Heersink Marius, Dovich Jesse A
University of Alabama School of Medicine, Birmingham, AL, USA.
Pacific Eye Institute, Upland, CA, USA.
Clin Ophthalmol. 2019 Aug 12;13:1533-1542. doi: 10.2147/OPTH.S215667. eCollection 2019.
Evaluate outcomes of trabecular meshwork (TM) bypass (iStent GTS100) with cataract extraction (CE) and TM-bypass + ab interno canaloplasty (CP) (VISCO360) with CE in patients with primary open-angle glaucoma (POAG).
Private surgical center for a comprehensive ophthalmology practice.
Retrospective analysis of 186 eyes from 130 consecutive patients with 6 months follow-up.
Eligible eyes had POAG, indicated for CE, and had received CE + TM-bypass or CE + TM-bypass + CP. Exclusions: glaucomas not POAG, SLT within 6 months, or previous ALT. IOP, visual acuity, and medication use assessed at baseline, months 1, 3, and 6. Endpoints were mean reduction in IOP from baseline at 6 months, proportion with IOP reduction at 6 months of ≥20% and IOP <18 mmHg on same or fewer medications, mean medication reduction, and proportion medication independent.
Eighty-six eyes comprised the CE + TM-bypass + CP group; 100 eyes in the CE + TM-bypass group. At 6 months: mean IOP reduction was 2.9±3.6 mmHg for CE + TM-bypass + CP and 1.7±3.1 mmHg for CE + TM-bypass group (<0.05); the proportion with IOP reduction of ≥20% and an IOP <18 mmHg on the same or fewer medications was 46% for CE + TM-bypass + CP and 35% for CE + TM-bypass; for both CE + TM-bypass + CP and CE + TM-bypass, mean number of medications was decreased (0.9 and 0.7, <0.0001) with 56% and 48% off all medication. The most common AE were inflammation (6%) for CE + TM-bypass + CP group and VA loss (8%) for CE + TM-bypass.
At six months, a greater proportion of CE + TM-bypass + CP patients achieved IOP reduction of ≥20% and an IOP <18 mmHg on the same or fewer medications than for TM-bypass + CE.
评估原发性开角型青光眼(POAG)患者小梁网(TM)旁路术(iStent GTS100)联合白内障摘除术(CE)以及TM旁路术 + 内路房角成形术(CP)(VISCO360)联合CE的治疗效果。
一家综合性眼科诊疗的私立手术中心。
对130例连续患者的186只眼进行回顾性分析,随访6个月。
符合条件的眼睛患有POAG,需行CE,并接受了CE + TM旁路术或CE + TM旁路术 + CP。排除标准:非POAG青光眼、6个月内接受过选择性激光小梁成形术(SLT)或既往接受过氩激光小梁成形术(ALT)。在基线、第1、3和6个月评估眼压、视力和药物使用情况。观察终点为6个月时眼压较基线的平均降低值、6个月时眼压降低≥20%且使用相同或更少药物时眼压<18 mmHg的比例、平均药物减少量以及药物停用比例。
CE + TM旁路术 + CP组有86只眼;CE + TM旁路术组有100只眼。6个月时:CE + TM旁路术 + CP组眼压平均降低2.9±3.6 mmHg,CE + TM旁路术组眼压平均降低1.7±3.1 mmHg(<0.05);CE + TM旁路术 + CP组在使用相同或更少药物时眼压降低≥20%且眼压<18 mmHg的比例为46%,CE + TM旁路术组为35%;CE + TM旁路术 + CP组和CE + TM旁路术组的平均用药数量均减少(分别为0.9和0.7,<0.0001),停药比例分别为56%和48%。最常见的不良事件是CE + TM旁路术 + CP组的炎症(6%)和CE + TM旁路术组的视力下降(8%)。
6个月时,与TM旁路术 + CE相比,CE + TM旁路术 + CP组有更大比例的患者在使用相同或更少药物的情况下眼压降低≥20%且眼压<18 mmHg。