Literature DB >> 27347814

Quality of life of patients with Duchenne muscular dystrophy: from adolescence to young men.

Yi-Jing Lue1,2, Shun-Sheng Chen3, Yen-Mou Lu4,5.   

Abstract

PURPOSE: This study investigated quality of life (QOL) in adolescent and young men with Duchenne muscular dystrophy (DMD).
METHODS: Health-related QOL and global QOL were assessed with the Short Form 36 (SF-36) and World Health Organization Quality of Life-BREF (WHOQOL-BREF). Associations between functional status and QOL were assessed.
RESULTS: All domains of the SF-36 were below Taiwan norms (effect size: -14.2 to -0.5), especially Physical Function, Role Physical, and Social Function. Three of the four domains of the WHOQOL-BREF were below Taiwan norms (effect size: -2.0 to -0.7). The Physical Function of the SF-36 was moderately correlated with functional status (mobility, basic activities of daily living, and arm function). The Social Function of the SF-36 and Social Relationships of the WHOQOL-BREF were also moderately correlated with functional status (impairment, basic activities of daily living, and arm function).
CONCLUSION: The adolescent and young men with DMD had poor health-related and global QOL. Poor QOL was related to both physical condition and social health. We suggest that rehabilitation programs focus on using assistive devices to facilitate arm function and encouraging participation in social activities to improve the QOL of patients with DMD. Implications for rehabilitation Duchenne muscular dystrophy (DMD) is a progressive muscle weakness disease that not only impacts physical health but also leads to poor quality of life in many domains. A valuable rehabilitation goal for patients with DMD is to encourage participation in social activities. Medical care and educational programs should plan a formal transition processes for patients with DMD from pediatric to adult care to maximum their quality of life. Arm function is associated with many domains of global quality of life, so a key element in improving quality of life may be to improve arm function.

Entities:  

Keywords:  Duchenne muscular dystrophy; World Health Organization; quality of life; short form 36

Mesh:

Year:  2016        PMID: 27347814     DOI: 10.1080/09638288.2016.1196398

Source DB:  PubMed          Journal:  Disabil Rehabil        ISSN: 0963-8288            Impact factor:   3.033


  5 in total

Review 1.  Developing multidisciplinary clinics for neuromuscular care and research.

Authors:  Sabrina Paganoni; Katie Nicholson; Fawn Leigh; Kathryn Swoboda; David Chad; Kristin Drake; Kellen Haley; Merit Cudkowicz; James D Berry
Journal:  Muscle Nerve       Date:  2017-08-29       Impact factor: 3.217

Review 2.  Incomplete description of the current body of evidence of the health economics of Duchenne muscular dystrophy.

Authors:  Erik Landfeldt; Hanns Lochmüller; Peter Lindgren
Journal:  Orphanet J Rare Dis       Date:  2019-04-02       Impact factor: 4.123

3.  Facilitators and Barriers to Wearing Hand Orthoses by Adults with Duchenne Muscular Dystrophy: A Mixed Methods Study Design.

Authors:  S L S Houwen-van Opstal; Y M E M van den Elzen; M Jansen; M A A P Willemsen; E H C Cup; I J M De Groot
Journal:  J Neuromuscul Dis       Date:  2020

4.  User-centred assistive SystEm for arm Functions in neUromuscuLar subjects (USEFUL): a randomized controlled study.

Authors:  Valeria Longatelli; Alberto Antonietti; Emilia Biffi; Eleonora Diella; Maria Grazia D'Angelo; Mauro Rossini; Franco Molteni; Marco Bocciolone; Alessandra Pedrocchi; Marta Gandolla
Journal:  J Neuroeng Rehabil       Date:  2021-01-06       Impact factor: 4.262

5.  Evaluation of a Chair-Mounted Passive Trunk Orthosis: A Pilot Study on Able-Bodied Subjects.

Authors:  Ahmad Zahid Rao; Muhammad Abul Hasan
Journal:  Sensors (Basel)       Date:  2021-12-15       Impact factor: 3.576

  5 in total

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