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玻璃体内注射后眼内炎:发病率、表现、管理及视力预后

Endophthalmitis After Intravitreal Injections: Incidence, Presentation, Management, and Visual Outcome.

作者信息

Dossarps Denis, Bron Alain M, Koehrer Philippe, Aho-Glélé Ludwig S, Creuzot-Garcher Catherine

机构信息

Department of Ophthalmology, Burgundy University, Dijon, France.

Department of Ophthalmology, Burgundy University, Dijon, France; Eye and Nutrition Research Group, CSGA, UMR 1324 INRA, 6265 CNRS, Burgundy University, Dijon, France.

出版信息

Am J Ophthalmol. 2015 Jul;160(1):17-25.e1. doi: 10.1016/j.ajo.2015.04.013. Epub 2015 Apr 16.

Abstract

PURPOSE

To report the incidence and characteristics of endophthalmitis after intravitreal injections of anti-vascular endothelial growth factor agents or corticosteroids and to describe the clinical and bacteriologic characteristics, management, and outcome of these eyes with acute endophthalmitis in France.

DESIGN

Retrospective, nationwide multicenter case series.

METHODS

From January 2, 2008 to June 30, 2013, a total of 316,576 intravitreal injections from 25 French ophthalmic centers were included. For each center, the number of intravitreal injections was determined using billing codes and the injection protocol was recorded. A registry and hospital records were reviewed to identify patients treated for endophthalmitis after injection during the same time period. The main outcome measures were the incidence of clinical endophthalmitis and visual acuity of endophthalmitis cases.

RESULTS

During the study period, 65 cases of presumed endophthalmitis were found, giving an overall incidence of 0.021% (2.1 in 10,000 injections) (95% confidence interval [CI], 0.016%-0.026%). The median number of days from injection to presentation was 4 [1-26] days. The most common symptom was vision loss. Bacterial identification was achieved in 43.4%. The most frequent pathogens were gram-positive bacteria (91.3%), including coagulase-negative Staphylococcus in 78.3%. Neither the interval between injection and presentation for endophthalmitis nor the clinical signs differentiated culture-positive from culture-negative cases. In multivariate analysis, the use of a disposable conjunctival mould assist device and the use of prophylaxis with an antibiotic or antiseptic were significantly associated with an increased incidence of endophthalmitis (P = .001). The majority of patients had worse visual acuity after 3 months of follow-up when compared with acuity before endophthalmitis.

CONCLUSIONS

The incidence of presumed endophthalmitis after intravitreal injections of anti-vascular endothelial growth factors or corticosteroids was low and the prognosis poor. Prevention and management remain challenging. It remains to be determined whether the findings of this study are relevant for other countries using different techniques for intravitreal injections.

摘要

目的

报告玻璃体内注射抗血管内皮生长因子药物或皮质类固醇后眼内炎的发生率及特征,并描述法国这些急性眼内炎患者的临床和细菌学特征、治疗及预后。

设计

回顾性全国多中心病例系列研究。

方法

纳入2008年1月2日至2013年6月30日期间法国25个眼科中心共316,576次玻璃体内注射。对每个中心,使用计费代码确定玻璃体内注射次数,并记录注射方案。查阅登记册和医院记录,以确定同期注射后接受眼内炎治疗的患者。主要观察指标为临床眼内炎的发生率及眼内炎病例的视力。

结果

研究期间,共发现65例疑似眼内炎病例,总体发生率为0.021%(每10,000次注射中有2.1例)(95%置信区间[CI],0.016% - 0.026%)。从注射到出现症状的中位天数为4[1 - 26]天。最常见的症状是视力下降。43.4%的病例实现了细菌鉴定。最常见的病原体是革兰氏阳性菌(91.3%),其中凝固酶阴性葡萄球菌占78.3%。眼内炎注射与出现症状的间隔时间及临床体征均无法区分培养阳性与培养阴性病例。多因素分析显示,使用一次性结膜模具辅助装置以及使用抗生素或防腐剂预防与眼内炎发生率增加显著相关(P = .001)。与眼内炎发作前的视力相比,大多数患者在随访3个月后的视力更差。

结论

玻璃体内注射抗血管内皮生长因子或皮质类固醇后疑似眼内炎的发生率较低,但预后较差。预防和治疗仍然具有挑战性。本研究结果是否适用于采用不同玻璃体内注射技术的其他国家仍有待确定。

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