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辅助性类固醇疗法与单纯抗生素疗法治疗眼内手术后急性眼内炎的对比

Adjunctive steroid therapy versus antibiotics alone for acute endophthalmitis after intraocular procedure.

作者信息

Kim Carole H, Chen Monica F, Coleman Anne L

机构信息

Stein Eye Institute, UCLA, 100 Stein Plaza, Los Angeles, California, USA, 90095.

出版信息

Cochrane Database Syst Rev. 2017 Feb 22;2(2):CD012131. doi: 10.1002/14651858.CD012131.pub2.

Abstract

BACKGROUND

Endophthalmitis refers to severe infection within the eye that involves the aqueous humor or vitreous humor, or both, and threatens vision. Most cases of endophthalmitis are exogenous (i.e. due to inoculation of organisms from an outside source), and most exogenous endophthalmitis is acute and occurs after an intraocular procedure. The mainstay of treatment is emergent administration of broad-spectrum intravitreous antibiotics. Due to their anti-inflammatory effects, steroids in conjunction with antibiotics have been proposed to be beneficial in endophthalmitis management.

OBJECTIVES

To assess the effects of antibiotics combined with steroids versus antibiotics alone for the treatment of acute endophthalmitis following intraocular surgery or intravitreous injection.

SEARCH METHODS

We searched the Cochrane Central Register of Controlled Trials (CENTRAL) (which contains the Cochrane Eyes and Vision Trials Register) (2016, Issue 11), MEDLINE Ovid (1946 to 8 December 2016), Embase Ovid (1980 to 8 December 2016), LILACS (Latin American and Caribbean Health Sciences Literature Database) (1982 to 8 December 2016), the ISRCTN registry (www.isrctn.com/editAdvancedSearch); searched 8 December 2016, ClinicalTrials.gov (www.clinicaltrials.gov); searched 8 December 2016, and the WHO International Clinical Trials Registry Platform (ICTRP) (www.who.int/ictrp/search/en); searched 8 December 2016. We did not use any date or language restrictions in the electronic searches for trials.

SELECTION CRITERIA

We included randomized controlled trials comparing the effectiveness of adjunctive steroids with antibiotics alone in the management of acute, clinically diagnosed endophthalmitis following intraocular surgery or intravitreous injection. We excluded trials with participants with endogenous endophthalmitis unless outcomes were reported by source of infection. We imposed no restrictions on the method or order of administration, dose, frequency, or duration of antibiotics and steroids.

DATA COLLECTION AND ANALYSIS

Two review authors independently screened the search results, assessed risk of bias, and extracted data using methods expected by Cochrane. We contacted study authors to try to obtain missing information or information to clarify risk of bias. We conducted a meta-analysis for any outcomes that were reported by at least two studies. Outcomes reported from single studies were summarized in the text. We assessed the certainty of the evidence using GRADE.

MAIN RESULTS

We included three trials with a total of 95 randomized participants in this review and identified one ongoing trial. The studies were conducted in South Africa, India, and the Netherlands. Out of the 92 analyzed participants, 91 participants were diagnosed with endophthalmitis following cataract surgery. In the remaining participant, endophthalmitis was attributable to penetrating keratoplasty. All studies used intravitreous dexamethasone for adjunctive steroid therapy and a combination of two intravitreous antibiotics that provided gram-positive and gram-negative coverage for the antibiotic therapy. We judged one trial to be at overall low risk of bias and two studies to be at overall unclear risk of bias due to lack of reporting of study methods. None of the three trials had been registered in a clinical trial register.While none of the included studies reported the primary outcome of complete resolution of endophthalmitis as defined in our protocol, one study reported combined anatomical and functional success (i.e. proportion of participants with intraocular pressure of at least 5 mmHg and visual acuity of at least 6/120). Very low-certainty evidence suggested no difference in combined success when comparing adjunctive steroid antibiotics alone (risk ratio (RR) 1.08, 95% confidence interval (CI) 0.80 to 1.45; 32 participants). Low-certainty evidence from two studies showed that a higher proportion of participants who received adjunctive dexamethasone had a good visual outcome (Snellen visual acuity 6/6 to 6/18) at three months compared with those in the antibiotics-alone group (RR 1.95, 95% CI 1.05 to 3.60; 60 participants). Similarly, low-certainty evidence from one study suggested that more participants in the dexamethasone group had a good visual outcome at 12 months compared to those who did not receive dexamethasone (RR 2.00, 95% CI 0.98 to 4.08; 28 participants). Investigators of one study reported improvement in visual acuity, but we could not estimate the effect of adjunctive steroid therapy because the study investigators did not provide standard deviations or standard errors. Two studies reported adverse events (retinal detachment, hypotony, proliferative vitreoretinopathy, and seclusion of pupil). The total numbers of adverse events were 8 out of 30 (26.7%) for those who received dexamethasone versus 6 out of 30 (20.0%) for those who did not. We could only perform a pooled analysis for the occurrence of retinal detachment; any difference between the two treatment groups was uncertain (RR 1.57, 95% CI 0.50 to 4.90; 60 participants) (very low-certainty evidence). No study reported intraocular pressure or cost outcomes.

AUTHORS' CONCLUSIONS: Current evidence on the effectiveness of adjunctive steroid therapy versus antibiotics alone in the management of acute endophthalmitis after intraocular surgery is inadequate. We found no studies that had enrolled cases of acute endophthalmitis following intravitreous injection. A combined analysis of two studies suggests adjunctive steroids may provide a higher probability of having a good visual outcome at three months than not using adjunctive steroids. However, considering that most of the confidence intervals crossed the null and that this review was limited in scope and applicability to clinical practice, it is not possible to conclude whether the use adjunctive steroids is effective at this time. Any future trials should examine whether adjunctive steroids may be useful in certain clinical settings such as type of causative organism or etiology. These studies should include outcomes that take patient's symptoms and clinical examination into account, report outcomes in a uniform and consistent manner, and follow up at short- and long-term intervals.

摘要

背景

眼内炎是指眼内发生的严重感染,累及房水或玻璃体,或两者均受累,并威胁视力。大多数眼内炎病例为外源性(即由于外界病原体接种所致),且大多数外源性眼内炎为急性,发生于眼内手术后。主要治疗方法是紧急玻璃体内注射广谱抗生素。由于具有抗炎作用,有人提出将类固醇与抗生素联合使用对眼内炎的治疗有益。

目的

评估抗生素联合类固醇与单纯使用抗生素治疗眼内手术或玻璃体内注射后急性眼内炎的效果。

检索方法

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11期)、MEDLINE Ovid(1946年至2016年12月8日)、Embase Ovid(1980年至2016年12月8日)、LILACS(拉丁美洲和加勒比健康科学文献数据库)(1982年至2016年12月8日)、ISRCTN注册库(www.isrctn.com/editAdvancedSearch);于2016年12月8日检索;检索ClinicalTrials.gov(www.clinicaltrials.gov);于2016年12月8日检索;检索世界卫生组织国际临床试验注册平台(ICTRP)(www.who.int/ictrp/search/en);于2016年12月8日检索。在电子检索试验时,我们未使用任何日期或语言限制。

入选标准

我们纳入了比较辅助类固醇与单纯抗生素治疗眼内手术或玻璃体内注射后急性临床诊断眼内炎有效性的随机对照试验。除非按感染源报告结果,否则我们排除了患有内源性眼内炎参与者的试验。我们对抗生素和类固醇的给药方法、顺序、剂量、频率或持续时间未作限制。

数据收集与分析

两位综述作者独立筛选检索结果、评估偏倚风险并使用Cochrane期望的方法提取数据。我们联系研究作者以获取缺失信息或澄清偏倚风险的信息。对于至少两项研究报告的任何结局,我们进行了荟萃分析。单篇研究报告的结局在正文中进行了总结。我们使用GRADE评估证据的确定性。

主要结果

本综述纳入了三项试验,共95名随机参与者,并确定了一项正在进行的试验。这些研究在南非、印度和荷兰进行。在92名分析参与者中,91名参与者在白内障手术后被诊断为眼内炎。在其余参与者中,眼内炎归因于穿透性角膜移植术。所有研究均使用玻璃体内地塞米松进行辅助类固醇治疗,并使用两种玻璃体内抗生素联合治疗,这些抗生素对革兰氏阳性菌和革兰氏阴性菌均有覆盖。由于缺乏研究方法报告,我们判断一项试验总体偏倚风险较低,两项研究总体偏倚风险不明确。三项试验均未在临床试验注册库中注册。虽然纳入的研究均未报告我们方案中定义的眼内炎完全消退的主要结局,但一项研究报告了解剖和功能联合成功(即眼压至少为5 mmHg且视力至少为6/120的参与者比例)。极低确定性证据表明,比较辅助类固醇与单纯抗生素时,联合成功率无差异(风险比(RR)1.08,95%置信区间(CI)0.80至1.45;32名参与者)。两项研究的低确定性证据表明,与单纯抗生素组相比,接受辅助地塞米松治疗的参与者在三个月时视力良好(Snellen视力6/6至6/18)的比例更高(RR 1.95,95% CI 1.05至3.60;60名参与者)。同样,一项研究的低确定性证据表明,与未接受地塞米松治疗的参与者相比,地塞米松组在12个月时视力良好的参与者更多(RR 2.00,95% CI 0.98至4.08;28名参与者)。一项研究的研究者报告了视力改善情况,但由于研究研究者未提供标准差或标准误,我们无法估计辅助类固醇治疗的效果。两项研究报告了不良事件(视网膜脱离、低眼压、增生性玻璃体视网膜病变和瞳孔闭锁)。接受地塞米松治疗的参与者中,不良事件总数为30例中的8例(26.7%),未接受地塞米松治疗的参与者中为30例中的6例(20.0%)。我们只能对视网膜脱离的发生情况进行汇总分析;两个治疗组之间的任何差异均不确定(RR 1.57,95% CI 0.50至4.90;60名参与者)(极低确定性证据)。没有研究报告眼压或成本结局。

作者结论

目前关于辅助类固醇治疗与单纯抗生素治疗眼内手术后急性眼内炎有效性的证据不足。我们未发现纳入玻璃体内注射后急性眼内炎病例的研究。两项研究的综合分析表明,辅助类固醇可能比不使用辅助类固醇在三个月时获得良好视力结局的概率更高。然而,考虑到大多数置信区间跨越无效值,且本综述在范围和对临床实践的适用性方面存在局限性,目前无法得出辅助类固醇使用是否有效的结论。未来的任何试验都应研究辅助类固醇在某些临床环境中(如致病微生物类型或病因)是否有用。这些研究应包括考虑患者症状和临床检查的结局,以统一和一致的方式报告结局,并进行短期和长期随访。

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