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玻璃体内注射贝伐单抗和雷珠单抗后持续性眼内高压。

Persistent ocular hypertension following intravitreal bevacizumab and ranibizumab injections.

机构信息

Department of Ophthalmology and Visual Science, Yale University School of Medicine, New Haven, Connecticut 06510, USA.

出版信息

J Ocul Pharmacol Ther. 2010 Feb;26(1):105-10. doi: 10.1089/jop.2009.0076.

Abstract

PURPOSE

To study ocular hypertension (OHT) following intravitreal injections of bevacizumab and/or ranibizumab in patients with age-related macular degeneration (AMD).

METHODS

Retrospective case series. Patients with AMD who were treated at a tertiary referral center with intravitreal bevacizumab and/or ranibizumab injections from January 1, 2006 to December 31, 2008 were studied. The development of OHT following these injections was investigated.

RESULTS

Four out of 116 patients with AMD (3.45%) developed sustained elevated intraocular pressure (IOP) after multiple intravitreal injections of bevacizumab 1.5 mg/0.06 mL and/or ranibizumab 0.5 mg/0.05 mL. An analysis of 4 cases revealed: None of the patients had a previous diagnosis or family history of glaucoma/OHT. Two patients had both bevacizumab and ranibizumab injections. Two patients developed OHT after recent intravitreal ranibizumab and 2 patients after recent intravitreal bevacizumab injection. Two patients were pseudophakic with a history of YAG capsulotomy. The range of preinjection IOP was 8-15 mmHg (mean, 13 mmHg). The range of postinjection IOP was 28-36 mmHg (mean, 31.75 mmHg). The range of IOP increase was 17-21 mmHg (mean, 18.75 mmHg). Mean number of pan-anti-VEGF injections prior to OHT was 13.3 (range, 3-19). A disrupted posterior capsule might predispose patients to the development of OHT.

CONCLUSIONS

Persistent OHT may occur after intravitreal anti-VEGF injection in patients with no previous diagnosis of glaucoma or OHT. OHT may persist across several visits and patients may require IOP-lowering therapy. Sustained elevation in IOP usually occurs after multiple injections.

摘要

目的

研究与年龄相关的黄斑变性(AMD)患者玻璃体腔内注射贝伐单抗和/或雷珠单抗后发生的眼压升高(OHT)。

方法

回顾性病例系列研究。对 2006 年 1 月 1 日至 2008 年 12 月 31 日在一家三级转诊中心接受玻璃体腔内贝伐单抗和/或雷珠单抗注射治疗的 AMD 患者进行了研究。研究了这些注射后 OHT 的发展情况。

结果

在 116 例接受 AMD 治疗的患者中,有 4 例(3.45%)在接受多次玻璃体腔内注射 1.5mg/0.06mL 贝伐单抗和/或 0.5mg/0.05mL 雷珠单抗后出现持续的眼压升高。对 4 例患者的分析表明:无青光眼/OHT 的既往诊断或家族史。2 例患者同时接受贝伐单抗和雷珠单抗注射。2 例患者在最近接受玻璃体腔内雷珠单抗注射后出现 OHT,2 例患者在最近接受玻璃体腔内贝伐单抗注射后出现 OHT。2 例患者为白内障术后患者,有 YAG 后囊切开术史。注射前眼压范围为 8-15mmHg(平均 13mmHg)。注射后眼压范围为 28-36mmHg(平均 31.75mmHg)。眼压升高范围为 17-21mmHg(平均 18.75mmHg)。发生 OHT 前接受全抗-VEGF 注射的平均次数为 13.3 次(范围 3-19 次)。后囊破裂可能使患者易发生 OHT。

结论

无青光眼或 OHT 既往诊断的患者玻璃体腔内注射抗 VEGF 药物后可能会发生持续性 OHT。OHT 可能会持续数诊,并可能需要降低眼压治疗。眼压升高通常发生在多次注射后。

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