Literature DB >> 9447806

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

L J Kristjanson1, A Leis, P M Koop, K C Carrière, B Mueller.   

Abstract

Psychometric properties of assessment tools designed for use with English-speaking family members of advanced cancer patients in different care settings and different geographic locations were evaluated in this study. The robustness of the theoretical framework guiding the study and the factors identified with care satisfaction were also tested. Seventy-two family members drawn equally from medical hospital units, palliative care units, and home care programs in Alberta, Saskatchewan, and Manitoba participated. Instruments used included the F-Care Expectations Scale, F-Care Perceptions Scale, FAMCARE Scale, and the General Functioning Scale of the Family Assessment Device. All four tools yielded acceptable reliability estimates. Discrepancy theory predicted family care satisfaction in a highly significant manner (p < 0.0001). Family members of patients who had been diagnosed for longer than two years had more positive perceptions of palliative care than did family members of patients diagnosed for less than two years (p = 0.05). Older family members reported better family functioning than younger family members (p < 0.001). Spouses reported less discrepancy between care expectations and perceptions than did other relatives (p < 0.05).

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Mesh:

Year:  1997        PMID: 9447806

Source DB:  PubMed          Journal:  J Palliat Care        ISSN: 0825-8597            Impact factor:   2.250


  14 in total

1.  The Senate report on end-of-life care: the ball is in our court.

Authors:  H M Chochinov
Journal:  CMAJ       Date:  2001-03-20       Impact factor: 8.262

Review 2.  What is a health expectation? Developing a pragmatic conceptual model from psychological theory.

Authors:  Jennifer Amy Janzen; James Silvius; Sarah Jacobs; Susan Slaughter; William Dalziel; Neil Drummond
Journal:  Health Expect       Date:  2006-03       Impact factor: 3.377

Review 3.  A systematic review of measures of end-of-life care and its outcomes.

Authors:  Richard A Mularski; Sydney M Dy; Lisa R Shugarman; Anne M Wilkinson; Joanne Lynn; Paul G Shekelle; Sally C Morton; Virginia C Sun; Ronda G Hughes; Lara K Hilton; Margaret Maglione; Shannon L Rhodes; Cony Rolon; Karl A Lorenz
Journal:  Health Serv Res       Date:  2007-10       Impact factor: 3.402

Review 4.  Family functioning in the context of an adult family member with illness: A concept analysis.

Authors:  Yingzi Zhang
Journal:  J Clin Nurs       Date:  2018-08       Impact factor: 3.036

5.  Caregiver satisfaction with out-patient oncology services: utility of the FAMCARE instrument and development of the FAMCARE-6.

Authors:  Gregory Leigh Carter; Terry J Lewin; Louisa Gianacas; Kerrie Clover; Catherine Adams
Journal:  Support Care Cancer       Date:  2010-03-28       Impact factor: 3.603

Review 6.  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

7.  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

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

Authors:  Christopher Lo; Debika Burman; Gary Rodin; Camilla Zimmermann
Journal:  Qual Life Res       Date:  2009-06-10       Impact factor: 4.147

9.  The Italian version of the FAMCARE scale: a validation study.

Authors:  Rabih Chattat; Giovanni Ottoboni; Anita Zeneli; Maria Alejandra Berardi; Veronica Cossu; Marco Maltoni
Journal:  Support Care Cancer       Date:  2016-04-11       Impact factor: 3.603

10.  Relationship quality and burden among caregivers for late-stage cancer patients.

Authors:  Linda E Francis; Julie Worthington; Georgios Kypriotakis; Julia H Rose
Journal:  Support Care Cancer       Date:  2009-11-08       Impact factor: 3.603

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