Mitomycin C 0.2 mg/ml versus Mitomycin C 0.4 mg/ml during the Implantation of an Ab Externo Polystyrene-isobutylene-styrene Microshunt

IF 2.8 Q1 OPHTHALMOLOGY
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引用次数: 0

Abstract

Purpose

To compare the effectiveness and adverse event profile of standalone polystyrene-isobutylene-styrene (SIBS) microshunt implantation with adjunct mitomycin C (MMC) 0.2 mg/ml and MMC 0.4 mg/ml.

Design

Mega-analysis using individual patient data from international prospective and retrospective clinical studies.

Participants

Patients with glaucoma who underwent implantation of a SIBS microshunt with MMC as a standalone procedure.

Methods

A comparison of eyes that received MMC 0.2 mg/ml or 0.4 mg/ml.

Main Outcomes Measures

Primary outcome was complete success defined as the proportion of eyes at 1 year with all of the following: (1) no 2 consecutive intraocular pressures (IOPs) > 17 mmHg; (2) no clinical hypotony; (3) ≥ 20% IOP reduction from baseline; and (4) no use of glaucoma medications. Secondary outcomes included IOP thresholds of 12 mmHg, 14 mm Hg, and 21 mmHg, median IOP, number of medications, risk factors for failure, interventions, adverse events, and reoperations.

Results

At 1 year, the complete success rate was significantly higher (71.3% vs. 50.46%; P < 0.001) and the median IOP was significantly lower (13.0 vs 14.2 mmHg; P < 0.05) in the MMC 0.4 mg/ml group. Mitomycin C 0.2 mg/ml was found to be a significant risk factor for failure (hazard ratio 1.75; 95% confidence interval 1.14–2.67). Needling and surgical revision occurred at a lower rate in the MMC 0.4 mg/ml group (7% vs 18.8%; P = 0.002 and 4.3% vs 13.7% P = 0.0087, respectively). Adverse events occurred at a similar frequency in both groups (26.6% MMC 0.2 mg/ml vs 29.6% MMC 0.4 mg/ml; P = 0.46), most of which were early and transient.

Conclusion

Polystyrene-isobutylene-styrene microshunt implantation with MMC 0.4 mg/ml resulted in a higher success rate with greater IOP reduction compared with MMC 0.2 mg/ml. Higher MMC concentration was not associated with increased serious adverse events.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
在植入体外 SIBS 微分流术时,0.2 毫克/毫升的丝裂霉素与 0.4 毫克/毫升的丝裂霉素:一项大型分析。
目的:比较独立SIBS微分流植入术与辅助MMC 0.2 mg/ml和MMC 0.4 mg/ml的有效性和不良事件概况:设计:利用国际前瞻性和回顾性临床研究中的单个患者数据进行大规模分析:研究对象:接受SIBS微分流术并将MMC作为独立手术植入的青光眼患者:主要结果测量:主要结果是完全成功,定义为一年后具备以下所有条件的眼睛比例:(1)无连续两次眼压>17 mmHg;(2)无临床低眼压症状;(3)眼压较基线下降≥20%;(4)未使用青光眼药物。次要结果包括 12 毫米汞柱、14 毫米汞柱和 21 毫米汞柱的眼压阈值、中位眼压、用药次数、失败的风险因素、干预措施、不良事件和再次手术:结果:1 年后的完全成功率明显更高(71.3% 对 50.46%,P=0.05):与 MMC 0.2 mg/ml 相比,使用 MMC 0.4 mg/ml 植入 SIBS 微分流术的成功率更高,眼压降低幅度更大。较高浓度的 MMC 与严重不良事件的增加无关。
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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