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iStent 小梁微分流管支架植入联合超声乳化术治疗开角型青光眼:日本上市后 2 年的随访研究。

iStent Trabecular Micro-bypass Stent Implantation Combined with Phacoemulsification for Open-Angle Glaucoma: A 2-Year Post-marketing Surveillance Study in Japan.

机构信息

Department of Ophthalmology, Faculty of Medical Sciences, University of Fukui, 23-3 Shimoaizuki, Matsuoka, Eiheiji, Yoshida, Fukui, 910-1193, Japan.

Glaukos Corporation, Tokyo, Japan.

出版信息

Adv Ther. 2022 Sep;39(9):4076-4093. doi: 10.1007/s12325-022-02207-0. Epub 2022 Jul 5.

Abstract

INTRODUCTION

We report 2-year outcomes after implantation of iStent trabecular micro-bypass stent with phacoemulsification, in Japanese patients with mild-moderate open-angle glaucoma (OAG).

METHODS

This was a 24-month, prospective, longitudinal, observational, post-marketing study conducted between July 2017 and September 2020. Patients consisted of adults with OAG on antiglaucoma medications who had cataract surgery combined with one iStent implantation. Outcome measures included intraocular pressure (IOP), antiglaucoma medications, treatment success rates (defined as eyes having lower IOP with same or reduced number of medications from baseline, or same IOP with reduced number of medications from baseline, and not requiring secondary glaucoma surgeries postoperatively), and safety. Outcomes were analyzed in the overall cohort and in glaucoma subtypes: primary OAG, normal-tension glaucoma, and exfoliative glaucoma.

RESULTS

Overall, 232 eyes were enrolled. At 24 months, mean ± standard deviation IOP decreased from 17.6 ± 4.0 mmHg preoperatively to 14.3 ± 3.0 mmHg (p < 0.05), and mean number of medications reduced from 2.2 ± 1.2 preoperatively to 0.7 ± 1.2 (p < 0.05). Similar trends were observed across glaucoma subtypes. In the overall cohort, 96.7%, 95.3%, and 93.7% of patients achieved treatment success at 6, 12, and 24 months, respectively. There were 67.6% medication-free eyes at 24 months compared to 3.2% medication-free eyes preoperatively (p < 0.0001). Safety profile was favorable over the 2-year period.

CONCLUSIONS

Following iStent implantation with phacoemulsification, clinically relevant and statistically significant reductions in IOP and number of medications were observed in Japanese eyes with OAG over 2 years, with favorable safety profile. These reductions were observed across all glaucoma subtypes.

摘要

简介

我们报告了在日本轻中度开角型青光眼(OAG)患者中,行超声乳化白内障吸除术联合植入 iStent 小梁微旁路支架后的 2 年结果。

方法

这是一项为期 24 个月的前瞻性、纵向、观察性、上市后研究,于 2017 年 7 月至 2020 年 9 月进行。患者为接受抗青光眼药物治疗的 OAG 成年人,他们行白内障手术并联合植入一枚 iStent。主要观察指标包括眼内压(IOP)、抗青光眼药物、治疗成功率(定义为眼压降低,且用药种类与基线相比相同或减少,或眼压相同但用药种类减少,且术后无需进行二次青光眼手术)和安全性。在总体队列和青光眼亚型(原发性 OAG、正常眼压性青光眼和剥脱性青光眼)中分析了结果。

结果

总体而言,共纳入 232 只眼。24 个月时,平均(±标准差)IOP 从术前的 17.6±4.0mmHg 降至 14.3±3.0mmHg(p<0.05),用药种类从术前的 2.2±1.2 降至 0.7±1.2(p<0.05)。在所有青光眼亚型中均观察到类似的趋势。在总体队列中,分别有 96.7%、95.3%和 93.7%的患者在 6、12 和 24 个月时达到治疗成功,与术前相比,24 个月时药物无依赖的眼占比为 67.6%,而术前仅为 3.2%(p<0.0001)。2 年期间,安全性良好。

结论

在 OAG 日本患者中,行超声乳化白内障吸除术联合植入 iStent 小梁微旁路支架后,2 年内观察到 IOP 和用药种类均有显著且有临床意义的降低,安全性良好。这些降低在所有青光眼亚型中均观察到。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ded/9402767/7793060ab4ca/12325_2022_2207_Fig1_HTML.jpg

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