Rystedt Alma, Zetterberg Lena, Burman Joachim, Nyholm Dag, Johansson Anders
*Department of Neuroscience, Neurology and †Department of Neuroscience, Physiotherapy, Uppsala University, Uppsala; and ‡Department of Clinical Neuroscience, Neurology R3:04, Karolinska Institutet, Karolinska University Hospital Solna, Stockholm, Sweden.
Clin Neuropharmacol. 2015 Sep-Oct;38(5):170-6. doi: 10.1097/WNF.0000000000000101.
Intramuscular injections of botulinum toxin (BTX) are used as symptomatic treatment for cervical dystonia. Botox and Dysport are commercial products containing BTX; however, dosage and concentration of the prepared solution vary considerably among studies. The concentration of BTX in the prepared solution affects clinical outcome. This double-blind, randomized crossover trial compares Botox and Dysport in 2 different dose conversion ratios (1:3 and 1:1.7) when diluted to the same concentration (100 U/mL).
Forty-six patients with cervical dystonia received 3 different treatments, Botox in 2 different doses and Dysport as control treatment. The efficacy was evaluated 4 and 12 weeks after treatment using 5 instruments, including Toronto Western Spasmodic Torticollis Rating Scale.
The primary outcome was the estimated median Toronto Western Spasmodic Torticollis Rating Scale total score, which was 1.96 points higher for Botox (1:3) compared with Dysport at week 4, but the difference was not statistically significant (confidence interval, -0.88-4.61; P = 0.0799). No significant differences were seen between Botox (1:1.7) and Dysport. At week 12, a statistically significant difference in effect between Botox (1:3) and Dysport was observed, suggesting a shorter duration of effect for Botox when this ratio (low dose) was used. Furthermore, the patients' assessments showed that the ratio 1:3 resulted in suboptimal efficacy of Botox. These secondary outcome observations indicate that the dose conversion ratio between Dysport 100 U/mL and Botox 100 U/mL may be lower than 1:3, but this must be further validated in a larger patient material.
肌肉注射肉毒杆菌毒素(BTX)用于颈部肌张力障碍的对症治疗。保妥适(Botox)和得保松(Dysport)是含有BTX的商业产品;然而,不同研究中配制溶液的剂量和浓度差异很大。配制溶液中BTX的浓度会影响临床疗效。这项双盲、随机交叉试验比较了保妥适和得保松在稀释至相同浓度(100 U/mL)时两种不同剂量转换比(1:3和1:1.7)的情况。
46例颈部肌张力障碍患者接受了3种不同治疗,即两种不同剂量的保妥适以及作为对照治疗的得保松。在治疗后4周和12周使用5种工具评估疗效,包括多伦多西部痉挛性斜颈评定量表。
主要结局指标是估计的多伦多西部痉挛性斜颈评定量表总分中位数,在第4周时,保妥适(1:3)的该分数比得保松高1.96分,但差异无统计学意义(置信区间,-0.88 - 4.61;P = 0.0799)。保妥适(1:1.7)和得保松之间未观察到显著差异。在第12周时,观察到保妥适(1:3)和得保松在疗效上有统计学显著差异,这表明使用该比例(低剂量)的保妥适时效果持续时间较短。此外,患者评估显示1:3的比例导致保妥适疗效欠佳。这些次要结局观察结果表明,得保松100 U/mL与保妥适100 U/mL之间的剂量转换比可能低于1:3,但这必须在更大规模的患者群体中进一步验证。