Philp, Fraser
ORCID: 0000-0002-8552-7869
(2023)
Effectiveness of conservative non- pharmacological interventions in people with muscular dystrophies: a systematic review and meta- analysis
Journal of Neurology, Neurosurgery and Psychiatry, 95 (5).
pp. 442-453.
ISSN 0022-3050, 1468-330X
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Abstract
<h4>Introduction</h4>Management of muscular dystrophies (MD) relies on conservative non-pharmacological treatments, but evidence of their effectiveness is limited and inconclusive.<h4>Objective</h4>To investigate the effectiveness of conservative non-pharmacological interventions for MD physical management.<h4>Methods</h4>This systematic review and meta-analysis followed Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines and searched Medline, CINHAL, Embase, AMED and Cochrane Central Register of Controlled Trial (inception to August 2022). Effect size (ES) and 95% Confidence Interval (CI) quantified treatment effect.<h4>Results</h4>Of 31,285 identified articles, 39 studies (957 participants), mostly at high risk of bias, were included. For children with Duchenne muscular dystrophy (DMD), trunk-oriented strength exercises and usual care were more effective than usual care alone in improving distal upper-limb function, sitting and dynamic reaching balance (ES range: 0.87 to 2.29). For adults with Facioscapulohumeral dystrophy (FSHD), vibratory proprioceptive assistance and neuromuscular electrical stimulation respectively improved maximum voluntary isometric contraction and reduced pain intensity (ES range: 1.58 to 2.33). For adults with FSHD, Limb-girdle muscular dystrophy (LGMD) and Becker muscular dystrophy (BMD), strength-training improved dynamic balance (sit-to-stand ability) and self-perceived physical condition (ES range: 0.83 to 1.00). A multicomponent programme improved perceived exertion rate and gait in adults with Myotonic dystrophy type 1 (DM1) (ES range: 0.92 to 3.83).<h4>Conclusions</h4>Low-quality evidence suggests that strength training, with or without other exercise interventions, may improve perceived exertion, distal upper limb function, static and dynamic balance, gait and well-being in MD. Although more robust and larger studies are needed, current evidence supports the inclusion of strength training in MD treatment, as it was found to be safe.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | Humans, Muscular Dystrophies, Muscular Dystrophy, Duchenne, Muscular Dystrophy, Facioscapulohumeral, Treatment Outcome, Exercise Therapy, Electric Stimulation Therapy, Adult, Child, Conservative Treatment |
| Divisions: | Faculty of Health & Life Sciences Faculty of Health & Life Sciences > Inst. Population Health Faculty of Health & Life Sciences > School of Life Sciences |
| Depositing User: | Symplectic Admin |
| Date Deposited: | 13 Dec 2023 09:41 |
| Last Modified: | 28 Feb 2026 17:31 |
| DOI: | 10.1136/jnnp-2023-331988 |
| Related Websites: | |
| URI: | https://livrepository.liverpool.ac.uk/id/eprint/3177290 |
| Disclaimer: | The University of Liverpool is not responsible for content contained on other websites from links within repository metadata. Please contact us if you notice anything that appears incorrect or inappropriate. |
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