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中国南方预防闭角型青光眼激光虹膜切开术随机对照试验的设计与方法:中山闭角型青光眼预防试验

Design and methodology of a randomized controlled trial of laser iridotomy for the prevention of angle closure in southern China: the Zhongshan angle Closure Prevention trial.

作者信息

Jiang Yuzhen, Friedman David S, He Mingguang, Huang Shengsong, Kong Xiangbin, Foster Paul J

机构信息

State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, China.

出版信息

Ophthalmic Epidemiol. 2010 Oct;17(5):321-32. doi: 10.3109/09286586.2010.508353.

DOI:10.3109/09286586.2010.508353
PMID:20868259
Abstract

PURPOSE

To summarize the design and methodology of a large-scale trial in southern China, the Zhongshan Angle Closure Prevention (ZAP) trial. This trial will determine if laser iridotomy (LI) is superior to no treatment for managing Chinese people who are Primary Angle Closure Suspects (PACS). In this trial, PACS was defined as having 6 or more clock hours of angle circumference in which the pigmented trabecular meshwork was not visible under static gonioscopy in both eyes without elevated intraocular pressure, peripheral anterior synechiae or glaucomatous neuropathy.

METHODS

Subjects were recruited from an urban district in Guangzhou. The target sample size was 870. Persons 50 years of age and older with 20/40 or better vision in both eyes identified as having 6 or more clock hours of angle circumference in which the pigmented trabecular meshwork was not visible under static gonioscopy in both eyes were enrolled. Each subject was randomized to undergo LI in one eye with the fellow eye left untreated. Follow up is planned for a minimum period of 3 years. Baseline examination included tonometry, limbal chamber depth grading, gonioscopy, fundus photography, anterior segment coherence tomography, ultrasound A scan, ultrasound biomicroscopy, specular microscopy and dark room provocative testing. Endpoints for the study include developing elevated intraocular pressure, peripheral anterior synechiae or experiencing acute primary angle closure.

CONCLUSION

The ZAP trial will determine if LI is safe and effective at preventing pathological angle closure in asymptomatic eyes with narrow angle configurations on gonioscopy. It will also provide data on what happens to untreated eyes in PACSs. Data collected at baseline will also help identify those at high risk for developing primary angle closure and primary angle closure glaucoma.

摘要

目的

总结中国南方一项大型试验——中山闭角预防(ZAP)试验的设计与方法。该试验将确定激光虹膜切开术(LI)在治疗原发性闭角型青光眼可疑患者(PACS)方面是否优于不治疗。在本试验中,PACS的定义为:双眼静态前房角镜检查时,在无眼压升高、周边前粘连或青光眼性神经病变的情况下,双眼小梁网色素沉着不可见的房角圆周达6个或更多钟点。

方法

研究对象从广州的一个市区招募。目标样本量为870例。纳入年龄在50岁及以上、双眼视力20/40或更好、双眼静态前房角镜检查时小梁网色素沉着不可见的房角圆周达6个或更多钟点的患者。每位受试者被随机分配一只眼睛接受LI治疗,另一只眼睛不治疗。计划随访至少3年。基线检查包括眼压测量、角膜缘前房深度分级、前房角镜检查、眼底照相、眼前段相干断层扫描、A超、超声生物显微镜检查、镜面显微镜检查和暗室激发试验。研究终点包括眼压升高、周边前粘连或发生急性原发性房角关闭。

结论

ZAP试验将确定LI在预防前房角镜检查显示房角狭窄的无症状眼睛发生病理性房角关闭方面是否安全有效。它还将提供有关PACS患者未治疗眼睛情况的数据。基线时收集的数据也将有助于识别那些发生原发性房角关闭和原发性闭角型青光眼高危患者。

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