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单日内玻璃体内注射污染贝伐单抗导致的急性细菌性眼内炎的处理和视力转归。

Management and Visual Outcomes of Acute Bacterial Endophthalmitis Following Intravitreal Injection of Contaminated Bevacizumab in a Single Day.

出版信息

Ophthalmic Surg Lasers Imaging Retina. 2020 Jun 1;51(6):346-352. doi: 10.3928/23258160-20200603-05.

Abstract

BACKGROUND AND OBJECTIVE

Bevacizumab requires compounding for off-label intravitreal injection, thus creating a risk of possible contamination during preparation.

PATIENTS AND METHODS

This retrospective, consecutive case series from a single site included patients who developed culture-proven acute endophthalmitis after intravitreal injection with contaminated bevacizumab. All patients suspected of endophthalmitis had vitreous biopsy and microbial cultures prior to initiation of treatment and were managed with immediate tap and injection of antibiotics followed early by pars plana vitrectomy. Main outcome measures included best-corrected visual acuity (BCVA) at 3-month follow-up after treatment.

RESULTS

Twenty-four patients developed acute bacterial endophthalmitis following intravitreal injection of contaminated bevacizumab single-dose syringes in a single day. Twenty-three cases (95.8%) grew Streptococcus species and one (4.2%) grew Enterococcus species. Six cases (25.0%) had optic nerve atrophy, three (12.5%) developed retinal detachment, one (4.2%) had vitreous hemorrhage, and one (4.2%) had band keratopathy. At 3-month follow-up, compared to BCVA at the time of initial presentation, 11 patients (45.8%) had improved vision, eight (33.3%) had unchanged BCVA, and five (20.8%) had worse BCVA. However, when compared to BCVA prior to endophthalmitis (baseline), 22 cases (91.7%) had significantly worse BCVA at 3-month follow-up.

CONCLUSIONS

Contamination of off-label bevacizumab poses devastating risk of endophthalmitis following intravitreal injection. Vigilance is needed to ensure all possible safeguards are in place to prevent contamination. [Ophthalmic Surg Lasers Imaging Retina. 2020;51:346-352.].

摘要

背景与目的

贝伐单抗需要进行非标签外的玻璃体腔内注射配制,因此在配制过程中存在潜在污染的风险。

患者与方法

本研究为单中心回顾性连续病例系列研究,纳入了接受污染的贝伐单抗玻璃体腔内注射后培养证实的急性眼内炎的患者。所有疑似眼内炎的患者在开始治疗前均进行了玻璃体活检和微生物培养,并采用立即进行玻璃体抽吸和抗生素注射,随后早期行玻璃体切割术进行治疗。主要观察指标包括治疗后 3 个月的最佳矫正视力(BCVA)。

结果

24 例患者在单日内接受污染的贝伐单抗单剂量注射器玻璃体腔内注射后发生急性细菌性眼内炎。23 例(95.8%)培养出链球菌属,1 例(4.2%)培养出肠球菌属。6 例(25.0%)发生视神经萎缩,3 例(12.5%)发生视网膜脱离,1 例(4.2%)发生玻璃体积血,1 例(4.2%)发生带状角膜病变。在 3 个月的随访时,与初始就诊时的 BCVA 相比,11 例(45.8%)视力改善,8 例(33.3%)BCVA 不变,5 例(20.8%)BCVA 更差。然而,与眼内炎发生前的 BCVA(基线)相比,22 例(91.7%)在 3 个月的随访时 BCVA 显著更差。

结论

非标签外贝伐单抗的污染会在玻璃体腔内注射后带来毁灭性的眼内炎风险。需要保持警惕,确保采取所有可能的预防措施来防止污染。

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