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DOI 10.1016/j.nmd.2019.02.011

Медицинская библиотека · Neuromuscular disorders : NMD · 2019

Participation and mental well-being of mothers of home-living patients with spinal muscular atrophy.

Cremers C H, Fischer M J, Kruitwagen-van Reenen E T, Wadman R I, Vervoordeldonk J J, Verhoef M, Visser-Meily J M, van der Pol W L, Schröder C D

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Аннотация

Proximal spinal muscular atrophy (SMA) causes severe physical limitations but also has a major impact on the lives of parents. The aim of this study was to investigate participation and mental well-being (burden, emotional distress and satisfaction with participation) of parents of home-living patients with SMA. Caregiver burden was assessed with the Caregiver Strain Index, emotional distress with the Hospital Anxiety and Depression Scale and satisfaction with participation with the Utrecht Scale for Evaluation of Rehabilitation-Participation. Because the majority of parents were mothers of home-living SMA patients (76%), further analyses were restricted to mothers. Seventy-seven percent of mothers of patients with SMA had paid work. A substantial proportion of mothers (76%) perceived high caregiver burden. Burden, emotional distress and satisfaction with participation were comparable between mothers of children and mothers of adults with SMA. Caregivers' participation in leisure activities was significantly related to their perceived level of caregiver burden, emotional distress and satisfaction with participation. Mothers engaging in more social and leisure activities reported lower emotional distress and caregiver burden. Considering the high level of burden attention should be paid to mental well-being of primary caregivers of patients with SMA. Caregivers should be motivated to keep participating in social/leisure activities.

Для цитирования: Cremers C H, Fischer M J, Kruitwagen-van Reenen E T, Wadman R I, Vervoordeldonk J J, Verhoef M, Visser-Meily J M, van der Pol W L, Schröder C D. Participation and mental well-being of mothers of home-living patients with spinal muscular atrophy.. Neuromuscular disorders : NMD. 2019. DOI: 10.1016/j.nmd.2019.02.011.

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