EMT Podcast:

Consent

Every consumer must be presumed to be competent unless there are reasonable grounds for believing that they are not. The common circumstances where a patient is not competent are where they are a young child, where they are unconscious, or where they are suffering from dementia, or have an intellectual disability.


The difficult cases are those who are conscious and would normally be competent but may not be currently due to head injury or alcohol and or other drugs

  • Do they know enough?
  • Are they able to think enough (time and competence)?
  • Are they free enough (free of coercive forces such as doctors, family, psychiatric illness, drugs)?

Assessing competence
  • Capacity to understand
    • LOC / GCS
    • Intoxication: clinical assessment +/- levels (but we are experts in intoxication)
    • Possibly a cognitive assessment (but probably not)
  • Understanding
    • Can s/he hear me?
    • Is his/her short term memory good enough?
    • Has s/he grasped the
      • Problem?
      • Options to address the problem?
      • Consequences of the options?
    • Can s/he express her/his decision
    • Is there reason behind her/his decision?
    • So it's mostly to do with understanding 
      • Of the problem
      • The options to address the problem
      • The pros and cons of each option

We must be reasonably confident that s/he knows enough, can think enough and is free enough.  If we are not confident of that, then we must be reasonably confident that if s/he knew enough, could think enough and was free enough, s/he would most likely give the same answer she is giving now.

We might prevent someone from going home if
  • There were good beneficent and non-maleficent justifications [eg there stroppy behaviour could be due to an extra dural haematoma]
AND
  • The patient was unable to appreciate adequately the threat, due to being ill-informed, impaired competence or coercive influences (ie the wish they expressed may not be their own autonomous choice)

Documentation
eg "Discussed with patient, told him of the possibility of EDH etc.  He displayed good understanding of the condition, the risks and the options ...."
or
"Discussed with patient, clearly impaired, unable to repeat things I had just told him, to understanding of the risk of his condition ..."

Patient is not required to "sign them self out against medical advice"

NZ Health and Disability Code  Section 7:

3) Where a consumer has diminished competence, that consumer retains the right to make informed choices and give informed consent, to the extent appropriate to his or her level of competence.

4) Where a consumer is not competent to make an informed choice and give informed consent, and no person entitled to consent on behalf of the consumer is available, the provider may provide services where -

a) It is in the best interests of the consumer; and

b) Reasonable steps have been taken to ascertain the views of the consumer; and

c) Either, -

i. If the consumer's views have been ascertained, and having regard to those views, the provider believes, on reasonable grounds, that the provision of the services is consistent with the informed choice the consumer would make if he or she were competent; or

ii. If the consumer's views have not been ascertained, the provider takes into account the views of other suitable persons who are interested in the welfare of the consumer and available to advise the provider.




Who can give consent on behalf of another?


The only individuals who are entitled to grant consent on behalf of a patient are

legal guardians (welfare guardians under the Protection of Personal Property

Rights Act, or parents/guardians under the Care of Children Act 2004 or someone

with enduring power of attorney). A spouse or next of kin cannot consent to or

refuse medical treatment on behalf of an incompetent person unless they hold

enduring power of attorney or are their welfare guardian. It is important to ask

someone who has enduring power of attorney, if they have powers in relation to

property, or personal care, or both.

If, in emergency, immediate action must be taken to preserve the life or health

of a patient, then you can provide the key services without consent. It is expected

that only those treatments that are necessary to preserve life or health will be done

at this time. Any procedure that can reasonably be delayed should be delayed until

an opportunity can be given for the patient to consent.


Care of Children Act 2004


All persons over the age of 16 are regarded as adults for the purposes of determining competence to give informed consent. People under the age of 16 are not automatically prohibited from consenting to medical, surgical, or dental procedures so judgment is needed in each instance.


It also covers how the consent of children should be obtained for medical procedures and the right of health practitioners to administer blood transfusions to children without consent in certain conditions (to save life being

the principal condition)[See Blood Product Transfusions for Jehovah's Witnesses] Section 38 of the Act addresses the issue of obtaining consent for abortion for children (a female of any age has the right to consent to or

refuse to consent to any medical or surgical procedure for the purpose of terminating her pregnancy).


Ethical dilemmas


All the issues surrounding consent for the treatment of children have not been

settled and doctors will still face dilemmas. New Zealand has had three high

profile cases since the year 2000 where parents withheld consent for medical

treatment for their children under circumstances that resulted in all three children

dying of their diseases. The way the police and the courts treated these cases was

inconsistent and in the first of these cases, the lack of a police prosecution

followed intense nationwide public support for the parent’s decision to decline to

accept conventional medical treatment. In the other two cases the parents were

prosecuted. The courts imposed a suspended sentence on the parents in the second

case, and sentenced the parents in the third case to 5 years in prison. It would

appear, for the time being at least, that the ability to persuade the court will be the

most significant factor in determining outcomes.

Doctors should regard court orders against parents as an absolute last resort, and

all other means to persuade parents should be exhausted first. Professor Don

Evans, director of Otago University’s Bioethics Centre has stated “There is a huge

price to be paid for that last step. It pretty well destroys any collaboration for the

future between parents and health carers”. If you are likely to find yourself in

conflict with a child’s guardian about the treatment of serious life threatening

conditions, you should read this new legislation and seek advice from the medical

protection society, lawyers, or employers. There are situations where doctors and

care givers may jointly seek a court order for consent, for example to terminate

treatment to allow a patient to die peacefully, or sterilisation of a patient who is

unable to consent but for whom the family and other carers, supported by medical

opinion, request the operation to enhance the quality of life or to prevent

deterioration in physical or mental health.

In summary, informed consent, long an ethical obligation, is in

New Zealand a legal requirement. It is one of the cornerstones of good patient

care, and recognises that the doctor patient relationship is for the benefit of the

patient. Not all issues in informed consent have simple solutions. Consult with

other doctors and professional advisers when you are uncertain.


References

New Zealand Medical Council: Cole’s MEDICAL PRACTICE IN NEW ZEALAND 2009 http://www.mcnz.org.nz/portals/0/publications/coles/cole%20chapter%2012.pdf


Ethics Toolkit by Prof M Ardagh, Christchurch ED http://www.nursingcouncil.org.nz/Ethics%20toolkit%2008.pdf Accessed 17/1/09

NZ Health and Disability Code 1996 http://www.hdc.org.nz/theact/theact-thecodedetail  Accessed 17/1/09

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