Özge Ertekin1, Serkan Özakbaş2, Egemen İdiman2. 1. Department of Physiotherapy and Rehabilitation, Sifa University Faculty of Health Sciences, Izmir, Turkey. 2. Department of Neurology, Dokuz Eylül University School of Medicine, Izmir, Turkey.
Abstract
BACKGROUND: 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). OBJECTIVES: 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.
BACKGROUND: 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). OBJECTIVES: This study was designed to compare according to the disability level (1) the walking ability, quality of life (QOL), and disease impact of the MSpatients (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 MSpatients were recruited, 47 MSpatients and their 47 caregivers finished the study. Disability, walking ability, QOL, disease impact of the MSparticipants; the burden, QOL, self-efficacy, life satisfaction of the caregivers were evaluated. RESULTS:MSPatients 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 MSpatients 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 MSpatients and their caregivers to improve the rehabilitation success.
Entities:
Keywords:
Multiple sclerosis; burden; caregiver; disability; life satisfaction; quality of life; self-efficacy
Authors: Tamara McKenzie; Mary Elizabeth Quig; Tuula Tyry; Ruth Ann Marrie; Gary Cutter; Edward Shearin; Kamau Johnson; James Simsarian Journal: Int J MS Care Date: 2015 Nov-Dec
Authors: Cécile Donzé; Bruno Lenne; Anne-Sophie Jean Deleglise; Christian Kempf; Yasmine Bellili; Patrick Hautecoeur Journal: Mult Scler Int Date: 2016-08-01