Article

The caregivers of Multiple Sclerosis (MS) individuals are usually
burdened with a wide range of MS-related caregiving tasks which may result in
damages of their daily life and quality of life (QOL). This study was
designed to compare according to the disability level (1) the walking ability,
quality of life (QOL), and disease impact of the MS patients (2) and the burden,
QOL, self-efficacy and life satisfaction of their caregivers; (3) to determine
the relationship between these outcome results, disease duration and caregivers'
age. METHODS: 772 MS patients were recruited, 47 MS patients and their 47
caregivers finished the study. Disability, walking ability, QOL, disease impact
of the MS participants; the burden, QOL, self-efficacy, life satisfaction of the
caregivers were evaluated. RESULTS: MS Patients with higher disability had
significantly worse scores on the MSWS-12, MUSIQOL, MSIS-29, and PDSS (p < 0.01).
The caregivers facing with higher disability had significantly worse scores on
CBI and CAREQOL (p < 0.01). CONCLUSIONS: The impairments on disability level,
walking and QOL of MS patients were related to OQL declines and increased burden
of their caregivers. Therefore, it may be important to provide acceptable
education and support strategies with individual intervention while defining the
needs and goals of the MS patients and their caregivers to improve the
rehabilitation success.

Langue : ANGLAIS