Literature DB >> 25877977

Self-reported severity among patients with multiple sclerosis in the U.S. and its association with health outcomes.

Shaloo Gupta1, Amir Goren2, Amy L Phillips3, Fernando Dangond4, Michelle Stewart5.   

Abstract

PURPOSE: Individuals with multiple sclerosis (MS) experience diminished health outcomes. However, little is known about how these outcomes differ according to disease severity. The aim of this study is to compare health-related quality of life (HRQoL), work productivity, activity impairment, and resource use between MS patients and controls, as well as across MS patients with varying self-reported disease severity.
METHODS: Data were analyzed from respondents reporting an MS diagnosis (n=536) and controls (n=74,451) in the U.S. 2009 National Health and Wellness Survey (administered online to a nationally representative adult population). Differences were assessed between those with and without MS, and across three MS severity groups: mild (38.4%), moderate (50%), and severe (11.6%).
RESULTS: MS patients vs. controls experienced significantly more activity impairment, decreased work productivity, increased healthcare utilization, and lower HRQoL (all p<0.001). Increasing MS severity was associated with greater activity impairment, lower work productivity, increased healthcare utilization, and lower HRQoL. More significant impairments emerged between individuals who perceived their disease severity as mild vs. moderate than moderate vs. severe.
CONCLUSION: MS patients reported greater impairment than controls, and impairment increased with disease severity (especially from mild to moderate). These findings show that increasing MS disease severity is associated with worse health outcomes.
© 2013 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Disease severity; Multiple sclerosis; Quality of life; Resource use; Self-report; Work productivity

Year:  2013        PMID: 25877977     DOI: 10.1016/j.msard.2013.06.002

Source DB:  PubMed          Journal:  Mult Scler Relat Disord        ISSN: 2211-0348            Impact factor:   4.339


  6 in total

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2.  Quality of life in adults with multiple sclerosis: a systematic review.

Authors:  Irene Gil-González; Agustín Martín-Rodríguez; Rupert Conrad; María Ángeles Pérez-San-Gregorio
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3.  Fatigue, Depression, and Anxiety Among Ambulating Multiple Sclerosis Patients.

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Journal:  Front Immunol       Date:  2022-03-29       Impact factor: 7.561

4.  Self-reported quality of life in multiple sclerosis patients: preliminary results based on the Polish MS Registry.

Authors:  Waldemar Brola; Piotr Sobolewski; Małgorzata Fudala; Stanisław Flaga; Konrad Jantarski; Danuta Ryglewicz; Andrzej Potemkowski
Journal:  Patient Prefer Adherence       Date:  2016-08-26       Impact factor: 2.711

5.  Health-related outcomes, health care resource utilization, and costs of multiple sclerosis in Japan compared with US and five EU countries.

Authors:  Kaoru Yamabe; Marco D DiBonaventura; Chris L Pashos
Journal:  Clinicoecon Outcomes Res       Date:  2019-01-07

6.  Burden of relapsing-remitting multiple sclerosis on workers in the US: a cross-sectional analysis of survey data.

Authors:  Jacqueline A Nicholas; Batul Electricwala; Lulu K Lee; Kristen M Johnson
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  6 in total

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