Ethical/Legal Aspects of Consent to Investigation or Treatment

March 17, 2003ISD II – MSK

Barbara BarrowmanAndrew Latus

Outline – Consent

General Significance Forms of Consent Elements of a Valid Consent Exceptions to Requirement of Consent

– Primary focus will be on legal aspects of consent

General Considerations

a mentally competent patient has right to refuse medical treatment, regardless of consequences and how beneficial or necessary treatment may be

– This is both a legal requirement as well as, to most, a moral requirement

consent is often viewed as the single most ethically important aspect of medical ethics

– “all of medical ethics is but a footnote to informed consent” (Mark Kuczewski, 1996)

– But why is consent so important?

Consent: Moral Significance main reason: the requirement of consent reflects the

ethical principle of patient autonomy

to some extent principles of beneficence/non-maleficence also support importance of consent

figuring out what is in a patient’s ‘best interests’ is notoriously difficult in some cases.

– Distinguish medical best interest from best interests ‘all things considered’

often we take the view that the patient is the best judge of what is in his own best interest ‘all things considered’

Consent: Legal Significance

save in exceptional circumstances, medical treatment must not be administered without obtaining patient’s valid consent

treatment/investigations performed without consent constitute “battery”

no liability results from decision to withhold or withdraw even life-sustaining treatment at request of competent patient

Forms of Consent - Written or Oral as general rule, no legal requirement that consent be

in written form

written consent = evidence

hospital practice to require written consent

consent not a piece of paper, but part of a process of communication between doctor and patient

– Beware of tendency to treat signs of consent as more important than consent itself

Forms of Consent - Express or Implied consent may often be implied by words or

conduct e.g. holding out arm for injection

many examinations, some procedures routinely performed with implied consent

prudent to document for anything but the most minor interventions

Withdrawing Consent

right to withdraw consent at any time

doctor must stop treatment once consent withdrawn unless life-threatening or immediate serious problems to health of patient to stop

if unclear whether consent being withdrawn, doctor must stop to ascertain

Elements of Consent

1. Voluntary

2. Capacity

3. Specific to Treatment & Person Administering It

4. Informed

1. Voluntary

Some factors interfering with voluntariness

– coercion by physician, family or others Line between coercion & legitimate influence can be

tricky

– pre-op sedation

– misrepresentation as to nature of treatment or procedure

2. Capacity

presumption that adults have legal capacity

capacity = ability to understand and appreciate nature and purpose of treatment and consequences of giving or refusing consent– See notes from Psychiatry

if patient has capacity, no one else’s consent required

problem areas - mental disability, minors

Capacity - (a) Mental Disability

impairment may be temporary or permanent

assessment of capacity is functional - specific to issue in question– i.e., not all or nothing

not automatically lacking capacity because of Dx of dementia, psychosis, etc.

refusal of treatment others see as beneficial or necessary does not imply incompetence

Capacity - Mental Disability

assessment - expert assistance

documentation

substitute consent

Advance Health Care Directives

Capacity - (b) Minors

legislation in some provinces

common law - regardless of age, child capable of consenting if able to appreciate nature and purpose of Rx and consequences of giving/refusing consent (“mature minor”)

if child has capacity, parental consent not required, nor can they override child

common practice to get parental consent

Capacity – Minors

if child lacks capacity, parents have (joint) legal authority to make treatment decision

parental refusal can be overridden by court order if not in child’s best interests (child protection legislation)

many controversial areas e.g. contraception, abortion, religious beliefs

Capacity - Minors

Interaction between mature minor principle & child welfare legislation is a difficult & controversial area

E.g., B.H. Case Will be discussed in pediatrics course

3. Treatment and Treating MD

patient should only receive that treatment to which (s)he has consented, apart from emergency

importance of clear communication

consent specific to doctor who will carry out care or treatment

presence and role of house staff should be made clear to patient

Treatment and Treating MD

consent should be obtained by person who will carry out care or treatment

role of obtaining informed consent may be delegated (e.g. resident), but before delegating, treating MD should be confident delegate has knowledge and experience to provide adequate explanations to patient

responsibility rests with delegating MD

4. Informed Consent

Four points

(a) importance

(b) standard of disclosure

(c) research/experimental treatment

(d) documentation

(a) Importance

gives meaning to patient’s right to medical self-determination, profound impact on nature of doctor-patient relationship

focus on effective communication

frequent basis of litigation - failure to obtain informed consent may constitute “negligence” or substandard care

(b) Standard of Disclosure

…in obtaining the consent of a patient for a surgical operation, the surgeon, generally, should answer any specific questions posed by the patient as to the risks involved and should, without being questioned, disclose to him the nature of the operation, its gravity, any material risks and any special or unusual risks…

(Reibl v. Hughes, S.C.C. 1980)

Standard of Disclosure

professional disclosure standard vs. reasonable patient standard

Canadian Standard: what a reasonable person in the patient’s position would want to know– Reibl vs. Hughes– compromise between reasonable person standard and

subjective standard

material risks include common risks and risks which are mere possibilities but have serious consequences, e.g. death, paralysis

Standard of Disclosure

insofar as possible, tell patient the diagnosis

if uncertainty, explain this

explain nature of proposed treatment, its gravity, chances of success and risks

give patient opportunity to ask questions

be alert to patient’s individual concerns and circumstances and deal with them

Standard of Disclosure

patient should be told consequences of non-treatment - no coercion but entitled to information

accepted alternative forms of treatment (no obligation to discuss unconventional Rx)

optimism should not allow misinterpretation of guaranteed results

Standard of Disclosure

although patient may waive explanations, have no questions and be prepared to submit to treatment, doctors must be cautious in accepting such waivers

“therapeutic privilege” (withholding or generalizing information due to patient’s emotional condition) - use very cautiously– once much more widely accepted than today– part of shift away from paternalism

Standard of Disclosure

consent for cosmetic or other “medically non-necessary” procedures - take special care re. risks and expected results– courts may impose higher standard of disclosure

patients must be informed re. planned delegation of care

supplements to consent explanations - pamphlets, etc.

(c) Research/Experimental Rx full disclosure required, “therapeutic privilege” not

applicable

consent requirements even stronger morally than in standard treatment situation – less possibility of appeal to beneficence if treatment is

untested, so respecting patient autonomy is more important

caution re. coercion if doctor-patient relationship with researcher

patient must understand possibility of placebo/alternative treatment

research and minors/incompetents

(d) Documentation

consent form - identification, acknowledgement of explanations, anesthesia, added/alternative procedures, delegation, signatures, witness

contemporaneous note - brief summary of informed consent discussion, risks discussed, any special concerns/questions

Exceptions to Requirement of Consent

emergency situations

legislation

1. Emergencies

may treat without consent if:

1. injury life-threatening or imminent threat to patient’s health,

2. patient not able to give consent, e.g., comatose, severe injuries, incompetent, and

3. substitute decision maker not readily available

2. Legislation

mental health legislation - detention +/- treatment of patients with mental disorder who are danger to selves or others

other examples of law providing for compulsory treatment

Charter of Rights issues

Controversies about Informed Consent

idea of the absolute centrality of informed consent is relatively recent

some challenge the importance of informed consent on the grounds that it reflects an unrealistic picture of patients’ ability to understand what they are consenting to– see studies cited in Bunch (2000)

Informed Shared Decision-Making

not a legal term, but in some ways a better term to describe ideal process of medical decision-making

emphasis on discussion, working together with patients in deciding best way to proceed

“meeting between experts” - MD expert in disease, patient expert in own experience of disease and in their preferences

– emphasis placed on consent can hide the appropriately collaborative nature of medical treatment