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不同青光眼亚型和严重程度的超声乳化术中第二代小梁微管旁路支架(iStent inject)的 3 年疗效。

Three-Year Outcomes of Second-generation Trabecular Micro-bypass Stents (iStent inject) With Phacoemulsification in Various Glaucoma Subtypes and Severities.

机构信息

Department of Ophthalmology, Faculty of Medicine.

Montreal Glaucoma Institute.

出版信息

J Glaucoma. 2021 Mar 1;30(3):266-275. doi: 10.1097/IJG.0000000000001716.

Abstract

PRECIS

This longitudinal case series provides valuable long-term data on the safety and efficacy of iStent inject with concomitant cataract surgery. Patients experienced significant and durable reductions in both intraocular pressure (IOP) and medication burden through 3 years postoperative.

PURPOSE

The purpose of this study was to examine the 3-year effectiveness and safety of iStent inject second-generation trabecular micro-bypass stent implantation with concomitant phacoemulsification cataract surgery in eyes with various glaucoma subtypes and severities.

METHODS

This was a single-center consecutive case series. Three-year outcomes included mean IOP and medications, the proportions of eyes with IOP ≤18, ≤15, and ≤12 mm Hg, and success (absence of secondary glaucoma interventions). Safety included best-corrected visual acuity (BCVA), cup-to-disc ratio, visual field (VF) mean deviation, retinal nerve fiber layer (RNFL), and ganglion cell-inner plexiform layer (GCIPL) thickness, and adverse events.

RESULTS

A total of 124 eyes with different glaucoma subtypes and severities were included. At 3 years postoperative, mean IOP reduced from 16.90±3.85 mm Hg preoperatively to 13.17±2.83 mm Hg (22% reduction, P<0.001) and mean medication burden decreased from 2.38±1.29 medications preoperatively to 1.16±1.22 medications (51% reduction, P<0.001). At 3 years, 96% of eyes achieved IOP ≤18 mm Hg (vs. 69% preoperatively), 80% of eyes achieved IOP ≤15 mm Hg (vs. 40% preoperatively), and 42% of eyes achieved IOP ≤12 mm Hg (vs. 7% preoperatively) with 76% of eyes eliminating ≥1 medication and 37% of eyes eliminating ≥2 medications versus preoperative medication burden. The 3-year cumulative survival rate was 74%. Postphacoemulsification BCVA improvement was preserved, and cup-to-disc ratio, VF mean deviation, and RNFL and GCIPL thickness remained stable. A favorable safety profile included no intraoperative complications and few, transient, postoperative adverse events.

CONCLUSION

Significant and sustained IOP and medication reductions were achieved through 3 years after iStent inject implantation with cataract surgery in a real-world clinical population with mild-to-severe glaucoma, along with favorable safety including stable BCVA, VF, and RNFL and GCIPL thickness.

摘要

目的

本研究旨在评估第二代 iStent inject 小梁微旁路支架植入联合白内障超声乳化术治疗各种青光眼亚型和严重程度患者的 3 年疗效和安全性。

方法

这是一项单中心连续病例系列研究。3 年的结果包括平均眼压(IOP)和药物使用情况、IOP≤18mmHg、IOP≤15mmHg 和 IOP≤12mmHg 的眼比例以及成功率(无继发性青光眼干预)。安全性包括最佳矫正视力(BCVA)、杯盘比、视野(VF)平均偏差、视网膜神经纤维层(RNFL)和神经节细胞内丛状层(GCIPL)厚度以及不良事件。

结果

共纳入 124 只不同青光眼亚型和严重程度的眼。术后 3 年,平均眼压从术前的 16.90±3.85mmHg 降至 13.17±2.83mmHg(降低 22%,P<0.001),平均药物使用量从术前的 2.38±1.29 种药物降至 1.16±1.22 种药物(降低 51%,P<0.001)。术后 3 年,96%的眼达到 IOP≤18mmHg(术前为 69%),80%的眼达到 IOP≤15mmHg(术前为 40%),42%的眼达到 IOP≤12mmHg(术前为 7%),76%的眼减少了≥1 种药物,37%的眼减少了≥2 种药物,与术前的药物负担相比。3 年累积生存率为 74%。白内障超声乳化术后 BCVA 改善得以维持,杯盘比、VF 平均偏差以及 RNFL 和 GCIPL 厚度保持稳定。安全性良好,包括术中无并发症和少数短暂的术后不良事件。

结论

在轻度至重度青光眼的真实世界临床人群中,与白内障手术联合应用第二代 iStent inject 小梁微旁路支架植入可显著、持续地降低眼压和减少药物使用,安全性良好,包括稳定的 BCVA、VF 和 RNFL 及 GCIPL 厚度。

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