Chapter

Assessing Quality of Life in Palliative Care

Russell K. Portenoy and Eduardo Bruera

in Issues in Palliative Care Research

Published in print September 2003 | ISBN: 9780195130652
Published online November 2011 | e-ISBN: 9780199999842 | DOI: http://dx.doi.org/10.1093/acprof:oso/9780195130652.003.0015
Assessing Quality of Life in Palliative Care

Show Summary Details

Preview

Palliative care providers who wish to evaluate the full impact of their care must measure changes in quality of life (QOL) as well as improvements in areas specifically targeted by particular interventions such as pain and depression. Since palliative care considers the family as the unit of care, patient QOL, family member QOL, and the QOL of the family unit are all primary outcomes of palliative care. This chapter suggests that the best indicator of the quality of whole-person care is the QOL of the care recipient. The importance of measuring QOL has been widely recognized in the health care literature in the last two decades. Unfortunately, this has led to a great pressure to measure QOL at all phases of cancer and HIV disease, even though the measures are not adequately developed to show primary outcomes.

Keywords: quality of life; health care; family; patient care; cancer; HIV

Chapter.  5043 words. 

Subjects: Palliative Medicine

Full text: subscription required

How to subscribe Recommend to my Librarian

Buy this work at Oxford University Press »

Users without a subscription are not able to see the full content. Please, subscribe or login to access all content.