Department of Ophthalmology, Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, Florida 33136, USA.
Am J Ophthalmol. 2012 Feb;153(2):204-208.e1. doi: 10.1016/j.ajo.2011.11.035.
To report a series of patients with Streptococcus endophthalmitis after injection with intravitreal bevacizumab prepared by the same compounding pharmacy.
Noncomparative consecutive case series.
Medical records and microbiology results of patients who presented with endophthalmitis after injection with intravitreal bevacizumab between July 5 and July 8, 2011, were reviewed.
Twelve patients were identified with endophthalmitis, presenting 1 to 6 days after receiving an intravitreal injection of bevacizumab. The injections occurred at 4 different locations in south Florida. All patients received bevacizumab prepared by the same compounding pharmacy. None of the infections originated at the Bascom Palmer Eye Institute, Miami, Florida, although 9 patients presented to its tertiary-care ophthalmic emergency room for treatment, and 3 additional patients were seen in consultation. All patients were treated initially with a vitreous tap and injection; 8 patients subsequently received a vitrectomy. Microbiology cultures for 10 patients were positive for Streptococcus mitis/oralis. Seven unused syringes of bevacizumab prepared by the compounding pharmacy at the same time as those prepared for the affected patients also were positive for S. mitis/oralis. After 4 months of follow-up, all but 1 patient had count fingers or worse visual acuity, and 3 required evisceration or enucleation. Local, state, and federal health department officials have been investigating the source of the contamination.
In this outbreak of endophthalmitis after intravitreal bevacizumab injection, Streptococcus mitis/oralis was cultured from the majority of patients and from all unused syringes. Visual outcomes were generally poor. The most likely cause of this outbreak was contamination during syringe preparation by the compounding pharmacy.
报告一系列在同一家药房配制的玻璃体腔内注射用贝伐单抗注射后发生眼内炎的患者。
非对照连续病例系列。
回顾了 2011 年 7 月 5 日至 7 月 8 日期间因注射玻璃体腔内贝伐单抗而发生眼内炎的患者的病历和微生物学结果。
共发现 12 例眼内炎患者,在接受贝伐单抗玻璃体腔内注射后 1 至 6 天出现症状。这些注射发生在佛罗里达州南部的 4 个不同地点。所有患者均接受同一家药房配制的贝伐单抗治疗。尽管 9 例患者在佛罗里达州迈阿密的 Bascom Palmer 眼科研究所的三级眼科急诊室接受治疗,另外 3 例患者在会诊时接受了治疗,但没有一例感染源自该研究所。所有患者最初均接受玻璃体抽取和注射治疗;8 例患者随后接受玻璃体切除术。10 例患者的微生物培养结果均为缓症链球菌/变异链球菌阳性。同时为受影响患者配制的贝伐单抗,以及同批配制的 7 个未使用的注射器,也均为缓症链球菌/变异链球菌阳性。在 4 个月的随访中,除 1 例患者外,其余患者均出现指数视力或更差的视力,3 例患者需要眼球摘除或眼内容剜除。地方、州和联邦卫生部门官员一直在调查污染的源头。
在这次玻璃体腔内注射贝伐单抗后发生的眼内炎爆发中,缓症链球菌/变异链球菌从大多数患者和所有未使用的注射器中培养出来。视力结果普遍较差。此次爆发最有可能的原因是来自药房在注射器准备过程中的污染。