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局部滴眼药物治疗干眼的疗效:系统文献回顾。

Efficacy of topical ophthalmic drugs in the treatment of dry eye disease: A systematic literature review.

机构信息

Cincinnati Eye Institute, Edgewood, KY, USA.

McGill University, Montreal, Canada.

出版信息

Ocul Surf. 2019 Jul;17(3):412-423. doi: 10.1016/j.jtos.2019.02.012. Epub 2019 Mar 4.

Abstract

Dry eye disease (DED) is a multifactorial and complex disease of the ocular surface, with a high prevalence in adults. We systematically reviewed efficacy and safety data from published articles reporting results from prospective, controlled trials of topical ophthalmic drugs for DED. PubMed was searched for articles from January 1997 to October 2017. Twenty-six unique trials investigating 13 ophthalmic drugs were identified, including trials of the approved drugs cyclosporine A, cyclosporine A cationic emulsion, diquafosol, rebamipide and lifitegrast. All identified studies provided level 1 evidence. None of the large (N > 100) studies demonstrated statistical significance of primary endpoints for both a sign and a symptom endpoint versus a control treatment in the same published trial. Publications on lifitegrast reported statistical superiority in a symptom or sign endpoint versus the control group in a large (N > 200), multicenter trial, with results repeated in trials of similar design. The most common adverse events associated with the approved drugs related to ocular discomfort upon instillation, especially burning/stinging and ocular irritation. The trial design and endpoints used across the studies varied considerably, highlighting the importance of standardization in clinical trials for DED. Recent advances in drug delivery and improved understanding of DED should contribute to new ophthalmic drug approvals.

摘要

干眼症(DED)是一种多因素、复杂的眼表疾病,在成年人中发病率较高。我们系统地回顾了已发表的前瞻性对照试验报告,以评估局部眼科药物治疗 DED 的疗效和安全性数据。我们在 PubMed 上检索了 1997 年 1 月至 2017 年 10 月的文章。确定了 26 项独特的试验,共涉及 13 种眼科药物,包括已批准药物环孢素 A、环孢素 A 阳离子乳剂、地夸磷索、贝复舒和利福平特格拉司。所有确定的研究都提供了 1 级证据。在同一已发表的试验中,没有一项大型(N>100)研究在主要终点(症状和体征终点)方面显示出与对照组相比的统计学意义。利福平特格拉司的研究报告表明,在一项大型(N>200)、多中心试验中,与对照组相比,在一项症状或体征终点具有统计学优势,并且在类似设计的试验中也得到了重复。与已批准药物相关的最常见不良事件与滴眼时的眼部不适有关,尤其是烧灼感/刺痛和眼部刺激。研究之间的试验设计和终点使用差异很大,这突出表明在 DED 的临床试验中标准化的重要性。药物输送的最新进展和对 DED 的理解的提高应该有助于新的眼科药物批准。

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