Literature DB >> 19513815

Measuring patient satisfaction in oncology palliative care: psychometric properties of the FAMCARE-patient scale.

Christopher Lo1, Debika Burman, Gary Rodin, Camilla Zimmermann.   

Abstract

PURPOSE: We provide preliminary psychometric results concerning the use of a modified FAMCARE scale, adapted for patient use, to assess satisfaction with outpatient care in advanced stage cancer patients.
METHODS: Participants were 145 outpatients with advanced cancer who were participating in a phase II trial of an outpatient palliative care intervention. Patients completed our modified FAMCARE measure of patient satisfaction and the Edmonton Symptom Assessment Scale, a measure of symptom burden. Individuals were also assessed for performance status using the Eastern Cooperative Oncology Group scale. We conducted an exploratory factor analysis of the patient satisfaction measure and performed correlations of satisfaction with symptom burden as well as with performance status.
RESULTS: Factor analysis of the satisfaction measure revealed a one-factor structure and suggested the removal of one nonloading item, producing a 16-item scale (FAMCARE-P16) with high internal reliability. Patient satisfaction was not correlated with performance status, but was inversely associated with symptom burden, particularly with depression and anxiety.
CONCLUSIONS: The FAMCARE-P16 may be used to assess satisfaction with outpatient palliative care interventions of patients with advanced stage cancer in both clinical settings and prospective trials.

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Year:  2009        PMID: 19513815     DOI: 10.1007/s11136-009-9494-y

Source DB:  PubMed          Journal:  Qual Life Res        ISSN: 0962-9343            Impact factor:   4.147


  35 in total

1.  Measuring quality of life at the end of life: validation of the QUAL-E.

Authors:  Karen E Steinhauser; Elizabeth C Clipp; Hayden B Bosworth; Maya McNeilly; Nicholas A Christakis; Corrine I Voils; James A Tulsky
Journal:  Palliat Support Care       Date:  2004-03

2.  Family members' care expectations, care perceptions, and satisfaction with advanced cancer care: results of a multi-site pilot study.

Authors:  L J Kristjanson; A Leis; P M Koop; K C Carrière; B Mueller
Journal:  J Palliat Care       Date:  1997       Impact factor: 2.250

3.  Measuring quality of care at the end of life: a statement of principles.

Authors:  J Lynn
Journal:  J Am Geriatr Soc       Date:  1997-04       Impact factor: 5.562

4.  An international prospective study of the EORTC cancer in-patient satisfaction with care measure (EORTC IN-PATSAT32).

Authors:  A Brédart; A Bottomley; J M Blazeby; T Conroy; C Coens; S D'Haese; Wei-Chu Chie; E Hammerlid; J I Arraras; F Efficace; C Rodary; S Schraub; M Costantini; A Costantini; F Joly; O Sezer; D Razavi; M Mehlitz; M Bielska-Lasota; N K Aaronson
Journal:  Eur J Cancer       Date:  2005-09       Impact factor: 9.162

Review 5.  Quality of life in palliative care: principles and practice.

Authors:  Stein Kaasa; Jon Håvard Loge
Journal:  Palliat Med       Date:  2003-01       Impact factor: 4.762

Review 6.  Pain assessment: global use of the Brief Pain Inventory.

Authors:  C S Cleeland; K M Ryan
Journal:  Ann Acad Med Singapore       Date:  1994-03       Impact factor: 2.473

7.  The Memorial Symptom Assessment Scale: an instrument for the evaluation of symptom prevalence, characteristics and distress.

Authors:  R K Portenoy; H T Thaler; A B Kornblith; J M Lepore; H Friedlander-Klar; E Kiyasu; K Sobel; N Coyle; N Kemeny; L Norton
Journal:  Eur J Cancer       Date:  1994       Impact factor: 9.162

8.  Family caregiver burden: results of a longitudinal study of breast cancer patients and their principal caregivers.

Authors:  Eva Grunfeld; Doug Coyle; Timothy Whelan; Jennifer Clinch; Leonard Reyno; Craig C Earle; Andrew Willan; Raymond Viola; Marjorie Coristine; Teresa Janz; Robert Glossop
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9.  Measuring quality of palliative care: psychometric properties of the FAMCARE Scale.

Authors:  Gerd Inger Ringdal; Marit S Jordhøy; Stein Kaasa
Journal:  Qual Life Res       Date:  2003-03       Impact factor: 4.147

10.  Does a palliative care clinic have a role in improving end-of-life care? Results of a pilot program.

Authors:  David J Casarett; Karen B Hirschman; John F Coffey; Lucy Pierre
Journal:  J Palliat Med       Date:  2002-06       Impact factor: 2.947

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  27 in total

1.  Structural and reliability analysis of a patient satisfaction with cancer-related care measure: a multisite patient navigation research program study.

Authors:  Pascal Jean-Pierre; Kevin Fiscella; Karen M Freund; Jack Clark; Julie Darnell; Alan Holden; Douglas Post; Steven R Patierno; Paul C Winters
Journal:  Cancer       Date:  2010-10-04       Impact factor: 6.860

2.  Health care providers' use and knowledge of the Edmonton Symptom Assessment System (ESAS): is there a need to improve information and training?

Authors:  Daniela Carli Buttenschoen; Jarad Stephan; Sharon Watanabe; Cheryl Nekolaichuk
Journal:  Support Care Cancer       Date:  2013-09-13       Impact factor: 3.603

3.  Psychometric Properties of a Spanish-Language Version of a Short-Form FAMCARE: Applications to Caregivers of Patients With Alzheimer's Disease and Related Dementias.

Authors:  Jeanne A Teresi; Katja Ocepek-Welikson; Mildred Ramirez; Katherine A Ornstein; Suzanne Bakken; Albert Siu; José A Luchsinger
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4.  Satisfaction with oncology care among patients with advanced cancer and their caregivers.

Authors:  Breffni Hannon; Nadia Swami; Monika K Krzyzanowska; Natasha Leighl; Gary Rodin; Lisa W Le; Camilla Zimmermann
Journal:  Qual Life Res       Date:  2013-02-23       Impact factor: 4.147

Review 5.  Measuring Experience With End-of-Life Care: A Systematic Literature Review.

Authors:  Jessica Penn Lendon; Sangeeta C Ahluwalia; Anne M Walling; Karl A Lorenz; Oluwatobi A Oluwatola; Rebecca Anhang Price; Denise Quigley; Joan M Teno
Journal:  J Pain Symptom Manage       Date:  2014-12-24       Impact factor: 3.612

6.  Psychometric validation and reliability analysis of a Spanish version of the patient satisfaction with cancer-related care measure: a patient navigation research program study.

Authors:  Pascal Jean-Pierre; Kevin Fiscella; Paul C Winters; Electra Paskett; Kristen Wells; Tracy Battaglia
Journal:  Support Care Cancer       Date:  2011-10-27       Impact factor: 3.603

7.  Exploratory analyses of the Danish Palliative Care Trial (DanPaCT): a randomized trial of early specialized palliative care plus standard care versus standard care in advanced cancer patients.

Authors:  Anna Thit Johnsen; Morten Aagaard Petersen; Per Sjøgren; Lise Pedersen; Mette Asbjoern Neergaard; Anette Damkier; Christian Gluud; Peter Fayers; Jane Lindschou; Annette S Strömgren; Jan Bjoern Nielsen; Irene J Higginson; Mogens Groenvold
Journal:  Support Care Cancer       Date:  2019-08-13       Impact factor: 3.603

8.  Measuring Patient-Centeredness of Care for Seriously Ill Individuals: Challenges and Opportunities for Accountability Initiatives.

Authors:  Rebecca Anhang Price; Marc N Elliott
Journal:  J Palliat Med       Date:  2017-11-01       Impact factor: 2.947

9.  Evaluation of measurement equivalence of the Family Satisfaction with the End-of-Life Care in an ethnically diverse cohort: tests of differential item functioning.

Authors:  Jeanne A Teresi; Katja Ocepek-Welikson; Mildred Ramirez; Marjorie Kleinman; Katherine Ornstein; Albert Siu
Journal:  Palliat Med       Date:  2014-08-26       Impact factor: 4.762

10.  Evaluation of measurement equivalence of the Family Satisfaction with the End-of-Life Care (FAMCARE): Tests of differential item functioning between Hispanic and non-Hispanic White caregivers.

Authors:  Jeanne A Teresi; Katja Ocepek-Welikson; Mildred Ramirez; Marjorie Kleinman; Katherine Ornstein; Albert Siu; Jose Luchsinger
Journal:  Palliat Support Care       Date:  2020-10
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