Efficacy of the XEN45 Implant in Advanced to End-stage Glaucoma Patients.

Q3 Medicine
Isaac Hindi, Eran Berkowitz, Inbar Waizer, Beatrice Tiosano
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Abstract

Purpose: To report the efficacy of the XEN45 implant in advanced to end-stage glaucoma patients, after a 6 months follow-up.

Methods: Retrospective, noncomparative electronic health record audit of patients who had undergone an XEN45 procedure. The main outcome measures were intraocular pressure (IOP) reduction and the number of antihypertensive medications. Secondary outcome measures were the rates of early postoperative complications. Complete and qualified success; failure and hypotony were defined according to the World Glaucoma Association guidelines (Shaarawy TM et al.). Needling rates and short-term complications were assessed and a subgroup analysis was performed.

Results: A total of 39 eyes with advanced to end stage-glaucoma were included. Twenty eyes (51%) had undergone combined cataract surgery and 19 (49%), the XEN45 procedure alone. Mean IOP decreased from 19.67 ± 7.87 mm Hg to 13.18 ± 6.09 mm Hg; the number of medications decreased from a median use of 4 (IQR 2-5) to 0 (IQR 0-1). Complete success was achieved in 24 (61.5%) of the eyes, qualified success in 10 (25.6%), and failure in five (12.82%). Needling was required in 15 (38.46%) of the eyes at 6 months. Choroidal detachment occurred in eight (20.51%) eyes, numerical hypotony (IOP ≤ 5 mm Hg) at day 1 was noted in seven (17.95%) eyes with a full resolution by 2 weeks.

Conclusion: In this short-term follow-up, we have seen that XEN45 is a viable, effective, and safe procedure utilized in advanced to end-stage glaucoma patients. Treating cases of significant hypotony using AC reformation with sulfur hexafluoride (SF6) is a safe and effective procedure.

How to cite this article: Hindi I, Berkowitz E, Waizer I, et al. Efficacy of the XEN45 Implant in Advanced to End-stage Glaucoma Patients. J Curr Glaucoma Pract 2022;16(2):84-90.

Abstract Image

Abstract Image

Abstract Image

XEN45植入体治疗晚期至终末期青光眼的疗效观察。
目的:在6个月的随访后,报告XEN45植入物在晚期至终末期青光眼患者中的疗效。方法:对接受XEN45手术的患者进行回顾性、非比较性电子健康记录审计。主要观察指标为眼压(IOP)降低和降压药物用量。次要观察指标为早期术后并发症发生率。圆满合格的成功;根据世界青光眼协会指南(Shaarawy TM等)定义失败和低斜视。评估针刺率和短期并发症,并进行亚组分析。结果:共纳入39只中晚期青光眼。20只眼(51%)接受了联合白内障手术,19只眼(49%)只接受了XEN45手术。平均眼压由19.67±7.87 mm Hg降至13.18±6.09 mm Hg;药物使用中位数从4 (IQR 2-5)降至0 (IQR 0-1)。完全成功24只(61.5%)眼,合格成功10只(25.6%)眼,失败5只(12.82%)眼。6个月时,有15只(38.46%)的眼睛需要针刺。8只(20.51%)眼发生脉络膜脱离,7只(17.95%)眼在第1天出现数值性低视(IOP≤5 mm Hg), 2周完全分辨。结论:在这项短期随访中,我们看到XEN45是一种可行、有效和安全的手术,可用于晚期至终末期青光眼患者。用六氟化硫(SF6)进行AC重整是一种安全有效的方法。如何引用本文:Hindi I, Berkowitz E, Waizer I, et al。XEN45植入体治疗晚期至终末期青光眼的疗效观察。中华青光眼杂志(英文版);2009;16(2):391 - 391。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Current Glaucoma Practice
Journal of Current Glaucoma Practice Medicine-Ophthalmology
CiteScore
1.00
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