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青光眼引流装置植入联合玻璃体内注射贝伐单抗治疗新生血管性青光眼:3年经验

Glaucoma drainage device implantation with adjunctive intravitreal bevacizumab in neovascular glaucoma: 3-year experience.

作者信息

Noor Nina Asrini, Mustafa Syukri, Artini Widya

机构信息

Ophthalmology Department.

Glaucoma Division, Ophthalmology Department, Cipto Mangunkusumo General Hospital, Jakarta, Indonesia.

出版信息

Clin Ophthalmol. 2017 Aug 7;11:1417-1422. doi: 10.2147/OPTH.S137470. eCollection 2017.

Abstract

PURPOSE

To evaluate the outcome of glaucoma drainage device (GDD) implantation with and without intravitreal bevacizumab (IVB) injection in treating neovascular glaucoma (NVG) at Cipto Mangunkusumo Hospital Jakarta, Indonesia.

PATIENTS AND METHODS

This retrospective study involved 39 eyes with NVG which underwent GDD implantation between 2012 and 2014. Thirty eyes underwent GDD implantation alone (control group) while 9 eyes underwent GDD implantation and IVB injection (IVB group). Visual acuity (VA), intraocular pressure (IOP), number of antiglaucoma medications, and success rate were compared between groups.

RESULTS

There were no significant differences in preoperative characteristics. On the last visit, VA was 2.6 (0.2-4.0) logMAR in the control group and 2.3 (0.4-4.0) logMAR in the IVB group (=0.97). In the control group, final VA was significantly worse compared to initial VA (<0.01), while in IVB group VA was apparently stable (=0.24). Final IOP was 16.3±10.3 mmHg in the control group and 12.0 (2.0-49.0) mmHg in IVB group (=0.40). The number of antiglaucoma medications was similar between groups (=0.57). Surgical success rate in the IVB group (66.7%) was better than the control group (56.7%), but this difference was not statistically significant (=0.71). Kaplan-Meier survival analysis showed the probability of success 37 months after surgery as 53.6% in the IVB group and 31.6% in the control group. No significant difference was found between the groups (=0.45).

CONCLUSION

In cases of NVG, GDD combined with IVB could maintain VA compared to GDD alone. However, there were no significant differences in final IOP, number of antiglaucoma medications, and surgical success rate.

摘要

目的

在印度尼西亚雅加达的西托·曼古库苏莫医院评估青光眼引流装置(GDD)植入联合或不联合玻璃体内注射贝伐单抗(IVB)治疗新生血管性青光眼(NVG)的效果。

患者与方法

这项回顾性研究纳入了2012年至2014年间接受GDD植入的39例NVG患者的眼睛。30只眼睛仅接受了GDD植入(对照组),而9只眼睛接受了GDD植入及IVB注射(IVB组)。比较两组之间的视力(VA)、眼压(IOP)、抗青光眼药物数量及成功率。

结果

术前特征无显著差异。在最后一次随访时,对照组的VA为2.6(0.2 - 4.0)logMAR,IVB组为2.3(0.4 - 4.0)logMAR(P = 0.97)。在对照组中,最终视力与初始视力相比显著更差(P < 0.01),而在IVB组中视力明显稳定(P = 0.24)。对照组的最终眼压为16.3±10.3 mmHg,IVB组为12.0(2.0 - 49.0)mmHg(P = 0.40)。两组之间抗青光眼药物的数量相似(P = 0.57)。IVB组的手术成功率(66.7%)高于对照组(56.7%),但这种差异无统计学意义(P = 0.71)。Kaplan - Meier生存分析显示,术后37个月IVB组成功的概率为53.6%,对照组为31.6%。两组之间未发现显著差异(P = 0.45)。

结论

在NVG病例中,与单独使用GDD相比,GDD联合IVB可维持视力。然而,最终眼压、抗青光眼药物数量及手术成功率方面无显著差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d6c/5557098/bf190fe5a94a/opth-11-1417Fig1.jpg

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