Methodological challenges for measuring quality of care at the end of life
Title
Methodological challenges for measuring quality of care at the end of life
Creator
Fowler FJ; Coppola KM; Teno JM
Identifier
Publisher
Journal Of Pain And Symptom Management
Date
1999
Subject
Humans; Research Design; Quality of Life/psychology; Quality Assurance; Terminal Care/standards; Health Care/methods; Health Care/statistics & numerical data
Description
Measurement is a fundamental step in improving the quality of care for dying patients and their families. Yet, there are important methodological challenges to be addressed. In conducting surveys about the patient and family experience, research is needed regarding the relative merits and cost-effectiveness of prospective or retrospective surveys after the patient’s death. Proxies are an important source of information given that the majority of patients can not be interviewed in the last week of life. Research is needed to understand who is best able to serve as a proxy and the validity of their reports. The cost-effectiveness and comparability of alternative data collection strategies need to be examined. These and other important issues need to be addressed in designing reliable, valid, and clinically manageable measures.
1999
Rights
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
Journal Article
Citation List Month
Backlog
URL Address
Citation
Fowler FJ; Coppola KM; Teno JM, “Methodological challenges for measuring quality of care at the end of life,” Pediatric Palliative Care Library, accessed March 16, 2025, https://pedpalascnetlibrary.omeka.net/items/show/12201.