000, 30(2); 295-306.

432 : Sullivan K Mental Capacity. Powers of Attorney and advance health directives (2005) Collier B, Coyne, Sullivan K. Leichardt :The Federation Press.

433 : Davis DHJ. “Subjective estimates of cognitive impairment in older surgical patients. Implications for giving informed consent” Journal of the American Geriatrics Society (2005), 53(10) 1842 -1843.

434 : Gurian, Baker, Jacobson, Lagerbom and Watts (1990).

435 : Sullivan K In Mental Capacity. Powers of Attorney and advance health directives Collier B, Coyne, Sullivan K. (2005) Leichardt :The Federation Press.

436 : Grisso T, Appelbaum PS (1995) “Comparison of standards for assessing patients' capacities to make treatment decisions” Am J Psychiatry. 152, 1033-1037.

437 : Roth LH, Meisel A, Lidz CW. “Tests of competency to consent to treatment” American Journal of Psychiatry (1977) 134: 279-284.

438 : Fitten LJ, Lusky R, Hamann C. “Assessing treatment decision making in elderly nursing home patients” Journal of the American Geriatrics Society (1990) 38: 1097-1104.

439 : Janofsky JS, McCarthy RJ, Folstein MF “The Hopkins Competency Assessment Test: A brief method for evaluating patients capacity to give informed consent” Hospital and Community Psychiatry (1992) 43(2): 132-136.

440 : Grisso T, Appelbaum PS (1995) “Comparison of standards for assessing patients' capacities to make treatment decisions” Am J Psychiatry. 152, 1033-1037.

441 : Grisso T, and Applebaum PS “The MacArthur Treatment Competence Study. I: Mental illness and competence to consent to treatment” Law Hum Behav. 1995 19(2):105-26.

442 : Grisso T, and Applebaum PS “The MacArthur Treatment Competence Study. II: Measures of abilities related to competence to consent to treatment” Law Hum Behav. (1995) 19(2):127-48.

443 : Grisso T, and Applebaum PS (1995) “The MacArthur Treatment Competence Study. III: Abilities of patients to consent to psychiatric and medical treatments” Law Hum Behav. (1995) 19(2):149-74.

444 : Gristo T, Appelbaum PS, Hill-Fotouhi C. 'The MacCat -T: a clinical tool to assess patients' capacities to make treatment decisions' Psychiatry Serv. 1997 Nov; 48(11):1415-9.

445 : Etchells E, Darzins P, Silberfeld M, Singer PA, McKenny J, Naglie G, Katz M, Guyatt GH, Molloy DW, Strang D. “Assessment of patient capacity to consent to treatment” J Gen Intern Med. (1999) 14 (1):27-34.

446 : Marson DC, Ingram KK, Cody HA, Harrell LE. “Assessing the competency of patients with Alzheimer’s disease under different legal standards” Arch Neurol 1995; 52: 949–954.

447 : Darzins, P, Molloy DW, Strang D. (Ed) Who can decide? The six step capacity assessment process (2000) Memory Australia Press, Adelaide, 58-71.

448 : Stewart C, Biegler P A “Primer on the law of competence to refuse medical treatment” Australian Law Journal (2004) 78: 325-342.

449 : Sullivan K In Mental Capacity. Powers of Attorney and advance health directives Collier B, Coyne, Sullivan K. Leichardt :The Federation Press, p128.

450 : Dunn LB,Nowrangi MA, Palmer BW, Jeste DV, Saks ER “Assessing decisional capacity for clinical research or treatment: a review of instruments” Am J Psychiatry. 2006 Aug;163(8):1323-34.

451 : Darzins, P, Molloy DW, Strang D. (Ed) op. cit.(footnote 377), p 6.

452 : Parker M, Cartright M, In: Mental capacity in medical practice and advance care planning : clinical ethical and legal issues In Collier B, Coyne C, Sullivan Mental Capacity Federation Press: Annandale 2005 p74.

453 : Re T [1992] EWCA Civ 18; [1993] Fam 95, 113; Re MB [1997] EWCA Civ 1361 and Re B [2002] EWHC 429 (Fam) [31].

454 : Parker M, Cartright M, In: Mental capacity in medical practice and advance care planning : clinical ethical and legal issues In Collier B, Coyne C, Sullivan Mental Capacity Federation Press: Annandale 2005 p74.

455 : Hertogh CMPM Autonomy, competence and advance directives. In: Jones GGM, Miesen BML. (eds) Caregiving in dementia. Research and applications. (Vol 3) New York London, Brunner Routledge, 2004, p391-403.a.

456 : Darzins, P, Molloy DW, Strang D. (Ed) op. cit.(footnote 379) p64-67.

457 : Parker M., and Cartright C: Mental capacity in medical practice and advance care planning : clinical ethical and legal issues In Collier B, Coyne C, Sullivan Mental Capacity Federation Press: Leichhardt 2005 p74.

458 : D.Moye J, Karel MJ, Gurrera RJ, Azar AR “Neuropsychological predictors of decision-making capacity over 9 months in mild-to-moderate dementia” J Gen Intern Med. 2006 21(1):78-83.

459 : Palmer BW Jeste DV “Relationship of individual cognitive abilities to specific components of decisional capacity among middle-aged and older patients with schizophrenia” Schizophr Bull. 2006 32(1):98-106.

460 : Rogers DM. Crookston KP “The approach to the patient who refuses blood transfusion” Transfusion (2006) 46: 1471-1477.

461 : Stamou SC, White T, Barnett S, Boyce SW, Corso PJ, Lefrak EA. “Comparisons of Cardiac Surgery Outcomes in Jehovah's Versus Non-Jehovah's Witnesses” Am J Cardiol. 2006; 98(9):1223-5.

462 : Massiah N, Abdelmagied A, Samuels D, Evans F, Okolo S, Yoong W. “An audit of gynaecological procedures in Jehovah's Witnesses in an inner city hospital” J Obstet Gynaecol. 2006 26(2):149-51

463 : Stamou SC, White T, Barnett S, Boyce SW, Corso PJ, Lefrak EA. “Comparisons of Cardiac Surgery Outcomes in Jehovah's Versus Non-Jehovah's Witnesses” Am J Cardiol . 2006; 98(9):1223-5.

464 : [2009] NSWSC 761.

465 : KB [1999] NSWGT 2.

466 : Ibid. 10.

467 : KB [1999] NSWGT 2.

468 : Re AF (unreported, NSW Guardianship Tribunal, matter no 2004/1867, 6 April 2004).

469 : Stewart, C “Advance directives: Disputes and dilemmas” in Freckelton, I and Petersen, K, op cit pp 49-50. For a case in which the former Guardianship and Administration Board of Victoria did not, in an emergency situation, pursue the likelihood that a person refusing a blood transfusion may have been a Jehovah’s Witness and may have had an advance directive in the form of a “blood card” see, Qumsieh v Guardianship and Administration Board (1998) 14 VAR 46. See also Stewart’s discussion of that case, and related matters, in Stewart, C, “Qumsieh’s Case, Civil Liability and the Right to Refuse Medical Treatment”, (2000) 8 JLM 56.

470 : For a case in which the Tribunal refused consent to a blood transfusion see, MA [2001] NSWGT 2. For cases in which the Tribunal gave consent to blood transfusions see, Re JJ (unreported, Guardianship Tribunal Matter No. 1999/5085, 20 October 1999), Re IL (unreported, Guardianship Tribunal Matter No. 1994/2383, 18 July 1994) and NKQ [2008] NSWGT 21.

471 : NSW Kids and Families (2014). Youth Health Resource Kit: An Essential Guide for Workers. NSW Kids and Families: Sydney. Section 3.5 Medico-legal issues (Kang, M & Sanders, J) Retrieved from http://www.kidsfamilies.health.nsw.gov.au/media/318781/youth-health-resource-kit-revised.pdf

472 : [1985] UKHL 7; [1986] AC 112 at 188-89.

473 : Ibid. See [1985] UKHL 7; [1986] AC 112 at 188-89.

474 : Cea CD, Fisher C.B. "Health care decision-making by adults with mental retardation." Mental Retardation 2003; 41(2): 78-87.

475 : Ibid.

476 : Ibid.

477 : Secretary, Department of Health and Community Services v JWB and SMB [1992] HCA 15; [1992] 175 CLR 218; (Marion’s Case).

478 : Cea CD, Fisher C.B. "Health care decision-making by adults with mental retardation." Mental Retardation 2003; 41(2): 78-87.

479 : British Medical Association Medical ethics today. 2nd ed. London: BMJ Publishing Group, 2004: 230–1.

480 : X v The Sydney Children’s Hospitals Network [2013] NSWCA 320.

481 : Minors (Property and Contracts) Act 1970 s 49 (1) and (2).

482 : See Kerridge, I, Lowe, M, and Stewart, C, in Ethics and Law for the Health Professions, Leichhardt, The Federation Press, 4th ed 2013, pp 589-90.

483 : Guardianship Act 1987 (NSW) s 34. The purpose of that Act was to provide a regime for doctors and dentists obtaining substitute consent to medical or dental treatment proposed by them for a person unable to give a valid consent to the proposed treatment. Consequently, a person who is under 16 years of age and who is Gillick competent to give (or refuse) consent to medical or dental treatment proposed for them is not affected by that Act. As the Guardianship Act was enacted after the Minors (Property and Contracts) Act and has particular provisions relating to substitute consent to medical and dental treatment, those provisions will prevail over the provisions of the Minors (Property and Contracts) Act, including s 49 of that Act, to the extent of any inconsistency. However, as the relevant provisions of the Minors (Property and Contracts) Act are aimed at the issue of liability for assault or battery for giving medical or dental treatment without consent, the likelihood of a conflict between the two pieces of legislation is slight.

484 : Consent to Medical Treatment and Palliative Care Act 1995 (SA) ss 4 and 6.

485 : Ibid. s.12.

486 : The principle is dealt with more detail in 12.2.1. However, s 13(5) of the Act applies in relation children in need of urgent treatment in South Australia. The subsection provides that if a parent or guardian of the child is available to decide whether the medical treatment should be administered, their consent to the treatment must be sought. However, the subsection (s 13(5)) states, in terms, that the child's health and well-being are paramount and that, if the parent or guardian refuses consent, the treatment may be administered despite the refusal if it is in the best interests of the child's health and well-being [that they receive the treatment].

487 : Wong J.G. Clare ICH, Holland A.J., Watson P.C., Gunn M. “The capacity of people with a “mental disability” to make a health care decision” Psychological Medicine 2000, 30(2); 295-306.

488 : In re C [1994] 1 All ER 819, 822 and 824; Re MB [1997] EWCA Civ 1361; Re B [EWHC 429 (Fam) [33]; Re NK (unreported Guardianship Tribunal NSW, C/28379, Matter Nos 2004/1672 and 2004/1673, 3 June 2004).

489 : Parker M., and Cartright C: Mental capacity in medical practice and advance care planning : clinical ethical and legal issues In Collier B, Coyne C, Sullivan Mental Capacity Federation Press; Leichhardt 2005 p 67.


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