Augenklinik Innenstadt, Ludwig-Maximilians-Universität, München, Germany.
Ophthalmologica. 2011;226(2):51-6. doi: 10.1159/000327364. Epub 2011 May 5.
To assess the duration of the effect of intracameral bevacizumab in patients presenting with rubeosis iridis and neovascular glaucoma (NVG).
Retrospective analysis of 24 consecutive eyes of 24 patients with decompensated NVG (> 21 mm Hg) treated with a single intracameral injection of bevacizumab over a minimum follow-up of 6 months. The endpoint of the study was the need for retreatment due to recurrence of raised intraocular pressure (IOP). Secondary outcome was the course of visual acuity (VA) and IOP over 6 months.
A Kaplan-Meier calculation revealed a mean duration of the treatment effect of 23 ± 4.4 days. Compared to mean IOP before treatment (26.3 mm Hg), decreases to 17.5 mm Hg at 1 week after treatment (p < 0.002) and to 17.1 mm Hg (p < 0.005) at 6 months following a single injection were seen. At 6 months, additional treatment was performed in 87.5% (n = 21) of eyes. VA remained stable or improved in 75% (n = 18) of all cases.
The IOP-lowering effect of intracameral bevacizumab can be seen 1 week after the injection, but is limited to a period of approximately 3 weeks. However, the fast and effective response to intracameral bevacizumab injection opens a time window for additional treatments, which are often necessary.
评估玻璃体内注射贝伐单抗治疗虹膜新生血管和新生血管性青光眼(NVG)患者后虹膜红变的持续时间。
对 24 例(24 只眼)NVG 失代偿(眼压>21mmHg)患者进行回顾性分析,这些患者均接受了单次玻璃体内注射贝伐单抗治疗,随访时间至少为 6 个月。本研究的终点是因眼压升高而需要再次治疗的情况。次要结局是 6 个月内视力(VA)和眼压的变化。
Kaplan-Meier 计算显示,治疗效果的平均持续时间为 23±4.4 天。与治疗前平均眼压(26.3mmHg)相比,治疗后 1 周眼压下降至 17.5mmHg(p<0.002),6 个月后下降至 17.1mmHg(p<0.005)。6 个月时,87.5%(n=21)的眼需要进一步治疗。75%(n=18)的所有病例的 VA 保持稳定或改善。
玻璃体内注射贝伐单抗后 1 周即可观察到眼压降低,但效果仅持续约 3 周。然而,玻璃体内注射贝伐单抗可迅速有效地缓解眼压,为进一步治疗提供了时间窗口,而进一步治疗通常是必要的。