- Emily Collis, consultant in palliative medicine1,
- Katherine E Sleeman, clinical lecturer in palliative medicine2
- 1Pembridge Palliative Care Centre, Central London Community Healthcare Trust, St Charles’ Hospital, London W10 6DZ, UK
- 2Cicely Saunders Institute, King’s College London, London, UK
- Correspondence to: E Collis
Patients have the right to make informed decisions about their healthcare. Informed consent, and the process of balancing risks and benefits of treatment, is a fundamental ethical principle.1 This principle is no less relevant for a patient with terminal illness, for whom an awareness of the incurable and life limiting nature of their underlying condition is essential to decision making.
Knowledge gives power
Decision making in terminal illness extends from the medical treatments and supportive care to decisions around advance planning of care, finances, guardianship, power of attorney, and voicing preferences for place of death. Worryingly, such decisions are not always fully informed. A recent study showed that 69% of 710 US patients with incurable lung cancer (and 81% of 483 patients with colorectal cancer) who received palliative chemotherapy were not aware that this was unlikely to cure the cancer.2 On the other hand, being …