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展示一款在线工具,以辅助管理式医疗目录循证决策:前列腺素类似物疗效的荟萃分析。

Demonstration of an online tool to assist managed care formulary evidence-based decision making: meta-analysis of topical prostaglandin analog efficacy.

机构信息

Department of Ophthalmology and Visual Sciences, Washington University School of Medicine, St Louis, MO, USA.

出版信息

Ther Clin Risk Manag. 2011;7:283-90. doi: 10.2147/TCRM.S20495. Epub 2011 Jul 12.

Abstract

BACKGROUND

The purpose of this paper was to demonstrate the use of an online service for conducting a systematic review and meta-analysis of the efficacy of topical prostaglandin analogs in reducing intraocular pressure (IOP) in glaucoma and ocular hypertension.

METHODS

An online service provider (Doctor Evidence) reviewed and extracted data from the peer-reviewed literature through September 2009. Randomized controlled studies of at least three months' duration assessing at least two prostaglandin analogs in patients with primary open-angle glaucoma, ocular hypertension, or normal-tension glaucoma were included. The primary endpoint was mean IOP. Summary estimates were created using random-effects models. The Q Chi-square test was used to assess statistical heterogeneity.

RESULTS

Sixteen studies satisfied the inclusion criteria and were analyzed. On average, greater IOP-lowering was seen with bimatoprost relative to latanoprost (1 mmHg, P = 0.025) and travoprost (0.8 mmHg, P = 0.033) based on mean IOP after 12-26 weeks of treatment. No statistical difference was observed in IOP-lowering between latanoprost and travoprost (P = 0.841). Findings were similar to previously published meta-analyses of topical prostaglandin analogs.

CONCLUSION

Systematic reviews relying on meta-analytic techniques to create summary statistics are considered to be the "gold standard" for synthesizing evidence to support clinical decision-making. However, the process is time-consuming, labor-intensive, and outside the capability of most formulary managers. We have demonstrated the effectiveness of a commercial service that facilitates the process of conducting such reviews.

摘要

背景

本文旨在展示一种在线服务在进行系统评价和荟萃分析中的应用,以评估局部前列腺素类似物在降低青光眼和高眼压症患者眼内压(IOP)方面的疗效。

方法

一家在线服务提供商(Doctor Evidence)通过 2009 年 9 月对同行评审文献进行了审查和数据提取。纳入了至少持续三个月、评估至少两种前列腺素类似物在原发性开角型青光眼、高眼压症或正常眼压性青光眼患者中的随机对照研究。主要终点为平均 IOP。使用随机效应模型创建汇总估计值。使用 Q 卡方检验评估统计异质性。

结果

符合纳入标准并进行分析的研究有 16 项。基于治疗 12-26 周后的平均 IOP,与拉坦前列素(1mmHg,P=0.025)和曲伏前列素(0.8mmHg,P=0.033)相比,贝美前列素的降压效果更大。拉坦前列素和曲伏前列素之间的降压效果无统计学差异(P=0.841)。这些发现与之前发表的局部前列腺素类似物荟萃分析相似。

结论

依靠荟萃分析技术来创建汇总统计数据的系统评价被认为是综合证据以支持临床决策的“金标准”。然而,该过程耗时、劳动强度大,超出了大多数处方管理者的能力。我们已经证明了一种商业服务的有效性,该服务可以促进进行此类综述的过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a32/3150474/1add64e9a61a/tcrm-7-283f1.jpg

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