Pradhan Eli, Duwal Sushma, Bajimaya Sanyam, Thapa Raba, Sharma Sanjita, Manandhar Anu
Tilganga Institute of Ophthalmology.
Nepal J Ophthalmol. 2018 Jan;10(19):107-110. doi: 10.3126/nepjoph.v10i1.21727.
There are many reports of endophthalmitis following Anti- VEG F use in developed countries and from India, but there are none from Nepal yet. Therefore, the aim of this study was to report the prevalence and management of acute endophthalmitis after intravitreal injection of bevacizumab.
This is a clinical, retrospective, non-comparative study, performed in Tilganga Institute of Ophthalmology, Kathmandu, Nepal from Jan 2015 till Dec 2016. All consecutive cases of intravitreal 1.25 mg of bevacizumab injections during the study period were collected from Bevacizumab registry of the operation theatre. A total number of endophthalmitis, following intravitreal bevacizumab injections were collected from Endophthalmitis registry. The statistical analysis was carried out by SPSS for percentage calculation and its 95% Confidence Interval (CI) calculation.
There were 4182 injections performed during the study period for various retinal conditions. Two eyes of two patients with acute postoperative endophthalmitis were identified in the first week following intravitreal injections of 1.25 mg bevacizumab among a total of 4128 injections with a prevalence of 0.048% (95% CI: 0.00 to 0.12.).
The prevalence of acute endophthalmitis following intravitreal Bevacizumab in our retrospective series was 0.048% and was comparable with the other studies conducted elsewhere. Acute post-injection endophthalmitis following intravitreal bevacizumab can result in severe loss of vision. Therefore prompt recognition and treatment are important part of its management in such patients.
在发达国家和印度有许多关于抗血管内皮生长因子(Anti-VEGF)使用后发生眼内炎的报道,但尼泊尔尚无此类报道。因此,本研究的目的是报告玻璃体内注射贝伐单抗后急性眼内炎的发生率及处理情况。
这是一项临床回顾性非对照研究,于2015年1月至2016年12月在尼泊尔加德满都的蒂尔冈加眼科研究所进行。研究期间所有连续接受1.25毫克玻璃体内贝伐单抗注射的病例均从手术室的贝伐单抗登记册中收集。玻璃体内注射贝伐单抗后发生眼内炎的所有病例均从眼内炎登记册中收集。采用SPSS进行统计分析,计算百分比及其95%置信区间(CI)。
在研究期间,因各种视网膜疾病共进行了4182次注射。在总共4128次1.25毫克玻璃体内注射贝伐单抗后,有2例患者的2只眼在术后第一周发生急性眼内炎,发生率为0.048%(95%CI:0.00至0.12)。
在我们的回顾性系列研究中,玻璃体内注射贝伐单抗后急性眼内炎的发生率为0.048%,与其他地方进行的其他研究结果相当。玻璃体内注射贝伐单抗后急性注射后眼内炎可导致严重视力丧失。因此,及时识别和治疗是此类患者管理的重要组成部分。