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PRESERFLO™ 微分流器:25号与27号针道的1年结果

PRESERFLO™ Microshunt: 1-Year Results of a 25-Gauge vs. 27-Gauge Needle Tract.

作者信息

Steiner Stefan, Resch Hemma, Kiss Barbara, Vass Clemens

机构信息

Department of Ophthalmology, Medical University of Vienna, 1090 Vienna, Austria.

Department of Ophthalmology, Sanatorium Hera, 1090 Vienna, Austria.

出版信息

J Clin Med. 2024 Mar 29;13(7):1979. doi: 10.3390/jcm13071979.

Abstract

The purpose of this study was to evaluate the effectiveness and safety of the PreserFlo™ microshunt (PMS) using a 25-Gauge vs. 27-Gauge needle tract. : This is a prospective postoperative examination of 60 glaucoma eyes that received a PMS. The main outcome measures were intraocular pressure (IOP), glaucoma drug score (GDS), Kaplan-Meier success rates, complications, and secondary intervention rates. Two subgroups were formed for data comparison: 27-Gauge (27G), and 25-Gauge (25G). Success was defined as IOP < 18 mmHg together with ≥20% IOP reduction with medication allowed (qualified success = QS18) or not (full success = FS18). : IOP and GDS were reduced from baseline to the 1-year study visit as follows: All eyes from 23.4 ± 8.6 mmHg (3.1 ± 0.9) to 15.1 ± 5.9 mmHg (0.8 ± 1.1); 25G from 24.2 ± 7.3 mmHg (3.0 ± 0.8) to 12.7 ± 2.7 mmHg (0.5 ± 0.8); and 27G from 23.1 ± 9.2 mmHg (3.1 ± 1.0) to 16.2 ± 6.7 mmHg (0.9 ± 1.2). IOP at one year was lower in the 25G group compared to the 27G group ( = 0.035). Bleb needling was required in eight (13.3%) eyes and open bleb revisions in three (5.0%). Transient hypotony occurred in 21% and choroidal effusion in 8% of all eyes. Choroidal effusions were more frequent in the 25G group (21%) compared to the 27G group (2%, = 0.031). One-year success rates were significantly higher in the 25G group compared to the 27G group for both QS18 (25G: 67.9% vs. 27G: 35.7%, = 0.002) and FS18 (25G: 63.6% vs. 27G: 29.2%, = 0.007). : The PreserFlo microshunt is an effective and safe glaucoma surgery with a low rate of bleb revisions or needlings. We show that the 25G needle tract might be more efficient for IOP control at the cost of increased IOP-related complications compared to 27G.

摘要

本研究的目的是评估使用25号与27号针道的PreserFlo™微型分流器(PMS)的有效性和安全性。这是一项对60只接受PMS的青光眼患眼进行的前瞻性术后检查。主要观察指标为眼压(IOP)、青光眼药物评分(GDS)、Kaplan-Meier成功率、并发症及二次干预率。为进行数据比较形成了两个亚组:27号(27G)和25号(25G)。成功定义为眼压<18 mmHg且允许使用药物使眼压降低≥20%(合格成功=QS18)或未使用药物使眼压降低≥20%(完全成功=FS18)。眼压和GDS从基线至1年研究访视时的降低情况如下:所有患眼从23.4±8.6 mmHg(3.1±0.9)降至15.1±5.9 mmHg(0.8±1.1);25G组从24.2±7.3 mmHg(3.0±0.8)降至12.7±2.7 mmHg(0.5±0.8);27G组从23.1±9.2 mmHg(3.1±1.0)降至16.2±6.7 mmHg(0.9±1.2)。25G组1年时的眼压低于27G组(P=0.035)。8只(13.3%)患眼需要进行滤泡针刺,3只(5.0%)需要进行开放滤泡修复。所有患眼中21%出现短暂性低眼压,8%出现脉络膜渗漏。25G组脉络膜渗漏(21%)比27G组(2%,P=0.031)更常见。25G组QS18(25G:67.9% vs. 27G:35.7%,P=0.002)和FS18(25G:63.6% vs. 27G:29.2%,P=0.007)的1年成功率均显著高于27G组。PreserFlo微型分流器是一种有效且安全的青光眼手术,滤泡修复或针刺率低。我们发现,与27G相比,25G针道可能在控制眼压方面更有效,但代价是增加了与眼压相关的并发症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8004/11012831/8868c4a796bf/jcm-13-01979-g001.jpg

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