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Palliative Care

Palliative care is defined by the World Health Organisation as an approach that improves the quality of life of patients (adults and children) and their families who are facing problems associated with life-limiting illness, usually progressive. It prevents and relieves suffering through the early identification, correct assessment and treatment of pain and other problems whether physical, psychosocial or spiritual. 
In England, the term ‘end of life care’ refers to the last year of life. [Source]

In this topic guide you are able to access key texts available in print or electronically within UHD/DHUFT, useful websites, and links to relevant journals. Please note that you may need to logon using your OpenAthens password to access many of these resources.

If there are books that you would like to recommend, please let us know. Or contact us to make any suggestions to improve this topic guide.

Articles In Our Latest Bulletin

End of life care in children: Summary.

‘What end of life care do people who die in a care home receive, and how has this changed over time?’

‘Beyond the Reach of Palliative Care’: A Qualitative Study of Patient and Public Experiences and Anticipation of Death and Dying.”

Electronic Health Record Tracking of Psychosocial Care in the Context of Serious Illness: A Narrative Review.”

Useful Links

BMJ Best Practice

ClinicalKey

Library Catalogue

OpenAthens

Requests

Visible Body

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