Two-year outcomes of Xen 45 gel stent implantation in patients with open-angle glaucoma: real-world data from the Fight Glaucoma Blindness registry.

IF 3.7 2区 医学 Q1 OPHTHALMOLOGY
Louis Arnould, Elise Balsat, Yohei Hashimoto, Andrew White, George Kong, Hamish Dunn, Leo Fan, Pierre-Henry Gabrielle, Alain M Bron, Catherine P Creuzot-Garcher, Mitchell Lawlor
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引用次数: 0

Abstract

Objective: To evaluate efficacy and safety outcomes of the Xen 45 gel stent implant over 24 months of follow-up.

Methods: A retrospective analysis of prospectively collected data from the Fight Glaucoma Blindness observational registry. Complete success (CS) was defined as intraocular pressure (IOP) reduction ≥20% from preoperative and an IOP ≤18 mm Hg and ≥6 mm Hg with no secondary procedure at 2 years and without IOP-lowering medications. Qualified success (QS) was defined similarly, allowing the use of IOP-lowering medications.

Results: The Xen 45 gel stent implant was implanted in 646 eyes of 515 patients. Preoperative IOP was 21.4±7.6 (mean±SD) mm Hg on 2.7±1.3 IOP-lowering medication and mean deviation was -10.2±8.4 dB. After 24-month follow-up, IOP was 16.8±7.3 mm Hg (mean reduction of 21.7%) on 1.2±1.4 IOP-lowering medications. CS and QS rates at 24 months were 26% and 48%, respectively. CS and QS were higher in the Xen stand-alone group (33% and 52%, respectively) than in the Xen+cataract group (16% and 42%, respectively). Bleb needling was performed in 28.4% of cases, and 18% underwent a secondary procedure.

Conclusions: The Xen 45 gel stent implant offers acceptable long-term efficacy for the treatment of open-angle glaucoma. However, there is a significant rate of reoperation and needling, and outcomes are less effective if combined with cataract surgery.

开角型青光眼患者 Xen 45 凝胶支架植入术两年后的疗效:来自抗击青光眼致盲登记处的真实数据。
目的:评估 Xen 45 凝胶支架植入物 24 个月随访的疗效和安全性:评估 Xen 45 凝胶支架植入物在 24 个月随访期间的疗效和安全性:方法:对抗击青光眼致盲观察登记处前瞻性收集的数据进行回顾性分析。完全成功(CS)的定义是眼压(IOP)比术前降低≥20%,眼压≤18 mm Hg,且≥6 mm Hg,2年内无二次手术,未服用降眼压药物。合格成功(QS)的定义类似,允许使用降眼压药物:结果:515 名患者的 646 只眼睛植入了 Xen 45 凝胶支架。术前使用 2.7±1.3 降眼压药物时,眼压为 21.4±7.6(平均值±SD)毫米汞柱,平均偏差为 -10.2±8.4 分贝。随访 24 个月后,使用 1.2±1.4 种降低眼压药物时,眼压为 16.8±7.3mmHg(平均降低 21.7%)。24个月时的CS和QS率分别为26%和48%。Xen独立组的CS和QS率(分别为33%和52%)高于Xen+白内障组(分别为16%和42%)。28.4%的病例进行了出血针刺,18%的病例进行了二次手术:结论:Xen 45凝胶支架植入体在治疗开角型青光眼方面具有可接受的长期疗效。结论:Xen 45 凝胶支架植入体在治疗开角型青光眼方面具有可接受的长期疗效,但再次手术和针刺的比例较高,而且如果与白内障手术结合使用,疗效较差。
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来源期刊
CiteScore
10.30
自引率
2.40%
发文量
213
审稿时长
3-6 weeks
期刊介绍: The British Journal of Ophthalmology (BJO) is an international peer-reviewed journal for ophthalmologists and visual science specialists. BJO publishes clinical investigations, clinical observations, and clinically relevant laboratory investigations related to ophthalmology. It also provides major reviews and also publishes manuscripts covering regional issues in a global context.
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