This section of the website contains the main policy documents relating to children’s palliative care in Northern Ireland and the Republic of Ireland.
This policy provides a foundation upon which children’s palliative care services can be developed in Ireland. It is divided into three sections. The first section defines and describes palliative care for children with lifelimiting conditions and draws on national and international developments in this small and highly specialised field of health care. The second section describes services as they are currently provided. The third section gives clear direction for the future development of palliative care for children.
Link to Document: Palliative Care For Children With Life-Limiting Conditions In Ireland- A National Policy
This policy provides a foundation upon which children’s palliative care services can be developed in Ireland. It is divided into three sections. The first section defines and describes palliative care for children with lifelimiting conditions and draws on national and international developments in this small and highly specialised field of health care. The second section describes services as they are currently provided. The third section gives clear direction for the future development of palliative care for children.
This policy provides a foundation upon which children’s palliative care services can be developed in Ireland. It is divided into three sections. The first section defines and describes palliative care for children with lifelimiting conditions and draws on national and international developments in this small and highly specialised field of health care. The second section describes services as they are currently provided. The third section gives clear direction for the future development of palliative care for children.
Link to Document: Palliative Care For Children With Life-Limiting Conditions In Ireland- A National Policy
The Northern Ireland Regional Paediatric Palliative Care Network (RPPCN) have developed a resource to support families and professionals where a diagnosis of a potentially life limiting, or life-threatening condition has been made at antenatal stage.
The resource will help inform parental decisions and promote effective communication between professionals to ensure the most effective supports are put in place.
Link To Document: Antenatal Pathway
This pathway guides community services in meeting the needs of families, children and young people, aged up to 18 years, who have complex physical healthcare needs. This is defined as: Children (and young people) with complex physical healthcare needs are those who require a range of additional support services beyond the type and amount required by children generally and those usually provided to children with impairments and long-term illnesses.
Link To Document: Integrated Care Pathway for Children with Complex Physical Health Care Needs
This document sets out the strategic direction for the palliative and end-of-life care of ill and dying children and young people in the North for the next ten years. It follows public consultation in early 2014 on 18 proposed recommendations aimed at enhancing the existing care and support for children and young people with life-limiting or life-threatening conditions, as well as their families.
Link To Document: Providing High Quality Palliative Care for Our Children. A Strategy For Children’s Palliative And End-Of-Life Care 2016-26
The report evaluates the impact, outcomes and added value that ‘step down’ care provides to children, families, health and social care providers, and commissioners, in a children’s hospice setting and puts forward six recommendations which centre on the need for a holistic care approach. It ascertains that children who are considered ‘medically stable’ should not remain in an acute hospital setting for any longer than is clinically necessary and explores the potential for children’s hospice’s to provide an alternate setting for care within a ‘step down’ model.
