首页> 外文期刊>BMC Ophthalmology >Combined pars plana glaucoma drainage device placement and vitrectomy using a vitrectomy sclerotomy site for tube placement: a case series
【24h】

Combined pars plana glaucoma drainage device placement and vitrectomy using a vitrectomy sclerotomy site for tube placement: a case series

机译:使用玻璃体切除术核心术部位的管放置综合Pars Plana Glaucoma排水装置放置和玻璃体切除术:案例系列

获取原文
           

摘要

The purpose of this study is to report the safety and efficacy of pars plana glaucoma drainage devices with pars plana vitrectomy using one of the vitrectomy sclerotomy sites for tube placement in patients with refractory glaucoma. Retrospective case series of 28 eyes of 28 patients who underwent combined pars plana glaucoma drainage device and pars plana vitrectomy between November 2016 and September 2019 at Massachusetts Eye and Ear. Main outcome measures were intraocular pressure (IOP), glaucoma medication burden, best corrected visual acuity, and complications. Statistical tests were performed with R and included Kaplan-Meier analyses, Wilcoxon paired signed-rank tests, and Fisher tests. Mean IOP decreased from 22.8?mmHg to 11.8?mmHg at 1.5?years (p?=?0.002), and mean medication burden decreased from 4.3 to 2.1 at 1.5?years (p?=?0.004). Both IOP and medication burden were significantly lower at all follow-up time points. The probability of achieving 5 2 lines. Two eyes required subsequent pars plana vitrectomies for tube obstruction, and one eye had transient hypotony. The results of pars plana glaucoma drainage device and pars plana vitrectomy using one of the vitrectomy sclerotomy sites for tube placement are promising, resulting in significant IOP and medication-burden reductions through postoperative year 1.5 without additional risk of postoperative complications. Inserting glaucoma drainage devices into an existing vitrectomy sclerotomy site may potentially save surgical time by obviating the need to create another sclerotomy for tube placement and suture one of the vitrectomy ports.
机译:本研究的目的是使用耐火绿酶患者的玻璃体切除术治疗术中的玻璃体切除术核心位点,报告Pars Plana glaucoma引流装置的安全性和有效性。回顾性案例系列28只接受Pars Plana青光眼扩散装置的28名患者的眼睛,2016年11月和2019年9月在马萨诸塞州的眼睛和耳朵。主要结果措施是人工压力(IOP),青光眼药物负担,最佳矫正视力和并发症。统计测试与R并包括Kaplan-Meier分析,Wilcoxon配对级别测试和Fisher测试。平均IOP从22.8?mmhg减少到11.8?mmhg 1.5?年(p?= 0.002),并且平均用药负担从4.3到2.1减少1.5岁(p?= 0.004)。在所有后续时间点,IOP和药物负担都显着降低。实现5 2条线的概率。两只眼睛需要随后的管道玻璃体切除术进行管梗阻,一只眼睛有瞬态的低音。使用玻璃体切除术治疗部门的玻璃体切除术部位的Pars Plana青光眼引流装置和Pars Plana Vitectomy的结果是有前途的,导致术后年份的IOP和药物负担减少,而无需额外的术后并发症。将青光眼引流装置插入现有的玻璃体切除术中可能会通过避免为管置和缝合术口的缝合口之一产生另一种硬化术来节省手术时间。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号