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MINIject 在患有药物控制不佳的开角型青光眼患者中的性能和安全性的欧洲研究(STAR-II)。

A European Study of the Performance and Safety of MINIject in Patients With Medically Uncontrolled Open-angle Glaucoma (STAR-II).

机构信息

Departamento de Oftalmologia, Hospital Clinico San Carlos, Universidad Complutense, OFTARED, Madrid, Spain.

Department of Ophthalmology, Hôpital de la Croix-Rousse, Lyon.

出版信息

J Glaucoma. 2020 Oct;29(10):864-871. doi: 10.1097/IJG.0000000000001632.

Abstract

PRECIS

In this European study (STAR-II), MINIject, a novel, ab-interno, supraciliary minimally invasive glaucoma surgery device, effectively lowered intraocular pressure (IOP) and the need for IOP-lowering medications in patients with primary open-angle glaucoma.

PURPOSE

This study evaluates the safety and performance of a minimally invasive supraciliary glaucoma drainage device (MINIject DO627) for surgical treatment of primary open-angle glaucoma in patients refractory to topical hypotensive medications.

METHODS

In a prospective, interventional, single-arm, multicenter, European study (STAR-II), MINIject was successfully implanted in a stand-alone procedure in 29 of 31 patients in 8 sites in 3 countries. The primary endpoint was the success rate 6 months after surgery >60% (defined as diurnal IOP ≤21 and >5 mm Hg with ≥20% IOP reduction from baseline, with/without glaucoma hypotensive medication). ClinicalTrials.gov: NCT03624361.

RESULTS

At the 6-month follow-up, the primary endpoint was fulfilled, with 75.9% of patients reaching prospectively defined success. The mean IOP was reduced by 40.2% (9.9 mm Hg) to 14.7±6.0 mm Hg at 6 months from 24.6±3.8 mm Hg at baseline. The use of IOP-lowering medication ingredients was reduced by 63.4% from 2.9±1.2 at baseline to 1.0±1.3. Furthermore, 79.3% of the patients had mean IOP ≤18 mm Hg, 82.8% achieved a ≥20% IOP reduction, and 55.2% were medication free at 6 months. Six device-related serious adverse events were reported in the study eye: IOP increase (3/31 patients, 9.7%), and single reports of eye pain, corneal erosion, and chorioretinal folds (1/31, 3.2%), all of which resolved. There was minimal change to corneal endothelial cell density.

CONCLUSION

Ab-interno supraciliary surgical implantation using MINIject DO627 in a stand-alone procedure significantly lowers IOP by 40% at the 6-month follow-up, while reducing the need for IOP-lowering medication.

摘要

简介

在这项欧洲研究(STAR-II)中,MINIject 是一种新型的经巩膜、睫状体下微创青光眼手术设备,能有效降低原发性开角型青光眼患者的眼压(IOP)并减少对 IOP 降低药物的需求。

目的

本研究评估了微创型经巩膜睫状体下青光眼引流装置(MINIject DO627)用于治疗对局部降压药物难治的原发性开角型青光眼的安全性和性能。

方法

在一项前瞻性、干预性、单臂、多中心、欧洲研究(STAR-II)中,在 3 个国家的 8 个地点的 31 例患者中,成功地单独进行了 MINIject 植入手术。主要终点是术后 6 个月时成功率>60%(定义为白天 IOP≤21mmHg,且较基线降低≥20%,同时伴有或不伴有青光眼降压药物)。ClinicalTrials.gov:NCT03624361。

结果

在 6 个月的随访中,主要终点达到,75.9%的患者达到了预期的成功标准。与基线时的 24.6±3.8mmHg 相比,6 个月时平均 IOP 降低了 40.2%(9.9mmHg),降至 14.7±6.0mmHg。IOP 降低药物成分的使用量从基线时的 2.9±1.2 减少到 1.0±1.3。此外,79.3%的患者平均 IOP≤18mmHg,82.8%的患者眼压降低≥20%,55.2%的患者在 6 个月时无需药物治疗。研究眼中报告了 6 例与设备相关的严重不良事件:眼压升高(31 例患者中有 3 例,9.7%),单眼报告眼痛、角膜侵蚀和脉络膜皱褶(31 例患者中有 1 例,3.2%),均已解决。角膜内皮细胞密度有轻微变化。

结论

MINIject DO627 经巩膜睫状体下微创外科植入术可在 6 个月的随访中使 IOP 显著降低 40%,同时减少对 IOP 降低药物的需求。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1bb/7647427/873971236825/ijg-29-864-g001.jpg

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