Boscia Francesco, Ferreri Paolo, Sisto Dario, Niro Alfredo, Boscia Giacomo, Scotti Giacomo, Viggiano Pasquale, Sborgia Alessandra, Sborgia Giancarlo, Giancipoli Ermete, Alessio Giovanni
Eye Clinic, Department of Medical Science, Neuroscience and Sense Organs, University of Bari, 70124, Bari, Italy.
Eye Clinic, "SS. ANNUNZIATA" Hospital, ASL TA, 74010, Taranto, Italy.
Eur J Ophthalmol. 2025 Mar;35(2):591-601. doi: 10.1177/11206721241272273. Epub 2024 Aug 7.
To evaluate the effectiveness and safety of the XEN-Stent for managing unresponsive to medical therapy secondary glaucoma after silicone oil (SO) removal.
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.
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.
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.
评估XEN支架治疗硅油(SO)取出后药物治疗无效的继发性青光眼的有效性和安全性。
本回顾性病历研究纳入了12例行玻璃体切除术和SO眼内填充术的患者。尽管使用了最大耐受量的青光眼药物,他们在SO取出后仍出现眼压(IOP)升高。11只眼植入了XEN支架,1只眼在植入XEN支架的同时行超声乳化白内障吸除术/人工晶状体植入术。主要结局是达到成功标准:眼压<18 mmHg且未使用药物(完全成功)或使用药物(合格成功)时眼压降低>20%,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)和青光眼药物使用数量(青光眼药物评分-GMS)。
基线特征包括男性占比66.6%,平均年龄61.8±5.7岁,BCVA为0.69±0.3 logMAR,眼压为30±4.2 mmHg,GMS为3.1±0.5。与基线相比,M12时眼压显著降低14±1.9 mmHg,GMS降低0.27±0.6(p<0.01),但BCVA无显著变化(p=0.21)。完全成功率在M3时降至50%,针刺后在M6和M12时升至75%。2例患者在M12时达到合格成功。6只眼进行了针刺,其中3只眼需要二次手术。1只眼需要植入Ex-PRESS。1只眼出现低眼压和前房积血,1周内消退。
XEN支架植入术可能是治疗SO取出后持续性青光眼的初始治疗方法,并发症极少。针刺手术有助于维持或恢复手术成功率。