Liu Zhi-sheng, Chen Yan-hui, Zhong You-quan, Zou Li-ping, Wang Hua, Sun Dan, Wang Da-bin, Liao Jian-xiang
Department of Neurology, Wuhan Children's Hospital, Wuhan 430016, China.
Zhonghua Er Ke Za Zhi. 2011 Aug;49(8):572-6.
To evaluate the efficacy and safety of aripiprazole in the treatment of children with Tourette syndrome.
A prospective, multi-center, controlled clinical trial was conducted in 195 children aged 5-17 years with Tourette syndrome. The patients were assigned to two groups: aripiprazole group (n=98) and tiapride group (n=97), with the treatment dosage of 5-25 mg/d and 100-500 mg/d, respectively. After 12 weeks treatment, the clinical efficacy was assessed by the Yale Global Tic Severity Scale (YGTSS) score, and adverse reactions were observed by side effects symptoms scale, blood biochemical indexes, and electrocardiography.
Significant pre- and post-treatment differences were ascertained for motor tic, phonic tic, function damage and total scores of YGTSS in the both groups from the second week of treatment (P<0.0001). Compared with the tiapride group, the aripiprazole group showed a more significantly decreased function damage score of YGTSS by the second week of treatment (P<0.05). After 12 weeks treatment, total scores of YGTSS in the aripiprazole group decreased from 53.74±15.71 at baseline to 24.36±16.38, while in the tiapride group from 51.66±13.63 to 23.26±15.31. The mean reduction scores of YGTSS were 29.38 in the aripiprazole group and 28.40 in the tiapride group at the end of treatment, and the clinical response rates were 60.21% and 63.92%, respectively. There were no significant differences between the 2 groups (P>0.05). The incidence of adverse reactions was similar in the aripiprazole and tiapride groups, with 29.6% and 27.8% respectively. There were no significant differences in the incidence of adverse reactions between aripiprazole and tiapride groups and no severe adverse events were found in either group.
The results showed that aripiprazole showed similar therapeutic effect to tiapride in treatment of children with Tourette syndrome. Aripiprazole was safe and well tolerated in Chinese population, and can be considered as a new valid option for the treatment of tic disorders.
评估阿立哌唑治疗抽动秽语综合征患儿的疗效和安全性。
对195例年龄在5至17岁的抽动秽语综合征患儿进行一项前瞻性、多中心、对照临床试验。将患者分为两组:阿立哌唑组(n = 98)和硫必利组(n = 97),治疗剂量分别为5 - 25mg/d和100 - 500mg/d。治疗12周后,采用耶鲁综合抽动严重程度量表(YGTSS)评分评估临床疗效,通过副作用症状量表、血液生化指标和心电图观察不良反应。
两组从治疗第二周起,运动性抽动、发声性抽动、功能损害及YGTSS总分在治疗前后均有显著差异(P < 0.0001)。与硫必利组相比,阿立哌唑组在治疗第二周时YGTSS功能损害评分下降更显著(P < 0.05)。治疗12周后,阿立哌唑组YGTSS总分从基线时的53.74±15.71降至24.36±16.38,而硫必利组从51.66±13.63降至23.26±15.31。治疗结束时,阿立哌唑组YGTSS平均减分29.38,硫必利组为28.40,临床有效率分别为60.21%和63.92%。两组间无显著差异(P > 0.05)。阿立哌唑组和硫必利组不良反应发生率相似,分别为29.6%和27.8%。阿立哌唑组与硫必利组不良反应发生率无显著差异,两组均未发现严重不良事件。
结果表明,阿立哌唑在治疗抽动秽语综合征患儿方面显示出与硫必利相似的治疗效果。阿立哌唑在中国人群中安全且耐受性良好,可被视为治疗抽动障碍的一种新的有效选择。