1 Geriatric and General Medicine, Leeds General Infirmary, Leeds LS3
2 Elderly Medicine, Beckett Wing, St James's University Hospital, Beckett
Street, Leeds LS9 7TF, UK
Correspondence to: Professor Graham Mulley E-mail: Graham.Mulley{at}leedsth.nhs.uk
| INTRODUCTION |
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| IMPACT OF THE HUMAN RIGHTS ACT |
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| INVOLVEMENT OF THE FAMILY IN DECISION-MAKING |
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Family members will often have knowledge of the previously held views and wishes of a now incompetent or seriously ill patient, but care must be taken not to worsen their distress by asking them to make decisions about management in the terminal phase: the ultimate decision is the doctor's and should not be delegated.
In the case of incompetent patients, involvement of family members is desirable. The law varies in different parts of the UK. The Mental Capacity Bill of England and Wales favours 'lasting powers of attorney' whereby a trusted friend or relative is able to refuse or consent to medical treatment if previously authorized to do so by the patient.8 In Scotland, the Adults with Incapacity (Scotland) Act 2000 has since 2002 allowed a proxy's decision to be legally binding.9
| FACTORS THAT CAN AFFECT DECISION-MAKING |
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Age
Ethical decisions should be free from
ageism12 (article
14 of the Human Rights Act specifies the right to be free from such
discriminatory practices) and should be made without regard to resource
constraints.13 In
practice, physicians are as likely to attempt cardiopulmonary resuscitation as
to withhold it in an aged
patient;2 however,
age can legitimately enter the discussion. When dealing with patients and
relatives, doctors need to make clear that 'do not resuscitate' is
not a sign of abandonmentin other words, the patient will continue to
receive comfort, symptom control, dignified care and psychological
support.
Competence
Competence signifies that the individual comprehends and retains pertinent
information, is able to believe and weigh up the information and can make a
decision on treatment. The issue of mental capacity arises when an individual
wants to make an 'advance statement' or when there is doubt about
his or her understanding concerning a particular treatment being proposed.
An adult is presumed to be competent until the contrary is proved. The burden of proof rests on those who are ascertaining incapacity. Once someone is judged to be incompetent, this state is presumed to continue. Competence can fluctuate; a decision taken during a lucid interval is considered valid. Doctors have to ensure that decisions on treatment are made without manipulation or coercion in any form. When the patient is judged incompetent, his or her previously held wishes (where known) should be taken into account; and where these wishes are not known the doctor must act in the patient's best interest, in the light of what is known of his or her past and present feelings together with clinical factors. Information from those close to the patient (including the general practitioner) may be helpful.
Patient autonomy
There has been a move in medicine from benign paternalism to patient
autonomy and shared decision-making. Patients have higher expectations than
formerly, people are living longer, and doctors are increasingly facing
patients with complex disorders. In the USA, under the Patient Self
Determination Act, every individual has a statutory right to accept or refuse
medical care and to execute a written advance
directive.14 In
Britain there is no such mandatory requirement, but article 10 of the Human
Rights Act (the right to hold opinions and receive information) relates to the
involvement of patients in decisions.
Doctors are not always skilled in anticipating the wishes of their patients.15 Even frail elderly patients are often pleased when their physicians initiate discussions about future choices. By raising the subject of death, doctors can allow patients to express their hopes and fears, and families too may appreciate the opportunity to talk of these things.17 Sometimes an obstacle to such discussions is distress and lack of understanding on the part of the physician.18
| SPECIFIC CLINICAL QUESTIONS |
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According to article 2 of the Human Rights Act every individual has the right to life. However, it is clear that in certain circumstancesthe patient with severe broncho-pneumonia, or bedfast with metastatic cancer, or with sepsis and multiple organ failure, or with acute major stroke, or with dementia requiring long-term care24 cardiopulmonary resuscitation has a negligible chance of success. Doctors are not obliged to offer treatments they believe to be inappropriate or futile; nevertheless, dilemmas at times of crisis can often be avoided by earlier discussion and the provision of information to patient and family.
Transplantation
Some people may decide long before death to donate organs but omit to
inform their close relatives; and even when the patient has made a clear
decision on organ donation through an advanced statement or a donor card the
relatives may still be unwilling to allow it to happen. There are no clear
guidelines on whose wish is to be
followed,25 but it
certainly helps if during the final illness the individual has confirmed that
his or her previous wishes still apply. The same principle applies to donating
the body or organs for the benefit of medical science (e.g. anatomy
teaching).
Artificial nutrition and hydration
Artificial nutrition and hydration are legally established as medical
treatments in the UK, though this definition is not universally
accepted.26 Under
the Medical Treatment Act of 1988 the competent patient has the right to
refuse these interventions in the same way as other treatments. However, if
tube feeding is regarded as a means of sustaining life, withdrawal of food and
fluid could lay a doctor open to a charge of murder. At present a court order
is needed in England, Wales, and Northern Ireland, though not in Scotland, to
withdraw these interventions in patients with persistent vegetative state or a
similarly low awareness.
There is an argument for extension of these provisions to patients with advanced dementia and severe stroke.27 In one study28 of hypothetical life-sustaining treatment (involving 339 hospital physicians and 987 randomly selected elderly people) physicians favoured artificial feeding over cardiopulmonary resuscitation, whereas the elderly participants took the opposite view. This difference may reflect the inflated public notion of cardiopulmonary resuscitation. The professional dilemmas are illustrated by the finding that, in a hypothetical situation of metastatic cancer, physicians would want less life-sustaining treatment for themselves than they would give to an elderly patient. Current guidelines recommend the withholding or withdrawal of artificial nutrition and hydration when death is imminent or the burdens or risks of providing fluid and nutrition outweigh the benefits.25 It would be helpful to have the patient's clearly expressed views on such treatments that delay an inevitable death, when the wishes of relatives and the judgment of the clinician are in conflict.
Ventilation
Artificial ventilation in a young person with severe asthma is very
different from artificial ventilation in an 80-year-old patient with end-stage
chronic obstructive pulmonary disease. Mechanical ventilation in elderly
people is sometimes initiated because of lack of advance care
planning.29 Most of
these patients will never previously have entered an intensive therapy unit or
seen a ventilator, hence the need for earlier information and discussion when
possible. Documentation in the medical notes of the patient's expressed
views on matters such as ventilation would help clinicians make decisions in a
crisis.
Surgery
Sometimes a patient admitted with an apparently straightforward problem
(for example, collapse) turns out to have a condition such as critical aortic
stenosis or leaking abdominal aortic aneurysm that would normally require
major surgery. If the patient is unable to decide whether to have the
operation, the doctor will again be much helped by knowing the patient's
views on major surgery expressed at the time of admission or before.
| ADVANCE DIRECTIVE (LIVING WILL) |
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An advance directive may be a written document, a witnessed oral statement or a note in the patient's file following a discussion with a healthcare professional. An advance directive made by a competent adult is binding under common law and can relieve both the relatives and healthcare professionals of the burden of best-guessing the patient's wishes (or deciding between the views of different relatives). In these documents there is no provision for refusing, in advance, basic care of the sort needed to keep an individual comfortable. A doctor must be satisfied that a living will has not been revoked and that there is no indication of a change of mind or a change in circumstances affecting the decision. This might be confirmed during the current illness.30 Patients are entitled to make an advance directive without discussion with family members or a doctor.31 It would be wrong, however, to assume that those who make advance directives are opposed to aggressive treatment: a Finnish study has shown similar preferences for cardiopulmonary resuscitation between those with and without a living will.32 Implementation of advance directives has the potential to reduce the use of health services without affecting patient satisfaction or mortality.33 Less formal directives (e.g. informal conversation, the most frequent form of advance directive) can also help in determining the patient's values and desires and guide doctors in reaching clinical decisions.34 In an American study35 15% (32/214) of individuals aged 65-90 years had written a living will and some two-thirds of respondents planned to do so. By contrast, among 74 London inpatients (mean age 81) more than three-quarters had not even heard of living wills.36
We suggest that doctors should initiate discussions about advance directives as part of general healthcare. The BMA supports the idea of the general practitioner or the practice nurse doing this during routine consultations, since hospital admission 'is not generally a good time to raise the subject of anticipatory choice'.37 The main barriers are an expectation that decisions on treatment options will be made by doctors and the feeling that such issues are only relevant to those who are old or in poor health. Discussions of death and dying do not usually cause distress to the patient,38 but some patients may feel that the signing of such a document amounts to giving up or may present a risk that they will receive less treatment than they deserve.39 Many find the document lengthy and the wording ambiguous. For doctors the main barrier is lack of time.40 Doctors with a positive attitude to advanced directives are the ones most likely to initiate such discussions with their patients.41
| AN ETHICS HISTORY |
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When such history-taking was tested in a hospital study,5 no patient admitted to having been distressed by the questions; indeed, there is evidence12,15 that these discussions are not as stressful to patients as doctors might suppose. A few minutes spent in this way seem greatly preferable to subsequent long conversations with relatives expressing various opinions on what should be done. Doctors should ask patients periodically whether there has been any change in previously expressed wishes.18
We propose the following key questions, the answers to which may be helpful in decision-making in the advent of a subsequent medical crisis.
If you were seriously ill:
| REFERENCES |
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This article has been cited by other articles:
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A. K. Das, L. Das, and G. P. Mulley Awareness of living wills in the United Kingdom Age Ageing, September 1, 2006; 35(5): 543 - 543. [Full Text] [PDF] |
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C. Seton-Jones Taking an 'ethics history' J R Soc Med, October 1, 2005; 98(10): 442 - 442. [Full Text] [PDF] |
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F-E M Murtagh and A. Thorns Taking an 'ethics history' J R Soc Med, October 1, 2005; 98(10): 442 - 443. [Full Text] [PDF] |
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G. M Sayers, A K Das, and G P Mulley Taking an 'ethics history' * Authors' reply J R Soc Med, September 1, 2005; 98(9): 435 - 436. [Full Text] [PDF] |
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C. Schwartz Decision making at the end of life: shifting sands J R Soc Med, July 1, 2005; 98(7): 297 - 298. [Full Text] [PDF] |
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