Comcali Sebile, Tasci Yelda Yildiz, Onen Mehmet, Gulhan Busra, Sahin Muzaffer, Cavdarli Cemal, Bilgic Omer Mustafa, Yorgun Mucella Arikan, Toklu Yasin, Alp Mehmet Numan, Yazar Zeliha
Department of Ophthalmology, Ankara Bilkent City Hospital, Ankara, Turkey.
Department of Ophthalmology, Ankara Bilkent City Hospital Ankara, Yildirim Beyazit University, Ankara, Turkey.
BMC Ophthalmol. 2025 May 7;25(1):278. doi: 10.1186/s12886-025-04093-w.
To investigate the incidence, contributing factors, management, and long-term outcomes of endophthalmitis following intravitreal injections performed in our clinic.
This retrospective study included all patients who received intravitreal bevacizumab, aflibercept, ranibizumab, or dexamethasone injections between 2019 and 2024 at four retina clinics of Ankara Bilkent City Hospital. Demographic characteristics of the patients, visual acuity, intravitreal injection etiology, comorbidities, and treatments applied were recorded. Patients who received antibiotic prophylaxis after intravitreal injections (IVI) were categorized as Group 1, while those who did not receive prophylaxis were classified as Group 2.
A total of 4171 patients and 21,339 intravitreal injections were evaluated. Of the participants, 47.2% were female and 52.8% were male, with a mean age of 66.3 ± 10.3 years (range: 40-98). Group 1 included 13,121 injections (61%), while Group 2 had 8,218 injections (39%). Endophthalmitis was observed in 13 patients (3.0 per 1000 patients-8.1 per 10,000 injections). Patients who developed endophthalmitis had an average of 6.1 ± 4.1 prior injections (range: 2-16), and the mean time to presentation after the last injection was 7.6 ± 3.4 days (range: 2-14). Endophthalmitis cases were distributed as 7 in Group 1 (5.3 per 10,000) and 6 in Group 2 (4.4 per 10,000). The endophthalmitis rate in Group 1 was not statistically significantly different from Group 2 (p > 0.05). All patients received vitreous taps and intravitreal vancomycin-ceftazidime injections at initial presentation. Eleven patients (85%) underwent a pars plana vitrectomy within 24 h. The mean follow-up period was 32 ± 20 months, and any case did not require evisceration surgery.
Early surgical intervention in cases of endophthalmitis is the most critical approach for preserving the eye and achieving visual rehabilitation. Notably, endophthalmitis was more common in people who got intravitreal bevacizumab or dexamethasone injections, and antibiotic prophylaxis did not appear to reduce the risk of its occurrence.
研究我院门诊玻璃体内注射后眼内炎的发生率、相关因素、治疗及长期预后。
这项回顾性研究纳入了2019年至2024年期间在安卡拉比尔肯特市医院的四家视网膜诊所接受玻璃体内注射贝伐单抗、阿柏西普、雷珠单抗或地塞米松的所有患者。记录患者的人口统计学特征、视力、玻璃体内注射病因、合并症及应用的治疗方法。玻璃体内注射(IVI)后接受抗生素预防的患者归为第1组,未接受预防的患者归为第2组。
共评估了4171例患者和21339次玻璃体内注射。参与者中,47.2%为女性,52.8%为男性,平均年龄为66.3±10.3岁(范围:40 - 98岁)。第1组包括13121次注射(61%),第2组有8218次注射(39%)。13例患者发生眼内炎(每1000例患者中有3.0例 - 每10000次注射中有8.1例)。发生眼内炎的患者之前平均注射6.1±4.1次(范围:2 - 16次),最后一次注射后出现症状的平均时间为7.6±3.4天(范围:2 - 14天)。眼内炎病例在第1组有7例(每10000例中有5.3例),第2组有6例(每10000例中有4.4例)。第1组的眼内炎发生率与第2组无统计学显著差异(p>0.05)。所有患者在初次就诊时均接受了玻璃体穿刺和玻璃体内注射万古霉素 - 头孢他啶。11例患者(85%)在24小时内接受了玻璃体切割术。平均随访期为32±20个月,无一例需要眼球摘除手术。
眼内炎病例的早期手术干预是保护眼睛和实现视力恢复的最关键方法。值得注意的是,眼内炎在接受玻璃体内注射贝伐单抗或地塞米松的人群中更为常见,抗生素预防似乎并未降低其发生风险。