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首页> 外文期刊>Therapeutics and Clinical Risk Management >Demonstration of an online tool to assist managed care formulary evidence-based decision making: meta-analysis of topical prostaglandin analog efficacy
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Demonstration of an online tool to assist managed care formulary evidence-based decision making: meta-analysis of topical prostaglandin analog efficacy

机译:演示在线工具,以帮助管理式护理制定循证决策:局部前列腺素类似物功效的荟萃分析

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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.
机译:背景:本文的目的是证明在线服务对局部前列腺素类似物在降低青光眼和高眼压中的眼内压(IOP)的功效方面进行系统的回顾和荟萃分析。方法:一个在线服务提供商(Evidence医生)对直到2009年9月为止的同行评审文献进行了回顾和提取。对至少三个月时间的随机对照研究,评估了原发性开角型青光眼,眼的至少两种前列腺素类似物包括高血压或正常血压的青光眼。主要终点是平均眼压。使用随机效应模型创建汇总估算。 Q卡方检验用于评估统计异质性。结果:16项研究符合纳入标准并进行了分析。平均而言,比马前列素相对于拉坦前列素(1 mmHg,P = 0.025)和特拉沃前列素(0.8 mmHg,P = 0.033),在治疗12–26周后平均IOP降低更大。拉坦前列素和曲伏前列素在降低眼压方面没有统计学差异(P = 0.841)。研究结果与以前发表的局部前列腺素类似物的荟萃分析相似。结论:依靠荟萃分析技术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“黄金标准”。但是,该过程耗时,劳动密集并且超出大多数配方管理者的能力。我们已经证明了商业服务的有效性,该服务有助于进行此类审查。

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