Physical training of wheelchair users with neuromuscular disorders: A systematic review.

IF 3.4 4区 医学 Q2 CLINICAL NEUROLOGY
Journal of neuromuscular diseases Pub Date : 2025-05-01 Epub Date: 2025-03-04 DOI:10.1177/22143602241313114
Nanna Scharff Poulsen, Lærke Rykær Kraglund, John Vissing
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引用次数: 0

Abstract

Objective: Wheelchair users with neuromuscular disorders have symptoms related to the disease and complications to the sedentary lifestyle, such as constipation and lower back pain. Physical training might be beneficial. This systematic review investigates the potential benefits and harms of physical training for wheelchair users with neuromuscular disorders.

Methods: We systematically searched PubMed including studies published until July 2024.

Inclusion criteria: 1) participants with a neuromuscular disorder, 2) at least 60% of participants in a study were wheelchair users, 3) physical training and its effects were investigated, 4) studies were prospective, and 5) English language was used. Non-peer-reviewed articles were excluded. Search results were screened by title, abstract, and full text. Two independent authors assessed the quality with the Downs and Black Quality Index.

Results: We included 14 studies of 140 patients from 5 types of neuromuscular disorders (Duchenne muscular atrophy, spinal muscular atrophy, limb-girdle muscular atrophy, facioscapulohumeral muscular dystrophy, and amyotrophic lateral sclerosis). The mean quality was low (16/32) due to flaws in study design, selection bias, and power. Even though many were of low quality and lacked descriptions of adverse events, they all showed positive effects. Most studies investigated physical training of mastication or respiration with improvements in both. Other findings were improvements in endurance, extremity strength, and range of motion.

Conclusions: Physical training of wheelchair users with neuromuscular disorders is not well investigated. Physical training seems safe and beneficial, but training of respiratory and masticatory muscles is the only well-documented exercise modality that can be advised in patients with Duchenne Muscular Dystrophy or Duchenne Muscular Dystrophy/Spinal Muscular Atrophy, respectively. Larger, high-quality trials, including other neuromuscular disorders, are needed to assess the effects and adverse events of physical training.

有神经肌肉疾病的轮椅使用者的体能训练:一个系统的回顾。
目的:患有神经肌肉疾病的轮椅使用者有与疾病相关的症状和久坐生活方式的并发症,如便秘和下背部疼痛。体育锻炼可能是有益的。本系统综述调查了患有神经肌肉疾病的轮椅使用者进行体育锻炼的潜在益处和危害。方法:我们系统地检索PubMed,包括截至2024年7月发表的研究。纳入标准:1)患有神经肌肉障碍的受试者,2)至少60%的研究参与者是轮椅使用者,3)调查了体育训练及其效果,4)研究是前瞻性的,5)使用英语。未经过同行评审的文章被排除在外。搜索结果按标题、摘要和全文筛选。两位独立作者用Downs和Black质量指数对质量进行了评估。结果:我们纳入了来自5种神经肌肉疾病(杜氏肌萎缩症、脊髓性肌萎缩症、肢带性肌萎缩症、面肩肱骨肌萎缩症和肌萎缩侧索硬化症)的140例患者的14项研究。平均质量较低(16/32)是由于研究设计的缺陷、选择偏差和权力。尽管许多研究质量不高,缺乏对不良事件的描述,但它们都显示出积极的效果。大多数研究调查了咀嚼或呼吸的身体训练,两者都有改善。其他发现还包括耐力、四肢力量和活动范围的改善。结论:对轮椅使用者神经肌肉障碍的体能训练研究尚不充分。体育训练似乎是安全和有益的,但呼吸肌和咀嚼肌的训练是唯一有充分证据的锻炼方式,可以分别建议杜氏肌营养不良症或杜氏肌营养不良症/脊髓性肌萎缩症患者。需要更大规模、高质量的试验,包括其他神经肌肉疾病,来评估体育训练的效果和不良事件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of neuromuscular diseases
Journal of neuromuscular diseases Medicine-Neurology (clinical)
CiteScore
5.10
自引率
6.10%
发文量
102
期刊介绍: The Journal of Neuromuscular Diseases aims to facilitate progress in understanding the molecular genetics/correlates, pathogenesis, pharmacology, diagnosis and treatment of acquired and genetic neuromuscular diseases (including muscular dystrophy, myasthenia gravis, spinal muscular atrophy, neuropathies, myopathies, myotonias and myositis). The journal publishes research reports, reviews, short communications, letters-to-the-editor, and will consider research that has negative findings. The journal is dedicated to providing an open forum for original research in basic science, translational and clinical research that will improve our fundamental understanding and lead to effective treatments of neuromuscular diseases.
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