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A型肉毒毒素注射治疗上肢原发性震颤的运动学研究。

Botulinum Toxin Type A Injections as Monotherapy for Upper Limb Essential Tremor Using Kinematics.

机构信息

1Department of Clinical Neurological Sciences,London Health Sciences Centre,Lawson Health Research Institute,London,Ontario,Canada.

出版信息

Can J Neurol Sci. 2018 Jan;45(1):11-22. doi: 10.1017/cjn.2017.260. Epub 2017 Nov 21.

Abstract

BACKGROUND

There is a significant need for a targeted therapy for essential tremor (ET), as medications have not been developed specifically for ET, and the ones prescribed are often not well-tolerated, so that many patients remain untreated. Recent work has shown that, unlike previous experience, kinematically guided individualized botulinum toxin type A (BoNT-A) injections provide benefit along with minimal weakness. Ours is the first long-term (96-week) safety and efficacy study of BoNT-A as monotherapy for ET using kinematically driven injection parameters.

METHODS

Ten ET patients were administered six serial BoNT-A treatments every 16 weeks and were assessed at 6 weeks following treatment. During each study visit, the Fahn-Tolosa-Marin (FTM) scale, the Unified Parkinson's Disease Rating Scale, and the Quality of Life for Essential Tremor Questionnaire (QUEST) were administered along with kinematic assessment of the treated limb. Participants performed scripted tasks with motion sensors placed over each arm joint. Dosing patterns were determined using the movement disorder neurologist's interpretation of muscles contributing to the kinematically analyzed upper limb tremor biomechanics.

RESULTS

There was a 33.8% (p<0.05) functional improvement (FTM part C) and a 39.8% (p<0.0005) improvement in QUEST score at week 96 compared to pretreatment scores at week 0. Although there was a 44.6% (p<0.0005) non-dose-dependent reduction in maximal grip strength, only 2 participants complained of mild weakness. Following the fourth serial treatment, mean action tremor score was reduced by 62.9% (p=0.001) in the treated and by 44.4% (p=0.03) in the untreated arm at week 96 compared to week 48.

CONCLUSIONS

Individualized BoNT-A dosing patterns to each individual's tremor biomechanics provided an effective monotherapy for ET as function improved without functionally limiting muscle weakness.

摘要

背景

特发性震颤(ET)需要一种靶向治疗方法,因为目前还没有专门针对 ET 的药物,而开的药物往往不能耐受,因此许多患者未得到治疗。最近的研究表明,与以往的经验不同,运动学引导的个体化肉毒毒素 A(BoNT-A)注射不仅提供益处,而且肌肉无力最小。我们是第一项使用运动学驱动的注射参数对 BoNT-A 进行特发性震颤单药治疗的长达 96 周的安全性和有效性研究。

方法

10 例 ET 患者每 16 周接受 6 次连续 BoNT-A 治疗,并在治疗后 6 周进行评估。在每次研究访视中,进行 Fahn-Tolosa-Marin(FTM)量表、统一帕金森病评定量表和特发性震颤生活质量问卷(QUEST)评估,同时对治疗肢体进行运动学评估。参与者用放置在每个手臂关节上的运动传感器执行脚本任务。剂量模式是根据运动障碍神经科医生对有助于运动学分析上肢震颤生物力学的肌肉的解释来确定的。

结果

与治疗前第 0 周相比,第 96 周时功能改善(FTM 部分 C)为 33.8%(p<0.05),QUEST 评分改善 39.8%(p<0.0005)。尽管最大握力有 44.6%(p<0.0005)的非剂量依赖性下降,但只有 2 名参与者抱怨轻度无力。在第 4 次连续治疗后,第 96 周时治疗臂的动作性震颤评分降低 62.9%(p=0.001),而未治疗臂降低 44.4%(p=0.03)。

结论

根据每个个体的震颤生物力学为个体化 BoNT-A 剂量模式为 ET 提供了有效的单药治疗方法,因为功能改善而不会导致肌肉无力的功能限制。

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