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白内障手术后眼内炎的治疗模式是否遵循眼内炎玻璃体切除术研究建议?:一项美国眼科学会眼内炎症反应研究(IRIS)注册分析。

Do Treatment Patterns for Endophthalmitis after Cataract Surgery Follow the Endophthalmitis Vitrectomy Study Recommendations?: An Academy IRIS® Registry Analysis.

机构信息

Vickie and Jack Farber Vision Research Center at Wills Eye, Wills Eye Hospital, Philadelphia, Pennsylvania.

Mid Atlantic Retina, Wills Eye Hospital, Philadelphia, Pennsylvania; Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania.

出版信息

Ophthalmol Retina. 2024 Nov;8(11):1035-1043. doi: 10.1016/j.oret.2024.07.014. Epub 2024 Jul 22.

Abstract

OBJECTIVE

To evaluate whether treatment patterns for endophthalmitis after cataract surgery in American Academy of Ophthalmology IRIS® (Intelligent Research in Sight) Registry patients are in line with evidence-based guidelines established by the 1995 Endophthalmitis Vitrectomy Study (EVS), which showed that patients who present with light perception (LP) vision have better visual outcomes with immediate vitrectomy (VIT) compared with vitreous tap with antibiotic injection (TAP).

DESIGN

Retrospective cohort study.

SUBJECTS

Intelligent Research in Sight Registry patients undergoing cataract surgery between 2014 and 2022 (identified by Current Procedural Terminology codes), presenting with endophthalmitis (identified by International Classification of Diseases 10 codes) within 42 days postcataract surgery, and having a record of being treated with VIT or TAP on the same or 1 day after endophthalmitis diagnosis were identified.

METHODS

Potential covariates of age, sex, race, ethnicity, geographic region, insurance status, and visual acuity on the day of endophthalmitis diagnosis were evaluated using multivariable logistic regression.

MAIN OUTCOME MEASURES

Treatment with VIT or TAP.

RESULTS

Of the 2425 patients who met the inclusion criteria, 14% (345) underwent VIT and 86% (2080) underwent TAP. Notably, 80% of patients (1946) presented with endophthalmitis within 14 days from cataract surgery (median = 6 days). Notably, 66% (173/263) of the patients presenting with LP vision underwent TAP instead of VIT. In a multivariable logistic regression model, receiving VIT instead of TAP was positively associated with poor vision at endophthalmitis presentation (LP - odds ratio [OR] = 5.4; confidence interval [CI], 2.9-10.6; counting fingers, hand motions - OR = 1.9; CI, 1.1-3.6) versus (20/20-20/40) vision; Asian versus White race (OR = 2.6; CI, 1.3-5.2); Hispanic versus non-Hispanic ethnicity (OR = 1.9; CI, 1.1-3.2); living in the West (OR = 1.6; CI, 1.1-2.2) and Midwest (OR = 1.5; CI, 1.1-2.0) (vs. South), but not with age, sex, and insurance coverage (P > 0.05).

CONCLUSIONS

In the IRIS Registry, treatment patterns for postcataract surgery endophthalmitis did not match evidence-based recommendations of the EVS, a randomized controlled clinical trial. More work is needed to evaluate whether the current treatment patterns are optimal for patients with postcataract surgery endophthalmitis.

FINANCIAL DISCLOSURE(S): Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.

摘要

目的

评估美国眼科学会(ARVO)IRIS®(智能眼研究)注册患者白内障手术后眼内炎的治疗模式是否符合 1995 年眼内炎玻璃体切除术研究(EVS)制定的循证指南,该研究表明,与玻璃体抽吸联合抗生素注射(TAP)相比,视力为光感(LP)的患者行立即玻璃体切除术(VIT)可获得更好的视力结局。

设计

回顾性队列研究。

受试者

在 2014 年至 2022 年间(通过当前程序术语代码确定)接受白内障手术且在白内障手术后 42 天内发生眼内炎(通过国际疾病分类第 10 版代码确定)并在眼内炎诊断后同一天或第 1 天接受 VIT 或 TAP 治疗的 ARVO 注册患者。

方法

使用多变量逻辑回归评估年龄、性别、种族、民族、地理位置、保险状况和眼内炎诊断当天视力等潜在混杂因素。

主要结局指标

VIT 或 TAP 治疗。

结果

在符合纳入标准的 2425 名患者中,14%(345 名)接受了 VIT,86%(2080 名)接受了 TAP。值得注意的是,80%(1946 名)的患者在白内障手术后 14 天内(中位数=6 天)发生眼内炎。值得注意的是,66%(173/263)视力为 LP 的患者接受了 TAP 而不是 VIT。在多变量逻辑回归模型中,与视力较差(LP-比值比[OR] = 5.4;95%置信区间[CI],2.9-10.6;指数 finger-OR = 1.9;CI,1.1-3.6)相比,接受 VIT 而不是 TAP 与较差的视力呈正相关(20/20-20/40);亚洲人种与白人种族(OR = 2.6;CI,1.3-5.2);西班牙裔与非西班牙裔(OR = 1.9;CI,1.1-3.2);居住在西部(OR = 1.6;CI,1.1-2.2)和中西部(OR = 1.5;CI,1.1-2.0)(与南部相比);但与年龄、性别和保险范围无关(P>0.05)。

结论

在 IRIS 登记处,白内障手术后眼内炎的治疗模式不符合 EVS 的循证建议,即一项随机对照临床试验。需要进一步研究评估当前的治疗模式是否最适合白内障手术后眼内炎患者。

金融披露

本文末尾的脚注和披露中可能存在专有或商业披露。

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