“It is estimated that there are approximately 8 million Jehovah’s Witnesses worldwide, with 140,000 currently resident in the UK. Jehovah’s Witnesses have refused allogenic blood transfusion and primary components (red cells, white cells, platelets and plasma) on religious grounds.
In addition to Jehovah’s Witnesses, a growing number of patients are choosing to decline blood transfusions; many of whom do so for reasons other than religious faith. Fears about the safety of blood transfusion as well as the scarcity of donors and changing patient expectations are leading some patients to withhold consent for blood transfusion.” (Royal College of Surgeons of England, p3, 2018).
NHS Borders aims to respect the wishes of all patients, adults and children and their families, and to provide high quality health care acceptable to them. All patients have the right to be treated with respect and staff must be sensitive to their individual needs, acknowledging their values and beliefs.
1.1 Principles of Consent
Consent refers to a patient’s autonomous agreement for a health professional to provide care, and it must be confirmed in writing. For consent to be valid, it must be:
Given by a person with the capacity to make the decision in question.
- Given voluntarily.
- Based on appropriate information (informed) and understood.
If one or more of these factors is missing, the patient is not considered to have given permission to proceed to treatment.
All patients in the UK with mental capacity have the absolute legal and ethical right to refuse treatment or any aspect of treatment. To administer blood against a patient’s wishes may be unlawful and could lead to criminal and/or civil proceedings.
It is the right of an adult patient to withhold consent to treatment, even when doing so would be potentially fatal (British Medical Association, 2019). It is also the case for pregnant women choosing to refuse treatment even if it might lead to harm for their unborn child (Royal College of Surgeons of England, 2018).
Doctors must listen to patients and respect their views about their health. The options for treatment should be discussed in relation to the patient’s own values and wishes. Working in partnership with patients requires learning their views and expectations regarding their treatment and working together to inform patients of their options for achieving the best outcome for them as individuals.
Patients must be made aware of their right to refuse or to give consent to treatment at any time and assumptions must not be made about the patients’ awareness of their right to make treatment decisions.
Patients should be asked explicitly whether any refusal of treatment extends to situations where loss of life or limb without these treatments is likely. The patient’s decision should be recorded and placed in their clinical record.
When supporting a patient to reach a decision about treatment, doctors must be satisfied that the patient gave or withheld consent to treatment themselves, without coercion or unwelcome influence from other persons. Although patients may value the aid of a friend, family member or other supporter to provide comfort through their decision-making process, it is important to ensure that any decision represents the patient’s own views and is not unduly influenced by the wishes of another person.
At the end of the consent discussion, the doctor should review with the patient the potential implications of any choices that could be contrary to their wellbeing. This should include any risks and benefits associated with such choices. This review should not, however, be intended to influence the patient to take a course of action that is not in keeping with their values and wishes (General Medical Council, 2019).