Gonzalez-Gonzalez Luis A, Knickelbein Jared E, Doft Bernard H, Balasubramani G K, Wisniewski Stephen
University of Pittsburgh Medical Center, Pittsburgh, PA, USA.
Retina Vitreous Consultants, 300 Oxford Drive, Suite 300, Pittsburgh, PA, USA.
Int Ophthalmol. 2023 Mar;43(3):867-876. doi: 10.1007/s10792-022-02489-x. Epub 2022 Sep 14.
To describe the incidence and factors predicting visual outcome in patients with infectious endophthalmitis following intravitreal anti-VEGF injection.
Retrospective, single-site, cohort study. Patients with acute endophthalmitis within 6 weeks of intravitreal anti-VEGF injection who were referred to our practice after inciting injection or were injected by us between January 2010 and July 2017 were included. All patients received intravitreal antibiotics with either vitreous/anterior chamber tap (TAP) or pars plana vitrectomy. Visual outcomes pre/post treatment, baseline variables (age, gender, ocular disease) and cultures results were studied.
Seventy eyes of 69 patients were included. Presenting VA was the strongest factor associated with final visual outcome after adjusting for other variables including culture status and baseline VA (p = .0002). Cultures were positive in 62.8% of eyes and were associated with worse visual outcome (p = .0087). Growth of Streptococcus or microorganisms other than coagulase negative Staphylococci (CNS) was also associated with worse prognosis, regardless of baseline and presenting VA (p = .0002). The crude incidence of post-injection endophthalmitis was 0.028% in our practice (40 eyes in 143,628 injections) during the study time. No significant difference was found between pre-filled bevacizumab versus ranibizumab or aflibercept drawn from a vial.
In a large, single center, retrospective study, the incidence of acute endophthalmitis post anti-VEGF injection was relatively low. Worse visual acuity at presentation of endophthalmitis and growth of Streptococcus or organisms other than CNS were associated with the worst visual outcomes.
描述玻璃体内注射抗血管内皮生长因子(VEGF)后感染性眼内炎患者的发生率及预测视力预后的因素。
回顾性、单中心队列研究。纳入在2010年1月至2017年7月期间,因玻璃体内抗VEGF注射后6周内发生急性眼内炎而前来就诊或由我们进行注射的患者。所有患者均接受玻璃体内抗生素治疗,同时进行玻璃体/前房穿刺(TAP)或玻璃体切割术。研究治疗前后的视力预后、基线变量(年龄、性别、眼部疾病)及培养结果。
纳入69例患者的70只眼。在校正包括培养结果和基线视力等其他变量后,初始视力是与最终视力预后相关的最强因素(p = 0.0002)。62.8%的眼培养结果为阳性,且与较差的视力预后相关(p = 0.0087)。无论基线和初始视力如何,链球菌或凝固酶阴性葡萄球菌(CNS)以外的微生物生长也与较差的预后相关(p = 0.0002)。在研究期间,我们机构注射后眼内炎的粗发病率为0.028%(143,628次注射中有40只眼)。预充式贝伐单抗与从药瓶中抽取的雷珠单抗或阿柏西普之间未发现显著差异。
在一项大型单中心回顾性研究中,抗VEGF注射后急性眼内炎的发生率相对较低。眼内炎发病时较差的视力以及链球菌或CNS以外的微生物生长与最差的视力预后相关。