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随机对照试验:短期奥昔哌汀控释片对患有注意缺陷多动障碍的年轻男性囚犯的症状和行为结果的影响:CIAO-II 研究。

Randomised controlled trial of the short-term effects of osmotic-release oral system methylphenidate on symptoms and behavioural outcomes in young male prisoners with attention deficit hyperactivity disorder: CIAO-II study.

机构信息

Social Genetic and Developmental Psychiatry, Institute of Psychiatry Psychology and Neuroscience, King's College London, UK.

Department of Biostatistics and Health Informatics, Institute of Psychiatry Psychology and Neuroscience, King's College London, UK.

出版信息

Br J Psychiatry. 2023 Jan;222(1):7-17. doi: 10.1192/bjp.2022.77.

Abstract

BACKGROUND

Research has shown that 20-30% of prisoners meet the diagnostic criteria for attention-deficit hyperactivity disorder (ADHD). Methylphenidate reduces ADHD symptoms, but effects in prisoners are uncertain because of comorbid mental health and substance use disorders.

AIMS

To estimate the efficacy of an osmotic-release oral system methylphenidate (OROS-methylphenidate) in reducing ADHD symptoms in young adult prisoners with ADHD.

METHOD

We conducted an 8-week parallel-arm, double-blind, randomised placebo-controlled trial of OROS-methylphenidate versus placebo in male prisoners (aged 16-25 years) meeting the DSM-5 criteria for ADHD. Primary outcome was ADHD symptoms at 8 weeks, using the investigator-rated Connors Adult ADHD Rating Scale (CAARS-O). Thirteen secondary outcomes were measured, including emotional dysregulation, mind wandering, violent attitudes, mental health symptoms, and prison officer and educational staff ratings of behaviour and aggression.

RESULTS

In the OROS-methylphenidate arm, mean CAARS-O score at 8 weeks was estimated to be reduced by 0.57 points relative to the placebo arm (95% CI -2.41 to 3.56), and non-significant. The responder rate, defined as a 20% reduction in CAARS-O score, was 48.3% for the OROS-methylphenidate arm and 47.9% for the placebo arm. No statistically significant trial arm differences were detected for any of the secondary outcomes. Mean final titrated dose was 53.8 mg in the OROS-methylphenidate arm.

CONCLUSIONS

ADHD symptoms did not respond to OROS-methylphenidate in young adult prisoners. The findings do not support routine treatment with OROS-methylphenidate in this population. Further research is needed to evaluate effects of higher average dosing and adherence to treatment, multi-modal treatments and preventative interventions in the community.

摘要

背景

研究表明,20-30%的囚犯符合注意力缺陷多动障碍 (ADHD) 的诊断标准。哌甲酯可减轻 ADHD 症状,但由于合并精神健康和物质使用障碍,其在囚犯中的效果不确定。

目的

评估渗透型控释口服哌甲酯 (OROS-methylphenidate) 治疗成年 ADHD 年轻囚犯的疗效。

方法

我们对符合 DSM-5 ADHD 标准的成年囚犯(年龄 16-25 岁)进行了一项为期 8 周的平行臂、双盲、随机安慰剂对照试验,评估 OROS-methylphenidate 与安慰剂的疗效。主要结局是 8 周时的 ADHD 症状,使用研究者评定的 Connors 成人 ADHD 评定量表(CAARS-O)。测量了 13 个次要结局,包括情绪失调、心不在焉、暴力态度、心理健康症状,以及狱警和教育工作者对行为和攻击的评定。

结果

在 OROS-methylphenidate 组中,与安慰剂组相比,8 周时 CAARS-O 评分估计平均降低 0.57 分(95%CI-2.41 至 3.56),无统计学意义。响应率定义为 CAARS-O 评分降低 20%,OROS-methylphenidate 组为 48.3%,安慰剂组为 47.9%。未检测到任何次要结局有统计学意义的试验组差异。OROS-methylphenidate 组的平均最终滴定剂量为 53.8mg。

结论

成年 ADHD 年轻囚犯对 OROS-methylphenidate 无反应。结果不支持在该人群中常规使用 OROS-methylphenidate 治疗。需要进一步研究评估更高平均剂量和治疗依从性、多模式治疗和社区预防干预的效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad32/10895500/2bd97f504d8d/S0007125022000770_fig1.jpg

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