Literature DB >> 20471782

Psychological well-being and quality of care: a factor-analytic examination of the palliative care outcome scale.

Richard J Siegert1, Wei Gao, Frank H Walkey, Irene J Higginson.   

Abstract

CONTEXT: The Palliative Care Outcome Scale (POS) is a widely used outcome measure in palliative care research, and has good psychometric properties. It has been used for clinical or research purposes in specialist cancer centers, nursing homes, day hospice units, and hospice settings in a growing number of countries. However, the POS has not yet been examined using factor analysis.
OBJECTIVE: The aim of the present study was to examine the internal factor structure of the POS.
METHODS: Confirmatory and exploratory factor analyses were used for secondary analysis of two existing POS data sets of British patients, most of whom were cancer patients.
RESULTS: We began with a confirmatory factor analysis (CFA), which indicated that the POS is not a unidimensional scale. This was followed by an exploratory factor analysis that suggested two factors-one reflecting a psychological well-being dimension and the other consisting of three items relating to the standard of professional care. A similar two-factor structure also was identified in the second sample using CFA.
CONCLUSION: The POS appears to capture two factors, psychological status and quality of care, and to have three items that function independently (family anxiety, symptoms, and pain control). Our findings suggest that future evaluations of palliative care services should include assessment not only of symptoms and well-being or quality of life, but also of quality of care, and that unidimensional measures will not capture all relevant aspects in palliative care. Copyright 2010 U.S. Cancer Pain Relief Committee. Published by Elsevier Inc. All rights reserved.

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Mesh:

Year:  2010        PMID: 20471782     DOI: 10.1016/j.jpainsymman.2009.11.326

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


  19 in total

1.  Reliability and concurrent validity of the Palliative Outcome Scale, the Rotterdam Symptom Checklist, and the Brief Pain Inventory.

Authors:  Marta Pelayo-Alvarez; Santiago Perez-Hoyos; Yolanda Agra-Varela
Journal:  J Palliat Med       Date:  2013-06-28       Impact factor: 2.947

2.  Measuring health-related quality of life in patients with advanced cancer: a systematic review of self-administered measurement instruments.

Authors:  Janneke van Roij; Heidi Fransen; Lonneke van de Poll-Franse; Myrte Zijlstra; Natasja Raijmakers
Journal:  Qual Life Res       Date:  2018-02-10       Impact factor: 4.147

3.  Expert opinion on detecting and treating depression in palliative care: A Delphi study.

Authors:  Lauren Rayner; Annabel Price; Matthew Hotopf; Irene J Higginson
Journal:  BMC Palliat Care       Date:  2011-05-27       Impact factor: 3.234

4.  Proxy assessment of patients before and after radiotherapy for brain metastases. Results of a prospective study using the DEGRO brain module.

Authors:  D Steinmann; D Vordermark; H Geinitz; R Aschoff; A Bayerl; J Gerstein; M Hipp; B van Oorschot; H J Wypior; C Schäfer
Journal:  Strahlenther Onkol       Date:  2012-11-18       Impact factor: 3.621

5.  Cognitive interviewing of bereaved relatives to improve the measurement of health outcomes and care utilisation at the end of life in a mortality followback survey.

Authors:  Barbara Gomes; Paul McCrone; Sue Hall; Julia Riley; Jonathan Koffman; Irene J Higginson
Journal:  Support Care Cancer       Date:  2013-06-08       Impact factor: 3.603

6.  Predictors of Quality of Life in Elderly Hospice Patients with Cancer.

Authors:  Christopher M Garrison; Janine Overcash; Susan C McMillan
Journal:  J Hosp Palliat Nurs       Date:  2011-09       Impact factor: 1.918

7.  Quality of Life in Palliative Care.

Authors:  Mellar P Davis; David Hui
Journal:  Expert Rev Qual Life Cancer Care       Date:  2017-11-08

Review 8.  The Palliative Outcome Scale (POS) applied to clinical practice and research: an integrative review.

Authors:  Fernanda Capella Rugno; Marysia Mara Rodrigues do Prado De Carlo
Journal:  Rev Lat Am Enfermagem       Date:  2016-08-15

9.  Symptoms and quality of life in late stage Parkinson syndromes: a longitudinal community study of predictive factors.

Authors:  Irene J Higginson; Wei Gao; Tariq Zaffer Saleem; K Ray Chaudhuri; Rachel Burman; Paul McCrone; Peter Nigel Leigh
Journal:  PLoS One       Date:  2012-11-07       Impact factor: 3.240

10.  Palliative patients cared for at home by PAMINO-trained and other GPs - health-related quality of life as measured by QLQ-C15-PAL and POS.

Authors:  Katja Hermann; Peter Engeser; Joachim Szecsenyi; Antje Miksch
Journal:  BMC Palliat Care       Date:  2012-08-21       Impact factor: 3.234

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