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抗血管内皮生长因子眼内注射治疗后持续性眼内压升高的临床预测因子。

Clinical predictors of sustained intraocular pressure elevation due to intravitreal anti-vascular endothelial growth factor therapy.

机构信息

Vitreous Retina Macula Consultants of New York, New York 10022, USA.

出版信息

Retina. 2013 Jan;33(1):179-87. doi: 10.1097/IAE.0b013e318261a6f7.

Abstract

PURPOSE

We assess for frequency and predictive factors related to sustained intraocular pressure (IOP) elevation in eyes with neovascular age-related macular degeneration receiving intravitreal injections of ranibizumab and/or bevacizumab.

METHODS

A total of 328 patients with neovascular age-related macular degeneration (449 eyes) who presented to a single physician over a 6-month period were retrospectively assessed for baseline demographic/clinical information, total number of bevacizumab and/or ranibizumab injections, and sustained IOP elevation on 2 or more consecutive visits (absolute IOP >25 mmHg, increase above baseline >10 mmHg, or IOP of >21 mmHg and increase of >5 mmHg). Cox regression survival analysis and multivariate logistic regression were performed to assess the influence of intravitreal injections on experiencing sustained IOP elevation.

RESULTS

Overall, 32 eyes (7.1%) experienced sustained IOP elevation. Survival analysis showed a significant effect of the number of anti-vascular endothelial growth factor injections on sustained IOP elevation (hazard ratio, 1.085; 95% confidence interval: 1.06-1.11, P < 0.001). Also, there was an increased odds ratio (16.1, P = 0.008) of sustained IOP elevation in eyes receiving ≥29 injections compared with ≤12 injections. After controlling for the confounder (prior intravitreal steroid injection), total number of injections still showed a statistically significant association (P = 0.002).

CONCLUSION

A greater number of intravitreal anti-vascular endothelial growth factor injections is associated with an increased risk for sustained IOP elevation in eyes with neovascular age-related macular degeneration receiving intravitreal ranbizumab and/or bevacizumab.

摘要

目的

评估接受玻璃体内雷珠单抗和/或贝伐单抗注射的新生血管性年龄相关性黄斑变性患者眼内持续性眼压升高的频率和相关预测因素。

方法

回顾性评估了在 6 个月内由一名医生就诊的 328 名新生血管性年龄相关性黄斑变性(449 只眼)患者的基线人口统计学/临床资料、贝伐单抗和/或雷珠单抗注射总数以及 2 次或以上连续就诊时的持续性眼压升高(绝对眼压>25mmHg,较基线升高>10mmHg,或眼压>21mmHg,升高>5mmHg)。采用 Cox 回归生存分析和多变量逻辑回归评估玻璃体内注射对持续性眼压升高的影响。

结果

总体而言,32 只眼(7.1%)发生持续性眼压升高。生存分析显示,抗血管内皮生长因子注射次数对持续性眼压升高有显著影响(风险比,1.085;95%置信区间:1.06-1.11,P<0.001)。此外,与接受≤12 次注射的眼相比,接受≥29 次注射的眼发生持续性眼压升高的优势比(16.1,P=0.008)增加。在控制混杂因素(先前玻璃体内类固醇注射)后,注射总数仍显示出统计学上的显著相关性(P=0.002)。

结论

在接受玻璃体内雷珠单抗和/或贝伐单抗治疗的新生血管性年龄相关性黄斑变性患者中,玻璃体内抗血管内皮生长因子注射次数越多,持续性眼压升高的风险越高。

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