Alessandro Di Lisi, Simona Pupo, Marco Menchetti, Lorenzo Pelizza
{"title":"Antipsychotic Treatment in People at Clinical High Risk for Psychosis: A Narrative Review of Suggestions for Clinical Practice.","authors":"Alessandro Di Lisi, Simona Pupo, Marco Menchetti, Lorenzo Pelizza","doi":"10.1097/JCP.0000000000001891","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>The \"early intervention\" paradigm in psychiatry holds significant promise for preventing psychosis. Recent evidence showed that individuals at clinical high risk for psychosis (CHR-P) with antipsychotic (AP) prescription at baseline have higher psychosis transition rates compared with those without AP, although the underlying cause remains unclear. In this article, we reviewed international guidelines on early intervention in CHR-P people, paying specific attention to clinical recommendations on AP treatment. Then, we comment on these suggestions in the light of recent empirical evidence examining AP prescription in CHR-P populations within \"real-world\" clinical settings.</p><p><strong>Methods: </strong>This search was conducted on PubMed/MEDLINE, PsycINFO, EMBASE, and Google, looking for both \"Guidelines AND CHR-P OR UHR OR Early Psychosis.\"</p><p><strong>Results: </strong>International guidelines generally recommend not using AP as first-line treatment, but only when psychosocial interventions have failed. CHR-P people with AP drug showed high prevalence rates and had more severe clinical picture at entry. Is this a \"warning signal\" for potentially higher psychosis transition risk? Is it a direct AP iatrogenic effect? Is it possible to detect specific CHR-P subgroup that may benefit from AP? These are the questions that this article seeks to explore.</p><p><strong>Conclusions: </strong>The current framework for identifying CHR-P subjects has defined psychometric criteria mainly based on positive symptoms. In our opinion, this is reductive, especially for evaluating therapeutic outcomes and prognosis. A more comprehensive assessment considering quality of life, psychiatric comorbidity, persistent negative symptoms, subjective experience of CHR-P psychopathology, and social/personal recovery is thus needed.</p>","PeriodicalId":15455,"journal":{"name":"Journal of Clinical Psychopharmacology","volume":"44 5","pages":"502-508"},"PeriodicalIF":2.9000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11460766/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Clinical Psychopharmacology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1097/JCP.0000000000001891","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/8/5 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose: The "early intervention" paradigm in psychiatry holds significant promise for preventing psychosis. Recent evidence showed that individuals at clinical high risk for psychosis (CHR-P) with antipsychotic (AP) prescription at baseline have higher psychosis transition rates compared with those without AP, although the underlying cause remains unclear. In this article, we reviewed international guidelines on early intervention in CHR-P people, paying specific attention to clinical recommendations on AP treatment. Then, we comment on these suggestions in the light of recent empirical evidence examining AP prescription in CHR-P populations within "real-world" clinical settings.
Methods: This search was conducted on PubMed/MEDLINE, PsycINFO, EMBASE, and Google, looking for both "Guidelines AND CHR-P OR UHR OR Early Psychosis."
Results: International guidelines generally recommend not using AP as first-line treatment, but only when psychosocial interventions have failed. CHR-P people with AP drug showed high prevalence rates and had more severe clinical picture at entry. Is this a "warning signal" for potentially higher psychosis transition risk? Is it a direct AP iatrogenic effect? Is it possible to detect specific CHR-P subgroup that may benefit from AP? These are the questions that this article seeks to explore.
Conclusions: The current framework for identifying CHR-P subjects has defined psychometric criteria mainly based on positive symptoms. In our opinion, this is reductive, especially for evaluating therapeutic outcomes and prognosis. A more comprehensive assessment considering quality of life, psychiatric comorbidity, persistent negative symptoms, subjective experience of CHR-P psychopathology, and social/personal recovery is thus needed.
目的:精神病学中的 "早期干预 "模式在预防精神病方面大有可为。最近的证据显示,基线处方抗精神病药物(AP)的临床高危精神病(CHR-P)患者与未处方AP的患者相比,精神病转归率更高,但其根本原因仍不清楚。在这篇文章中,我们回顾了有关对临床高危人群进行早期干预的国际指南,特别关注了有关抗精神病药物治疗的临床建议。然后,我们根据最近在 "真实世界 "的临床环境中对慢性阻塞性肺病患者进行 AP 处方治疗的经验证据,对这些建议进行了评论:方法:在 PubMed/MEDLINE、PsycINFO、EMBASE 和 Google 上进行搜索,同时搜索 "指南 AND CHR-P OR UHR OR Early Psychosis":国际指南普遍建议不要将 AP 作为一线治疗,只有在社会心理干预无效时才使用。患有 AP 药物的 CHR-P 患者发病率较高,入院时的临床表现更为严重。这是否是潜在的较高精神病转变风险的 "预警信号"?这是 AP 的直接先天效应吗?是否有可能发现可能受益于 AP 的特定 CHR-P 亚群?这些都是本文试图探讨的问题:目前用于识别CHR-P受试者的框架主要根据阳性症状来定义心理测量标准。我们认为,这是一种简化的方法,尤其是在评估治疗效果和预后时。因此,需要进行更全面的评估,考虑生活质量、精神病合并症、持续性阴性症状、CHR-P 心理病理学的主观体验以及社会/个人恢复情况。
期刊介绍:
Journal of Clinical Psychopharmacology, a leading publication in psychopharmacology, offers a wide range of articles reporting on clinical trials and studies, side effects, drug interactions, overdose management, pharmacogenetics, pharmacokinetics, and psychiatric effects of non-psychiatric drugs. The journal keeps clinician-scientists and trainees up-to-date on the latest clinical developments in psychopharmacologic agents, presenting the extensive coverage needed to keep up with every development in this fast-growing field.