Literature DB >> 21276697

Exploring generalizability in a study of costs for community-based palliative care.

M Ruth Lavergne1, Grace M Johnston, Jun Gao, Serge Dumont, Fred I Burge.   

Abstract

CONTEXT: Palliative care researchers face challenges recruiting and retaining study subjects.
OBJECTIVES: This article investigates selection, study site, and participation biases to assess generalizability of a cost analysis of palliative care program (PCP) clients receiving care at home.
METHODS: Study subjects' sociodemographic, geographic, survival, disease, and treatment characteristics were compared for the same year and region with those of three populations. Comparison I was with nonstudy subjects enrolled in the PCP to assess selection bias. Comparison II was with adults who died of cancer to assess study site bias. Comparison III was with study-eligible persons who declined to participate in order to assess participation bias.
RESULTS: Comparison I: When compared with the other 1010 PCP clients, the 50 study subjects were on average 3.6 years younger (P=0.03), enrolled 70 days longer in the PCP (P<0.001), lived 6.7 km closer to the PCP (P<0.0001), and were more likely to have cancer (96.0% vs. 86.4%, P=0.05). Comparison II: Compared with all cancer decedents, the 45 study subjects who died of cancer were on average 7.0 years younger (P<0.001), lived 2.7 km closer to the PCP (P<0.001), and were more likely to have had radiotherapy (62.2% vs. 33.8%, P<0.0001) and medical oncology (28.9% vs. 14.8%, P=0.01) consultations. Comparison III: The 50 study subjects lived on average 42 days longer after their diagnosis (P=0.03) and 2.6 km closer to the PCP (P=0.01) than the 110 eligible persons who declined to participate.
CONCLUSION: If the study findings are applied to populations that differ from the study subjects, inaccurate conclusions are possible.
Copyright © 2011 U.S. Cancer Pain Relief Committee. Published by Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Year:  2011        PMID: 21276697      PMCID: PMC3747103          DOI: 10.1016/j.jpainsymman.2010.07.010

Source DB:  PubMed          Journal:  J Pain Symptom Manage        ISSN: 0885-3924            Impact factor:   3.612


  15 in total

1.  Clinical research in palliative care: patient populations, symptoms, interventions and endpoints.

Authors:  C Mazzocato; C Sweeney; E Bruera
Journal:  Palliat Med       Date:  2001-03       Impact factor: 4.762

Review 2.  Why are trials in palliative care so difficult?

Authors:  G E Grande; C J Todd
Journal:  Palliat Med       Date:  2000-01       Impact factor: 4.762

3.  Palliative medicine--a research challenge.

Authors:  B Glimelius
Journal:  Acta Oncol       Date:  2000       Impact factor: 4.089

4.  Population-based trends in referral of the elderly to a comprehensive palliative care programme.

Authors:  F Burge; G Johnston; B Lawson; R Dewar; I Cummings
Journal:  Palliat Med       Date:  2002-05       Impact factor: 4.762

5.  Challenges in palliative care research; recruitment, attrition and compliance: experience from a randomized controlled trial.

Authors:  M S Jordhøy; S Kaasa; P Fayers; T Ovreness; G Underland; M Ahlner-Elmqvist
Journal:  Palliat Med       Date:  1999-07       Impact factor: 4.762

Review 6.  A framework for generalizability in palliative care.

Authors:  David C Currow; Jane L Wheeler; Paul A Glare; Stein Kaasa; Amy P Abernethy
Journal:  J Pain Symptom Manage       Date:  2008-09-21       Impact factor: 3.612

Review 7.  Methodologic issues in effectiveness research on palliative cancer care: a systematic review.

Authors:  G C Rinck; G A van den Bos; J Kleijnen; H J de Haes; E Schadé; C H Veenhof
Journal:  J Clin Oncol       Date:  1997-04       Impact factor: 44.544

8.  Palliative care program effectiveness research: developing rigor in sampling design, conduct, and reporting.

Authors:  Marie A Bakitas; Kathleen Doyle Lyons; Jane Dixon; Tim A Ahles
Journal:  J Pain Symptom Manage       Date:  2006-03       Impact factor: 3.612

9.  Complexities in prognostication in advanced cancer: "to help them live their lives the way they want to".

Authors:  Elizabeth B Lamont; Nicholas A Christakis
Journal:  JAMA       Date:  2003-07-02       Impact factor: 56.272

10.  Costs associated with resource utilization during the palliative phase of care: a Canadian perspective.

Authors:  Serge Dumont; Philip Jacobs; Konrad Fassbender; Donna Anderson; Véronique Turcotte; François Harel
Journal:  Palliat Med       Date:  2009-10-16       Impact factor: 4.762

View more
  3 in total

1.  Identifying population groups with low palliative care program enrolment using classification and regression tree analysis.

Authors:  Jun Gao; Grace M Johnston; M Ruth Lavergne; Paul McIntyre
Journal:  J Palliat Care       Date:  2011       Impact factor: 2.250

2.  Use of opioid analgesics among older persons with colorectal cancer in two health districts with palliative care programs.

Authors:  Judith Fisher; Robin Urquhart; Grace Johnston
Journal:  J Pain Symptom Manage       Date:  2012-09-24       Impact factor: 3.612

3.  Bereaved family member perceptions of patient-focused family-centred care during the last 30 days of life using a mortality follow-back survey: does location matter?

Authors:  Fred Burge; Beverley Lawson; Grace Johnston; Yukiko Asada; Paul F McIntyre; Eva Grunfeld; Gordon Flowerdew
Journal:  BMC Palliat Care       Date:  2014-05-14       Impact factor: 3.234

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.