Department of Ophthalmology, Istanbul Bilim University, Istanbul, Turkey.
Eye (Lond). 2009 Dec;23(12):2187-93. doi: 10.1038/eye.2009.7.
The aim of this study was to report the incidence and management of acute endophthalmitis after intravitreal injection of Avastin (bevacizumab), and visual acuity outcomes of three eyes of three patients who developed acute endophthalmitis following intravitreal injection of Avastin.
This clinical retrospective, non-comparative study included 3022 intravitreal injections of 1.25 mg bevacizumab consecutively performed for 1822 eyes with exudative age-related macular degeneration and other retinal diseases. Of 3022 injections, 1200 were reinjections. After clinical appearance of post-injection endophthalmitis, immediate intervention was performed, including injection of intravitreal antibiotics and early pars plana vitrectomy.
Three eyes of three patients with acute postoperative endophthalmitis were identified in the first week following intravitreal injections of 1.25 mg bevacizumab. Among of these patients, two cases were culture-positive and one case was culture-negative. Compared with presenting visual acuities, all of three patients improved at the end of follow-up time. The overall incidence rate of post-injection culture-proven endophthalmitis was 0.066%.
Acute culture-proven endophthalmitis is still a potential complication of intravitreal bevacizumab injection (approximately 0.066%) despite using maximal sterile techniques. Acute post-injection endophthalmitis following intravitreal bevacizumab occurs rapidly and can result in severe loss of vision. Prompt recognition and treatment are key in maximizing outcomes in patients who developed endophthalmitis after intravitreal injection of bevacizumab.
本研究旨在报告玻璃体腔注射阿瓦斯汀(贝伐单抗)后发生急性眼内炎的发生率和处理方法,并报告三例玻璃体腔注射阿瓦斯汀后发生急性眼内炎患者的三只眼的视力结果。
本临床回顾性、非对照研究纳入了 1822 只眼 3022 例连续进行的 1.25mg 贝伐单抗玻璃体腔注射,这些眼患有渗出性年龄相关性黄斑变性和其他视网膜疾病。3022 例注射中有 1200 例为再注射。在出现注射后眼内炎的临床症状后,立即进行干预,包括玻璃体腔内注射抗生素和早期玻璃体切割术。
在玻璃体腔注射 1.25mg 贝伐单抗后第一周,发现三例患者的三只眼发生急性术后眼内炎。在这些患者中,两例为培养阳性,一例为培养阴性。与就诊时视力相比,所有患者在随访结束时视力均有所提高。注射后培养证实的眼内炎总发生率为 0.066%。
尽管采用了最大无菌技术,但急性培养证实的眼内炎仍是玻璃体腔注射贝伐单抗的潜在并发症(约 0.066%)。玻璃体腔注射贝伐单抗后发生的急性注射后眼内炎发病迅速,可导致严重视力丧失。及时识别和治疗是最大限度提高接受贝伐单抗玻璃体腔注射后发生眼内炎患者治疗效果的关键。