Literature DB >> 15684848

Terminal care for persons with advanced dementia in the nursing home and home care settings.

Susan L Mitchell1, John N Morris, Pil S Park, Brant E Fries.   

Abstract

BACKGROUND: Many older persons with advanced dementia receive terminal care in nursing homes, others remain in the community with home care services.
OBJECTIVES: To describe and compare the end-of-life experience of persons dying with advanced dementia in the nursing home and home care settings.
DESIGN: Retrospective cohort study. SETTING/
SUBJECTS: Persons 65 years or older with advanced dementia who died within 1 year of admission to either a nursing home in Michigan between July 1, 1998 until December 31, 2000 (n = 2730), or the state's publicly funded home and community-based services from October 1, 1998 until December 31, 2001 (n = 290). MEASUREMENTS: Data were derived from the Minimum Data Set (MDS)-Nursing home Version 2.0 for the institutionalized sample, and the MDS-Home Care for the community-based sample. Variables from the MDS assessment completed within 180 days of death were used to describe the end-of-life experiences of these two groups.
RESULTS: Nursing home residents dying with advanced dementia were older, had greater functional impairment, and more behavior problems compared to home care clients. Few subjects in the nursing home (10.3%) and home care (15.6%) cohorts were perceived to have less than 6 months to live. Only 5.7% of nursing home residents and 10.7% home care clients were referred to hospice. Hospitalizations were frequent: nursing home, 43.7%; home care, 31.5%. Pain and shortness of breath were common in both settings. End-of-life variables independently associated with nursing home versus home care included: hospice (adjusted odds ratio [AOR] 0.26, 95% confidence interval [CI], 0.16-0.43), life expectancy less than 6 months (AOR 0.31; 95% CI, 0.20-0.48), advance directives (AOR, 1.48; 95% CI, 1.11-1.96), pain (AOR, 0.38; 95% CI, 0.29-0.50), shortness of breath (AOR 0.20; 95% CI (0.13-0.28), and oxygen therapy (AOR, 2.47; 95% CI, 1.51-4.05).
CONCLUSIONS: Persons dying with advanced dementia admitted to nursing homes have different characteristics compared to those admitted to home care services. Their end-of-life experiences also differ in these two sites of care. However, palliative care was not optimal in either setting.

Entities:  

Mesh:

Year:  2004        PMID: 15684848     DOI: 10.1089/jpm.2004.7.808

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


  44 in total

1.  Hospice care for persons with dementia: The growth of access in US nursing homes.

Authors:  Susan C Miller; Julie C Lima; Susan L Mitchell
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2.  Medicare Expenditures and Health Care Utilization in a Multiethnic Community-based Population With Dementia From Incidence to Death.

Authors:  Katherine A Ornstein; Carolyn W Zhu; Evan Bollens-Lund; Melissa D Aldridge; Howard Andrews; Nicole Schupf; Yaakov Stern
Journal:  Alzheimer Dis Assoc Disord       Date:  2018 Oct-Dec       Impact factor: 2.703

3.  The Impact of Dementia Special Care Units on Quality of Care: An Instrumental Variables Analysis.

Authors:  Nina R Joyce; Thomas G McGuire; Stephen J Bartels; Susan L Mitchell; David C Grabowski
Journal:  Health Serv Res       Date:  2018-05-07       Impact factor: 3.402

Review 4.  [Palliative care in nursing homes: central issues and further research].

Authors:  S Pleschberger
Journal:  Z Gerontol Geriatr       Date:  2006-10       Impact factor: 1.281

5.  A study protocol for the development of a multivariable model predicting 6- and 12-month mortality for people with dementia living in residential aged care facilities (RACFs) in Australia.

Authors:  Ross Bicknell; Wen Kwang Lim; Andrea B Maier; Dina LoGiudice
Journal:  Diagn Progn Res       Date:  2020-10-07

6.  Influence of hospice on nursing home residents with advanced dementia who received Medicare-skilled nursing facility care near the end of life.

Authors:  Susan C Miller; Julie C Lima; Susan L Mitchell
Journal:  J Am Geriatr Soc       Date:  2012-10-30       Impact factor: 5.562

Review 7.  Withholding, discontinuing and withdrawing medications in dementia patients at the end of life: a neglected problem in the disadvantaged dying?

Authors:  Carole Parsons; Carmel M Hughes; A Peter Passmore; Kate L Lapane
Journal:  Drugs Aging       Date:  2010-06-01       Impact factor: 3.923

8.  Dying with dementia: symptom burden, quality of care, and place of death.

Authors:  Luis Carlos Escobar Pinzon; Matthias Claus; Klaus Maria Perrar; Kirsten Isabel Zepf; Stephan Letzel; Martin Weber
Journal:  Dtsch Arztebl Int       Date:  2013-03-22       Impact factor: 5.594

9.  Does Caregiving Strain Increase as Patients With and Without Dementia Approach the End of Life?

Authors:  Judith B Vick; Katherine A Ornstein; Sarah L Szanton; Sydney M Dy; Jennifer L Wolff
Journal:  J Pain Symptom Manage       Date:  2018-11-17       Impact factor: 3.612

10.  Characteristics and outcomes of hospice enrollees with dementia discharged alive.

Authors:  Kimberly S Johnson; Katja Elbert-Avila; Maragatha Kuchibhatla; James A Tulsky
Journal:  J Am Geriatr Soc       Date:  2012-08-20       Impact factor: 5.562

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