Literature DB >> 30954388

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

C H Cremers1, M J Fischer2, E T Kruitwagen-van Reenen2, R I Wadman3, J J Vervoordeldonk1, M Verhoef2, J M Visser-Meily4, W L van der Pol3, C D Schröder2.   

Abstract

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.
Copyright © 2019 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Burden; Caregiver; Emotional distress; Participation; Satisfaction; Spinal muscular atrophy

Mesh:

Year:  2019        PMID: 30954388     DOI: 10.1016/j.nmd.2019.02.011

Source DB:  PubMed          Journal:  Neuromuscul Disord        ISSN: 0960-8966            Impact factor:   4.296


  6 in total

Review 1.  Parents as informal caregivers of children and adolescents with spinal muscular atrophy: a systematic review of quantitative and qualitative data on the psychosocial situation, caregiver burden, and family needs.

Authors:  Maja Brandt; Lene Johannsen; Laura Inhestern; Corinna Bergelt
Journal:  Orphanet J Rare Dis       Date:  2022-07-19       Impact factor: 4.303

Review 2.  The adult multidisciplinary respiratory neuromuscular clinic.

Authors:  Neeraj M Shah; Patrick B Murphy; Georgios Kaltsakas
Journal:  Breathe (Sheff)       Date:  2020-09

3.  Quality of life of children with spinal muscular atrophy and their caregivers from the perspective of caregivers: a Chinese cross-sectional study.

Authors:  Mei Yao; Ying Ma; Ruiying Qian; Yu Xia; Changzheng Yuan; Guannan Bai; Shanshan Mao
Journal:  Orphanet J Rare Dis       Date:  2021-01-06       Impact factor: 4.123

4.  Health economic evaluation of gene replacement therapies: methodological issues and recommendations.

Authors:  Samuel Aballéa; Katia Thokagevistk; Rimma Velikanova; Steven Simoens; Lieven Annemans; Fernando Antonanzas; Pascal Auquier; Clément François; Frank-Ulrich Fricke; Daniel Malone; Aurélie Millier; Ulf Persson; Stavros Petrou; Omar Dabbous; Maarten Postma; Mondher Toumi
Journal:  J Mark Access Health Policy       Date:  2020-10-11

5.  Improving Care and Empowering Adults Living with SMA: A Call to Action in the New Treatment Era.

Authors:  Maggie C Walter; Claudia Chiriboga; Tina Duong; Nathalie Goemans; Anna Mayhew; Laëtitia Ouillade; Maryam Oskoui; Ros Quinlivan; Juan F Vázquez-Costa; John Vissing; Laurent Servais
Journal:  J Neuromuscul Dis       Date:  2021

6.  Burden of Spinal Muscular Atrophy (SMA) on Patients and Caregivers in Canada.

Authors:  H J McMillan; B Gerber; T Cowling; W Khuu; M Mayer; J W Wu; B Maturi; K Klein-Panneton; C Cabalteja; H Lochmüller
Journal:  J Neuromuscul Dis       Date:  2021
  6 in total

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