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经晶状体眼房水引流管植入术联合 OMNI 系统小梁切开术治疗闭角型青光眼合并白内障患者的疗效观察:ROMEO 研究。

Canaloplasty and Trabeculotomy with the OMNI System in Pseudophakic Patients with Open-Angle Glaucoma: The ROMEO Study.

机构信息

Vold Vision, Fayetteville, Arkansas.

The Williamson Eye Center, Baton Rouge, Louisiana.

出版信息

Ophthalmol Glaucoma. 2021 Mar-Apr;4(2):173-181. doi: 10.1016/j.ogla.2020.10.001. Epub 2020 Oct 9.

Abstract

PURPOSE

Provide outcomes up to 12 months postsurgically for sequential canaloplasty and trabeculotomy with the OMNI surgical system (Sight Sciences, Inc) in pseudophakic patients with mild to moderate open-angle glaucoma.

DESIGN

Retrospective, multicenter, single-arm study conducted at 10 multi-subspecialty ophthalmology practices and surgery centers located in 7 states (Arkansas, California, Kansas, Louisiana, Missouri, New York, and Texas).

PARTICIPANTS

Eligible patients were pseudophakic, with mild/moderate open-angle glaucoma, 12-month follow-up, and medicated intraocular pressure (IOP) ≤36 mmHg on ≤4 medications preoperatively. One eye per patient was enrolled.

METHODS

Institutional Review Board approved. All available cases meeting eligibility criteria were enrolled. Analysis of secondary end points was stratified by baseline (BL) IOP (>18 mmHg in group 1 and ≤18 mmHg in group 2) recognizing that treatment goals differed depending on BL IOP.

MAIN OUTCOME MEASURES

Primary success was defined as the proportion of patients with ≥20% reduction in IOP from BL or IOP between 6 and 18 mmHg (inclusive) and on the same or fewer medications without secondary surgical intervention (SSI). Other effectiveness end points included mean IOP and number of medications at 12 months. Safety end points were best-corrected visual acuity (BCVA), adverse events (AEs), and SSIs.

RESULTS

Forty-eight patients were enrolled, 24 in each group. Primary success was met by 73%. Mean IOP was reduced in group 1 (21.8 to 15.6 mmHg, P < 0.0001) and remained controlled in group 2 (15.4 to 13.9 mmHg, P = 0.24). Medications went from 1.7 ± 1.3 to 1.2 ± 1.3 (P = 0.024) in group 1 and from 2.0 ± 1.3 to 1.3 ± 1.3 (P = 0.003) in group 2. Adverse events were typical for the patient population undergoing angle surgery. Those reasonably related to the procedure were mild inflammation (13%), IOP spikes (6%), hyphema, corneal edema, and BCVA loss (all 4%). Five patients (10%) required an SSI.

CONCLUSIONS

The sequential combination of canaloplasty followed by trabeculotomy performed as stand-alone procedures using the OMNI system in pseudophakic patients with open-angle glaucoma provides effective IOP reduction or sustained IOP control and meaningful medication reduction for up to 12 months postoperatively.

摘要

目的

在伴有轻度至中度开角型青光眼的白内障术后患者中,提供使用 OMNI 手术系统(Sight Sciences,Inc.)进行连续房角切开术和小梁切开术的术后 12 个月的结果。

设计

在位于 7 个州(阿肯色州、加利福尼亚州、堪萨斯州、路易斯安那州、密苏里州、纽约州和德克萨斯州)的 10 个多专科眼科诊所和手术中心进行的回顾性、多中心、单臂研究。

参与者

符合条件的患者为白内障术后,患有轻度/中度开角型青光眼,随访 12 个月,术前接受 ≤4 种药物治疗时眼压(IOP)≤36mmHg。每位患者的一只眼被纳入研究。

方法

机构审查委员会批准。所有符合入选标准的可评估病例均被纳入研究。根据基线(BL)IOP(第 1 组>18mmHg,第 2 组≤18mmHg)对次要终点进行分层分析,因为治疗目标取决于 BL IOP。

主要观察指标

主要成功定义为眼压从基线降低≥20%或眼压在 6 至 18mmHg(含)之间,且使用相同或更少药物治疗且无二次手术干预(SSI)的患者比例。其他有效性终点包括 12 个月时的平均眼压和药物数量。安全性终点为最佳矫正视力(BCVA)、不良事件(AE)和 SSI。

结果

共纳入 48 例患者,每组 24 例。主要成功的比例为 73%。第 1 组的平均眼压从 21.8mmHg 降至 15.6mmHg(P<0.0001),第 2 组保持在 15.4mmHg 至 13.9mmHg(P=0.24)。第 1 组的药物从 1.7±1.3 降至 1.2±1.3(P=0.024),第 2 组从 2.0±1.3 降至 1.3±1.3(P=0.003)。不良事件是接受角手术的患者群体中常见的。与手术相关的不良反应为轻度炎症(13%)、眼压升高(6%)、前房积血、角膜水肿和 BCVA 丧失(均为 4%)。5 例患者(10%)需要 SSI。

结论

在白内障术后伴有开角型青光眼的患者中,使用 OMNI 系统作为独立手术进行连续房角切开术联合小梁切开术,可提供有效的眼压降低或持续眼压控制,并在术后长达 12 个月时显著减少药物治疗。

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