Department of Rehabilitation Medicine, Jikei University School of Medicine, Tokyo, Japan.
Eur J Phys Rehabil Med. 2012 Mar;48(1):47-55. Epub 2011 Nov 9.
For spastic upper limb hemiparesis after stroke, we developed triple-element protocol of botulinum toxin type A (BoNTA) injection, low-frequency repetitive transcranial magnetic stimulation (LF-rTMS), and intensive occupational therapy (OT). Aim. To investigate the safety and feasibility of the protocol. Design. A preliminary study. Setting. At a university hospital. Population. Fourteen post-stroke patients with spastic upper limb hemiparesis (mean age: 54.9±9.2 years, time after onset: 87.1±48.2 months, ±SD).
In all patients, BoNTA was injected into spastic muscles of the affected upper limb (maximum total dose: 240 units). Four weeks later, they were hospitalized to receive 22 sessions of 20-min LF-rTMS and 120-min intensive OT daily over 15 days. Motor function of the affected upper limb was evaluated mainly using Fugl-Meyer Assessment (FMA), Wolf Motor Function Test (WMFT), motor activity log (MAL), and the severity of spasticity was measured with modified Ashworth scale (MAS) at BoNTA injection, discharge and four weeks post-discharge.
All patients completed the protocol without any adverse effects. The FMA score and MAL scores, but not WMFT performance time, improved significantly at discharge. The MAS score of all examined muscles decreased significantly between BoNTA and discharge. The beneficial effect of the protocol on motor function and spasticity was almost maintained until four weeks after discharge.
The protocol is safe and feasible, although further larger studies are needed to confirm its efficacy.
The protocol is a potentially useful neurorehabilitative approach for this patient population.
对于脑卒中后痉挛性上肢偏瘫,我们开发了包含肉毒毒素 A(BoNTA)注射、低频重复经颅磁刺激(LF-rTMS)和强化作业治疗(OT)的三重方案。目的:研究该方案的安全性和可行性。设计:初步研究。设置:在一所大学医院。人群:14 例脑卒中后痉挛性上肢偏瘫患者(平均年龄:54.9±9.2 岁,发病后时间:87.1±48.2 个月,±SD)。
所有患者的患侧上肢痉挛肌肉均接受 BoNTA 注射(最大总剂量:240 单位)。4 周后,他们住院接受 22 次 20 分钟 LF-rTMS 和 120 分钟强化 OT,每天一次,共 15 天。主要采用 Fugl-Meyer 评估(FMA)、Wolf 运动功能测试(WMFT)、运动活动日志(MAL)评估患侧上肢运动功能,改良 Ashworth 量表(MAS)评估痉挛严重程度,分别在 BoNTA 注射时、出院时和出院后 4 周进行评估。
所有患者均完成了方案,无任何不良反应。出院时 FMA 评分和 MAL 评分明显提高,而 WMFT 表现时间无明显变化。所有检查肌肉的 MAS 评分在 BoNTA 和出院时均显著降低。该方案对运动功能和痉挛的有益作用在出院后 4 周内几乎保持不变。
该方案安全可行,但需要进一步的更大规模研究来证实其疗效。
该方案可能是这一患者群体的一种有用的神经康复方法。