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The effectiveness of aripiprazole in the management of problem behaviour in people with intellectual disabilities, developmental disabilities and/or autistic spectrum disorder - A systematic review

机译:阿立哌唑在智力障碍,发育障碍和/或自闭症谱系障碍患者行为管理中的有效性-系统评价

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The management of problem behaviours (PB) in individuals with intellectual disabilities (ID), developmental disabilities (DD) and/or autistic spectrum disorders (ASD) can be challenging. Antipsychotic medications are commonly prescribed where other strategies have failed. A systematic review (SR) was conducted to establish the research evidence for the efficacy of aripiprazole in the management of PB in adults and children with ID, DD and/or ASD. Although included studies supported the efficacy of aripiprazole for this indication, the overall quality of studies was poor. Of the 20 studies included in this systematic review there were only two randomised controlled trials (RCTs) on children with ASD and/or ID/DD, both of which were conducted by the pharmaceutical company that manufactures aripiprazole, and it is not clear whether a number of same participants were included in both RCTs. One of the RCTs was extended into an open label long term follow up, which showed that aripiprazole's efficacy lasted over 52 weeks and the adverse effects were tolerable. Four studies were open label prospective studies, 11 were retrospective case reports which included four single case reports, and two were prospective case series. Most studies reported adverse effects from aripiprazole in the form of weight gain, increased appetite, sedation, tiredness, drooling and tremor. However, aripiprazole improved serum prolactin level in some participants and overall did not show any adverse effect on QTc interval. There is a need for more carefully designed RCTs into the use of aripiprazole in the management of PB in people with ID/DD and/or ASD, which should be carried out independent of pharmaceutical companies.
机译:对智障者(ID),发育障碍者(DD)和/或自闭症谱系障碍(ASD)的问题行为(PB)的管理可能具有挑战性。通常在其他策略失败的地方开抗精神病药物。进行了系统评价(SR),以建立阿立哌唑在ID,DD和/或ASD成人和儿童PB治疗中的疗效研究证据。尽管纳入的研究支持阿立哌唑对这种适应症的疗效,但总体研究质量较差。在该系统评价中包括的20项研究中,只有两项针对ASD和/或ID / DD患儿的随机对照试验(RCT),均由生产阿立哌唑的制药公司进行,目前尚不清楚两个RCT中都包含相同的参与者数量。其中一项随机对照试验被扩展到开放标签的长期随访中,这表明阿立哌唑的疗效持续超过52周,并且不良反应是可以忍受的。有4项研究是开放标签的前瞻性研究,有11项是回顾性病例报告,其中包括4项单例报告,还有2项是前瞻性病例系列。大多数研究报告了阿立哌唑的不良影响,包括体重增加,食欲增加,镇静,疲倦,流口水和震颤。但是,阿立哌唑改善了部分参与者的血清催乳素水平,总体上未显示对QTc间隔的任何不利影响。需要对ID / DD和/或ASD患者的PB管理中使用阿立哌唑进行更精心设计的RCT,这些RCT应独立于制药公司进行。

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