Advanced Search

Journal Navigation

Journal Home

Subscriptions

Archive

Contact Us

Table of Contents

CiteULike is a free service for managing and discovering scholarly references - click here to get started.

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
Right arrow Citation Map
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 McCarthy, M.
Right arrow Search for Related Content
PubMed
Right arrow Articles by McCarthy, M.
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?

Hospice patients: a pilot study in 12 services

Mark McCarthy

Department of Community Medicine, University College, London

We have developed an instrument to record details of patients referred to hospice services. Twelve services across the UK, including inpatient units, support teams and home care teams, participated in a pilot study and were asked to record data on 20 consecutive patients. The 195 patients included in the study ranged in age from 7 to 94 years; 95% had cancer and 4% had AIDS. Two-thirds (68%) of the patients were at home on referral to the service. Symptom control (77%) and emotional support (60%) were the dominant problems recorded. In the month prior to referral, the patients had received treatments including analgesic and psychotropic drugs, steroids, radiotherapy and surgery. Current symptoms correlated with these previous treatments, although not closely. Emotional problems, especially anxiety, were noted in a majority of patients and their carers, and social issues, especially housing problems and isolation, in a minority. This pilot study suggests that a full survey of patients in hospice services in the UK is feasible. The results would be of use both locally and nationally.

Key Words: data collection • health surveys • hospices • palliative treatment

Palliative Medicine, Vol. 4, No. 2, 93-104 (1990)
DOI: 10.1177/026921639000400206


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
H. Murphy, S. Alexander, and P. Stone
Investigation of diagnostic criteria for cancer-related fatigue syndrome in patients with advanced cancer: a feasibility study
Palliative Medicine, June 1, 2006; 20(4): 413 - 418.
[Abstract] [PDF]


Home page
West J Nurs ResHome page
W.-R. Tang, L. S. Aaronson, and S. A. Forbes
Quality of Life in Hospice Patients with Terminal Illness
West J Nurs Res, February 1, 2004; 26(1): 113 - 128.
[Abstract] [PDF]


Home page
Palliat MedHome page
M Hotopf, J Chidgey, J Addington-Hall, and K L. Ly
Depression in advanced disease: a systematic review Part 1. Prevalence and case finding
Palliative Medicine, March 1, 2002; 16(2): 81 - 97.
[Abstract] [PDF]


Home page
Palliat MedHome page
R. Catterall
Clinical databases for hospices
Palliative Medicine, July 1, 1994; 8(3): 257 - 257.
[PDF]