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用于青光眼随机对照试验的临床结局变异:系统评价。

Variation of clinical outcomes used in glaucoma randomised controlled trials: a systematic review.

机构信息

Health Services Research Unit, University of Aberdeen, , Aberdeen, UK.

出版信息

Br J Ophthalmol. 2014 Apr;98(4):464-8. doi: 10.1136/bjophthalmol-2013-304323. Epub 2014 Jan 13.

Abstract

PURPOSE

In randomised clinical trials (RCTs) the selection of appropriate outcomes is crucial to the assessment of whether one intervention is better than another. The purpose of this review is to identify different clinical outcomes reported in glaucoma trials.

METHODS

We conducted a systematic review of glaucoma RCTs. A sample or selection of glaucoma trials were included bounded by a time frame (between 2006 and March 2012). Only studies in English language were considered. All clinical measured and reported outcomes were included. The possible variations of clinical outcomes were defined prior to data analysis. Information on reported clinical outcomes was tabulated and analysed using descriptive statistics. Other data recorded included type of intervention and glaucoma, duration of the study, defined primary outcomes, and outcomes used for sample size calculation, if nominated.

RESULTS

The search strategy identified 4323 potentially relevant abstracts. There were 315 publications retrieved, of which 233 RCTs were included. A total of 967 clinical measures were reported. There were large variations in the definitions used to describe different outcomes and their measures. Intraocular pressure was the most commonly reported outcome (used in 201 RCTs, 86%) with a total of 422 measures (44%). Safety outcomes were commonly reported in 145 RCTs (62%) whereas visual field outcomes were used in 38 RCTs (16%).

CONCLUSIONS

There is a large variation in the reporting of clinical outcomes in glaucoma RCTs. This lack of standardisation may impair the ability to evaluate the evidence of glaucoma interventions.

摘要

目的

在随机临床试验(RCT)中,选择适当的结局对于评估一种干预措施是否优于另一种干预措施至关重要。本研究的目的是确定青光眼试验中报告的不同临床结局。

方法

我们对青光眼 RCT 进行了系统评价。纳入了一个时间框架内(2006 年至 2012 年 3 月)的样本或选择的青光眼试验。仅考虑英语语言的研究。纳入所有临床测量和报告的结局。在数据分析之前,定义了可能的临床结局变化。将报告的临床结局信息列表并使用描述性统计进行分析。记录的其他数据包括干预类型和青光眼、研究持续时间、定义的主要结局以及用于样本量计算的结局(如果指定)。

结果

搜索策略确定了 4323 篇可能相关的摘要。共检索到 315 篇文献,其中包括 233 项 RCT。共报告了 967 项临床测量。用于描述不同结局及其测量的定义存在很大差异。眼压是最常报告的结局(在 201 项 RCT 中使用,占 86%),共有 422 项测量(44%)。145 项 RCT(62%)常报告安全性结局,而 38 项 RCT(16%)使用视野结局。

结论

青光眼 RCT 中临床结局的报告存在很大差异。这种缺乏标准化可能会影响评估青光眼干预证据的能力。

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