iStent inject trabecular microbypass stent implantation with cataract extraction in open-angle glaucoma: early clinical experience.

Eye and vision (London, England) Pub Date : 2020-05-20 eCollection Date: 2020-01-01 DOI:10.1186/s40662-020-00194-3
Tanner J Ferguson, Zachary Dockter, Adam Bleeker, Kayla L Karpuk, Justin Schweitzer, Mitch J Ibach, John P Berdahl
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引用次数: 24

Abstract

Background: Retrospective, consecutive case series to evaluate the implantation of two second-generation trabecular microbypass stents in combination with cataract surgery in a real-world, clinical setting.

Methods: The series included 56 eyes implanted with the iStent inject device with phacoemulsification. The series consisted of eyes with primary open-angle glaucoma (n = 52) and pseudoexfoliative glaucoma (n = 4). Primary outcome measures included intraocular pressure (IOP) and number of glaucoma medications. Safety outcomes included the need for secondary surgical intervention and the incidence of IOP spikes ≥10 mmHg and ≥ 15 mmHg.

Results: IOP was reduced by 21% to 14.7 ± 2.9 mmHg (p < 0.01) at 6 months postoperative from 18.7 ± 5.8 mmHg at baseline. Preoperatively, the mean number of glaucoma medications was 1.5 ± 0.9 and reduced by 39% to 0.9 ± 1.2 (p < 0.01) at 6 months. At 6 months, 68% of eyes had an IOP ≤15 mmHg, increased from 30% at baseline. 55% of eyes were medication-free at 6 months, up from 18% at baseline. There were no severe postoperative complications. No eyes underwent an additional glaucoma procedure.

Conclusions: Implantation of the iStent inject device with concomitant cataract surgery effectively provides a sustained reduction in IOP with a markedly improved medication burden out to 6 months postoperative. The safety profile is excellent.

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开角型青光眼静脉注射小梁微搭桥支架植入术联合白内障摘出的早期临床体会。
背景:在现实世界的临床环境中,回顾性、连续的病例系列来评估两种第二代小梁微搭桥支架植入与白内障手术的结合。方法:对56只眼进行超声乳化植入术。该系列包括原发性开角型青光眼(n = 52)和假剥脱性青光眼(n = 4)。主要结局指标包括眼压(IOP)和青光眼药物的数量。安全性指标包括是否需要二次手术干预以及IOP峰值≥10mmhg和≥15mmhg的发生率。结果:IOP降低21%,为14.7±2.9 mmHg (p p)。结论:在合并白内障手术中植入iStent注射装置有效地提供了持续的IOP降低,并显著改善了术后6个月的药物负担。它的安全性非常好。
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