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Failure of Healthcare Provision for Attention-Deficit/Hyperactivity Disorder in the United Kingdom: A Consensus Statement.英国注意力缺陷多动障碍医疗服务的缺失:一份共识声明。
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BATIR 研究:评估在押注意缺陷多动障碍患者中监狱内口服哌甲酯缓释片与安慰剂治疗效果的单中心、双盲、随机、优效性对照试验方案。

Protocol of a monocentric, double-blind, randomized, superiority, controlled trial evaluating the effect of in-prison OROS-methylphenidate vs. placebo treatment in detained people with attention-deficit hyperactivity disorder (BATIR).

机构信息

Institute of Primary Health Care (BIHAM), University of Bern, Bern, Switzerland.

Laboratory of Population Health (#PopHealthLab), University of Fribourg, Fribourg, Switzerland.

出版信息

Trials. 2024 Jan 4;25(1):23. doi: 10.1186/s13063-023-07827-7.

DOI:10.1186/s13063-023-07827-7
PMID:38178233
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10765778/
Abstract

BACKGROUND

Attention-deficit hyperactivity disorder (ADHD) is characterized by difficulty paying attention, poor impulse control, and hyperactive behavior. It is associated with several adverse health and social outcomes and leads to an increased risk of criminality and recidivism. Worldwide, ADHD is thus highly prevalent in prisons. However, ADHD treatment has been neglected in such environments. Stimulant medications such as osmotic-release oral system methylphenidate (OROS-MPH) are first-line treatments in the general population, but they are under-prescribed in prisons due to concerns about abuse, even though such claims are not empirically supported. This project aims to compare the efficacy of a 3-month in-prison OROS-MPH vs. placebo treatment on the severity of core ADHD symptoms and relevant in- and post-prison outcomes.

METHODS

This study is a phase III, double-blinded, randomized, superiority, controlled trial of OROS-MPH vs. placebo. After randomization, the participants will receive 3 months of treatment with OROS-MPH or placebo (1:1 ratio) while incarcerated. Upon release, all participants will be offered the treatment (OROS-MPH) for 1 year but will remain blinded to their initial study group. The study will be conducted at the Division of Prison Health, Geneva, Switzerland, among incarcerated men (n = 150). Measures will include (1) investigator-rated ADHD symptoms, (2) acute events collected by the medical and prison teams, (3) assessment of the risk of recidivism, (4) medication side effects, (5) medication adherence, (6) study retention, (7) health care/prison costs, and (8) 1-year recidivism. Analyses will include bivariable and multivariable modeling (e.g., regression models, mixed-effects models, survival analyses) and an economic evaluation (cost-benefit analysis).

DISCUSSION

We expect that early identification and treatment of ADHD in prison will be an important public health opportunity and a cost-effective approach that is likely to reduce the vulnerability of incarcerated individuals and promote pathways out of criminal involvement. The study will also promote standards of care for people with ADHD in prison and provide recommendations for continuity of care after release.

TRIAL REGISTRATION

ClinicalTrials.gov NCT05842330 . Registered on June 5, 2023. Kofam.ch SNCTP000005388. Registered on July 17, 2023.

摘要

背景

注意力缺陷多动障碍(ADHD)的特征是难以集中注意力、冲动控制能力差和多动行为。它与许多不良的健康和社会结果有关,并导致犯罪和累犯的风险增加。因此,ADHD 在全球监狱中非常普遍。然而,在这种环境中,ADHD 的治疗往往被忽视。在普通人群中,兴奋剂药物如渗透压控释口服系统哌甲酯(OROS-MPH)是一线治疗药物,但由于担心滥用,它们在监狱中的处方量较少,尽管这种说法没有得到经验证据的支持。本项目旨在比较监狱内 3 个月 OROS-MPH 与安慰剂治疗对核心 ADHD 症状严重程度及相关入狱前后结果的疗效。

方法

这是一项为期 3 个月的、双盲、随机、优效性、对照试验,比较 OROS-MPH 与安慰剂在监狱中的疗效。随机分组后,参与者将接受 3 个月的 OROS-MPH 或安慰剂(1:1 比例)治疗。释放后,所有参与者将获得 1 年的治疗(OROS-MPH),但仍对其最初的研究组保持盲态。该研究将在瑞士日内瓦监狱卫生科进行,纳入 150 名男性囚犯。研究的主要评估指标包括(1)研究者评估的 ADHD 症状,(2)医疗和监狱团队收集的急性事件,(3)累犯风险评估,(4)药物副作用,(5)药物依从性,(6)研究保留率,(7)医疗保健/监狱费用,以及(8)1 年累犯率。分析将包括单变量和多变量模型(如回归模型、混合效应模型、生存分析)和经济评估(成本效益分析)。

讨论

我们预计,在监狱中早期识别和治疗 ADHD 将是一个重要的公共卫生机会,也是一种具有成本效益的方法,可能会降低被监禁个体的脆弱性,并促进他们摆脱犯罪行为。该研究还将促进监狱中 ADHD 患者的护理标准,并为释放后的护理连续性提供建议。

试验注册

ClinicalTrials.gov NCT05842330,于 2023 年 6 月 5 日注册。Kofam.ch SNCTP000005388,于 2023 年 7 月 17 日注册。