Papazoglou Anthia, Höhn René, Schawkat Megir, Tappeiner Christoph, Iliev Milko, Gugleta Konstantin, Saletta Giulia, Wiencierz Andrea, Wagels Barbara, Todorova Margarita G, Krzyzanowska Iwona, Töteberg-Harms Marc, Tschopp Markus
Department of Ophthalmology, Cantonal Hospital Aarau, Aarau, Switzerland.
Medical Faculty, University of Zurich, Zurich, Switzerland.
Ophthalmol Ther. 2024 Jun;13(6):1513-1525. doi: 10.1007/s40123-024-00917-y. Epub 2024 Apr 6.
The aim of this study was to investigate the 2-year postoperative efficacy of the XEN45 Gel Stent by evaluating the reduction of intraocular pressure (IOP) and the need for eye pressure-lowering medications in a multicenter setting in Switzerland.
Patients with various types of glaucoma who received a XEN45 Gel Stent with or without combined phacoemulsification cataract surgery at five hospitals in Switzerland were retrospectively enrolled. Pre- and postoperative IOP, the number of antiglaucoma medications, and the need of subsequent interventions to control IOP were assessed. The success rate was defined as a ≥ 20% reduction of IOP 2 years postoperatively without the need for subsequent glaucoma surgery.
A total of 345 eyes were included: 44.3% with primary open-angle, 42.0% pseudoexfoliation, and 13.7% with other types of glaucoma. Of these, 206 patients were followed for 2 years. Preoperatively, the mean IOP was 26.3 ± 8.9 mmHg and the mean number of antiglaucoma medications administered was 3.0 ± 1.3. Two years postoperatively, the success rate was 66.0% (95% confidence interval 59.3-72.1%), the IOP had dropped by 43.8% to 14.8 ± 5.7 mmHg, and the number of medications was reduced by a mean of 2.0 ± 1.7 per day. Postoperative complications and the need for interventions remained low.
The XEN45 Gel Stent successfully reduced IOP and the number of antiglaucoma drugs in most patients at 2 years postoperatively.
本研究的目的是通过在瑞士的多中心环境中评估眼内压(IOP)的降低情况以及降低眼压药物的使用需求,来调查XEN45凝胶支架的术后2年疗效。
回顾性纳入在瑞士五家医院接受了XEN45凝胶支架植入术(无论是否联合白内障超声乳化手术)的各类青光眼患者。评估术前和术后的眼压、抗青光眼药物数量以及控制眼压所需的后续干预措施。成功率定义为术后2年眼压降低≥20%且无需后续青光眼手术。
共纳入345只眼:原发性开角型青光眼占44.3%,假性剥脱性青光眼占42.0%,其他类型青光眼占13.7%。其中,206例患者随访了2年。术前,平均眼压为26.3±8.9 mmHg,平均使用的抗青光眼药物数量为3.0±1.3种。术后2年,成功率为66.0%(95%置信区间59.3 - 72.1%),眼压下降了43.8%至14.8±5.7 mmHg,药物数量平均每天减少2.0±1.7种。术后并发症及干预需求仍然较低。
XEN45凝胶支架在术后2年成功降低了大多数患者的眼压及抗青光眼药物的使用数量。