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Updated: May 7, 2026

The Multiple Sclerosis Performance Test MSPT: An iPad-Based Disability Assessment Tool
Published on: June 30, 2014
Improving Quality of Life in Polish patients with multiple sclerosis: a multicentre analysis
Joanna Tarasiuk1, Katarzyna Kapica-Topczewska2, Agata Czarnowska2
1Department of Neurology, Medical University of Bialystok, Bialystok, Poland. amirtarasiuk@wp.pl.
Introduction:
Multiple sclerosis (MS) is a progressive disease leading to disability, that mostly affects young and middle-aged adults. This study was aimed at evaluating the impact of sociodemographic and clinical factors, including changes in access to disease-modifying therapies (DMTs), on the quality of life (QoL) of Polish individuals with MS and to compare the findings to earlier national studies.
Material And Methods:
Data was collected from patients with MS across 19 MS treatment centres in Poland between February and April 2024. QoL was assessed using the EuroQol five-dimension, five-level (EQ-5D-5L) index and the EQ Visual Analogue Scale (EQ-VAS). Sociodemographic and clinical data was obtained via a standardised questionnaire.
Results:
The study included 3,165 patients with MS (mean age: 42.03 years; disease duration: 10.6 ± 7.85 years; female-to-male ratio 2.2:1). The mean EQ-5D-5L index score was 0.89 (± 0.15), and the mean EQ-VAS score was 71.58 (± 18.67), indicating an overall moderate-to-good QoL in the studied cohort. Pain/discomfort (80.7%) and anxiety/depression (79.6%) were the most frequently reported problems. Higher QoL scores were associated with younger age, relapsing-remitting MS, lower disability (EDSS ≤ 3.5), shorter disease duration, lack of comorbidities, employment, urban residence, childlessness, DMT usage, and infrequent DMTs switches (p < 0.001). When compared to earlier Polish studies, these results suggest a meaningful improvement in QoL over the past decade.
Conclusions:
The QoL of Polish patients with MS remains diminished compared to that of the general population. However, there has been a notable improvement compared to previous national data. This trend probably reflects advances in MS care, including wider access to novel DMTs and optimised treatment strategies.

