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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的临床疗效及房水中血管内皮生长因子水平的变化:回顾性两剂量比较研究。

Clinical outcomes and changes in aqueous vascular endothelial growth factor levels after intravitreal bevacizumab for iris neovascularization and neovascular glaucoma: a retrospective two-dose comparative study.

机构信息

Department of Ophthalmology, Osaka University Graduate School of Medicine, Suita, Japan.

出版信息

J Ocul Pharmacol Ther. 2012 Feb;28(1):41-8. doi: 10.1089/jop.2011.0059. Epub 2011 Oct 12.

DOI:10.1089/jop.2011.0059
PMID:21992534
Abstract

PURPOSE

To evaluate the clinical outcomes and biologic effects on the aqueous humor concentrations of vascular endothelial growth factor (VEGF) in patients with neovascular glaucoma (NVG) treated with intravitreal bevacizumab (IVB).

METHODS

Twenty-nine consecutive patients (35 eyes) treated with 1.0- or 0.1-mg injections of IVB for NVG between January and December 2009 were enrolled in this retrospective, interventional pilot study. The visual prognosis and changes in intraocular pressure (IOP) were followed for >6 months after the initial injection. Aqueous humor samples were obtained at the initial IVB injection from all study eyes and 1 week after the first injection in eyes undergoing a second intervention to measure the VEGF concentration.

RESULTS

The VEGF concentrations in the 35 eyes significantly correlated (r=0.535, P<0.001) with the pretreatment IOP. The mean reductions of the VEGF levels 1 week after IVB did not differ significantly between the 1.0- and 0.1-mg groups (P=0.738). Despite more repeated injections in the 0.1-mg group and additional medical or surgical interventions in both groups, both dosages inhibited the neovascular activity. The ability to control the IOP after IVB did not differ significantly between groups at 1 week (P=0.625) and 6 months (P>0.99). Visual improvements also did not differ significantly between groups during the 6-month follow-up (P=0.437).

CONCLUSIONS

Aqueous humor levels of VEGF were significantly correlated with the IOP. Low-dose (0.1 mg) IVB was as effective as the currently used higher dose (1.0 mg) for treating NVG within at least 6 months after the initial injection.

摘要

目的

评估玻璃体内注射贝伐单抗(IVB)治疗新生血管性青光眼(NVG)患者的临床疗效和对房水中血管内皮生长因子(VEGF)浓度的影响。

方法

本回顾性、干预性初步研究共纳入 2009 年 1 月至 12 月期间接受 1.0 或 0.1mg IVB 治疗的 29 例(35 只眼)NVG 连续患者。初始注射后,超过 6 个月随访视力预后和眼压(IOP)变化。所有研究眼在初次 IVB 注射时以及行第二次介入治疗的眼在第一次注射后 1 周时采集房水样本,以测量 VEGF 浓度。

结果

35 只眼中的 VEGF 浓度与预处理IOP 显著相关(r=0.535,P<0.001)。IVB 后 1 周时,1.0mg 和 0.1mg 组的 VEGF 水平降低幅度无显著差异(P=0.738)。尽管 0.1mg 组重复注射次数更多,两组均接受了额外的药物或手术干预,但两种剂量均抑制了新生血管活性。IVB 后 1 周(P=0.625)和 6 个月(P>0.99)时,两组的眼压控制能力无显著差异。6 个月随访期间,两组的视力改善也无显著差异(P=0.437)。

结论

房水中 VEGF 水平与IOP 显著相关。在初始注射后至少 6 个月内,低剂量(0.1mg)IVB 与目前使用的高剂量(1.0mg)一样有效治疗 NVG。

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