The Effect of Nabiximols on Driving Ability in Adults with Chronic Tic Disorders: Results of a Substudy Analysis of the Double-Blind, Randomized, Placebo-Controlled CANNA-TICS Trial.

IF 3.1 4区 医学 Q2 PHARMACOLOGY & PHARMACY Cannabis and Cannabinoid Research Pub Date : 2024-10-01 Epub Date: 2024-01-23 DOI:10.1089/can.2023.0114
Kirsten R Müller-Vahl, Anna Pisarenko, Rieke Ringlstetter, Camelia-Lucia Cimpianu, Carolin Fremer, Elif Weidinger, Eva Beate Jenz, Richard Musil, Alexander Brunnauer, Anika Großhennig
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Abstract

Background: The multicenter, randomized, double-blind, parallel-group, phase IIIb CANNA-TICS (CANNAbinoids in the treatment of TICS) trial showed clear trends for improvement of tics, depression, and quality of life with nabiximols versus placebo in adult patients with Gilles de la Tourette syndrome and other chronic tic disorders. Although in general nabiximols was well tolerated, it is unclear whether treatment using this cannabis extract influences driving skills in patients with chronic tic disorders. Methods: Here we report results of the "Fitness to Drive" substudy of the CANNA-TICS trial. The key endpoint was fitness to drive as a binary criterion with a computerized assessment at baseline and after 9 weeks of stable treatment (week 13) with nabiximols or placebo. A patient was considered unfit to drive according to the German Federal Highway Research Institute guidelines. Results: In the substudy, a total of 64 patients (76.6% men, mean±standard deviation of age: 36.8±13.9) were recruited at two study sites. The number of patients who were fit to drive increased from 24 (55.8%) at baseline to 28 (71.8%) at week 13 among 43 patients treated with nabiximols, and decreased from 14 (66.7%) to 10 (52.6%) among 21 patients who received placebo. The risk difference (nabiximols - placebo) was 0.17 (95% confidence interval=-0.08 to 0.43) in favor of nabiximols. Specifically, only 2 of 24 (8.3%) patients in the nabiximols, but 4 of 14 (28.6%) patients in the placebo group changed for the worse from fit (at baseline) to unfit (at week 13) to drive, whereas 8 of 19 (42.1%) patients in the nabiximols, and only 2 of 7 (28.6%) patients in the placebo group improved from unfit to fit. Conclusion: Treatment with nabiximols does not impair skills relevant to driving in those patients with tic disorders who were fit to drive at baseline and even improved fitness to drive in a subset of patients who were unfit to drive before start of treatment. EudraCT number: 2016-000564-42.

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纳比昔莫司对慢性抽搐症成人驾驶能力的影响:双盲、随机、安慰剂对照的 CANNA-TICS 试验的子研究分析结果。
背景:多中心、随机、双盲、平行组、IIIb 期 CANNA-TICS(治疗 TICS 的 CANNAbinoids)试验显示,在吉勒-德拉图雷特综合征和其他慢性抽搐症的成年患者中,纳比西莫司与安慰剂相比,在改善抽搐、抑郁和生活质量方面有明显的趋势。虽然纳比西莫司的耐受性总体良好,但使用这种大麻提取物进行治疗是否会影响慢性抽搐症患者的驾驶技能尚不清楚。方法:我们在此报告 CANNA-TICS 试验的 "驾驶能力 "子研究结果。关键终点是在基线和接受纳比西莫司或安慰剂稳定治疗 9 周后(第 13 周),通过计算机评估将驾驶能力作为二元标准。根据德国联邦公路研究所的指导方针,患者被视为不适合驾驶。研究结果在次级研究中,两个研究地点共招募了 64 名患者(76.6% 为男性,平均年龄为 36.8±13.9)。在接受纳比昔莫司治疗的 43 名患者中,适合驾驶的患者人数从基线时的 24 人(55.8%)增加到第 13 周时的 28 人(71.8%),而在接受安慰剂治疗的 21 名患者中,适合驾驶的患者人数从 14 人(66.7%)减少到 10 人(52.6%)。风险差异(纳比西莫司-安慰剂)为 0.17(95% 置信区间=-0.08 至 0.43),纳比西莫司更胜一筹。具体来说,在纳比西莫司治疗组的 24 名患者中,只有 2 名(8.3%)从适合驾驶(基线时)变为不适合驾驶(第 13 周时),而在安慰剂治疗组的 14 名患者中,只有 4 名(28.6%)从不适合驾驶变为适合驾驶,而在纳比西莫司治疗组的 19 名患者中,有 8 名(42.1%)从不适合驾驶变为适合驾驶,而在安慰剂治疗组的 7 名患者中,只有 2 名(28.6%)从不适合驾驶变为适合驾驶。结论是对于基线时适合驾驶的抽搐症患者,使用纳比西莫司治疗不会损害他们的驾驶技能,甚至还能改善一部分在开始治疗前不适合驾驶的患者的驾驶能力。EudraCT 编号:2016-000564-42。
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来源期刊
Cannabis and Cannabinoid Research
Cannabis and Cannabinoid Research PHARMACOLOGY & PHARMACY-
CiteScore
6.80
自引率
7.90%
发文量
164
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