Literature DB >> 26529470

Cross-Sectional Examination of the Associations Between Symptoms, Community Integration, and Mental Health in Multiple Sclerosis.

Anna L Kratz1, Dawn M Ehde2, Marisol A Hanley3, Mark P Jensen2, Travis L Osborne4, George H Kraft2.   

Abstract

OBJECTIVE: To determine the frequency and severity of 8 symptoms in persons with multiple sclerosis (MS) and to examine the association between these symptoms and community integration and mental health.
DESIGN: Cross-sectional survey that assessed 8 symptoms (pain, fatigue, imbalance, numbness, weakness, shortness of breath, vision loss, and memory loss), disease progression (self-report version of the Expanded Disability Status Scale), community integration, and mental health.
SETTING: Community. PARTICIPANTS: Adults with self-reported MS who responded to a mailed survey (N=180).
INTERVENTIONS: Not applicable. MAIN OUTCOME MEASURES: The presence and intensity of symptoms were measured with a symptoms checklist. Community integration was assessed with the Community Integration Questionnaire, and mental health was measured by the Mental Health Index of the Medical Outcomes Study 36-Item Short-Form Health Survey.
RESULTS: The average number of symptoms reported was 5.07±2.18. The most common symptoms (fatigue, weakness, and imbalance) were also rated as the most severe. Not all symptoms were associated with level of disease progression or with MS subtype. Symptoms related to mobility were more likely to be associated with these variables. The 8 symptoms as a whole accounted for significant amounts of variance (range, 13%-21%) in measures of community integration and mental health, with specific symptoms making differential independent contributions to these measures.
CONCLUSIONS: This study demonstrates that most individuals with MS report a number of bothersome symptoms. Type of MS or level of progression does not tell the whole story regarding the impact of symptoms.
Copyright © 2016 American Congress of Rehabilitation Medicine. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Community integration; Fatigue; Multiple sclerosis; Pain; Rehabilitation

Mesh:

Year:  2015        PMID: 26529470      PMCID: PMC4769914          DOI: 10.1016/j.apmr.2015.10.093

Source DB:  PubMed          Journal:  Arch Phys Med Rehabil        ISSN: 0003-9993            Impact factor:   3.966


  57 in total

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2.  Major depression in multiple sclerosis: a population-based perspective.

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3.  Is there a differential impact of fatigue and physical disability on quality of life in multiple sclerosis?

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4.  Depressive symptoms and severity of illness in multiple sclerosis: epidemiologic study of a large community sample.

Authors:  Lydia Chwastiak; Dawn M Ehde; Laura E Gibbons; Mark Sullivan; James D Bowen; George H Kraft
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5.  Self-administered Expanded Disability Status Scale with functional system scores correlates well with a physician-administered test.

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6.  The community integration questionnaire with new scoring guidelines: concurrent validity and need for appropriate norms.

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Review 7.  The use of quality of life measures in multiple sclerosis research.

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8.  Chronic pain in a large community sample of persons with multiple sclerosis.

Authors:  Dawn M Ehde; Laura E Gibbons; Lydia Chwastiak; Charles H Bombardier; Mark D Sullivan; George H Kraft
Journal:  Mult Scler       Date:  2003-12       Impact factor: 6.312

9.  Efficacy of a Telephone-Delivered Self-Management Intervention for Persons With Multiple Sclerosis: A Randomized Controlled Trial With a One-Year Follow-Up.

Authors:  Dawn M Ehde; Jamie L Elzea; Aimee M Verrall; Laura E Gibbons; Amanda E Smith; Dagmar Amtmann
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10.  Pain in patients with multiple sclerosis: a population-based study.

Authors:  Kristina Bacher Svendsen; Troels Staehelin Jensen; Kim Overvad; Hans Jacob Hansen; Nils Koch-Henriksen; Flemming W Bach
Journal:  Arch Neurol       Date:  2003-08
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5.  Translation and initial validation of Chinese (Cantonese) version of Modified Fatigue Impact Scale (MFIS-C) in people with stroke.

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