Department of Ophthalmology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Retina. 2012 Jul;32(7):1295-301. doi: 10.1097/IAE.0b013e31823f0c95.
The purpose of this study was to report the rate of intraocular pressure (IOP) elevation after intravitreal injections of anti-vascular endothelial growth factor agents for exudative age-related macular degeneration.
Retrospective chart review of all patients receiving intravitreal ranibizumab and/or bevacizumab injections for exudative age-related macular degeneration from November 2005 to June 2010. Delayed ocular hypertension (OHT) was defined as either an IOP ≥22 mmHg on 2 consecutive visits (with an increase from baseline >6 mmHg) or an IOP >26 mmHg on a single visit with a concomitant initiation or augmentation of IOP-lowering treatment. Noninjected fellow eyes served as controls. Incidence of delayed OHT was analyzed using survival analyses, with risk assessed by Cox proportional hazards regression models. Eyes with glaucoma were evaluated separately.
Three hundred and two treated eyes and 226 control eyes met inclusion criteria. In eyes with exudative age-related macular degeneration without glaucoma, 3 of 270 injected eyes (0.51% incidence per eye-year) developed delayed OHT compared with 4 of 195 control eyes (1.00% incidence per eye-year), a difference that was not statistically significant (hazard ratio = 0.48; 95% confidence interval: 0.11-2.23). In eyes with exudative age-related macular degeneration and glaucoma, 2 of 32 injected eyes developed delayed OHT (3.1% incidence per eye-year) compared with 3 of 31 control eyes (5.7% incidence per eye-year), a difference that was not statistically significant (hazard ratio = 0.59; 95% confidence interval: 0.10-3.60).
The incidence of delayed OHT after intravitreal anti-vascular endothelial growth factor injections was low and did not differ between injected and control eyes, including eyes with glaucoma. These results argue against a significant risk of IOP elevation because of repeated anti-vascular endothelial growth factor therapy.
本研究旨在报告接受抗血管内皮生长因子药物玻璃体内注射治疗渗出性年龄相关性黄斑变性患者的眼压升高发生率。
回顾性分析 2005 年 11 月至 2010 年 6 月期间接受玻璃体内雷珠单抗和/或贝伐单抗注射治疗渗出性年龄相关性黄斑变性的所有患者的病历。延迟性高眼压(OHT)定义为连续两次就诊时眼压≥22mmHg(与基线相比升高>6mmHg)或单次就诊时眼压>26mmHg,同时开始或增加降眼压治疗。未注射的对侧眼作为对照。采用生存分析评估延迟性 OHT 的发生率,并采用 Cox 比例风险回归模型评估风险。单独评估青光眼眼。
302 只治疗眼和 226 只对照眼符合纳入标准。在无青光眼的渗出性年龄相关性黄斑变性眼中,270 只注射眼中有 3 只(每眼年 0.51%的发生率)发生延迟性 OHT,而 195 只对照眼中有 4 只(每眼年 1.00%的发生率),差异无统计学意义(风险比=0.48;95%置信区间:0.11-2.23)。在有渗出性年龄相关性黄斑变性和青光眼的眼中,32 只注射眼中有 2 只(每眼年 3.1%的发生率)发生延迟性 OHT,而 31 只对照眼中有 3 只(每眼年 5.7%的发生率),差异无统计学意义(风险比=0.59;95%置信区间:0.10-3.60)。
玻璃体内抗血管内皮生长因子注射后延迟性 OHT 的发生率较低,且在注射眼和对照眼中无差异,包括青光眼眼。这些结果表明,由于重复抗血管内皮生长因子治疗,眼压升高的风险并不显著。