Advanced Search

Journal Navigation

Journal Home

Subscriptions

Archive

Contact Us

Table of Contents

Sign In to gain access to subscriptions and/or personal tools.
Palliative Medicine
This Article
Right arrow Full Text (PDF)
Right arrow References
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Add to Saved Citations
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Request Reprints
Right arrow Add to My Marked Citations
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Right arrow Citing Articles via Scopus
Google Scholar
Right arrow Articles by Field, D.
Right arrow Articles by Biswas, B.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Field, D.
Right arrow Articles by Biswas, B.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

Care and information received by lay carers of terminally ill patients at the Leicestershire Hospice

David Field

Pauline Dand

Sam Ahmedzai

Bronwen Biswas

This paper is based on interviews with 59 lay carers of patients admitted to the Leicestershire Hospice. Carers were interviewed approximately a week after patient admission, and 37 carers were re-interviewed approximately three months after the death of the patient. Most lay carers were satisfied with the care and attention they received, although they were somewhat less satisfied with care and attention received from community nurses and GPs than from hospice nurses and doctors. Carers expressed satisfaction with the care received by hospice inpatients and indicated that the good care their relative or close friend received was an important factor in relieving their anxieties. They were also positive about the reassurance and care which they themselves received from hospice doctors and nurses. There was a generally high level of satisfaction about the information which they received from hospice staff, although a minority of carers had only limited contact with hospice staff, and it was these who were unhappy about the information which they had received.

Key Words: attitudes of carers (non-MeSH) • health survey • hospice • patient satisfaction • quality of life • terminal care

Palliative Medicine, Vol. 6, No. 3, 237-245 (1992)
DOI: 10.1177/026921639200600308


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:


Home page
Palliat MedHome page
E K Wilkinson, C Salisbury, N Bosanquet, P J Franks, S Kite, M Lorentzon, and A Naysmith
Patient and carer preference for, and satisfaction with, specialist models of palliative care: a systematic literature review
Palliative Medicine, April 1, 1999; 13(3): 197 - 216.
[Abstract] [PDF]


Home page
Palliat MedHome page
G. Johnston and C. Abraham
The WHO objectives for palliative care: to what extent are we achieving them?
Palliative Medicine, April 1, 1995; 9(2): 123 - 137.
[Abstract] [PDF]