Intermediate Outcomes of the Novel 63-μm Gelatin Microstent versus the Conventional 45-μm Gelatin Microstent

IF 2.8 Q1 OPHTHALMOLOGY
Isra M. Hussein MD, MSc , Ticiana De Francesco MD , Iqbal Ike K. Ahmed MD, FRCSC
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引用次数: 3

Abstract

Purpose

To determine intermediate intraocular pressure (IOP)-lowering and adverse event profile of the 63-μm gelatin microstent (Xen63) with mitomycin C (MMC) compared with the 45-μm gelatin microstent (Xen45) with MMC.

Design

Single center, consecutive, retrospective cohort study.

Participants

Eighty-four glaucomatous eyes (42 63-μm gelatin microstent and 42 45-μm gelatin microstent) with or without previous subconjunctival glaucoma surgery.

Methods

Consecutive eyes that underwent 63-μm gelatin microstent implantation with MMC from February 2020 to June 2021 were compared with eyes that underwent 45-μm gelatin microstent implantation with MMC. Standalone and combined cases with phacoemulsification were included.

Main Outcome Measures

Primary outcome was the hazard ratio of failure of 45-μm gelatin microstent vs. 63-μm gelatin microstent eyes at 12 months, with failure defined as 2 consecutive IOPs, (1) >17 mmHg, (2) <6 mmHg with 2 lines of vision loss, or (3) <20% reduction from baseline IOP, without (complete) or with (qualified) glaucoma medications. Secondary outcomes included IOP thresholds of 14 mmHg and 21 mmHg, postoperative IOP, medications, adverse events, interventions, and reoperations.

Results

The complete success rate was higher in the 63-μm gelatin microstent group (59.5% vs. 28.6%, P = 0.009) at the primary IOP threshold of 6 to 17 mmHg but did not differ significantly for qualified success (66.7% vs. 45.2%, P = 0.08). The crude hazard ratio of failure of 45-μm gelatin microstent relative to 63-μm gelatin microstent was 2.28 (95% confidence interval [CI], 1.21–4.32), and the adjusted hazard ratio was 7.90 (95% CI, 2.12–29.43). 63-μm gelatin microstent eyes had significantly lower mean IOP (12.7 ± 4.8 vs. 15.5 ± 5.1 mmHg, P = 0.001) and fewer medication classes (0.6 ± 1.1 vs. 1.7 ± 1.6 medications, P = 0.0005), with the degree of reduction in IOP and medication count being significantly greater in 63-μm gelatin microstent eyes. There were 28 and 21 distinct interventions in 63-μm gelatin microstent and 45-μm gelatin microstent eyes respectively, with 11.9% of eyes undergoing needling in each group. There were 34 and 19 distinct adverse events, in 63-μm gelatin microstent and 45-μm gelatin microstent eyes, respectively, most of which were early and transient. Nine Xen63 eyes (21.4%) and 6 45-μm gelatin microstent eyes (14.3%) underwent reoperation.

Conclusions

63-μm gelatin microstent resulted in higher surgical success rates and fewer medications compared with 45-μm gelatin microstent. This was tempered by more postoperative interventions and adverse events, although most were transient.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.

新型63-μm明胶微支架与传统45-μm明胶微支架的中期结果比较。
目的:比较含有丝裂霉素C (MMC)的63-μm明胶微支架(Xen63)与含有MMC的45-μm明胶微支架(Xen45)的中间眼内压(IOP)降低和不良事件情况。设计:单中心、连续、回顾性队列研究。参与者:84只青光眼(42只63 μm明胶微支架和42只45 μm明胶微支架),既往有或未做过结膜下青光眼手术。方法:将2020年2月至2021年6月连续行63 μm明胶MMC微支架植入术的眼与45 μm明胶MMC微支架植入术的眼进行比较。包括单独和联合超声乳化术的病例。主要结局指标:主要结局是45 μm明胶微支架组与63 μm明胶微支架组在12个月时眼睛失败的风险比,失败定义为连续2次IOP, (1) >17 mmHg,(2)结果:63 μm明胶微支架组在初始IOP阈值6 - 17 mmHg时完全成功率更高(59.5% vs 28.6%, P = 0.009),但在合格成功方面无显著差异(66.7% vs 45.2%, P = 0.08)。45 μm明胶微支架相对于63 μm明胶微支架失效的粗风险比为2.28(95%可信区间[CI], 1.21-4.32),校正风险比为7.90 (95% CI, 2.12-29.43)。63 μm明胶微支架眼的平均IOP较低(12.7±4.8 vs 15.5±5.1 mmHg, P = 0.001),药物种类较少(0.6±1.1 vs 1.7±1.6,P = 0.0005),且63 μm明胶微支架眼的IOP降低程度和药物计数明显大于63 μm明胶微支架眼。63 μm明胶微支架眼和45 μm明胶微支架眼分别有28和21种不同的干预措施,每组有11.9%的眼进行针刺。63 μm明胶微支架组和45 μm明胶微支架组分别有34例和19例明显不良事件,大多数为早期和短暂性不良事件。9只Xen63眼(21.4%)和6只45 μm明胶微支架眼(14.3%)再次手术。结论:与45 μm明胶微支架相比,63 μm明胶微支架具有更高的手术成功率和更少的药物。术后更多的干预和不良事件缓和了这一点,尽管大多数是短暂的。财务披露:专有或商业披露可在本文末尾的脚注和披露中找到。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Ophthalmology. Glaucoma
Ophthalmology. Glaucoma OPHTHALMOLOGY-
CiteScore
4.80
自引率
6.90%
发文量
140
审稿时长
46 days
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