Literature DB >> 18294811

Bereaved family members' evaluation of hospice care: what factors influence overall satisfaction with services?

Ramona L Rhodes1, Susan L Mitchell, Susan C Miller, Stephen R Connor, Joan M Teno.   

Abstract

As patients near the end of life, bereaved family members provide an important source of evaluation of the care they receive. A study was conducted to identify which processes of care were associated with greater satisfaction with hospice services from the perception of bereaved family members. A total of 116,974 surveys from 819 hospices in the United States were obtained via the 2005 Family Evaluation of Hospice Care, an online repository of surveys of bereaved family members' perceptions of the quality of hospice care maintained by the National Hospice and Palliative Care Organization. Overall satisfaction was dichotomized as "excellent" vs. "other" (very good, good, fair, and poor). Using multivariate logistic regression, the association between overall satisfaction and the individual item problem scores that compose the Family Evaluation of Hospice Care were examined. Bereaved family members were more likely to rate overall satisfaction with hospice services as "excellent" if they were regularly informed about their loved one's condition (adjusted odds ratio [AOR]=3.76, 95% confidence interval [CI]=3.61-3.91), they felt the hospice team provided the right amount of emotional support to them (AOR=2.21, 95% CI=2.07-2.38), they felt that the hospice team provided them with accurate information about the patient's medical treatment (AOR=2.16, 95% CI=2.06-2.27), and they could identify one nurse as being in charge of their loved one's care (AOR=2.02, CI=1.92-2.13). These four key processes of care appear to significantly influence an "excellent" rating of overall satisfaction with hospice care.

Entities:  

Mesh:

Year:  2008        PMID: 18294811     DOI: 10.1016/j.jpainsymman.2007.12.004

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


  34 in total

Review 1.  Parental bereavement needs in the pediatric intensive care unit: review of available measures.

Authors:  Kathleen L Meert; Stephanie Myers Schim; Sherylyn H Briller
Journal:  J Palliat Med       Date:  2011-06-01       Impact factor: 2.947

2.  'The worst thing about hospice is that they talk about death': contrasting hospice decisions and experience among immigrant Central and South American Latinos with US-born White, non-Latino cancer caregivers.

Authors:  Barbara Kreling; Claire Selsky; Monique Perret-Gentil; Elmer E Huerta; Jeanne S Mandelblatt
Journal:  Palliat Med       Date:  2010-06       Impact factor: 4.762

3.  Associations between Race and Dementia Status and the Quality of End-of-Life Care.

Authors:  Elizabeth A Luth; Holly G Prigerson
Journal:  J Palliat Med       Date:  2018-04-05       Impact factor: 2.947

Review 4.  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

5.  Spiritual and emotional support of primary informal end-of-life caregivers in Nova Scotia.

Authors:  Leila Sloss; Beverley Lawson; Frederick I Burge
Journal:  J Palliat Care       Date:  2012       Impact factor: 2.250

6.  Health Care Reform and Concurrent Curative Care for Terminally Ill Children: A Policy Analysis.

Authors:  Lisa C Lindley
Journal:  J Hosp Palliat Nurs       Date:  2011-03       Impact factor: 1.918

7.  Family caregiver participation in hospice interdisciplinary team meetings: how does it affect the nature and content of communication?

Authors:  Elaine Wittenberg-Lyles; Debra Parker Oliver; Robin L Kruse; George Demiris; L Ashley Gage; Ken Wagner
Journal:  Health Commun       Date:  2012-03-21

8.  Informal hospice caregiver pain management concerns: a qualitative study.

Authors:  Marjorie Kelley; George Demiris; Huong Nguyen; Debra P Oliver; Elaine Wittenberg-Lyles
Journal:  Palliat Med       Date:  2013-04-23       Impact factor: 4.762

9.  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

10.  Quality of End-of-Life Care Provided to Patients With Different Serious Illnesses.

Authors:  Melissa W Wachterman; Corey Pilver; Dawn Smith; Mary Ersek; Stuart R Lipsitz; Nancy L Keating
Journal:  JAMA Intern Med       Date:  2016-08-01       Impact factor: 21.873

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.