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急诊医学中的对照临床试验。

Controlled clinical trials in emergency medicine.

作者信息

Brown C G, Moser M, Moeschberger M, Kelen G D

出版信息

Am J Emerg Med. 1985 Jan;3(1):67-73. doi: 10.1016/0735-6757(85)90016-6.

Abstract

In this first article of a series on controlled clinical trials in emergency medicine, an overview of the structure of such studies and the relevant issues related to study design, data generation, statistical analysis, and reporting are presented. The importance of precise patient selection, randomization and stratification, blinding, and equivalent therapeutic intervention in study design has been discussed. In addition, precise outcome and measurement criteria, assessor qualifications, deficiencies in data, appropriate sample-size selection, and reporting are also presented. Although an idealized framework for the conduct and analysis of a controlled clinical trial is provided, it should be appreciated that design and analytical compromises may at times be difficult to avoid in clinical research. Future articles in this series will discuss randomization in clinical trials, alternatives to randomization, beta error and sample-size determination, the statistical and analytical issues related to imperfections in the execution of a trial, and issues related to the reporting of clinical trials.

摘要

在关于急诊医学对照临床试验系列的第一篇文章中,介绍了此类研究的结构概述以及与研究设计、数据生成、统计分析和报告相关的问题。讨论了在研究设计中精确选择患者、随机化和分层、盲法以及等效治疗干预的重要性。此外,还介绍了精确的结局和测量标准、评估者资质、数据缺陷、合适的样本量选择以及报告。虽然提供了一个进行对照临床试验和分析的理想化框架,但应该认识到,在临床研究中有时可能难以避免设计和分析上的妥协。本系列的后续文章将讨论临床试验中的随机化、随机化的替代方法、β错误和样本量确定、与试验执行不完善相关的统计和分析问题以及与临床试验报告相关的问题。

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