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>The Effect of Botulinum Neurotoxin-A (BoNT-A) on Muscle Strength in Adult-Onset Neurological Conditions with Focal Muscle Spasticity: A Systematic Review
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The Effect of Botulinum Neurotoxin-A (BoNT-A) on Muscle Strength in Adult-Onset Neurological Conditions with Focal Muscle Spasticity: A Systematic Review
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机译:肉毒杆菌神经毒素 A (BoNT-A) 对成人发病的局灶性肌肉痉挛神经系统疾病肌肉力量的影响:系统评价
Botulinum neurotoxin-A (BoNT-A) injections are effective for focal spasticity. However, the impact on muscle strength is not established. This study aimed to investigate the effect of BoNT-A injections on muscle strength in adult neurological conditions. Studies were included if they were Randomised Controlled Trials (RCTs), non-RCTs, or cohort studies (n ≥ 10) involving participants ≥18 years old receiving BoNT-A injection for spasticity in their upper and/or lower limbs. Eight databases (CINAHL, Cochrane, EMBASE, Google Scholar, Medline, PEDro, Pubmed, Web of Science) were searched in March 2024. The methodology followed Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines and was registered in the Prospective Register of Systematic Reviews (PROSPERO: CRD42022315241). Quality was assessed using the modified Downs and Black checklist and the PEDro scale. Pre-/post-injection agonist, antagonist, and global strength outcomes at short-, medium-, and long-term time points were extracted for analysis. Following duplicate removal, 8536 studies were identified; 54 met the inclusion criteria (3176 participants) and were rated as fair-quality. Twenty studies were analysed as they reported muscle strength specific to the muscle injected. No change in agonist strength after BoNT-A injection was reported in 74% of the results. Most studies’ outcomes were within six weeks post-injection, with few long-term results (i.e., >three months). Overall, the impact of BoNT-A on muscle strength remains inconclusive.
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机译:肉毒杆菌神经毒素 A (BoNT-A) 注射对局灶性痉挛有效。然而,对肌肉力量的影响尚未确定。本研究旨在调查 BoNT-A 注射对成人神经系统疾病肌肉力量的影响。如果研究是随机对照试验 (RCT)、非 RCT 或队列研究 (n ≥ 10),则纳入研究,涉及 ≥18 岁接受 BoNT-A 注射治疗上肢和/或下肢痉挛的参与者。2024 年 3 月检索了八个数据库(CINAHL、Cochrane、EMBASE、Google Scholar、Medline、PEDro、Pubmed、Web of Science)。该方法遵循系统评价和荟萃分析的首选报告项目 (PRISMA) 指南,并在系统评价前瞻性注册库 (PROSPERO: CRD42022315241) 中注册。使用改良的 Downs and Black 检查表和 PEDro 量表评估质量。提取短期、中期和长期时间点的注射前/后激动剂、拮抗剂和整体强度结局进行分析。重复删除后,确定了 8536 项研究;54 例符合纳入标准 (3176 名参与者) 并被评为一般质量。分析了 20 项研究,因为它们报告了注射肌肉特有的肌肉力量。74% 的结果报告了 BoNT-A 注射后激动剂强度的变化。大多数研究的结局是在注射后 6 周内,很少有长期结果(即 >3 个月)。总体而言,BoNT-A 对肌肉力量的影响仍无定论。
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