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艾哈迈德青光眼引流阀植入术后新生血管性青光眼与非新生血管性难治性青光眼的前瞻性对照研究

A prospective comparative study on neovascular glaucoma and non-neovascular refractory glaucoma following Ahmed glaucoma valve implantation.

作者信息

Li Zheng, Zhou Minwen, Wang Wei, Huang Wenbin, Chen Shida, Li Xingyi, Gao Xinbo, Zhang Xiulan

机构信息

Department of Ophthalmology, 1st People's Hospital affiliated to Chenzhou City, Nanhua University, Chenzhou, Hunan 423000, China.

Zhongshan Ophthalmic Center, State Key Laboratory of Ophthalmology, Sun Yat-Sen University, Guangzhou, Guangdong 510060, China.

出版信息

Chin Med J (Engl). 2014;127(8):1417-22.

Abstract

BACKGROUND

Neovascular glaucoma is a refractory disease, and difficult to manage. The aim of this study was to evaluate the clinical outcomes of Ahmed glaucoma valve implantation (AGVI) in neovascular glaucoma (NVG) and non-NVG patients.

METHODS

This prospective, non-randomized study included 55 eyes of 55 patients with refractory glaucoma; 27 had NVG (NVG group) and 28 had non-NVG (non-NVG group). All of the patients underwent AGVI. The NVG group was adjunctively injected with intravitreal ranibizumab/bevacizumab (IVR/IVB) before AGVI. Intraocular pressure (IOP) was the primary outcome measure in this study. Surgical success rate, number of antiglaucoma medications used, best corrected visual acuity (BCVA), and postoperative complications were analyzed between the groups.

RESULTS

All of the patients completed the study (follow-up of 12 months). Kaplan-Meier survival curve analysis indicated that the qualified success rates in the NVG and non-NVG groups at 12 months were 70.5% and 92.9%, respectively; this difference was significant (P = 0.036). The complete success rates in the NVG and non-NVG groups at 12 months were 66.7% and 89.3%, respectively (P = 0.049). Compared with preoperative examinations, the postoperative mean IOP and use of medications were significantly lower at all follow-up time points in both groups (all P < 0.05). There were significant differences in BCVA between the two groups at the 12-month follow-up (χ(2) = 9.86, P = 0.020). Cox proportional hazards regression showed NVG as a risk factor for surgical failure (RR = 15.08, P = 0.033). Postoperative complications were similar between the two groups.

CONCLUSIONS

AGVI is a safe and effective procedure in refractory glaucoma, but the success rate of surgery was related to the type of refractory glaucoma. The complete and qualified success rates of NVG patient adjunctive anti-vascular endothelial growth factor treatment are still lower than those of non-NVG patients.

摘要

背景

新生血管性青光眼是一种难治性疾病,难以处理。本研究的目的是评估艾哈迈德青光眼引流阀植入术(AGVI)在新生血管性青光眼(NVG)和非NVG患者中的临床效果。

方法

这项前瞻性、非随机研究纳入了55例难治性青光眼患者的55只眼;其中27例为NVG(NVG组),28例为非NVG(非NVG组)。所有患者均接受了AGVI。NVG组在AGVI前辅助玻璃体腔内注射雷珠单抗/贝伐单抗(IVR/IVB)。眼压(IOP)是本研究的主要观察指标。分析了两组之间的手术成功率、抗青光眼药物使用数量、最佳矫正视力(BCVA)和术后并发症。

结果

所有患者均完成了研究(随访12个月)。Kaplan-Meier生存曲线分析表明,NVG组和非NVG组在12个月时的合格成功率分别为70.5%和92.9%;差异有统计学意义(P = 0.036)。NVG组和非NVG组在12个月时的完全成功率分别为66.7%和89.3%(P = 0.049)。与术前检查相比,两组在所有随访时间点的术后平均眼压和药物使用均显著降低(所有P < 0.05)。两组在12个月随访时的BCVA有显著差异(χ(2)=9.86, P = 0.020)。Cox比例风险回归显示NVG是手术失败的危险因素(RR = 15.08, P = 0.033)。两组术后并发症相似。

结论

AGVI在难治性青光眼中是一种安全有效的手术,但手术成功率与难治性青光眼的类型有关。NVG患者辅助抗血管内皮生长因子治疗的完全成功率和合格成功率仍低于非NVG患者。

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