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week 2 vle
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informed consent
starting point for protecting rights and interests of individuals
consent is very powerful
informed consent is a legitimacy requirement for certain actions:
consent is needed to make certain actions legally and ethically permissible
lack of consent can turn a well-intended medical intervention into assault or battery
autonomy
complex and debated philosophical concept
self rule that is free from both controlling interference by others and from certain limitations such as inadequate understanding that prevents meaningful choice
respecting autonomy is part of respecting rights and interests of patients
deontology
rules govern actions and we have a duty to abide by them regardless of cost
contrasted with emphasis on outcomes
“the right is prior to the good”
often seeks to respect autonomy
it’s the only way to respecting an individual’s right to determine their own life
4 principles of biomedical ethics
respect for autonomy
beneficence
non-maleficence
justice
consent in healthcare
treatment
investigation
examination
disclosure of information
research
education
battery- English law and consent
to avoid a charge of battery, a doctor must have valid conset
for a pt to give consent, they must understand the broad nature of the procedure
the pt need not be harmed by procedure to claim damages if battery is proved
GMC guidance
encourages a proportionate approach to consent
emphasises that obtaining consent doesn’t need to be a formal, time consuming process
need to exercise your own judgement
3 basic elements of consent
competence/capacity
information
voluntariness
attempts should generally be made to maximise quality of consent
capacity
assessment of a person’s capacity must be based on their ability to make a specific decision at the time it needs to be made
a person is unable to make a decision if they can’t do one or more of the following:
understand the information given to them that is relevant to the decision
retain that information long enough to be able to make the decision
use/weigh up information as part of the decision-making process
communicate their decision
working on capacity
assume: every adult patient has capacity to make decisions
do not assume that because of someone’s age, disability or communication difficulties that they lack capacity
they may simply need extra support to help make/communicate decisions
capacity can be decision-dependent and can change: a pt may be able to make simple decisions (but not complex ones) at a particular moment
special considerations apply to adult who lack capacity and to children
capacity and autonomy
capacity is a legal concept
autonomy is an ethical/philosophical concept
may overlap, but not exactly the same
information
consent needs to be sufficiently informed, but information provision should be tailored to specific patient and situation
you must give pts the information they want or need to make a decision
what information may include
diagnosis/prognosis
uncertainties about these
options for treating/managing condition
nature of each option, what would be involved, desired outcome
potential benefits/harms/likelihood of success
you should not rely on assumptions about
information a patient might want or need
factors a patient might consider significant
importance a patient might attach to different outcomes
voluntariness
consent should be freely given without coercion
some patients may be under pressure from employers, relatives or insurers to make particular decisions
if there are suspicions of external pressures, efforts should be made to speak to the patients by themselves to establish whether their decision is voluntary
voluntariness involves
explicit coercion
implicit coercion
power differentials in the pt/doctor relationship
pressure from family
different forms of consent
implied consent via compliance
a pt may roll up their sleeve to have their blood pressure taken
oral consent
appropriate for low risk procedures/treatments
written consent
generally sought for complex or higher-risk interventions
also if there are significant consequences for pt’s employnent, social or personal life
if clinical care is part of a research study
some specific treatments, such as fertility treatment, legally require written consent
written consent form
a signed consent form doesn’t mean that consent is valid
if pt:
lacked capacity
was not provided with sufficient info
did not give consent voluntarily
their consent will not be valid
written consent is evidence, rather than evidence of valid informed consent
therefore important to also document significant aspects of consent conversation