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本文引用的文献

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Costs associated with resource utilization during the palliative phase of care: a Canadian perspective.姑息治疗阶段相关资源利用的成本:加拿大视角。
Palliat Med. 2009 Dec;23(8):708-17. doi: 10.1177/0269216309346546. Epub 2009 Oct 16.
2
Characteristics and implications of attrition in health-related quality of life studies in palliative care.
Palliat Med. 2009 Jul;23(5):432-40. doi: 10.1177/0269216309104057. Epub 2009 Mar 20.
3
A population-based study of age inequalities in access to palliative care among cancer patients.一项基于人群的癌症患者获得姑息治疗的年龄不平等研究。
Med Care. 2008 Dec;46(12):1203-11. doi: 10.1097/MLR.0b013e31817d931d.
4
Palliative care and Parkinson's disease: managing the chronic-palliative interface.姑息治疗与帕金森病:处理慢性-姑息治疗的衔接
Chronic Illn. 2009 Mar;5(1):46-55. doi: 10.1177/1742395309102819.
5
Use of the Palliative Performance Scale (PPS) for end-of-life prognostication in a palliative medicine consultation service.在姑息医学咨询服务中使用姑息治疗表现量表(PPS)进行临终预后评估。
J Pain Symptom Manage. 2009 Jun;37(6):965-72. doi: 10.1016/j.jpainsymman.2008.08.003. Epub 2009 Feb 20.
6
A framework for generalizability in palliative care.姑息治疗中可推广性的框架。
J Pain Symptom Manage. 2009 Mar;37(3):373-86. doi: 10.1016/j.jpainsymman.2008.03.020. Epub 2008 Sep 21.
7
Palliative care program effectiveness research: developing rigor in sampling design, conduct, and reporting.姑息治疗项目效果研究:在抽样设计、实施和报告方面提高严谨性。
J Pain Symptom Manage. 2006 Mar;31(3):270-84. doi: 10.1016/j.jpainsymman.2005.07.011.
8
Complexities in prognostication in advanced cancer: "to help them live their lives the way they want to".晚期癌症预后的复杂性:“帮助他们按自己想要的方式生活”。
JAMA. 2003 Jul 2;290(1):98-104. doi: 10.1001/jama.290.1.98.
9
Population-based trends in referral of the elderly to a comprehensive palliative care programme.基于人群的老年人转介至综合姑息治疗项目的趋势。
Palliat Med. 2002 May;16(3):255-6. doi: 10.1191/0269216302pm550xx.
10
Clinical research in palliative care: patient populations, symptoms, interventions and endpoints.
Palliat Med. 2001 Mar;15(2):163-8. doi: 10.1191/026921601668441770.

探讨基于社区的姑息治疗成本研究中的可推广性。

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

机构信息

Department of Community Health and Epidemiology, Dalhousie University, Halifax, Nova Scotia, Canada.

出版信息

J Pain Symptom Manage. 2011 Apr;41(4):779-87. doi: 10.1016/j.jpainsymman.2010.07.010. Epub 2011 Jan 28.

DOI:10.1016/j.jpainsymman.2010.07.010
PMID:21276697
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3747103/
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.

摘要

背景

姑息治疗研究人员在招募和保留研究对象方面面临挑战。

目的

本文旨在调查选择、研究地点和参与偏倚,以评估姑息治疗计划(PCP)患者在家中接受护理的成本分析的普遍性。

方法

比较研究对象的社会人口统计学、地理、生存、疾病和治疗特征,这些特征与同一地区和同一时期的三个群体进行比较。比较 1 是与未参加 PCP 的非研究对象进行比较,以评估选择偏倚。比较 2 是与死于癌症的成年人进行比较,以评估研究地点偏倚。比较 3 是与拒绝参加研究的符合条件的人进行比较,以评估参与偏倚。

结果

比较 1:与其他 1010 名 PCP 患者相比,50 名研究对象的平均年龄小 3.6 岁(P=0.03),参加 PCP 的时间长 70 天(P<0.001),距离 PCP 近 6.7 公里(P<0.0001),更有可能患有癌症(96.0%对 86.4%,P=0.05)。比较 2:与所有癌症死亡者相比,45 名死于癌症的研究对象的平均年龄小 7.0 岁(P<0.001),距离 PCP 近 2.7 公里(P<0.001),更有可能接受放疗(62.2%对 33.8%,P<0.0001)和医学肿瘤学咨询(28.9%对 14.8%,P=0.01)。比较 3:与拒绝参与的 110 名合格者相比,50 名研究对象在诊断后平均多活 42 天(P=0.03),距离 PCP 近 2.6 公里(P=0.01)。

结论

如果研究结果应用于与研究对象不同的人群,则可能得出不准确的结论。