Literature DB >> 12171422

Patient and caregiver satisfaction with end-of-life care: does high satisfaction mean high quality of care?

Linda L Steele1, Beth Mills, Marty R Long, Gloria A Hagopian.   

Abstract

The purpose of this study was to determine patient and caregiver satisfaction with a hospice program of care. The setting for the study was a home-care hospice in the southeastern United States that provides a full range of services for patients with life-limiting illness and supportive services for family caregivers. Two Likert-type instruments were used to determine satisfaction with staff, communication, education, information provided, symptom management, promptness with service, and overall satisfaction. Some 321 patients and 443 caregivers completed surveys over a two-year period of time. Data indicates the majority of patients and their caregivers were very satisfied with hospice services and the care they received. Providing quality care at the end of life is the goal of hospice. Satisfaction with delivery of care, management of symptoms, and communication with staff are all components of quality care and contribute to quality of life.

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Year:  2002        PMID: 12171422     DOI: 10.1177/104990910201900106

Source DB:  PubMed          Journal:  Am J Hosp Palliat Care        ISSN: 1049-9091            Impact factor:   2.500


  6 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

Review 2.  Informal caregiving of hospice patients.

Authors:  Colin G Pottie; Karen A Burch; Lori P Montross Thomas; Scott A Irwin
Journal:  J Palliat Med       Date:  2014-07       Impact factor: 2.947

3.  Missed Opportunity: Hospice Care and the Family.

Authors:  Jennifer Tabler; Rebecca L Utz; Lee Ellington; Maija Reblin; Michael Caserta; Margaret Clayton; Dale Lund
Journal:  J Soc Work End Life Palliat Care       Date:  2015

4.  Can you hear me now? The experience of a deaf family member surrounding the death of loved ones.

Authors:  Karen A Kehl; Constance M Gartner
Journal:  Palliat Med       Date:  2009-11-12       Impact factor: 4.762

5.  Psychometric properties and relations with coping and family strain of the Health Services and Caregiver Experience questionnaire (HSCE): an outcome measure of informal caregivers' experience for inpatient care in Italy.

Authors:  Anna Coluccia; Fabio Ferretti; Andrea Fagiolini; Andrea Pozza
Journal:  BMC Health Serv Res       Date:  2017-07-17       Impact factor: 2.655

6.  Measuring Family Members' Satisfaction with End-of-Life Care in Long-Term Care: Adaptation of the CANHELP Lite Questionnaire.

Authors:  Shevaun Nadin; Mohammed Ali Miandad; Mary Lou Kelley; Jill Marcella; Daren K Heyland
Journal:  Biomed Res Int       Date:  2017-06-19       Impact factor: 3.411

  6 in total

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