Botulinum toxin type A in post-stroke upper limb spasticity

被引:90
|
作者
Kaji, Ryuji [1 ]
Osako, Yuka [2 ]
Suyama, Kazuaki [2 ]
Maeda, Toshio [2 ]
Uechi, Yasuyuki [2 ]
Iwasaki, Masaru [2 ]
机构
[1] Univ Tokushima, Grad Sch, Dept Clin Neurosci, Inst Hlth Biosci, Tokushima 7708503, Japan
[2] GlaxoSmithKline KK, Tokyo, Japan
关键词
Botulinum toxin type A; Disability Assessment Scale; Modified Ashworth Scale; Spasticity; Upper limb; ASHWORTH SCALE; DOUBLE-BLIND; STROKE; NEUROTOXIN; RELIABILITY; INTERRATER; MANAGEMENT; TRIALS; SAFETY;
D O I
10.1185/03007995.2010.497103
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To evaluate the efficacy and safety of one-time injections of botulinum toxin type A (BoNTA) in Japanese patients with post-stroke upper limb spasticity. Research design and methods: In a multicentre, randomised, double-blind, parallel-group, placebo-controlled study, 109 patients with upper limb spasticity were randomised to receive a single treatment with lower-dose (120-150 U) or higher-dose (200-240 U) BoNTA or placebo into upper limb muscles. Clinical trial registration: NCT00460564 Main outcome measures: The tone of the wrist flexor was assessed at baseline and at weeks 0, 1, 4, 6, 8 and 12 using the Modified Ashworth Scale (MAS) for wrist, finger, thumb and disability in activities of daily living (ADL) was rated using the 4-point Disability Assessment Scale (DAS). The primary endpoint was area under the curve (AUC) of the change from baseline in the MAS wrist score in the higher-dose groups. Results: Subjects were randomised with 51 in the higher BoNTA group, 26 in the higher-dose placebo group, 21 in the lower BoNTA group and 11 in the lower-dose placebo group. Significant improvement in spasticity with higher-dose BoNTA was demonstrated by a mean difference in the AUC of the change from baseline in the MAS wrist score between the higher-dose BoNTA group and the higher-dose placebo group of -6.830 (p<0.001, t-test), no significant different was demonstrated between the lower-dose BoNTA group and the lower-dose placebo group (p = 0.215, t-test). Significant improvements with higher-dose BoNTA were also observed in the DAS scores for limb position (p = 0.001-0.022) at all time points and dressing (p = 0.0180.038, Wilcoxon test) at weeks 6, 8 and 12. No clinically relevant difference was noted in the frequency of treatment-related adverse events between BoNTA-treated and placebo-treated patients. The long-term efficacy and safety, and the effects on rehabilitation of BoNTA on upper limb will be evaluated using the data obtained in the open-label phase. Conclusions: Higher-dose BoNTA reduced spasticity in upper limb muscles and improved ADL performance in terms of limb position and dressing. BoNTA is safe and effective in the treatment of post-stroke upper limb spasticity.
引用
收藏
页码:1983 / 1992
页数:10
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