Department of Clinical Neuroscience, Institute of Health Biosciences, Tokushima University Graduate School, 2-50-1 Kuramotocho, Tokushima, Tokushima 770-8503, Japan.
J Neurol. 2010 Aug;257(8):1330-7. doi: 10.1007/s00415-010-5526-3. Epub 2010 Apr 1.
Lower limb spasticity in post-stroke patients can impair ambulation and reduces activities of daily living (ADL) performance of patients. Botulinum toxin type A (BoNTA) has been shown effective for upper limb spasticity. This study assesses the treatment of lower limb spasticity in a large placebo-controlled clinical trial. In this multicenter, randomized, double-blind, parallel-group, placebo-controlled study, we evaluate the efficacy and safety of one-time injections of botulinum toxin type A (BoNTA) in Japanese patients with post-stroke lower limb spasticity. One hundred twenty patients with lower limb spasticity were randomized to a single treatment with BoNTA 300 U or placebo. The tone of the ankle flexor was assessed at baseline and through 12 weeks using the Modified Ashworth Scale (MAS). Gait pattern and speed of gait were also assessed. The primary endpoint was area under the curve (AUC) of the change from baseline in the MAS ankle score. Significant improvement in spasticity with BoNTA 300 U was demonstrated by a mean difference in the AUC of the change from baseline in the MAS ankle score between the BoNTA and placebo groups (-3.428; 95% CIs, -5.841 to -1.016; p = 0.006; t test). A significantly greater decrease from baseline in the MAS ankle score was noted at weeks 4, 6 and 8 in the BoNTA group compared to the placebo group (p < 0.001). Significant improvement in the Clinicians Global Impression was noted by the investigator at weeks 4, 6 and 8 (p = 0.016-0.048, Wilcoxon test), but not by the patient or physical/occupational therapist. Assessments of gait pattern using the Physician's Rating Scale and speed of gait revealed no significant treatment differences but showed a tendency towards improvement with BoNTA. No marked difference was noted in the frequency of treatment-related adverse events between BoNTA and placebo groups. This was the first large-scale trial to indicate that BoNTA significantly reduced spasticity in lower limb muscles.
脑卒中患者的下肢痉挛可影响其步行能力和日常生活活动(ADL)表现。A型肉毒毒素(BoNTA)已被证明对上肢痉挛有效。本研究在一项大型安慰剂对照临床试验中评估了 BoNTA 治疗下肢痉挛的效果。在这项多中心、随机、双盲、平行组、安慰剂对照研究中,我们评估了 BoNTA 单次注射治疗日本脑卒中后下肢痉挛患者的疗效和安全性。120 例下肢痉挛患者被随机分为 BoNTA 300U 或安慰剂单次治疗组。使用改良 Ashworth 量表(MAS)在基线和 12 周评估踝关节屈肌的肌张力。还评估了步态模式和步行速度。主要终点是 MAS 踝关节评分从基线变化的曲线下面积(AUC)。BoNTA 300U 治疗组 MAS 踝关节评分从基线变化的 AUC 有显著改善,BoNTA 组与安慰剂组之间的差值为-3.428(95%置信区间,-5.841 至-1.016;p=0.006;t 检验)。与安慰剂组相比,BoNTA 组在第 4、6 和 8 周时 MAS 踝关节评分的基线下降幅度显著更大(p<0.001)。研究者在第 4、6 和 8 周时注意到 Clinicians Global Impression 有显著改善(p=0.016-0.048,Wilcoxon 检验),但患者或物理治疗师未观察到改善。使用医师评定量表评估步态模式和步行速度显示治疗无显著差异,但 BoNTA 治疗有改善趋势。BoNTA 和安慰剂组之间治疗相关不良事件的频率无显著差异。这是首次表明 BoNTA 可显著降低下肢肌肉痉挛的大规模试验。