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基于德尔菲法的临床试验中治疗抵抗性抑郁症定义的共识指南。

A Delphi-method-based consensus guideline for definition of treatment-resistant depression for clinical trials.

机构信息

King's College London, Institute of Psychiatry, Psychology and Neuroscience, Department of Psychological Medicine, London, UK.

Neuroscience and Psychiatry Unit, Division of Neuroscience and Experimental Psychology, School of Biological Sciences, Faculty of Biological, Medical and Human Sciences, The University of Manchester and Manchester Academic Health Sciences Centre, Manchester, UK.

出版信息

Mol Psychiatry. 2022 Mar;27(3):1286-1299. doi: 10.1038/s41380-021-01381-x. Epub 2021 Dec 15.

Abstract

Criteria for treatment-resistant depression (TRD) and partially responsive depression (PRD) as subtypes of major depressive disorder (MDD) are not unequivocally defined. In the present document we used a Delphi-method-based consensus approach to define TRD and PRD and to serve as operational criteria for future clinical studies, especially if conducted for regulatory purposes. We reviewed the literature and brought together a group of international experts (including clinicians, academics, researchers, employees of pharmaceutical companies, regulatory bodies representatives, and one person with lived experience) to evaluate the state-of-the-art and main controversies regarding the current classification. We then provided recommendations on how to design clinical trials, and on how to guide research in unmet needs and knowledge gaps. This report will feed into one of the main objectives of the EUropean Patient-cEntric clinicAl tRial pLatforms, Innovative Medicines Initiative (EU-PEARL, IMI) MDD project, to design a protocol for platform trials of new medications for TRD/PRD.

摘要

治疗抵抗性抑郁症(TRD)和部分反应性抑郁症(PRD)作为重度抑郁症(MDD)的亚型,其定义并不明确。在本文件中,我们使用基于德尔菲法的共识方法来定义 TRD 和 PRD,并将其作为未来临床研究的操作性标准,特别是如果出于监管目的进行的研究。我们回顾了文献,并汇集了一组国际专家(包括临床医生、学者、研究人员、制药公司员工、监管机构代表和一位有过亲身经历的人),以评估当前分类的最新进展和主要争议。然后,我们就如何设计临床试验以及如何指导针对未满足需求和知识空白的研究提供了建议。本报告将为欧盟患者为中心的临床试验平台,创新药物倡议(EU-PEARL,IMI)MDD 项目的主要目标之一提供信息,该项目旨在为 TRD/PRD 的新药物平台试验设计方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28e0/9095475/858f94813b0f/41380_2021_1381_Fig1_HTML.jpg

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