The National Confidential Enquiry into Patient Outcome and Death has just released a new report: Planning for the End A Review of the Quality of Care Provided to Adult Patients towards the End of Life.
There are five big findings:
- Not enough patients had access to early palliative care alongside existing treatments to improve symptoms and quality of life
- Death and dying was not discussed as often as it could have been. More people need to have their end of life care wishes recorded.
- Care co-ordinators are an accepted standard in cancer services but were less common for other advanced chronic conditions.
- Specialist palliative care services were not always available in hospitals nor involved when needed.
- Training to identify when palliative or end of life care will help was not always provided or available.

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