Abstract | CONTEXT: The difficulties in defining a palliative care patient accentuate the need to provide stringent descriptions of the patient population in palliative care research. OBJECTIVES: To conduct a systematic literature review with the aim of identifying which key variables have been used to describe adult palliative care cancer populations in randomized controlled trials (RCTs). METHODS: The data sources used were MEDLINE (1950 to January 25, 2010) and Embase (1980 to January 25, 2010), limited to RCTs in adult cancer patients with incurable disease. Forty-three variables were systematically extracted from the eligible articles. RESULTS: The review includes 336 articles reporting RCTs in palliative care cancer patients. Age (98%), gender (90%), cancer diagnosis (89%), performance status (45%), and survival (45%) were the most frequently reported variables. A large number of other variables were much less frequently reported. CONCLUSION: A substantial variation exists in how palliative care cancer populations are described in RCTs. Few variables are consistently registered and reported. There is a clear need to standardize the reporting. The results from this work will serve as the basis for an international Delphi process with the aim of reaching consensus on a minimum set of descriptors to characterize a palliative care cancer population.
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Authors | Katrin Ruth Sigurdardottir, Line Oldervoll, Marianne Jensen Hjermstad, Stein Kaasa, Anne Kari Knudsen, Erik Torbjørn Løhre, Jon Håvard Loge, Dagny Faksvåg Haugen |
Journal | Journal of pain and symptom management
(J Pain Symptom Manage)
Vol. 47
Issue 5
Pg. 906-914.e17
(May 2014)
ISSN: 1873-6513 [Electronic] United States |
PMID | 24018205
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review, Systematic Review)
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Copyright | Copyright © 2014 U.S. Cancer Pain Relief Committee. Published by Elsevier Inc. All rights reserved. |
Topics |
- Humans
- Neoplasms
(therapy)
- Palliative Care
- Randomized Controlled Trials as Topic
(methods)
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