首页> 外文期刊>Neuropsychiatric Disease and Treatment >Real-World Effectiveness and Safety of Antipsychotics in Individuals at Clinical High-Risk for Psychosis: Study Protocol for a Prospective Observational Study (ShangHai at Risk for Psychosis-Phase 2)
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Real-World Effectiveness and Safety of Antipsychotics in Individuals at Clinical High-Risk for Psychosis: Study Protocol for a Prospective Observational Study (ShangHai at Risk for Psychosis-Phase 2)

机译:临床高风险对临床高风险的抗精神病药的现实世界效力和安全性:预期观察研究的研究议定书(上海心理阶段风险2)

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Background: The clinical high-risk (CHR) state is identified as a critical period for early prevention and intervention during the development of psychosis and early treatment may reduce the risk of conversion to psychosis. However, it remains controversial whether antipsychotics are effective in CHR populations. Limited previous randomised controlled trials of antipsychotic treatment of CHR individuals indicated possible short-term efficacy on psychotic symptoms with unclear long-term effects. To answer this question, it is necessary to establish a high-quality real-world cohort study with large sample size to explore the effectiveness and safety of antipsychotics in CHR individuals. Methods: We plan to consecutively recruit 600 CHR individuals from Shanghai Mental Health Centre in the ongoing SHARP-2 (ShangHai At Risk for Psychosis-Phase 2) project between 2019 and 2022. At baseline, participants will be assessed by the Structured Interview for Prodromal Syndromes, the MATRICS Consensus Cognitive Battery, demographic information, and clinical medication history. They will be followed up in a naturalistic way in which the research team will not prescribe antipsychotics or provide pharmacological consultation. First, CHR participants and their families will be trained to record their medication daily and self-evaluate symptoms through smart-phone application-based assessment and report their information weekly. Second, telephone calls will be arranged monthly so that the researchers are informed about the participants’ symptoms, medications and daily functions. Third, face-to-face interviews will be conducted annually for repeating assessment of baseline. The primary outcomes will include conversion to psychosis and functional outcome (scored with less than 60 in the Global Assessment of Function) at the end of the follow-up period. Conclusion: The current study will improve our knowledge on the effectiveness and safety of the use of antipsychotics at the prodromal phase, and will eventually facilitate optimisation of individualised interventions for psychosis prevention and treatment.
机译:背景:临床高风险(CHR)状态被确定为早期预防和干预在精神病发展期间的临界期的关键时期,早期治疗可能会降低对精神病转换的风险。然而,抗精神病药在CHR人群中是否有争议仍然存在争议。有限的先前随机对照试验的抗精神病药治疗CHR个体表示可能对精神症状的可能性短期疗效,不明确的长期效应。为了回答这个问题,有必要建立一个高质量的现实队列研究,具有大的样本量,以探讨抗抗精神病学的效果和安全性。方法:我们计划在2019年至2022年间,在持续的夏普-2(上海)在2019年至2022年期间,在持续的夏普-2(上海的身上)招募来自上海心理健康中心的600克朗个体。在基线,参与者将通过为前驱的结构性访谈进行评估综合征,基质共识认知电池,人口统计学信息和临床药物历史。他们将以自然主义方式随访,其中研究团队不会规定抗精神病药或提供药理学咨询。首先,CHR参与者及其家属将接受培训,以通过基于智能手机应用的评估和报告他们的信息每周报告他们的药物每日和自我评估症状。其次,将每月安排电话,以便研究人员了解参与者的症状,药物和日常功能。第三,将每年进行面对面的面试,以重复对基线的评估。在随访期结束时,主要成果将包括转换为精神病和功能结果(在全球职能评估中以少于60分)。结论:目前的研究将提高我们对产品在前期抗精神病药的有效性和安全性的知识,并最终促进个性化干预措施进行精神病预防和治疗。

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