Leslie Citrome, Marko A Mychaskiw, Alma Cortez, Mark Opler, Liza Sopina, Sameer Kotak
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引用次数: 0
Abstract
Objective: The complexity inherent in the treatment of schizophrenia results in a multitude of outcome assessments being employed when conducting clinical trials. Subjective outcome assessments and minimal clinically important differences (MCIDs) to evaluate clinical meaningfulness have gained traction; however, the extent of application in evaluation of treatments for schizophrenia is unknown. A scoping review was conducted to assess the availability of published psychometric evaluations, including MCIDs, for clinical outcome assessments used to evaluate treatments for schizophrenia.
Method of research: Key databases (PubMed®, Embase®, APA PsycINFO®, International Society for Pharmacoeconomics and Outcomes Research) were searched for studies on schizophrenia published from 2010 to 2020. Secondary sources (ClinicalTrials.gov, PROLABELS™, FDA.gov) were also reviewed. Clinical outcome assessments were organized by type (patient-reported outcomes [PROs], clinician-reported outcomes [ClinROs], observer-reported outcomes [ObsROs]) and further classified by intended use (generic, mental health, schizophrenia). Reliability and internal consistency were evaluated using Cronbach's α. External validity was evaluated by intraclass correlation coefficient (ICC).
Results: Across 140 studies, 66 clinical outcome assessments were identified. MCIDs were reported for eight of the 66 studies. Of these, two were PROs (generic) and six were ClinROs/ObsROs (three mental health-specific, three schizophrenia-specific). Reliability was good across generic, mental health-specific, and schizophrenia-specific categories, whereas external validity was strong mainly for schizophrenia-specific PROs. Overall, ClinROs/ObsROs that focused on mental health had good reliability and strong external validity.
Conclusion: This review provides a comprehensive overview of the clinical outcome assessments used in schizophrenia research during the past ten years. Results highlight the heterogeneity of existing outcomes and a growing interest in PROs for schizophrenia.
目的:在进行临床试验时,精神分裂症治疗固有的复杂性导致了大量的结果评估。主观结果评估和最小临床重要差异(MCIDs)来评估临床意义得到了关注;然而,在精神分裂症治疗评估中的应用程度尚不清楚。进行了一项范围审查,以评估已发表的心理测量评估的可用性,包括MCIDs,用于评估精神分裂症治疗的临床结果评估。研究方法:检索关键数据库(PubMed®,Embase®,APA PsycINFO®,International Society for Pharmacoeconomics and Outcomes research),检索2010年至2020年发表的精神分裂症相关研究。次要来源(ClinicalTrials.gov, PROLABELS™,FDA.gov)也进行了审查。临床结果评估按类型(患者报告的结果[PROs]、医生报告的结果[ClinROs]、观察者报告的结果[ObsROs])组织,并进一步按预期用途分类(一般用途、心理健康、精神分裂症)。采用Cronbach’s α评价信度和内部一致性。采用类内相关系数(ICC)评价外效度。结果:在140项研究中,确定了66项临床结果评估。66项研究中有8项报告了mcd。其中,2个是PROs(非专利),6个是ClinROs/ObsROs(3个是精神健康特异性,3个是精神分裂症特异性)。信度在一般类别、精神健康特定类别和精神分裂症特定类别中都很好,而外部效度主要在精神分裂症特定类别中很强。总体而言,关注心理健康的ClinROs/ObsROs具有良好的信度和较强的外部效度。结论:本综述对过去十年精神分裂症研究中使用的临床结果评估进行了全面概述。结果强调了现有结果的异质性,以及对精神分裂症pro治疗的兴趣日益增加。