Performance and Safety of a New Ab Intern Gelatin Stent in Refractory Glaucoma at 12 Months

被引:203
|
作者
Grover, Davinder S. [1 ]
Flynn, William J. [2 ]
Bashford, Kent P. [3 ]
Lewis, Richard A. [4 ]
Duh, Yi-Jing [5 ]
Nangia, Rupali S. [6 ]
Niksch, Barbara [6 ]
机构
[1] Glaucoma Associates Texas, 10740 N Cent Expressway, Dallas, TX 75231 USA
[2] Rashid Rice Flynn & Reilly Eye Associates, San Antonio, TX USA
[3] Eye Ctr Northern Colorado, Ft Collins, CO USA
[4] Sacramento Eye Consultants, Sacramento, CA USA
[5] StatServe Consulting Inc, Chino Hills, CA USA
[6] Allergan Plc, Irvine, CA USA
关键词
QUALITY-OF-LIFE; OPEN-ANGLE GLAUCOMA; HEALTH-CARE COSTS; VISUAL-FIELD LOSS; AHMED GLAUCOMA; TREATMENT-OUTCOMES; CLINICAL-EXPERIENCE; VALVE IMPLANT; FOLLOW-UP; PROJECTED INCREASE;
D O I
10.1016/j.ajo.2017.07.023
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE: To evaluate the intraocular pressure (IOP)lowering performance and safety of an ab interno gelatin stent (XEN 45 Gel Stent, Allergan plc, Irvine, California, USA), a minimally invasive glaucoma surgery device, in refractory glaucoma. DESIGN: Single-arm, open-label, multicenter clinical study. METHODS: Following mitomycin C pretreatment, the stent was placed ab intern in patients who failed prior filtering/cilioablative procedure or had uncontrolled IOP on maximum-tolerated medical therapy, with medicated IOP >= 20 and <= 35 mm Hg and visual field mean deviation <=-3 dB. Primary performance outcomes: patients (%) achieving >= 20% IOP reduction from baseline on the same or fewer medications and mean lop change from baseline at month 12. Procedure-related complications and ocular adverse events (AEs) were assessed. RESULTS: Sixty-five patients were implanted (intentto-treat/safety population). At 12 months, 75.4% (46/61; observed data) reported >= 2.0% IOP lowering from baseline on the same or fewer medications. Mean IOP change from baseline was -9.1 mm Hg (95% confidence interval [CI]: -10.7, -7.5) (n = 52; observed data) at 12 months, excluding patients with missing data (n = 4) and those requiring a glaucoma-related secondary surgical intervention (n = 9). Mean medication count decreased from 3.5 (baseline) to 1.7 (12 months). No intraoperative complications or unexpected postoperative AEs were reported. Most AEs were mild/moderate; common AEs included needling (without sight threatening complications), nonpersistent loss of best corrected visual acuity, and transient hypotony (requiring no surgical intervention). CONCLUSIONS: The gelatin stent reduced IOP and medication use without raising unexpected safety concerns, offering a minimally invasive surgical option for refractory glaucoma patients. (C) 2017 The Authors. Published by Elsevier Inc.
引用
收藏
页码:25 / 36
页数:12
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