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Br J Ophthalmol. 2015 Jan;99(1):54-8. doi: 10.1136/bjophthalmol-2013-304625. Epub 2014 Jul 29.
2
Outcomes of corneal transplantation for irreversible corneal decompensation secondary to corneal endotheliitis in Asian eyes.亚洲人眼角膜内皮炎导致的不可逆转角膜失代偿行角膜移植的结果。
Am J Ophthalmol. 2013 Aug;156(2):260-266.e2. doi: 10.1016/j.ajo.2013.03.020. Epub 2013 Apr 24.
3
Clinical significance of owl eye morphologic features by in vivo laser confocal microscopy in patients with cytomegalovirus corneal endotheliitis.体内激光共聚焦显微镜观察巨细胞病毒性角膜内皮炎患者“猫头鹰眼”形态特征的临床意义。
Am J Ophthalmol. 2012 Mar;153(3):445-53. doi: 10.1016/j.ajo.2011.07.026. Epub 2011 Oct 25.
4
Viral anterior uveitis.病毒性前葡萄膜炎。
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Treatment outcome and risk factors for visual loss in Cytomegalovirus endotheliitis.巨细胞病毒血管炎致盲的治疗结果和危险因素。
Graefes Arch Clin Exp Ophthalmol. 2012 Mar;250(3):383-9. doi: 10.1007/s00417-011-1813-7. Epub 2011 Sep 3.
6
Detection of cytomegalovirus DNA from cytomegalovirus corneal endotheliitis after penetrating keratoplasty.检测穿透性角膜移植术后巨细胞病毒角膜内皮炎的巨细胞病毒 DNA。
Cornea. 2010 Jun;29(6):683-5. doi: 10.1097/ICO.0b013e3181c325e2.
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Cytomegalovirus endotheliitis in Descemet's stripping endothelial keratoplasty.角膜后弹力层剥除内皮移植术中的巨细胞病毒内皮炎
Ophthalmology. 2009 Apr;116(4):624-30. doi: 10.1016/j.ophtha.2008.10.031. Epub 2009 Feb 4.
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Clinical features of cytomegalovirus anterior uveitis in immunocompetent patients.免疫功能正常患者巨细胞病毒性前葡萄膜炎的临床特征。
Am J Ophthalmol. 2008 May;145(5):834-40. doi: 10.1016/j.ajo.2007.12.015. Epub 2008 Feb 6.
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Cytomegalovirus as an etiologic factor in corneal endotheliitis.巨细胞病毒作为角膜内皮炎的一个病因因素。
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巨细胞病毒相关眼前段炎症的管理干预措施。

Interventions for the management of CMV-associated anterior segment inflammation.

作者信息

Anshu Arundhati, Tan Donald, Chee Soon-Phaik, Mehta Jod S, Htoon Hla M

机构信息

Singapore National Eye Centre, 11 Third Hospital Avenue, Singapore, Singapore, 168751.

出版信息

Cochrane Database Syst Rev. 2017 Aug 24;8(8):CD011908. doi: 10.1002/14651858.CD011908.pub2.

DOI:10.1002/14651858.CD011908.pub2
PMID:28838031
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6483705/
Abstract

BACKGROUND

Cytomegalovirus (CMV) is a virus that usually affects people with reduced immunity. In recent years, this virus has been thought to cause repeated inflammation in the eye, in otherwise healthy people. This form of inflammation can cause damage to the cornea (the outer layer of the eye) or to the optic nerve by causing secondary glaucoma, or to both, leading to visual loss.

OBJECTIVES

Our primary objective was to assess the effects of drug therapies for the treatment of CMV-associated anterior segment inflammation.Our secondary objective was to determine the optimal dose and duration of treatment with respect to recurrence and adverse effects.

SEARCH METHODS

We searched the Cochrane Central Register of Controlled Trials (CENTRAL) (which contains the Cochrane Eyes and Vision Trials Register) (2017, Issue 2), MEDLINE Ovid (1946 to 21 March 2017), Embase Ovid (1947 to 21 March 2017), the ISRCTN registry (www.isrctn.com/editAdvancedSearch); searched 21 March 2017, ClinicalTrials.gov (www.clinicaltrials.gov); searched 21 March 2017, and the WHO International Clinical Trials Registry Platform (ICTRP) (www.who.int/ictrp/search/en); searched 21 March 2017. We did not use any date or language restrictions in the electronic searches for trials. Two review authors independently reviewed the titles and abstracts.

SELECTION CRITERIA

We searched for randomised controlled trials (RCTs) on the management of CMV-associated anterior segment inflammation.

DATA COLLECTION AND ANALYSIS

We planned to have two review authors independently extract data from reports of included studies and analyse data based on methods expected by Cochrane.

MAIN RESULTS

We did not identify any RCTs that met our inclusion criteria.

AUTHORS' CONCLUSIONS: There is currently no good-quality evidence on the management of CMV-associated anterior segment inflammation. Ideally, a well-designed RCT is needed to evaluate the effectiveness of different anti-CMV medications as well as the optimal dose and duration.

摘要

背景

巨细胞病毒(CMV)是一种通常感染免疫力低下人群的病毒。近年来,人们认为这种病毒会在原本健康的人群中引发眼部反复炎症。这种炎症形式可通过引发继发性青光眼对角膜(眼球外层)或视神经造成损害,或同时对两者造成损害,导致视力丧失。

目的

我们的主要目的是评估药物治疗巨细胞病毒相关性眼前节炎症的效果。我们的次要目的是确定关于复发和不良反应方面的最佳治疗剂量和疗程。

检索方法

我们检索了考克兰对照试验中心注册库(CENTRAL)(其中包含考克兰眼科和视力试验注册库)(2017年第2期)、MEDLINE Ovid(1946年至2017年3月21日)、Embase Ovid(1947年至2017年3月21日)、国际标准随机对照试验编号注册库(www.isrctn.com/editAdvancedSearch);于2017年3月21日进行检索,检索了美国国立医学图书馆临床试验注册库(ClinicalTrials.gov)(www.clinicaltrials.gov);于2017年3月21日进行检索,以及世界卫生组织国际临床试验注册平台(ICTRP)(www.who.int/ictrp/search/en);于2017年3月21日进行检索。我们在电子检索试验时未使用任何日期或语言限制。两名综述作者独立审阅了标题和摘要。

选择标准

我们检索了关于巨细胞病毒相关性眼前节炎症管理的随机对照试验(RCT)。

数据收集与分析

我们计划让两名综述作者独立从纳入研究的报告中提取数据,并根据考克兰预期的方法进行数据分析。

主要结果

我们未识别出任何符合我们纳入标准的随机对照试验。

作者结论

目前尚无关于巨细胞病毒相关性眼前节炎症管理的高质量证据。理想情况下,需要进行一项设计良好的随机对照试验来评估不同抗巨细胞病毒药物的有效性以及最佳剂量和疗程。