Citation

Schmidt S, Jöstingmeyer P. Mult. Scler. Relat. Disord. 2019; 35: 262-269.

Affiliation

Neurologische, Gemeinschaftspraxis, Kölnstr. 54 53111 Bonn, Germany.

Copyright

(Copyright © 2019, Elsevier Publishing)

DOI

10.1016/j.msard.2019.07.029

PMID

31437741

Abstract

BACKGROUND: Quality of life (QoL) is significantly impaired in patients with Multiple Sclerosis (MS). As the expanded disability status scale (EDSS) inadequately reflects the impact of clinical symptoms on QoL, the present study aimed to identify factors associated with reduced QoL in MS patients.

DESIGN: Single-center cross-sectional study in 260 MS patients.

METHODS: QoL was assessed by the Multiple Sclerosis International QoL Questionnaire (MusiQoL), depression by the Center for Epidemiological Studies Depression Scale (CES-D scale), and fatigue by the Fatigue Scale for motor function and cognition (FSMC).

RESULTS: 79.6% patients were female and 21.4% male. The mean age was 44.5 ± 11.2 years and the median EDSS 3.0 (range 0.0-8.5). 35.8% had depression and 56.9% moderate to severe fatigue. The mean MusiQoL index score was 73.9 ± 11.3. Using linear regression, depression, fatigue, family status, physical activity, and occupation were associated with QoL. EDSS was only associated with QoL in patients with an EDSS 0.5.0.

CONCLUSIONS: Depression, fatigue, family status, physical activity, and occupational status were closely associated with QoL in MS patients. Potential measures to improve QoL include assessment and treatment of depression, physical exercise, and maintaining patients employed in accordance with their physical and mental disabilities.

Copyright © 2019. Published by Elsevier B.V.

Language: en

Keywords

Depression; Edss; Fatigue; Multiple sclerosis; Quality of life