通过配对联想刺激提高脊髓损伤患者的运动能力:对初步证据的系统回顾。

Alex Martino Cinnera, Mirjam Bonanno, Rocco Salvatore Calabrò, Alessio Bisirri, Martina D'Arienzo, Alessia D'Acunto, Irene Ciancarelli, Giovanni Morone, Giacomo Koch
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引用次数: 0

摘要

简介:脊髓损伤(SCI)通常会导致运动障碍和终身残疾:脊髓损伤(SCI)通常会导致运动障碍和终身残疾:本系统综述符合 PRISMA 指南,旨在评估皮质脊髓配对联想刺激(PAS)对 SCI 患者运动效果的影响。查阅了 PubMed、Scopus/EMBASE、Pedro 和 Cochrane 数据库中从开始到 2023/01/12 的资料:在 1021 篇文章中,有 10 项涉及 84 名患者的研究符合纳入标准,其中 7 项为病例系列/研究,3 项为临床试验。尽管存在轻微差异,但纳入的研究均采用了皮质外周 PAS,使用单次经颅磁刺激和高频外周神经电刺激,治疗次数一致(>20 次)。所有纳入的研究都报告了通过临床和/或神经生理学评估记录的运动效果改善情况:结论:现有证据显示,PAS 刺激后运动效果有所改善。事实上,临床和神经生理学结果都表明,对患有 SCI 的慢性患者进行大量 PAS 治疗是有效的。由于研究数量有限且研究设计不尽人意,因此需要设计良好的研究性试验来证实这些方法的潜力,并明确PAS在SCI人群中的适当剂量-反应:该方案已在 PROSPERO 数据库(CRD42023485703)中注册。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Paired associative stimulation to enhance motor outcome in spinal cord injury: a systematic review of first evidence.

Introduction: Spinal cord injuries (SCI) often result in motor impairment and lifelong disability.

Methods: This systematic review, conducted in agreement with PRISMA guidelines, aimed to evaluate the effects of cortico-spinal paired associative stimulation (PAS) on motor outcomes in individuals with SCI. PubMed, Scopus/EMBASE, Pedro, and Cochrane databases were consulted from inception to 2023/01/12.

Results: In 1021 articles, 10 studies involving 84 patients meet the inclusion criteria, 7 case series/study, and 3 clinical trials. Despite light differences, the included studies performed a cortico-peripheral PAS using a single transcranial magnetic stimulation and high frequency electrical peripheral nerve stimulation for a consistent number of sessions (>20). All included studies reported improvement in motor outcomes recorded via clinical and/or neurophysiological assessment.

Conclusion: Available evidence showed an increase in motor outcomes after PAS stimulation. Indeed, both clinical and neurophysiological outcomes suggest the effectiveness of a high number of PAS sessions in chronic individuals with SCI. Due to a limited number of studies and an unsatisfactory study design, well-designed RCTs are needed to confirm the potentiality of these approaches and clarify the adequate dose-response of PAS in the SCI population.

Registration id: The protocol was registered on the PROSPERO database (CRD42023485703).

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