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贝伐单抗(阿瓦斯汀)用于治疗前房新生血管化和新生血管性青光眼。

Bevacizumab (Avastin) for the management of anterior chamber neovascularization and neovascular glaucoma.

作者信息

Brouzas Dimitrios, Charakidas Antonios, Moschos Marilita, Koutsandrea Chryssanthi, Apostolopoulos Michael, Baltatzis Stefanos

机构信息

1st Department of Ophthalmology, University of Athens, Athens, Greece.

出版信息

Clin Ophthalmol. 2009;3:685-8. doi: 10.2147/opth.s7698. Epub 2009 Dec 29.

Abstract

PURPOSE

To establish the efficacy and safety of intravitreal bevacizumab in reducing iris and anterior chamber angle neovascularization and managing neovascular glaucoma.

DESIGN

Prospective interventional case series.

PATIENT AND METHODS

Eleven eyes of 11 patients with iris and anterior chamber angle neovascularization with refractory intraocular pressure were treated with intravitreal injection of 1.25 mg bevacizumab (Avastin((R))). The study group included eight males and three females aged 23 to 77 years (average, 62 years). Out of the 11 cases, five had proliferative diabetic retinopathy, of whom two had undergone vitrectomy for tractional retinal detachment and vitreous hemorrhage, and six were secondary to ischemic central retinal vein occlusion (CRVO). All patients were followed for eight to 16 months (average, 10 months).

RESULTS

Iris and anterior chamber angle neovascularization receded in all eyes after one to three injections at monthly intervals. In five eyes, neovascularization recurred during the follow-up period. The intraocular pressure normalized in one eye. Four eyes were controlled with anti-glaucoma drops. A cyclodestructive procedure was required in two eyes. An Ahmet drainage valve was implanted in four eyes, including one controlled with additional antiglaucoma drops and one in which the intraocular pressure remained high while on maximum antiglaucoma medication and a cyclodestructive procedure was scheduled.

CONCLUSIONS

Bevacizumab appears to be effective in reducing iris and anterior chamber angle neovascularization and is likely to extend our therapeutic options in the management of neovascular glaucoma.

摘要

目的

确定玻璃体内注射贝伐单抗在减少虹膜和前房角新生血管形成以及治疗新生血管性青光眼方面的疗效和安全性。

设计

前瞻性干预病例系列。

患者与方法

对11例患有虹膜和前房角新生血管形成且眼压难治的患者的11只眼进行玻璃体内注射1.25mg贝伐单抗(阿瓦斯汀(R))治疗。研究组包括8名男性和3名女性,年龄23至77岁(平均62岁)。11例中,5例患有增殖性糖尿病视网膜病变,其中2例因牵引性视网膜脱离和玻璃体积血接受了玻璃体切除术,6例继发于缺血性中央视网膜静脉阻塞(CRVO)。所有患者均随访8至16个月(平均10个月)。

结果

所有眼睛在每月间隔注射1至3次后,虹膜和前房角新生血管消退。5只眼在随访期间新生血管复发。1只眼眼压恢复正常。4只眼用抗青光眼滴眼液控制。2只眼需要进行睫状体破坏手术。4只眼植入了阿赫梅特引流阀,其中1只眼用额外的抗青光眼滴眼液控制,1只眼在使用最大剂量抗青光眼药物且计划进行睫状体破坏手术时眼压仍高。

结论

贝伐单抗似乎在减少虹膜和前房角新生血管形成方面有效,并且可能会扩展我们在新生血管性青光眼治疗中的选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e04/2801638/5cfa83475afd/opth-3-685f1.jpg

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