Providing palliative and end-of-life care for children and young people provides many complexities for health professionals. There are unique legal and ethical aspects of caring for children in a palliative or end-of-life setting due to the altered capacity of children dependent on their age. There is a difference between law and ethics: laws are binding and instructive of decisions and actions whereas ethics comprise principles and guidelines that inform decisions and actions in health care.
Law
The United Nations Convention on the Rights of the Child (UNCRC) 1990 defines a child as anyone under 18 years of age. Until a child reaches 18 years of age, an adult (usually their parent—see the Children Act 1989) should have responsibility for this child and therefore the decisions about their care. However, the Mental Capacity Act 2005 states that everyone over the age of 16 has the presumption of capacity. This means that
To view the rest of this content login below or request a demo
