Velez-Montoya Raul, Sanchez-Santos Idaira, Galvan-Chavez Mauricio, Wu Lihteh, Arevalo J Fernando, Berrocal María H, Alezzandrini Arturo A, Figueroa Marta S, Gallego-Pinazo Roberto, Dolz-Marco Rosa, Martinez-Rubio Clara, Gonzalez-Salinas Roberto
Retina Department, Asociación para Evitar le Ceguera en México IAP, México City 04030, Mexico.
Asociados de Macula, Vitreo y Retina de Costa Rica, San Jose City 10102, Costa Rica.
J Ophthalmol. 2021 Oct 11;2021:5591865. doi: 10.1155/2021/5591865. eCollection 2021.
To assess the risk for capsular rupture during routine phacoemulsification in patients with a history of anti-VEGF injections and other possible risk modifiers such as treatment patterns, type of anti-VEGF agent, and experience of the surgeon, among others.
This study reviewed the medical records of 11,129 patients from 7 different hospitals in 5 countries. The study included 939 patients that underwent routine phacoemulsification and had a history of anti-VEGF therapy. We excluded patients with known risk factors for capsular rupture, as well as patients with a history of other retinal procedures. The study extracted data regarding general demographics, the number of previous injections, type of anti-VEGF agent, details of cataract surgery, and anti-VEGF treatment patterns.
Overall prevalence of posterior capsular rupture: 7.45% (95% CI: 5.9-9.32%). The mean number of injections per patient was 3.37 ± 2.8. More than 50% of the patients received their last anti-VEGF injection within three months before cataract surgery. The complication rate during intravitreal injections was 1.07%. In the univariate analysis, the experience of the cataract surgeon (inexperience surgeons; OR: 2.93) and the history of prior anti-VEGF therapy (OR: 1.77) were significant risk indicators for PCR ( < 0.05). However, after controlling for age in the multivariate analysis, the trend did not reach a statistical significance.
The risk for capsular rupture is higher in patients with a history of intravitreal anti-VEGF injections.
评估有抗血管内皮生长因子(VEGF)注射史的患者在常规超声乳化白内障吸除术中发生囊膜破裂的风险,以及其他可能的风险因素,如治疗模式、抗VEGF药物类型和手术医生的经验等。
本研究回顾了来自5个国家7家不同医院的11129例患者的病历。该研究纳入了939例行常规超声乳化白内障吸除术且有抗VEGF治疗史的患者。我们排除了已知有囊膜破裂风险因素的患者以及有其他视网膜手术史的患者。该研究提取了有关一般人口统计学、既往注射次数、抗VEGF药物类型、白内障手术细节和抗VEGF治疗模式的数据。
后囊膜破裂的总体发生率为7.45%(95%可信区间:5.9 - 9.32%)。每位患者的平均注射次数为3.37±2.8次。超过50%的患者在白内障手术前三个月内接受了最后一次抗VEGF注射。玻璃体内注射的并发症发生率为1.07%。在单因素分析中,白内障手术医生的经验(经验不足的医生;比值比:2.93)和既往抗VEGF治疗史(比值比:1.77)是后囊膜破裂的显著风险指标(P<0.05)。然而,在多因素分析中控制年龄后,该趋势未达到统计学显著性。
有玻璃体内抗VEGF注射史的患者发生囊膜破裂的风险更高。