Literature DB >> 34374872

A qualitative study on the impact of caring for an ambulatory individual with nonsense mutation Duchenne muscular dystrophy.

Katharina Buesch1, Sarah Acaster2, Kate Williams3, Ian Davidson4, Mark Rance4.   

Abstract

BACKGROUND: Duchenne muscular dystrophy is a rare genetic neuromuscular disorder, which can result in early death due to disease progression. Ataluren is indicated for the treatment of nonsense mutation Duchenne muscular dystrophy, in ambulatory individuals aged two years and older. This study explored the impact of caring for an ambulatory individual with nonsense mutation Duchenne muscular dystrophy, as well as the impact of treatment with ataluren on the caregiver experience, using retrospective recall.
METHODS: Qualitative interviews were conducted with caregivers in the UK. Interviews were conducted by telephone, were recorded and transcribed. Data were analysed using thematic analysis and saturation was recorded.
RESULTS: Ten interviews were conducted with parents of individuals aged 4-19 years. Caregivers reported proximal impacts (physical, emotional, time-related), and distal impacts (work, relationships, social life) of caring for their sons. The relationships between these impacts were illustrated in a conceptual model. Changes to the caregiver experience since initiation with their son's treatment were discussed.
CONCLUSION: Caring for an ambulatory individual with nonsense mutation Duchenne muscular dystrophy has a substantial multifaceted impact on caregivers. Treatments which have the potential to improve symptoms or delay progression, may also have a positive impact on the quality of life of caregivers.
© 2021. The Author(s).

Entities:  

Keywords:  Ataluren; Caregiver; Carer; Duchenne muscular dystrophy; Nonsense mutation; Qualitative

Year:  2021        PMID: 34374872     DOI: 10.1186/s41687-021-00344-8

Source DB:  PubMed          Journal:  J Patient Rep Outcomes        ISSN: 2509-8020


  11 in total

1.  Subjective caregiver burden of parents of adults with Duchenne muscular dystrophy.

Authors:  Robert F Pangalila; Geertrudis A M van den Bos; Henk J Stam; N Job A van Exel; Werner B F Brouwer; Marij E Roebroeck
Journal:  Disabil Rehabil       Date:  2011-12-09       Impact factor: 3.033

2.  Siblings of young people with Duchenne muscular dystrophy--a qualitative study of impact and coping.

Authors:  Joy Read; Maria Kinali; Francesco Muntoni; Timothy Weaver; M Elena Garralda
Journal:  Eur J Paediatr Neurol       Date:  2010-08-21       Impact factor: 3.140

Review 3.  Current status of pharmaceutical and genetic therapeutic approaches to treat DMD.

Authors:  Christophe Pichavant; Annemieke Aartsma-Rus; Paula R Clemens; Kay E Davies; George Dickson; Shin'ichi Takeda; Steve D Wilton; Jon A Wolff; Christine I Wooddell; Xiao Xiao; Jacques P Tremblay
Journal:  Mol Ther       Date:  2011-04-05       Impact factor: 11.454

Review 4.  Duchenne muscular dystrophy and caregiver burden: a systematic review.

Authors:  Erik Landfeldt; Josefin Edström; Filippo Buccella; Janbernd Kirschner; Hanns Lochmüller
Journal:  Dev Med Child Neurol       Date:  2018-06-14       Impact factor: 5.449

5.  Social/economic costs and health-related quality of life in patients with Duchenne muscular dystrophy in Europe.

Authors:  Marianna Cavazza; Yllka Kodra; Patrizio Armeni; Marta De Santis; Julio López-Bastida; Renata Linertová; Juan Oliva-Moreno; Pedro Serrano-Aguilar; Manuel Posada-de-la-Paz; Domenica Taruscio; Arrigo Schieppati; Georgi Iskrov; Márta Péntek; Johann Matthias Graf von der Schulenburg; Panos Kanavos; Karine Chevreul; Ulf Persson; Giovanni Fattore
Journal:  Eur J Health Econ       Date:  2016-04-02

6.  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

7.  Health-related quality of life in patients with Duchenne muscular dystrophy: a multinational, cross-sectional study.

Authors:  Erik Landfeldt; Peter Lindgren; Christopher F Bell; Michela Guglieri; Volker Straub; Hanns Lochmüller; Katharine Bushby
Journal:  Dev Med Child Neurol       Date:  2015-10-19       Impact factor: 5.449

Review 8.  The burden, epidemiology, costs and treatment for Duchenne muscular dystrophy: an evidence review.

Authors:  S Ryder; R M Leadley; N Armstrong; M Westwood; S de Kock; T Butt; M Jain; J Kleijnen
Journal:  Orphanet J Rare Dis       Date:  2017-04-26       Impact factor: 4.123

9.  Characterizing health state utilities associated with Duchenne muscular dystrophy: a systematic review.

Authors:  Shelagh M Szabo; Ivana F Audhya; Daniel C Malone; David Feeny; Katherine L Gooch
Journal:  Qual Life Res       Date:  2019-12-06       Impact factor: 4.147

Review 10.  Global epidemiology of Duchenne muscular dystrophy: an updated systematic review and meta-analysis.

Authors:  Salvatore Crisafulli; Janet Sultana; Andrea Fontana; Francesco Salvo; Sonia Messina; Gianluca Trifirò
Journal:  Orphanet J Rare Dis       Date:  2020-06-05       Impact factor: 4.123

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  2 in total

1.  Evaluating the Feasibility and Reliability of Remotely Delivering and Scoring the North Star Ambulatory Assessment in Ambulant Patients with Duchenne Muscular Dystrophy.

Authors:  Nicholas Emery; Kate Strachan; Richa Kulshrestha; Jan Herman Kuiper; Tracey Willis
Journal:  Children (Basel)       Date:  2022-05-16

Review 2.  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

  2 in total

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