Lindholm Beata, Beckman Anders, Duzynski Wojciech, Ekvall Hansson Eva
Department of Clinical Sciences, Malmö Lund University Malmö Sweden.
Department of Neurology and Rehabilitation Medicine Skåne University Hospital Malmö Sweden.
Mov Disord Clin Pract. 2016 Aug 13;4(3):309-315. doi: 10.1002/mdc3.12411. eCollection 2017 May-Jun.
Striatal foot deformity can shorten the stance phase of gait and impair the ability to stand and walk. Botulinum neurotoxin type A (BoNT A) is a treatment option. However, no previous study has included clinical balance testing in the evaluation of treatment effects. The aim of this study was to evaluate gait and balance in patients with striatal foot deformities and Parkinson's disease (PD) before and after treatment with BoNT A injections.
The study included 10 patients with PD and striatal foot deformity who visited a neurological clinic. The mean ± standard deviation age and PD-duration was 62.8 ± 8.8 years and 4.9 ± 3.6 years, respectively. Clinical assessment was made before and 4 and 16 weeks after injection and included 5 clinical gait and balance tests. The intensity of distress due to deformities was investigated with a visual analogue scale. Parkinsonian motor status was assessed with the Unified Parkinson's Disease Rating Scale part III (motor part). Based on ordinary clinical examination, electromyography-guided BoNT A injection was given in affected muscles. Clinically effective doses of BoNT A were used.
Improvements were observed regarding functional, dynamic, and standing balance as well as intensity of distress at 4 weeks but not at 16 weeks compared with baseline.
BoNT A injection treatment improved gait and balance in patients with PD and striatal foot deformities. Multicenter trials are needed; and, to achieve increased power, a randomized, double-blind controlled design is needed and should focus on the ability of tests to capture subtle changes in gait and balance.
纹状体足部畸形会缩短步态的站立期,并损害站立和行走能力。A型肉毒杆菌神经毒素(BoNT A)是一种治疗选择。然而,以往的研究均未在治疗效果评估中纳入临床平衡测试。本研究的目的是评估A型肉毒杆菌毒素注射治疗前后纹状体足部畸形合并帕金森病(PD)患者的步态和平衡。
本研究纳入了10名前往神经科门诊就诊的帕金森病合并纹状体足部畸形患者。平均年龄±标准差为62.8±8.8岁,帕金森病病程为4.9±3.6年。在注射前、注射后4周和16周进行临床评估,包括5项临床步态和平衡测试。使用视觉模拟量表调查畸形引起的痛苦强度。采用统一帕金森病评定量表第三部分(运动部分)评估帕金森运动状态。根据常规临床检查,在受影响的肌肉中进行肌电图引导下的A型肉毒杆菌毒素注射。使用临床上有效的A型肉毒杆菌毒素剂量。
与基线相比,在4周时观察到功能、动态和站立平衡以及痛苦强度有所改善,但在16周时未观察到改善。
A型肉毒杆菌毒素注射治疗改善了帕金森病合并纹状体足部畸形患者的步态和平衡。需要进行多中心试验;并且,为了提高检验效能,需要采用随机、双盲对照设计,并且应关注测试捕捉步态和平衡细微变化的能力。