Literature DB >> 29270087

Fatigue and Mood States in Nursing Home and Nonambulatory Home-Based Patients with Multiple Sclerosis.

Zilfah Younus, Caila B Vaughn, Shaik Ahmed Sanai, Katelyn S Kavak, Sahil Gupta, Muhammad Nadeem, Barbara E Teter, Katia Noyes, Robert Zivadinov, Keith Edwards, Patricia K Coyle, Andrew Goodman, Bianca Weinstock-Guttman.   

Abstract

BACKGROUND: Multiple sclerosis (MS) is a chronic, progressively disabling condition of the central nervous system. We sought to evaluate and compare mood states in patients with MS with increased disability residing in nursing homes and those receiving home-based care.
METHODS: We conducted a cross-sectional analysis of the New York State Multiple Sclerosis Consortium to identify patients with MS using a Kurtzke Expanded Disability Status Scale (EDSS) score of 7.0 or greater. The nursing home group was compared with home-based care patients regarding self-reported levels of loneliness, pessimism, tension, panic, irritation, morbid thoughts, feelings of guilt, and fatigue using independent-samples t tests and χ2 tests. Multivariate logistic regression analyses were used to investigate risk-adjusted differences in mood states.
RESULTS: Ninety-four of 924 patients with EDSS scores of at least 7.0 lived in a nursing home (10.2%). Nursing home patients were less likely to use disease-modifying therapy and had higher mean EDSS scores compared with home-based patients. However, nursing home patients were less likely than home-based patients to report fatigue (odds ratio [OR] for no fatigue, 3.8; 95% CI, 2.1-7.2), feeling tense (OR for no tension, 1.7; 95% CI, 1.1-2.7), and having feelings of pessimism (OR for no pessimism, 1.8; 95% CI, 1.2-2.8).
CONCLUSIONS: The nursing home patients with MS were less likely to report fatigue, pessimism, and tension than those receiving home-based care. Further studies should examine ways of facilitating a greater degree of autonomy and decision-making control in MS patients receiving home-based care.

Entities:  

Year:  2017        PMID: 29270087      PMCID: PMC5734713          DOI: 10.7224/1537-2073.2016-058

Source DB:  PubMed          Journal:  Int J MS Care        ISSN: 1537-2073


  23 in total

1.  Helplessness, self-efficacy, cognitive distortions, and depression in multiple sclerosis and spinal cord injury.

Authors:  Z M Shnek; F W Foley; N G LaRocca; W A Gordon; J DeLuca; H G Schwartzman; J Halper; S Lennox; J Irvine
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2.  The natural history of multiple sclerosis: a geographically based study. 2. Predictive value of the early clinical course.

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Journal:  Brain       Date:  1989-12       Impact factor: 13.501

3.  Caregiver perceptions associated with risk of nursing home admission for people with multiple sclerosis.

Authors:  Robert J Buchanan; Dagmar Radin; Chunfeng Huang; Li Zhu
Journal:  Disabil Health J       Date:  2009-11-03       Impact factor: 2.554

4.  Caregiver quality of life in multiple sclerosis: a multicentre Italian study.

Authors:  F Patti; M P Amato; M A Battaglia; M Pitaro; P Russo; C Solaro; M Trojano
Journal:  Mult Scler       Date:  2007-01-29       Impact factor: 6.312

5.  Concerns about the future among older adults with multiple sclerosis.

Authors:  Marcia Finlayson
Journal:  Am J Occup Ther       Date:  2004 Jan-Feb

Review 6.  Assessment of caregiver burden in families of persons with multiple sclerosis.

Authors:  Marijean Buhse
Journal:  J Neurosci Nurs       Date:  2008-02       Impact factor: 1.230

Review 7.  The impact of multiple sclerosis on family members: a review of the literature.

Authors:  Michele Messmer Uccelli
Journal:  Neurodegener Dis Manag       Date:  2014

8.  Assessments of nursing home guidelines for quality of care provided to residents with multiple sclerosis.

Authors:  Robert J Buchanan; Allison L Seibert; Adele Crudden; Sarah Minden
Journal:  J Soc Work Disabil Rehabil       Date:  2013

9.  Patterns of Objective and Subjective Burden of Informal Caregivers in Multiple Sclerosis.

Authors:  E Bayen; C Papeix; P Pradat-Diehl; C Lubetzki; M E Joël
Journal:  Behav Neurol       Date:  2015-05-20       Impact factor: 3.342

10.  Is There Extra Cost of Institutional Care for MS Patients?

Authors:  Katia Noyes; Alina Bajorska; Bianca Weinstock-Guttman; Dana B Mukamel
Journal:  Mult Scler Int       Date:  2013-09-14
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