Sample policy · Adult social care

End-of-life care policy (adult social care)

1. Purpose

This policy sets out how the Service supports people approaching the end of life, records their wishes, works with healthcare professionals, supports families and learns from deaths.

The Service must verify this policy against current NICE end-of-life guidance, local palliative-care pathways, ReSPECT source material, DNACPR guidance and CQC source material before adoption.

2. Sources to verify before adoption

3. Scope

This policy applies to people using the Service who may be approaching the end of life, are in the last days of life, or have died while receiving support from the Service.

It applies to:

The Service does not replace GP, community nursing or specialist palliative-care clinical responsibility.

4. Identifying the end-of-life phase

Staff remain alert to signs that a person may be approaching the end of life.

Triggers for senior review may include:

The Registered Manager or clinical lead seeks GP, community nursing or specialist palliative-care advice when staff identify deterioration.

Staff verify clinical indicators against current NICE NG31, local palliative-care pathway and the person's clinical team before adopting local wording.

5. Advance care planning

Advance care planning is a conversation process, not just a form.

Where the person wishes to take part, staff support discussions about:

The Service records advance care planning conversations in the care plan and reviews them when the person's condition, wishes or circumstances change.

Where the person may lack capacity, staff follow the Mental Capacity Act 2005 and involve lawful decision-makers or people interested in the person's welfare as appropriate.

6. ReSPECT-form recording

Where a ReSPECT process is used locally, the Service records:

Staff do not complete or alter ReSPECT clinical recommendations unless their role and local process authorise them to do so.

The Service verifies ReSPECT procedure against current Resuscitation Council UK source material and local NHS process before adoption.

7. DNACPR conversations and decisions

DNACPR is not the same as advance care planning.

The Service records DNACPR information separately from broader preferences about care and treatment.

Records include:

Staff do not make DNACPR clinical decisions. If staff identify uncertainty, distress or disagreement, they escalate to the GP, clinical lead or relevant healthcare professional.

8. Symptom management referral pathways

The Service escalates symptoms promptly to the appropriate clinical route.

The local pathway includes:

Staff record symptoms, advice sought, medicines administered, comfort measures and family contact.

The Service verifies symptom-management escalation against NICE NG31 and local palliative-care guidance before adoption.

9. Family support and bereavement

The Service supports family, carers and people important to the person.

Support includes:

Staff respect confidentiality and the person's wishes when sharing information.

10. After-death care

After a person dies, staff follow the local after-death procedure.

The procedure covers:

Staff do not release the body until the required local process has been completed.

11. Body release procedure

The Service keeps a local body release procedure that reflects the service type and local arrangements.

The record includes:

Where death is unexpected, suspicious or subject to coroner involvement, staff follow police, coroner, GP and local procedure before any release.

12. Learning from each death

The Registered Manager reviews each death.

The review considers:

Learning is recorded without blame and converted into improvement actions where needed.

13. Staff training

The Service maps end-of-life training to role.

The Service verifies training expectations against current NICE guidance, local NHS pathway and CQC source material before adoption.

Review cadence: annual or on regulatory change, whichever sooner. Owner: Registered Manager.

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Last reviewed 21 May 2026