Department of Ophthalmology, Dijon University Hospital, Dijon, France; The University of Sydney, Sydney Medical School, Discipline of Ophthalmology, Save Sight Institute, New South Wales, Australia.
The University of Sydney, Sydney Medical School, Discipline of Ophthalmology, Save Sight Institute, New South Wales, Australia.
Ophthalmol Retina. 2022 Nov;6(11):1044-1053. doi: 10.1016/j.oret.2022.05.008. Epub 2022 May 16.
To report the estimated incidence, probability, risk factors, and 1-year outcomes of rhegmatogenous retinal detachment (RRD) in eyes receiving intravitreal injections (IVTs) of VEGF inhibitors for various retinal conditions in routine clinical practice.
Retrospective analysis of data from a prospectively designed observational outcomes registry: the Fight Retinal Blindness!
Eyes of patients starting IVTs of VEGF inhibitors (ranibizumab, aflibercept, or bevacizumab) for neovascular age-related macular degeneration, diabetic macular edema, or retinal vein occlusion from January 1, 2006, to December 31, 2020. All eyes that developed RRD within 90 days of IVTs were defined as cases with RRD and were matched with control eyes.
Estimated incidence, probability, and hazard ratios (HRs) of RRD were measured using Poisson regression, Kaplan-Meier survival curve, and Cox proportional hazards models. Locally weighted scatterplot smoothing curves were used to compare visual acuity (VA) between cases and matched controls.
Estimated incidence of RRD.
We identified 16 915 eyes of 13 792 patients who collectively received 265 781 IVTs over 14 years. Thirty-six eyes were reported to develop RRD over the study period. The estimated incidence (95% confidence interval [CI]) per year per 1000 patients and per 10 000 injections was 0.77 (0.54-1.07) and 1.36 (0.95-1.89), respectively. The probability of RRD did not significantly increase at each successive injection (P = 0.95) with the time of follow-up. Older patients (HR [95% CI] = 1.81 [1.21-3.62] for every decade increase in age, P < 0.01) were at a higher risk of RRD, whereas patients with good presenting VA (HR [95% CI] = 0.85 [0.70-0.98] for every 10-letter increase in VA, P = 0.02) were at a lower risk. Neither the type of retinal disease (P = 0.52) nor the VEGF inhibitor (P = 0.09) was significantly associated with RRD risk. Cases with RRD lost 3 lines of vision on average compared with the prior RRD VA and had significantly fewer injections than matched controls over the year after the RRD.
Rhegmatogenous retinal detachment is a rare complication of VEGF inhibitor IVT in routine clinical practice with poor visual outcomes at 1 year.
报告在常规临床实践中,接受抗血管内皮生长因子(VEGF)抑制剂玻璃体内注射(IVT)治疗各种视网膜疾病的患者发生孔源性视网膜脱离(RRD)的估计发生率、概率、风险因素和 1 年结局。
对前瞻性设计的观察性结局登记处的数据进行回顾性分析:抗击视网膜盲!
2006 年 1 月 1 日至 2020 年 12 月 31 日,开始接受 IVT 抗 VEGF 抑制剂(雷珠单抗、阿柏西普或贝伐单抗)治疗新生血管性年龄相关性黄斑变性、糖尿病性黄斑水肿或视网膜静脉阻塞的患者的眼。所有在 IVT 后 90 天内发生 RRD 的眼均被定义为 RRD 病例,并与对照组相匹配。
使用泊松回归、Kaplan-Meier 生存曲线和 Cox 比例风险模型测量 RRD 的估计发生率、概率和风险比(HR)。局部加权散点平滑曲线用于比较病例和匹配对照组的视力(VA)。
RRD 的估计发生率。
我们共纳入了 13792 名患者的 16915 只眼,这些患者在 14 年期间共接受了 265781 次 IVT。研究期间报告了 36 只眼发生 RRD。估计的年发生率(95%置信区间[CI])为每 1000 例患者每年 0.77(0.54-1.07),每 10000 次注射为 1.36(0.95-1.89)。RRD 的发生概率并未随时间的推移而显著增加(P=0.95)。年龄每增加 10 岁(HR [95%CI]为 1.81 [1.21-3.62],P<0.01)的患者发生 RRD 的风险更高,而 VA (HR [95%CI]为 0.85 [0.70-0.98],每增加 10 个字母 VA,P<0.01)较好的患者风险较低。视网膜疾病的类型(P=0.52)和 VEGF 抑制剂(P=0.09)均与 RRD 风险无显著相关性。RRD 病例的平均视力丧失 3 行,与 RRD 之前的 VA 相比,在 RRD 后 1 年的视力结果较差。RRD 病例在 RRD 后一年的注射次数明显少于匹配对照组。
RRD 是抗 VEGF 抑制剂 IVT 在常规临床实践中的一种罕见并发症,1 年后视力预后较差。