Literature DB >> 21266290

A pilot study to explore next of kin's perspectives on end-of-life care in the nursing home.

Petra Flock1, Jill M Terrien.   

Abstract

OBJECTIVES: To explore next-of-kin's (NOK's) perceptions of end-of-life (EOL) care in the nursing home setting and to compare these perceptions for residents receiving hospice care plus usual care versus usual care only.
DESIGN: Mailed survey.
SETTING: Three nursing homes in central Massachusetts. PARTICIPANTS: Nursing home decedents' NOK MEASUREMENTS: Nursing home decedents' NOK were identified from nursing home records. Survey data were collected on NOK demographics and perceptions of decedents' EOL care. This care included nursing home care and services received by decedents, pain and symptom management, communication about decedents' care, and advance directives.
RESULTS: Of 164 surveys mailed, 114 surveys were returned (70% response rate) with 100 completed (61% used for analysis). NOK reported that nursing home decedents had a high symptom burden, with at least 70% experiencing pain, agitation, and/or anxiety, and 60% having shortness of breath or depression. Most NOK reported good-to-excellent symptom control for decedents (88%), feeling well informed about the decedent's condition (91%), satisfaction with medical and nursing care (90%), and the decedent having advance directives in place (89%). Respondents' impressions of decedents' symptom control, communication about decedents' care, level of care, or advance directives did not differ significantly between the hospice plus usual care and usual care only groups.
CONCLUSION: In this pilot study, NOK perceived that decedents' EOL care in the nursing home was of similarly good quality under hospice care plus usual care and usual care only. Our study provides an approach to assessing quality of EOL care in the nursing home setting.
Copyright © 2011 American Medical Directors Association. Published by Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 21266290     DOI: 10.1016/j.jamda.2010.07.017

Source DB:  PubMed          Journal:  J Am Med Dir Assoc        ISSN: 1525-8610            Impact factor:   4.669


  3 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.  Family Members' Experience With Hospice in Nursing Homes.

Authors:  L Ashley Gage; Karla Washington; Debra Parker Oliver; Robin Kruse; Alexandra Lewis; George Demiris
Journal:  Am J Hosp Palliat Care       Date:  2014-11-23       Impact factor: 2.500

3.  Hospice family members' perceptions of and experiences with end-of-life care in the nursing home.

Authors:  Debra Parker Oliver; Karla Washington; Robin L Kruse; David L Albright; Alexandria Lewis; George Demiris
Journal:  J Am Med Dir Assoc       Date:  2014-07-10       Impact factor: 4.669

  3 in total

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