Patient Agreement To Investigation Or Treatment - Heart Of England Nhs Foundation Trust Page 2

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Guidance to health professionals
(to be read in conjunction with The Consent to Treatment or Examination
policy)
When NOT to use this form
What a consent form is for
When a patient is below 18 and does not have the capacity to consent, you should
This form documents the patient’s agreement to go ahead with the investigation or
use consent form 2 (i.e. Parental (or person with parental responsibility) agreement to
treatment you have proposed. It is not a legal waiver - if patients, for example, do not
investigation or treatment for a child or young person). A patient lacks the capacity
receive enough information on which to base their decision, then the consent may not
to consent to the proposed treatment or investigation if they have an impairment of
be valid, even though the form has been signed. Patients are also entitled to change
the mind or brain or disturbance affecting the way their mind or brain works and they
their mind after signing the form, if they retain capacity to do so. The form should
cannot:
act as an aide-memoire to health professionals and patients, by providing a check-list
• understand the information about the decision to be made
of the kind of information patients should be offered, and by enabling the patient
• retain that information
to have a written record of the main points discussed. In no way, however, should the
• use or weigh that information as part of the process of making a decision
written information provided for the patient be regarded as a substitute for face-to-
• communicate their decision (by talking, using sign language or any other means)
face discussions with the patient.
You should always take all reasonable steps (e.g. involving more specialist colleagues)
to support a patient in making their own decision, before concluding that they lack
The law on consent
the capacity to do so.
Relatives cannot be asked to sign a form on behalf of an adult who lacks capacity to
The process of taking consent is underpinned by the common law, the Human Rights
consent for themselves unless they have been given the authority to do so under a
Act 1998 and the Mental Capacity Act 2005. All staff involved in providing care to
Lasting Power of Attorney or as a Court Appointed Deputy.
patients must be familiar with the Consent to Treatment or Examination policy.
Information
More information on consent and the legislation behind it can be found in the
Department of Health’s Reference Guide to Consent for Examination or Treatment at
Information about what the treatment will involve, its benefits and risks (including
or the Office of the Public Guardian at
side-effects and complications) and the alternatives to this procedure proposed is
crucial for patients when making up their minds. The courts have stated that patients
should be told about ‘significant’ risks which would affect the judgement of a
reasonable patient. ‘Significant’ has not been legally defined, but the GMC requires
Who can give consent
doctors to tell patients about significant, unavoidable and frequently occurring risks.
In addition if patients make it clear they have particular concerns about certain kinds
Everyone aged 16 or more is presumed to be competent to give consent for
of risk, you should make sure they are informed about these risks, even if they are
themselves, unless the opposite is demonstrated. If a child under the age of 16 has
very small or rare. You should always answer questions honestly. Sometimes, patients
“sufficient understanding and intelligence to enable him or her to understand fully
may make it clear that they do not want to have any information about the options,
what is proposed”, then he or she will be competent to give consent for himself or
but want you to decide on their behalf. In such circumstances, you should do your best
herself. Young people aged 16 and 17, and legally ‘competent’ younger children, may
to ensure that the patient receives at least the very basic information about what is
therefore sign this form for themselves, but may like a parent to counter sign as well.
proposed. Where information is refused, you should document this on this form and
However even where a child is able to give consent for himself or herself, you should
in the patient’s medical records.
always involve those with parental responsibility in the child’s care, unless the child
If consent is sought for the use of tissue/blood products from the patient for one or
specifically asks you not to do so. If a patient is mentally competent to give consent
more of the purposes identified in the consent form, information should be given to
but physically unable to sign a form, you should complete this form as usual, and ask
the patient about the nature and purpose of what is proposed so that the patient is
an independent witness to confirm that the patient has given consent.
able to make an informed decision. The patient should be told of any ‘significant’ risks
inherent in the way the tissue/blood products will be obtained, how the tissue/blood
products will be used and any risks or possible implications of its use. When taking
consent for the use of tissue/blood products, you should comply with the Human Tissue
Authority Code of Practice on Consent.

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