Juthani Viral V, Clearfield Elizabeth, Chuck Roy S
Department of Ophthalmology and Visual Sciences, Albert Einstein College of Medicine, Montefiore Medical Center, New York, New York, USA.
Cochrane Database Syst Rev. 2017 Jul 3;7(7):CD010516. doi: 10.1002/14651858.CD010516.pub2.
Cataract is a leading cause of blindness worldwide. Cataract surgery is commonly performed but can result in postoperative inflammation of the eye. Inadequately controlled inflammation increases the risk of complications. Non-steroidal anti-inflammatory drugs (NSAIDs) and corticosteroids are used to prevent and reduce inflammation following cataract surgery, but these two drug classes work by different mechanisms. Corticosteroids are effective, but NSAIDs may provide an additional benefit to reduce inflammation when given in combination with corticosteroids. A comparison of NSAIDs to corticosteroids alone or combination therapy with these two anti-inflammatory agents will help to determine the role of NSAIDs in controlling inflammation after routine cataract surgery.
To evaluate the comparative effectiveness of topical NSAIDs (alone or in combination with topical corticosteroids) versus topical corticosteroids alone in controlling intraocular inflammation after uncomplicated phacoemulsification. To assess postoperative best-corrected visual acuity (BCVA), patient-reported discomfort, symptoms, or complications (such as elevation of IOP), and cost-effectiveness with the use of postoperative NSAIDs or corticosteroids.
To identify studies relevant to this review, we searched the Cochrane Central Register of Controlled Trials (CENTRAL), which contains the Cochrane Eyes and Vision Trials Register (2016, Issue 12), MEDLINE Ovid (1946 to December 2016), Embase Ovid (1947 to 16 December 2016), PubMed (1948 to December 2016), LILACS (Latin American and Caribbean Health Sciences Literature Database) (1982 to 16 December 2016), the metaRegister of Controlled Trials (mRCT) (www.controlled-trials.com; last searched 17 June 2013), ClinicalTrials.gov (www.clinicaltrials.gov; searched December 2016), and the WHO International Clinical Trials Registry Platform (ICTRP) (www.who.int/ictrp/search/en; searched December 2016).
We included randomized controlled trials (RCTs) in which participants were undergoing phacoemulsification for uncomplicated cataract extraction. We included both trials in which topical NSAIDs were compared with topical corticosteroids and trials in which combination therapy (topical NSAIDs and corticosteroids) was compared with topical corticosteroids alone. The primary outcomes for this review were inflammation and best-corrected visual acuity (BCVA).
Two review authors independently screened the full-text articles, extracted data from included trials, and assessed included trials for risk of bias according to Cochrane standards. The two review authors resolved any disagreements by discussion. We graded the certainty of the evidence using GRADE.
This review included 48 RCTs conducted in 17 different countries and two ongoing studies. Ten included studies had a trial registry record. Fifteen studies compared an NSAID with a corticosteroid alone, and 19 studies compared a combination of an NSAID plus a corticosteroid with a corticosteroid alone. Fourteen other studies had more than two study arms. Overall, we judged the studies to be at unclear risk of bias. NSAIDs alone versus corticosteroids aloneNone of the included studies reported postoperative intraocular inflammation in terms of cells and flare as a dichotomous variable. Inflammation was reported as a continuous variable in seven studies. There was moderate-certainty evidence of no difference in mean cell value in the participants receiving an NSAID compared with the participants receiving a corticosteroid (mean difference (MD) -0.60, 95% confidence interval (CI) -2.19 to 0.99), and there was low-certainty evidence that the mean flare value was lower in the group receiving NSAIDs (MD -13.74, 95% CI -21.45 to -6.04). Only one study reported on corneal edema at one week postoperatively and there was uncertainty as to whether the risk of edema was higher or lower in the group that received NSAIDs (risk ratio (RR) 0.77, 95% CI 0.26 to 2.29). No included studies reported BCVA as a dichotomous outcome and no study reported time to cessation of treatment. None of the included studies reported the proportion of eyes with cystoid macular edema (CME) at one week postoperatively. Based on four RCTs that reported CME at one month, we found low-certainty evidence that participants treated with an NSAID alone had a lower risk of developing CME compared with those treated with a corticosteroid alone (RR 0.26, 95% CI 0.17 to 0.41). No studies reported on other adverse events or economic outcomes. NSAIDs plus corticosteroids versus corticosteroids aloneNo study described intraocular inflammation in terms of cells and flare as a dichotomous variable and there was not enough continuous data for anterior chamber cell and flare to perform a meta-analysis. One study reported presence of corneal edema at various times. Postoperative treatment with neither a combination treatment with a NSAID plus corticosteroid or with corticosteroid alone was favored (RR 1.07, 95% CI 0.98 to 1.16). We judged this study to have high risk of reporting bias, and the certainty of the evidence was downgraded to moderate. No included study reported the proportion of participants with BCVA better than 20/40 at one week postoperatively or reported time to cessation of treatment. Only one included study reported on the presence of CME at one week after surgery and one study reported on CME at two weeks after surgery. After combining findings from these two studies, we estimated with low-certainty evidence that there was a lower risk of CME in the group that received NSAIDs plus corticosteroids (RR 0.17, 95% CI 0.03 to 0.97). Seven RCTs reported the proportion of participants with CME at one month postoperatively; however there was low-certainty evidence of a lower risk of CME in participants receiving an NSAID plus a corticosteroid compared with those receiving a corticosteroid alone (RR 0.50, 95% CI 0.23 to 1.06). The few adverse events reported were due to phacoemulsification rather than the eye drops.
AUTHORS' CONCLUSIONS: We found insufficient evidence from this review to inform practice for treatment of postoperative inflammation after uncomplicated phacoemulsification. Based on the RCTs included in this review, we could not conclude the equivalence or superiority of NSAIDs with or without corticosteroids versus corticosteroids alone. There may be some risk reduction of CME in the NSAID-alone group and the combination of NSAID plus corticosteroid group. Future RCTs on these interventions should standardize the type of medication used, dosing, and treatment regimen; data should be collected and presented using the Standardization of Uveitis Nomenclature (SUN) outcome measures so that dichotomous outcomes can be analyzed.
白内障是全球失明的主要原因。白内障手术是常见的手术,但可能导致术后眼部炎症。炎症控制不佳会增加并发症风险。非甾体类抗炎药(NSAIDs)和皮质类固醇用于预防和减轻白内障手术后的炎症,但这两类药物的作用机制不同。皮质类固醇有效,但NSAIDs与皮质类固醇联合使用时可能在减轻炎症方面提供额外益处。比较NSAIDs与单独使用皮质类固醇或这两种抗炎药联合治疗,将有助于确定NSAIDs在常规白内障手术后控制炎症中的作用。
评估局部使用NSAIDs(单独或与局部皮质类固醇联合使用)与单独使用局部皮质类固醇在单纯性超声乳化术后控制眼内炎症方面的相对有效性。评估使用术后NSAIDs或皮质类固醇后的最佳矫正视力(BCVA)、患者报告的不适、症状或并发症(如眼压升高)以及成本效益。
为识别与本综述相关的研究,我们检索了Cochrane对照试验中心注册库(CENTRAL),其中包含Cochrane眼科和视力试验注册库(2016年第12期)、MEDLINE Ovid(1946年至2016年12月)、Embase Ovid(1947年至2016年12月16日)、PubMed(1948年至2016年12月)、拉丁美洲和加勒比健康科学文献数据库(LILACS)(1982年至2016年12月16日)、对照试验元注册库(mRCT)(www.controlled-trials.com;最后检索时间为2013年6月17日)、ClinicalTrials.gov(www.clinicaltrials.gov;2016年12月检索)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;2016年12月检索)。
我们纳入了随机对照试验(RCTs),其中参与者正在接受单纯性白内障摘除的超声乳化手术。我们纳入了将局部NSAIDs与局部皮质类固醇进行比较的试验,以及将联合治疗(局部NSAIDs和皮质类固醇)与单独使用局部皮质类固醇进行比较的试验。本综述的主要结局是炎症和最佳矫正视力(BCVA)。
两位综述作者独立筛选全文文章,从纳入的试验中提取数据,并根据Cochrane标准评估纳入试验的偏倚风险。两位综述作者通过讨论解决任何分歧。我们使用GRADE对证据的确定性进行分级。
本综述纳入了在17个不同国家进行的48项RCTs以及两项正在进行的研究。十项纳入研究有试验注册记录。十五项研究将一种NSAID与单独的皮质类固醇进行比较,十九项研究将NSAID加皮质类固醇的联合治疗与单独的皮质类固醇进行比较。其他十四项研究有两个以上研究组。总体而言,我们判断这些研究的偏倚风险不明确。单独使用NSAIDs与单独使用皮质类固醇:没有纳入的研究将术后眼内炎症的细胞和闪光作为二分变量进行报告。七项研究将炎症作为连续变量进行报告。有中等确定性证据表明,接受NSAID的参与者与接受皮质类固醇的参与者相比,平均细胞值无差异(平均差(MD)-0.60,95%置信区间(CI)-2.19至0.99),并且有低确定性证据表明接受NSAIDs组的平均闪光值较低(MD -13.74,95%CI -21.45至-6.04)。只有一项研究报告了术后一周的角膜水肿情况,接受NSAIDs组的水肿风险是更高还是更低尚不确定(风险比(RR)0.77,95%CI 0.26至2.29)。没有纳入的研究将BCVA作为二分结局进行报告,也没有研究报告治疗停止时间。没有纳入的研究报告术后一周有黄斑囊样水肿(CME)的眼的比例。基于四项在术后一个月报告CME的RCTs,我们发现低确定性证据表明,单独使用NSAID治疗的参与者与单独使用皮质类固醇治疗的参与者相比,发生CME的风险较低(RR 0.26,95%CI 0.17至0.41)。没有研究报告其他不良事件或经济结局。NSAIDs加皮质类固醇与单独使用皮质类固醇:没有研究将眼内炎症的细胞和闪光作为二分变量进行描述,并且没有足够的前房细胞和闪光的连续数据进行荟萃分析。一项研究报告了不同时间的角膜水肿情况。术后使用NSAID加皮质类固醇联合治疗或单独使用皮质类固醇治疗均无优势(RR 1.07,95%CI