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新型独立式 Ab Externo SIBS 微分流控阀联合丝裂霉素 C 的中期疗效。

Intermediate Outcomes of a Novel Standalone Ab Externo SIBS Microshunt With Mitomycin C.

机构信息

Department of Ophthalmology and Vision Sciences, University of Toronto, Toronto, Ontario, Canada.

Department of Ophthalmology, Université de Montréal, Montreal, Quebec, Canada; Department of Ophthalmology, Centre Hospitalier Universitaire de Montréal (CHUM), Montreal, Quebec, Canada.

出版信息

Am J Ophthalmol. 2020 Jul;215:141-153. doi: 10.1016/j.ajo.2020.02.020. Epub 2020 Mar 13.

Abstract

PURPOSE

To determine the efficacy, risk factors for failure, and adverse events of a standalone novel ab externo SIBS microshunt with mitomycin C (MMC) during 1-year follow-up.

DESIGN

Retrospective, interventional case series.

SUBJECTS

Glaucomatous eyes with an intraocular pressure (IOP) above target and/or progressing on maximally tolerated medical therapy.

METHODS

Consecutive patients with open-angle glaucoma (OAG) and no previous filtering surgery received an ab externo SIBS microshunt with MMC from July 2015 to November 2017. Main outcome measures were proportion of eyes at 1-year with (1) no 2 consecutive IOP readings >17 mm Hg or clinical hypotony without (complete) or with glaucoma medications (qualified); and (2) at least a 20% reduction from decision IOP. Secondary outcomes included upper IOP thresholds of 14 mm Hg and 21 mm Hg with and without a 20% IOP reduction from baseline, median IOP, medications, risk factors for failure, interventions, complications, and reoperations.

RESULTS

A total of 164 eyes in 132 patients were included. Complete success was achieved in 76.9% of eyes, qualified success in 92.5%. Complete success was 75.6% for an upper IOP cut-off of 14 mm Hg and 76.9% for 21 mm Hg, and qualified success was 91.9% and 92.5%. MMC dose of 0.2 vs 0.4-0.5 mg/mL (hazard ratio [HR] 2.51; 95% CI 1.12-5.65) and primary open-angle glaucoma vs secondary open-angle glaucoma (SOAG) (HR 2.51; 95% CI 1.01-6.23) represented the only risk factors for failure in multivariable analysis. Needling was performed in 8.5% of eyes. Two eyes received surgical revision, and 1 a reoperation.

CONCLUSIONS

One-year results of the ab externo SIBS microshunt demonstrated promising rates of qualified and complete success, decreased drop use, few complications, and infrequent postoperative interventions.

摘要

目的

在 1 年的随访中,确定新型经巩膜睫状体沟引流阀(SIBS)联合丝裂霉素 C(MMC)治疗的疗效、失败的危险因素和不良事件。

设计

回顾性、干预性病例系列。

受试者

眼压(IOP)高于目标值且/或经最大耐受药物治疗仍进展的青光眼患者。

方法

2015 年 7 月至 2017 年 11 月,连续收治行外路 SIBS 微引流阀联合 MMC 治疗的开角型青光眼(OAG)患者,不合并既往滤过性手术史。主要观察指标是 1 年时(1)无 2 次连续 IOP 读数>17mmHg 或临床低眼压而无需(完全)或需要青光眼药物(合格);和(2)与基线相比IOP 至少降低 20%的眼的比例。次要观察指标包括眼压为 14mmHg 和 21mmHg 时的上界阈值,以及与基线相比IOP 降低 20%时的中位数、药物、失败的危险因素、干预措施、并发症和再手术。

结果

共纳入 132 例患者的 164 只眼。76.9%的眼达到完全成功,92.5%的眼达到合格成功。眼压上限为 14mmHg 时完全成功率为 75.6%,眼压上限为 21mmHg 时为 76.9%,合格成功率分别为 91.9%和 92.5%。MMC 剂量为 0.2mg/mL 与 0.4-0.5mg/mL 相比(风险比[HR]2.51;95%置信区间[CI]1.12-5.65)和原发性开角型青光眼与继发性开角型青光眼(SOAG)相比(HR 2.51;95% CI 1.01-6.23)是多变量分析中唯一的失败危险因素。8.5%的眼需要行针刺术。2 只眼接受了手术修正,1 只眼接受了再手术。

结论

外路 SIBS 微引流阀治疗 1 年的结果显示出有前景的合格和完全成功率、减少滴眼次数、较少的并发症和术后干预频率。

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