Literature DB >> 25095627

Psychosocial challenges in family caregiving with children suffering from Duchenne muscular dystrophy.

Priya Treesa Thomas, Prakashi Rajaram, Atchayaram Nalini.   

Abstract

Families of children with Duchenne muscular dystrophy (DMD) go through significant challenges in dealing with the condition. Few studies have looked into the situation, especially in the sociocultural scenario that is unique to India. The authors' aim was to identify the psychosocial challenges for caregivers of children with DMD. A cross-sectional descriptive study was perfomed among the caregivers of 60 children with DMD who were attending the neuromuscular disorders clinic of a national tertiary referral center for neurological disorders. The knowledge and attitude, psychosocial needs, burden, and coping patterns were assessed in an interview. The findings showed that parents of children with DMD tended to have inadequate understanding of the disease but had a positive attitude, had a moderate family burden, and tended to rely more on religion, focus on and venting of emotions, and instrumental and emotional social support for coping. Caregivers of children with DMD would benefit from psychosocial intervention to address their understanding of and attitude toward the disease, as well as burden of dealing with it, and to help them develop their coping skills and meet their children's and their own needs.

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Year:  2014        PMID: 25095627     DOI: 10.1093/hsw/hlu027

Source DB:  PubMed          Journal:  Health Soc Work        ISSN: 0360-7283


  5 in total

1.  Understanding adherence to noninvasive ventilation in youth with Duchenne muscular dystrophy.

Authors:  John E Pascoe; Hemant Sawnani; Brooke Hater; Mark Sketch; Avani C Modi
Journal:  Pediatr Pulmonol       Date:  2019-09-01

2.  Palliative Care in Duchenne Muscular Dystrophy: A Study on Parents' Understanding.

Authors:  Arun Sadasivan; Manjusha G Warrier; Kiran Polavarapu; Veeramani Preethish-Kumar; Meera G Nair; M S Keerthipriya; Seena Vengalil; John Vijay Sagar; Thomas Kishore; Atchayaram Nalini; Priya Treesa Thomas
Journal:  Indian J Palliat Care       Date:  2021-02-17

3.  Quantifying the burden of caregiving in Duchenne muscular dystrophy.

Authors:  Erik Landfeldt; Peter Lindgren; Christopher F Bell; Michela Guglieri; Volker Straub; Hanns Lochmüller; Katharine Bushby
Journal:  J Neurol       Date:  2016-03-10       Impact factor: 4.849

Review 4.  An Integrative Review Exploring Psycho-Social Impacts and Therapeutic Interventions for Parent Caregivers of Young People Living with Duchenne's Muscular Dystrophy.

Authors:  Debra Porteous; Barbara Davies; Christine English; Joanne Atkinson
Journal:  Children (Basel)       Date:  2021-03-11

Review 5.  Measuring carer quality of life in Duchenne muscular dystrophy: a systematic review of the reliability and validity of self-report instruments using COSMIN.

Authors:  Jill Carlton; Philip A Powell
Journal:  Health Qual Life Outcomes       Date:  2022-04-02       Impact factor: 3.186

  5 in total

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