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XEN 凝胶支架单独应用或与超声乳化术联合应用于开角型青光眼的 3 年疗效和安全性:一项多中心研究。

Three-year effectiveness and safety of the XEN gel stent as a solo procedure or in combination with phacoemulsification in open-angle glaucoma: a multicentre study.

机构信息

Department of Ophthalmology and Optometry, University Clinic Salzburg, SALK/Paracelsus Medical University, Salzburg, Austria.

Department of Ophthalmology, Unidad Oftalmologica de Caracas, Caracas, Venezuela.

出版信息

Acta Ophthalmol. 2022 Feb;100(1):e233-e245. doi: 10.1111/aos.14886. Epub 2021 May 10.

Abstract

PURPOSE

To assess the 3-year effectiveness and safety of the XEN gel stent implanted ab interno in open-angle glaucoma (OAG).

METHODS

This study was a multicentre, retrospective chart review of consecutive patients with OAG who underwent ab-interno gel stent placement alone or combined with phacoemulsification between 1 January 2014 and 1 October 2015. Outcome measures included mean changes in intraocular pressure (IOP) and IOP-lowering medication count from medicated baseline at 1, 2, 3 (primary outcome) and 4 years (if available) postimplantation. Intraoperative complications, adverse events of special interest (AESIs) and secondary surgical interventions (SSIs) were recorded.

RESULTS

The safety and effectiveness populations included 212 eyes (primary and secondary) and 174 eyes (primary), respectively. Mean IOP and medication decreased from 20.7 mmHg and 2.5 at baseline (n = 163 primary/first implanted eyes) to 13.9 mmHg and 1.1 medications (n = 76) at 3 years postimplantation, respectively. Mean changes from baseline in IOP (-5.6, -6.2 and -6.6 mmHg) and IOP-lowering medication count (-1.8, -1.6 and -1.4) were statistically significant at 1, 2 and 3 years postimplantation, respectively. Results appeared comparable when implantation was performed with (n = 76) or without (n = 98) phacoemulsification. In primary eyes with 4-year IOP and medication count data (n = 27), mean IOP was 14.0 mmHg on 1.3 medications at 4 years postimplantation. Fifteen (7.1%) eyes had intraoperative complications, 31 (14.6%) experienced 46 postoperative AESIs, and 26 (12.3%) required SSI.

CONCLUSION

The gel stent effectively lowered IOP and IOP-lowering medication count over 3 years, with a predictable and acceptable safety profile, when implanted via the traditional ab-interno technique.

摘要

目的

评估 XEN 凝胶支架经内路植入治疗开角型青光眼(OAG)的 3 年疗效和安全性。

方法

本研究为多中心回顾性病例系列研究,纳入 2014 年 1 月 1 日至 2015 年 10 月 1 日期间,接受单纯内路凝胶支架植入或联合超声乳化白内障吸除术治疗的 OAG 连续患者。主要结局为术后 1、2、3 年(如适用)时,与药物治疗基线相比,眼压(IOP)和降眼压药物使用数量的平均变化。记录术中并发症、特殊关注的不良事件(AESI)和二次手术干预(SSI)。

结果

安全性和有效性人群分别纳入 212 只眼(原发性和继发性)和 174 只眼(原发性)。与药物治疗基线相比(n=163 只原发性/初次植入眼),术后 3 年时,平均 IOP 和药物使用数量分别降低至 13.9mmHg 和 1.1 种药物(n=76)。术后 1、2 和 3 年时,IOP (-5.6、-6.2 和-6.6mmHg)和 IOP 降低药物计数(-1.8、-1.6 和-1.4)的平均变化均具有统计学意义。当植入术联合(n=76)或不联合(n=98)超声乳化白内障吸除术时,结果相似。在具有 4 年 IOP 和药物计数数据的原发性眼(n=27)中,术后 4 年时,平均 IOP 为 14.0mmHg,使用 1.3 种药物。15 只眼(7.1%)发生术中并发症,31 只眼(14.6%)发生 46 例术后 AESI,26 只眼(12.3%)需要 SSI。

结论

当通过传统内路技术植入时,XEN 凝胶支架可在 3 年内有效降低 IOP 和 IOP 降低药物计数,具有可预测且可接受的安全性。

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