Xen gel stent implant for persistent glaucoma after silicone oil removal.

IF 1.4 4区 医学 Q3 OPHTHALMOLOGY European Journal of Ophthalmology Pub Date : 2025-03-01 Epub Date: 2024-08-07 DOI:10.1177/11206721241272273
Francesco Boscia, Paolo Ferreri, Dario Sisto, Alfredo Niro, Giacomo Boscia, Giacomo Scotti, Pasquale Viggiano, Alessandra Sborgia, Giancarlo Sborgia, Ermete Giancipoli, Giovanni Alessio
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Abstract

Purpose: To evaluate the effectiveness and safety of the XEN-Stent for managing unresponsive to medical therapy secondary glaucoma after silicone oil (SO) removal.

Methods: This retrospective chart reviewed 12 patients who underwent vitrectomy and SO endotamponade. They experienced intraocular pressure (IOP) elevation after SO removal despite taking the maximum tolerated glaucoma medication. Eleven eyes underwent an XEN-implant, while 1 underwent an XEN-implant with phacoemulsification/IOL implantation. The primary outcome was to achieve success criteria: IOP <18 mmHg and >20% IOP reduction without medication (complete success) or with medication (qualified success) and without a secondary IOP-lowering procedure. IOP, best-corrected visual acuity (BCVA), and the number of glaucoma medications (Glaucoma Medication Score-GMS) were recorded at baseline, 1 day, 1 week, 1 (M1), 3 (M3), 6 (M6), and 12 (M12) months postoperatively.

Results: Baseline characteristics included males percentage 66.6%, mean age of 61.8 ± 5.7 years, BCVA 0.69 ± 0.3 logMAR, IOP 30 ± 4.2 mmHg, and GMS 3.1 ± 0.5. There was a significant reduction in IOP by 14 ± 1.9 mmHg and GMS by 0.27 ± 0.6 at M12 compared to baseline (p < 0.01), but no significant change in BCVA (p = 0.21). Complete success dropped to 50% (M3), rising to 75% (M6, M12) after needling. Two patients achieved qualified success at M12. Needling was performed in 6 eyes, with 3 requiring a second procedure. Ex-PRESS was required in 1 eye. One eye experienced hypotony and hyphema, which resolved within a week.

Conclusion: XEN implant may be an initial treatment for persistent post SO removal glaucoma with minimal complications. Needling procedures can help maintain or restore surgical success.

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Xen 凝胶支架植入物治疗硅油去除后的顽固性青光眼。
目的:评估 XEN 支架治疗硅油(SO)去除术后对药物治疗无反应的继发性青光眼的有效性和安全性:该回顾性病历回顾了 12 位接受玻璃体切除术和硅油内填塞术的患者。尽管他们服用了最大耐受度的青光眼药物,但在去除硅油后仍出现了眼压(IOP)升高。其中 11 只眼睛接受了 XEN 植入术,1 只眼睛在接受 XEN 植入术的同时接受了超声乳化/人工晶体植入术。主要结果是达到成功标准:眼压降低 20%,无需药物治疗(完全成功)或药物治疗(合格成功),且无需二次降眼压手术。在基线、术后 1 天、1 周、1 个月(M1)、3 个月(M3)、6 个月(M6)和 12 个月(M12)记录眼压、最佳矫正视力(BCVA)和青光眼用药次数(青光眼用药评分-GMS):基线特征包括:男性占 66.6%,平均年龄为 61.8 ± 5.7 岁,BCVA 0.69 ± 0.3 logMAR,眼压 30 ± 4.2 mmHg,GMS 3.1 ± 0.5。与基线相比,在 M12 阶段,眼压明显降低了 14 ± 1.9 mmHg,GMS 降低了 0.27 ± 0.6(p 结论:XEN 植入物可作为眼科治疗的初始阶段:XEN植入物可作为SO摘除术后顽固性青光眼的初始治疗方法,且并发症极少。针刺过程有助于保持或恢复手术成功。
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来源期刊
CiteScore
3.60
自引率
0.00%
发文量
372
审稿时长
3-8 weeks
期刊介绍: The European Journal of Ophthalmology was founded in 1991 and is issued in print bi-monthly. It publishes only peer-reviewed original research reporting clinical observations and laboratory investigations with clinical relevance focusing on new diagnostic and surgical techniques, instrument and therapy updates, results of clinical trials and research findings.
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