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一项为期 4 年的回顾性研究:XEN45 在青光眼患者中的临床结局。

A 4-Year Retrospective Study: Clinical Outcomes of XEN45 in Patients with Glaucoma.

机构信息

Miguel Servet University Hospital, Zaragoza, Spain.

Opthalmology Innovation and Research Group, Zaragoza, Spain.

出版信息

Ophthalmic Res. 2024;67(1):478-487. doi: 10.1159/000539504. Epub 2024 Jul 17.

Abstract

INTRODUCTION

The main purpose of the current study was to evaluate the long-term effectiveness and safety of XEN45 implant, either alone or in combination with cataract surgery, in patients with glaucoma.

METHODS

Retrospective and single center study conducted on consecutive patients who underwent a XEN45 implant, either alone or in combination with cataract surgery, between November 2016 and October 2021. The primary endpoint was the mean intraocular pressure (IOP) lowering from preoperative values.

RESULTS

Among the 230 screened patients, 206 eyes (176 patients) were included. Fifty-three (25.7%) eyes had undergone XEN alone and 153 (74.3%) eyes had undergone a combined procedure (XEN+phacoemulsification). The mean preoperative IOP was significantly higher in the XEN-alone (22.2 ± 5.9 mm Hg) than in the XEN+Phaco (19.8 ± 4.5 mm Hg) group (p = 0.0035). In the overall study population, the mean preoperative IOP was significantly lowered from 20.5 ± 5.0 mm Hg to 15.8 ± 4.4 at year-4, p < 0.0001. The mean preoperative (95% confidence interval) IOP was significantly lowered from 22.2 (20.6-23.8) mm Hg and 19.8 (19.1-20.6) mm Hg to 15.6 (12.2-16.9) mm Hg and 15.9 (15.2-16.5) mm Hg at year-4 in the XEN-alone and XEN+Phaco groups, respectively (p < 0.0001 each, respectively). The number of ocular hypotensive medications was significant reduced from 2.6 ± 1.0 drugs to 1.3 ± 1.3 drugs, with no significant differences between XEN-alone and XEN+Phaco groups (p = 0.1671). On the first postoperative day, 62 (30.1%) eyes presented some type of complication. Fifteen (7.3%) eyes underwent a needling procedure.

CONCLUSION

XEN45, either alone or in combination with phacoemulsification, significantly lowered the IOP and reduced the need of ocular hypotensive medication in the long-term.

摘要

简介

本研究的主要目的是评估 XEN45 植入物单独或联合白内障手术治疗青光眼患者的长期疗效和安全性。

方法

对 2016 年 11 月至 2021 年 10 月间接受 XEN45 植入物治疗的连续患者进行回顾性、单中心研究,包括单独接受 XEN45 植入物治疗或联合白内障手术治疗的患者。主要终点是从术前值降低的平均眼内压(IOP)。

结果

在筛选出的 230 例患者中,206 只眼(176 例患者)纳入研究。53 只眼(25.7%)接受了 XEN 单独治疗,153 只眼(74.3%)接受了联合治疗(XEN+超声乳化白内障吸除术)。XEN 单独治疗组(22.2 ± 5.9 mm Hg)的平均术前IOP 明显高于 XEN+超声乳化白内障吸除术组(19.8 ± 4.5 mm Hg)(p = 0.0035)。在总体研究人群中,平均术前 IOP 从 20.5 ± 5.0 mm Hg 显著降低至 4 年后的 15.8 ± 4.4 mm Hg,p < 0.0001。XEN 单独治疗组和 XEN+超声乳化白内障吸除术组的平均术前(95%置信区间)IOP 分别从 22.2(20.6-23.8)mmHg 和 19.8(19.1-20.6)mmHg 显著降低至 4 年后的 15.6(12.2-16.9)mmHg 和 15.9(15.2-16.5)mmHg,p < 0.0001(分别)。降眼压药物的数量从 2.6 ± 1.0 种显著减少至 1.3 ± 1.3 种,XEN 单独治疗组和 XEN+超声乳化白内障吸除术组之间无显著差异(p = 0.1671)。术后第 1 天,62 只眼(30.1%)出现某种类型的并发症。15 只眼(7.3%)接受了针刺治疗。

结论

XEN45 单独或联合超声乳化白内障吸除术均可显著降低眼压,并减少长期降眼压药物的需求。

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