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用于青光眼的穹窿部结膜小梁切除术瓣与角膜缘部结膜小梁切除术瓣对比

Fornix-based versus limbal-based conjunctival trabeculectomy flaps for glaucoma.

作者信息

Al-Haddad Christiane, Abdulaal Marwan, Al-Moujahed Ahmad, Ervin Ann-Margret

机构信息

Ophthalmology Department, American University of Beirut Medical Center, Hamrah Street, PO Box 110236, Beirut, Lebanon.

出版信息

Cochrane Database Syst Rev. 2015 Nov 25;11(11):CD009380. doi: 10.1002/14651858.CD009380.pub2.

Abstract

BACKGROUND

Glaucoma is one of the leading largely preventable causes of blindness in the world. It usually is addressed first medically with topical intraocular pressure-lowering drops or by laser trabeculoplasty. In cases where such treatment fails, glaucoma-filtering surgery is considered, most commonly trabeculectomy surgery with variations in technique, for example, the type of conjunctival flap (fornix- or limbal-based). In a fornix-based flap, the surgical wound is performed at the corneal limbus; while in a limbal-based flap, the incision is further away. Many studies in the literature compare fornix- and limbal-based trabeculectomy with respect to outcomes and complications.

OBJECTIVES

To assess the comparative effectiveness of fornix- versus limbal-based conjunctival flaps in trabeculectomy for adult glaucoma, with a specific focus on intraocular pressure (IOP) control and complications (adverse effects).

SEARCH METHODS

We searched CENTRAL (which contains the Cochrane Eyes and Vision Trials Register) (2015, Issue 9), Ovid MEDLINE, Ovid MEDLINE In-Process and Other Non-Indexed Citations, Ovid MEDLINE Daily, Ovid OLDMEDLINE (January 1946 to October 2015), EMBASE (January 1980 to October 2015), Latin American and Caribbean Health Sciences Literature Database (LILACS) (January 1982 to October 2015), the ISRCTN registry (www.isrctn.com/editAdvancedSearch), ClinicalTrials.gov (www.clinicaltrials.gov) and the World Health Organization (WHO) International Clinical Trials Registry Platform (ICTRP) (www.who.int/ictrp/search/en). We did not use any date or language restrictions in the electronic searches for trials. We last searched the electronic databases on 23 October 2015.We reviewed the bibliographic references of identified randomised controlled trials (RCTs) in order to find trials not identified by the electronic searches. We contacted researchers and practitioners active in the field of glaucoma to identify other published and unpublished trials.

SELECTION CRITERIA

We included RCTs comparing the benefits and complications of fornix- versus limbal-based trabeculectomy for glaucoma, irrespective of glaucoma type, publication status, and language. We excluded studies on children less than 18 years of age, since wound healing is different in this age group and the rate of bleb scarring postoperatively is high.

DATA COLLECTION AND ANALYSIS

Two review authors independently extracted data and assessed trial quality. We contacted study authors for additional information.The primary outcome was the proportion of failed trabeculectomies at 24 months. Failure was defined as the need for repeat surgery or uncontrolled IOP (more than 22 mmHg), despite additional topical/systemic medications. Needling and 5-fluorouracil (5-FU) injections were allowed only during the first six months postoperatively; additional needling or 5-FU injections were considered as failure. Mean post-operative IOP at 12 and 24 months also was recorded.

MAIN RESULTS

The review included six trials with a total of 361 participants. Two studies were conducted in America and one each in Germany, Greece, India, and Saudi Arabia. The participants of four trials had open-angle glaucoma; one study included participants with primary open-angle or primary closed-angle glaucoma, and one study did not specify the type of glaucoma. Three studies used a combined procedure (phacotrabeculectomy). Trabeculectomy with mitomycin C (MMC) was performed in four studies, and trabeculectomy with 5-fluorouracil (5-FU) was performed in only one study.None of the included trials reported trabeculectomy failure at 24 months. Only one trial reported the failure rate of trabeculectomy as a late complication. Failure was higher among participants randomised to the limbal-based surgery: 1/50 eyes failed trabeculectomy in the fornix group compared with 3/50 in the limbal group (risk ratio (RR) 0.33, 95% confidence interval (95% CI) 0.04 to 3.10); therefore we are very uncertain as to the relative effect of the two procedures on failure rate.Four studies including 252 participants provided measures of mean IOP at 12 months. In the fornix-based surgeries, mean IOP ranged from 12.5 to 15.5 mmHg and similar results were noted in limbal-based surgeries with mean IOP ranging from 11.7 to 15.1 mmHg without significant difference. Mean difference was 0.44 mmHg (95% CI -0.45 to 1.33) and 0.86 mmHg, (95% CI -0.52 to 2.24) at 12 and 24 months of follow-up, respectively. Neither of these pooled analyses showed a statistically significant difference in IOP between groups (moderate quality of evidence).One trial reported number of anti-glaucoma medications at 24 months of follow-up with no difference noted between surgical groups. However, three trials reported the mean number of anti-glaucoma medications at 12 months of follow-up without significant difference in the mean number of postoperative IOP-lowering medications between the two surgical techniques. Mean difference was 0.02, (95% CI -0.15 to 0.19) at 12 months of follow-up (high quality of evidence).Because of the small numbers of events and total participants, the risk of many reported adverse events were uncertain and those that were found to be statistically significant may have been due to chance.For risk of bias assessment: although all six trials were randomised selection bias was mostly unclear, with unclear random sequence generation in four of the six studies and unclear allocation concealment in five of the six studies. Attrition bias was encountered in only one trial which also suffered from reporting bias. All other trials had an unclear risk of reporting bias as there was no access to study protocols. All included trials were judged to have high risk of detection bias due to lack of masking of the outcomes. Trabeculectomy is quite a standard procedure and unlikely to induce bias due to surgeon 'performance', hence performance bias was not evaluated.

AUTHORS' CONCLUSIONS: The main result of this review was that there was uncertainty as to the difference between fornix- and limbal-based trabeculectomy surgeries due to the small number of events and confidence intervals that cross the null. This also applied to postoperative complications, but without any impact on long-term failure rate between the two surgical techniques.

摘要

背景

青光眼是全球主要的可预防性致盲原因之一。通常首先采用局部降眼压滴眼液或激光小梁成形术进行药物治疗。若此类治疗失败,则考虑进行青光眼滤过手术,最常见的是小梁切除术,手术技术存在差异,例如结膜瓣的类型(穹窿部或角膜缘部)。在基于穹窿部的结膜瓣手术中,手术切口位于角膜缘;而在基于角膜缘的结膜瓣手术中,切口距离角膜缘更远。文献中的许多研究比较了基于穹窿部和角膜缘的小梁切除术的疗效和并发症。

目的

评估在成人青光眼小梁切除术中,基于穹窿部与基于角膜缘的结膜瓣的相对有效性,特别关注眼压控制和并发症(不良反应)。

检索方法

我们检索了Cochrane中心对照临床试验注册库(CENTRAL)(其中包含Cochrane眼科和视力试验注册库)(2015年第9期)、Ovid MEDLINE、Ovid MEDLINE在研及其他未索引的文献、Ovid MEDLINE每日更新、Ovid OLDMEDLINE(1946年1月至2015年10月)、EMBASE(1980年1月至2015年10月)、拉丁美洲和加勒比健康科学文献数据库(LILACS)(1982年1月至2015年10月)、国际标准随机对照试验编号注册库(ISRCTN registry)(www.isrctn.com/editAdvancedSearch)、美国国立医学图书馆临床试验数据库(ClinicalTrials.gov)(www.clinicaltrials.gov)以及世界卫生组织(WHO)国际临床试验注册平台(ICTRP)(www.who.int/ictrp/search/en)。在电子检索试验时,我们未设置任何日期或语言限制。我们最后一次检索电子数据库的时间为2015年10月23日。我们查阅了已识别的随机对照试验(RCT)的参考文献,以查找电子检索未识别的试验。我们联系了青光眼领域活跃的研究人员和从业者,以识别其他已发表和未发表的试验。

选择标准

我们纳入了比较基于穹窿部与基于角膜缘的小梁切除术治疗青光眼的益处和并发症的RCT,无论青光眼类型、发表状态和语言如何。我们排除了对18岁以下儿童的研究,因为该年龄组的伤口愈合情况不同,且术后滤过泡瘢痕形成率较高。

数据收集与分析

两位综述作者独立提取数据并评估试验质量。我们联系研究作者获取更多信息。主要结局是24个月时小梁切除术失败的比例。失败定义为尽管使用了额外的局部/全身药物,但仍需要重复手术或眼压未得到控制(超过22 mmHg)。仅在术后前六个月允许进行针刺和5-氟尿嘧啶(5-FU)注射;额外的针刺或5-FU注射被视为失败。还记录了术后12个月和24个月时的平均眼压。

主要结果

该综述纳入了六项试验,共361名参与者。两项研究在美国进行,德国、希腊、印度和沙特阿拉伯各进行了一项研究。四项试验的参与者患有开角型青光眼;一项研究纳入了原发性开角型或原发性闭角型青光眼的参与者,一项研究未明确青光眼类型。三项研究采用了联合手术(晶状体切除联合小梁切除术)。四项研究进行了丝裂霉素C(MMC)小梁切除术,仅有一项研究进行了5-氟尿嘧啶(5-FU)小梁切除术。纳入的试验均未报告24个月时小梁切除术失败的情况。仅有一项试验报告了小梁切除术作为晚期并发症的失败率。随机分配到基于角膜缘手术的参与者中失败率更高:穹窿部组50只眼中有1只小梁切除术失败,而角膜缘组50只眼中有3只失败(风险比(RR)0.33,95%置信区间(95%CI)0.04至3.10);因此,我们对两种手术方法对失败率的相对影响非常不确定。四项研究共252名参与者提供了12个月时平均眼压的测量值。在基于穹窿部的手术中,平均眼压范围为12.5至15.5 mmHg,基于角膜缘的手术也有类似结果,平均眼压范围为11.7至15.1 mmHg,无显著差异。随访12个月和24个月时的平均差值分别为0.44 mmHg(9�%CI -0.45至1.33)和0.86 mmHg(95%CI -0.52至2.24)。这两项汇总分析均未显示两组之间眼压有统计学显著差异(证据质量中等)。一项试验报告了随访24个月时抗青光眼药物的使用数量,手术组之间无差异。然而三项试验报告了随访12个月时抗青光眼药物的平均使用数量,两种手术技术术后降低眼压药物的平均使用数量无显著差异。随访12个月时的平均差值为0.02(95%CI -0.15至0.19)(证据质量高)。由于事件数量和总参与者数量较少,许多报告的不良事件风险不确定,那些被发现具有统计学显著性的事件可能是偶然因素导致的。对于偏倚风险评估:尽管所有六项试验均为随机分组,但选择偏倚大多不明确,六项研究中有四项随机序列生成不明确,六项研究中有五项分配隐藏不明确。仅在一项试验中遇到失访偏倚,该试验还存在报告偏倚。由于无法获取研究方案,所有其他试验的报告偏倚风险均不明确。由于结局未设盲,所有纳入的试验均被判定存在高检测偏倚风险。小梁切除术是一种相当标准的手术,不太可能因外科医生的“操作”而导致偏倚,因此未评估性能偏倚。

作者结论

本综述的主要结果是,由于事件数量少且置信区间包含无效值,基于穹窿部和基于角膜缘的小梁切除术之间的差异尚不确定。这也适用于术后并发症,但对两种手术技术的长期失败率没有任何影响。

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The effect of cataract extraction on intraocular pressure.白内障摘除术对眼压的影响。
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