Associated Retinal Consultants, PC., Department of Ophthalmology, Oakland University William Beaumont School of Medicine, Royal Oak, MI.
Department of Ophthalmology, USC Roski Eye Institute, Keck School of Medicine, University of Southern California, Los Angeles, CA; and.
Retina. 2021 Jun 1;41(6):1242-1250. doi: 10.1097/IAE.0000000000002998.
To evaluate the clinical course of patients with neovascular age-related macular degeneration (nAMD) after developing endophthalmitis during their treatment with intravitreal injections.
Multicenter, retrospective series.
From April 2013 to October 2018, 196,598 intravitreal anti-vascular endothelial growth factor (VEGF) injections were performed, with 75 cases of endophthalmitis (incidence 0.0381%). There was no association between intravitreal anti-VEGF drug (P = 0.29), anesthetic method (P = 0.26), povidone concentration (P = 0.22), or any intraprocedure variable and endophthalmitis incidence. Seventy-two patients (96%) were treated with intravitreal tap and inject , while 3 underwent immediate pars plana vitrectomy. After endophthalmitis resolution, 17 patients (22.7%) were not re-treated for nAMD (in 10 cases due to inactive disease; follow-up, 115 ± 8.4 weeks). Patients required less frequent anti-VEGF injections after infection (7.4 ± 0.61 weeks vs. 11.5 ± 1.8 weeks; P = 0.004). Preinfection logarithm of the minimum angle of resolution visual acuity was 0.585 ± 0.053 (∼20/77). It worsened with endophthalmitis (1.67 ± 0.08, ∼20/935; P < 0.001) and again on postendophthalmitis treatment day 1 (1.94 ± 0.064; count fingers; P < 0.001), but improved after reinitiating nAMD therapy (1.02 ± 0.11; ∼20/209; P < 0.001). Better visual acuity on postendophthalmitis week 1 (P = 0.002) and reinitiation of nAMD treatment (P = 0.008) were associated with better final visual acuity, and streptococcal culture with worse visual acuity (P = 0.028). The postendophthalmitis treatment interval was associated with the anti-VEGF drug used (aflibercept = ranibizumab > bevacizumab; P < 0.001).
Patients with nAMD required fewer injections after endophthalmitis, suggesting a biological change in disease activity. Neovascular age-related macular degeneration became quiescent in 13.3% of eyes. Most achieved better outcomes with anti-VEGF reinitiation.
评估接受玻璃体内抗血管内皮生长因子(VEGF)注射治疗的年龄相关性黄斑变性(AMD)患者发生眼内炎后的临床病程。
多中心回顾性系列研究。
2013 年 4 月至 2018 年 10 月,共进行了 196598 例玻璃体内抗 VEGF 注射,发生眼内炎 75 例(发生率 0.0381%)。玻璃体内抗 VEGF 药物(P = 0.29)、麻醉方法(P = 0.26)、聚维酮浓度(P = 0.22)或任何术中变量与眼内炎发生率均无相关性。72 例(96%)患者接受了玻璃体内抽吸和注射治疗,3 例患者行立即玻璃体切除术。眼内炎消退后,17 例(22.7%)患者不再接受 nAMD 治疗(10 例因疾病静止;随访 115 ± 8.4 周)。感染后患者需要接受的抗 VEGF 注射次数减少(7.4 ± 0.61 周 vs. 11.5 ± 1.8 周;P = 0.004)。感染前最小分辨角视力对数(logMAR)为 0.585 ± 0.053(20/77)。眼内炎时视力恶化(1.67 ± 0.08,20/935;P < 0.001),眼内炎治疗后第 1 天再次恶化(1.94 ± 0.064;指数视力;P < 0.001),但再次开始 nAMD 治疗后视力改善(1.02 ± 0.11;~20/209;P < 0.001)。眼内炎后第 1 周视力较好(P = 0.002)和再次开始 nAMD 治疗(P = 0.008)与最终视力较好相关,而链球菌培养与视力较差相关(P = 0.028)。眼内炎后治疗间隔与所用抗 VEGF 药物有关(阿柏西普 = 雷珠单抗 > 贝伐单抗;P < 0.001)。
眼内炎后 nAMD 患者需要接受的注射次数减少,表明疾病活动度发生了生物学变化。13.3%的眼内 nAMD 静止。大多数患者通过重新使用抗 VEGF 治疗获得更好的结果。