首页> 外文期刊>Progress in Neuro-Psychopharmacology & Biological Psychiatry: An International Research, Review and News Journal >Double-blind, placebo-controlled trial of risperidone plus topiramate in children with autistic disorder.
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Double-blind, placebo-controlled trial of risperidone plus topiramate in children with autistic disorder.

机译:利培酮加托吡酯治疗自闭症儿童的双盲,安慰剂对照试验。

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BACKGROUND: Autism is a complex neurodevelopmental disorder that forms part of a spectrum of related disorders referred to as Autism Spectrum Disorders. The present study assessed the effects of topiramate plus risperidone in the treatment of autistic disorder. METHOD: Forty children between the ages of 4 and 12 years with a DSM IV clinical diagnosis of autism who were outpatients from a specialty clinic for children were recruited. The children presented with a chief complaint of severely disruptive symptoms related to autistic disorder. Patients were randomly allocated to topiramate+risperidone (Group A) or placebo+risperidone (Group B) for an 8-week, double-blind, placebo-controlled study. The dose of risperidone was titrated up to 2 mg/day for children between 10 and 40 kg and 3 mg/day for children weighting above 40 kg. The dose of topiramate was titrated up to 200 mg/day depending on weight (100 mg/day for <30 kg and 200 mg/day for >30 kg). Patients were assessed at baseline and after 2, 4, 6 and 8 weeks after starting medication. Measure of outcome was the Aberrant Behavior Checklist-Community (ABC-C) Rating Scale. RESULTS: Difference between the two protocols was significant as the group that received topiramate had a greater reduction in ABC-C subscale scores for irritability, stereotypic behavior and hyperactivityoncompliance. CONCLUSION: The results suggest that the combination of topiramate with risperidone may be superior to risperidone monotherapy for children with autistic disorder. However the results need to be further confirmed by a larger randomized controlled trial.
机译:背景:自闭症是一种复杂的神经发育障碍,形成了一系列相关疾病的一部分,称为自闭症谱系障碍。本研究评估了托吡酯加利培酮在自闭症治疗中的作用。方法:招募了四名年龄在4到12岁之间,患有DSM IV自闭症临床诊断的儿童,他们来自儿童专科诊所的门诊。这些孩子主要表现出与自闭症有关的严重破坏性症状。将患者随机分配至托吡酯+利培酮(A组)或安慰剂+利培酮(B组),进行为期8周,双盲,安慰剂对照的研究。对于10至40公斤之间的儿童,利培酮的剂量最高可调整为2毫克/天,对于体重40公斤以上的儿童,最高可调整为3毫克/天。托吡酯的剂量最高可滴定至200毫克/天,具体取决于重量(<30千克为100毫克/天,而> 30千克为200毫克/天)。在基线时以及开始用药后2、4、6和8周后对患者进行评估。结果的度量标准是“异常行为清单-社区(ABC-C)评分量表”。结果:两种方案之间的差异是显着的,因为接受托吡酯的组在烦躁,刻板印象行为和多动/不依从性方面的ABC-C子量表得分降低幅度更大。结论:托吡酯联合利培酮治疗自闭症患儿可能优于利培酮单药治疗。但是,结果需要通过更大的随机对照试验进一步证实。

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