Literature DB >> 21288125

Can we make reports of end-of-life care quality more consumer-focused? results of a nationwide quality measurement program.

Dawn Smith1, Nicole Caragian, Elena Kazlo, Jennie Bernstein, Diane Richardson, David Casarett.   

Abstract

OBJECTIVES: The goal of this study was to define families' priorities for various aspects of end-of-life care, and to determine whether scores that reflect these priorities alter facilities' quality rankings.
DESIGN: Nationwide telephone survey.
SETTING: 62 VA medical centers, including acute and long term care. PARTICIPANTS: For each patient who died in a participating facility, one family member was invited to participate. MEASUREMENTS: A survey included 14 items describing key aspects of the patient's care in his or her last month of life, and one global rating. A weighted score was calculated based on the association between each item and the global rating.
RESULTS: Interviews were completed with family members for 3,897 of 7,110 patients (55%). Items showed an approximately 5-fold range of weights, indicating a wide variation in the importance that families placed on aspects of palliative care (low: pain management, weight = 0.54, 95% CI 0.38-0.70;/P/<0.001; high: providers were "kind, caring, and respectful: weight = 2.46, 95% CI 2.24-2.68;/P/<0.001). Weights were homogeneous across patient subgroups, and there were no significant changes in facilities' quality rankings when weights were used. Both weighted and unweighted scores showed similar evidence of the impact of process measures.
CONCLUSION: There appears to be wide variation in the importance that families place on several aspects of end-of-life care. However, the impact of weighting was generally even across patient subgroups and facilities. Therefore, the use of weights to account for families' priorities is not likely to alter a facility's quality score.

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Year:  2011        PMID: 21288125     DOI: 10.1089/jpm.2010.0321

Source DB:  PubMed          Journal:  J Palliat Med        ISSN: 1557-7740            Impact factor:   2.947


  5 in total

Review 1.  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

2.  Organization of nursing and quality of care for veterans at the end of life.

Authors:  Ann Kutney-Lee; Caitlin W Brennan; Mark Meterko; Mary Ersek
Journal:  J Pain Symptom Manage       Date:  2014-08-10       Impact factor: 3.612

3.  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

4.  The 3 Wishes Program Improves Families' Experience of Emotional and Spiritual Support at the End of Life.

Authors:  Thanh H Neville; Zachary Taich; Anne M Walling; Danielle Bear; Deborah J Cook; Chi-Hong Tseng; Neil S Wenger
Journal:  J Gen Intern Med       Date:  2022-05-17       Impact factor: 6.473

5.  Association of Family Ratings of Quality of End-of-Life Care With Stopping Dialysis Treatment and Receipt of Hospice Services.

Authors:  Claire A Richards; Paul L Hebert; Chuan-Fen Liu; Mary Ersek; Melissa W Wachterman; Leslie L Taylor; Lynn F Reinke; Ann M O'Hare
Journal:  JAMA Netw Open       Date:  2019-10-02
  5 in total

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