Suppr超能文献

第一代iStent旁路植入术与外路巩膜瓣成形术联合白内障超声乳化术治疗原发性开角型青光眼的12个月随访

First-Generation iStent Bypass Implantation versus ab Externo Canaloplasty Combined with Phacoemulsification in Patients with Primary Open Angle Glaucoma-12-Month Follow-Up.

作者信息

Gołaszewska Kinga, Obuchowska Iwona, Konopińska Joanna

机构信息

Department of Ophthalmology, Medical University of Białystok, 15-089 Białystok, Poland.

出版信息

J Clin Med. 2023 Sep 1;12(17):5711. doi: 10.3390/jcm12175711.

Abstract

This prospective, non-randomized, interventional clinical study evaluated the efficacy and safety profile of first-generation iStent bypass implantation versus ab externo canaloplasty, both combined with phacoemulsification, in patients with primary open-angle glaucoma (POAG) after 12-month follow-up. A total of 138 patients with POAG and their 138 eyes (69 phaco-iStent and 69 phacocanaloplasty) were included. Postoperatively at 12 months, the mean intraocular pressure (IOP) decreased from 18.44 ± 3.88 to 15.51 ± 2.50 mmHg and from 17.20 ± 4.04 to 14.97 ± 2.37 mmHg in the phaco-iStent (PiS) and phacocanaloplasty (PC) groups, respectively ( = 0.480). In both groups, 35.7% achieved >20% IOP reduction from baseline. A total of 86% and 71.4% of the eyes were medication-free at 12 months in the PiS and PC groups, respectively. In both groups, all eyes showed improvement in best-corrected visual acuity compared with baseline and demonstrated similar safety profiles throughout the 12-month follow-up period. This study showed equal hypotensive effects of PiS and PC. Both procedures significantly reduced the IOP and the requirement for IOP-lowering medications for at least 12 months postoperatively, with no significant differences between the groups.

摘要

这项前瞻性、非随机、干预性临床研究评估了第一代iStent旁路植入术与外路巩膜切开术联合超声乳化术在原发性开角型青光眼(POAG)患者中的疗效和安全性,随访12个月。共纳入138例POAG患者及其138只眼(69只眼行超声乳化-iStent植入术,69只眼行超声乳化-巩膜切开术)。术后12个月,超声乳化-iStent(PiS)组和超声乳化-巩膜切开术(PC)组的平均眼压(IOP)分别从18.44±3.88 mmHg降至15.51±2.50 mmHg,从17.20±4.04 mmHg降至14.97±2.37 mmHg(P = 0.480)。两组中,35.7%的患者眼压从基线降低超过20%。PiS组和PC组分别有86%和71.4%的患眼在12个月时无需使用降眼压药物。两组所有患眼的最佳矫正视力与基线相比均有改善,且在整个12个月的随访期内安全性相似。本研究表明PiS和PC的降压效果相当。两种手术均能显著降低眼压,并在术后至少12个月内减少降眼压药物的使用,两组间无显著差异。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验