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Glaukos iStent inject®小梁微旁路植入术与白内障并存的开角型青光眼或高眼压症患者的白内障手术相关:一项长期研究。

Glaukos iStent inject® Trabecular Micro-Bypass Implantation Associated with Cataract Surgery in Patients with Coexisting Cataract and Open-Angle Glaucoma or Ocular Hypertension: A Long-Term Study.

作者信息

Arriola-Villalobos Pedro, Martinez-de-la-Casa Jose Maria, Diaz-Valle David, Morales-Fernandez Laura, Fernandez-Perez Cristina, Garcia-Feijoo Julian

机构信息

Servicio de Oftalmología, Hospital Clínico San Carlos, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), Madrid, Spain; Cooperative Research Network on Age-Related Ocular Pathology, Visual and Life Quality, Instituto de Salud Carlos III, Madrid, Spain.

Cooperative Research Network on Age-Related Ocular Pathology, Visual and Life Quality, Instituto de Salud Carlos III, Madrid, Spain; Servicio de Oftalmología, Hospital Clínico San Carlos, Departamento de Oftalmología y ORL, Facultad de Medicina, Universidad Complutense de Madrid, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), Madrid, Spain.

出版信息

J Ophthalmol. 2016;2016:1056573. doi: 10.1155/2016/1056573. Epub 2016 Nov 1.

Abstract

. To evaluate the long-term efficacy and safety of the iStent device (Glaukos Corporation, Laguna Hills, CA) combined with phacoemulsification in patients with coexistent cataract and open-angle glaucoma or ocular hypertension (OHT). . A prospective, uncontrolled, nonrandomized, interventional case series study was conducted in patients with both mild or moderate open-angle glaucoma or OHT and cataract. Patients underwent cataract surgery along with the implant of two iStent devices. Outcome measures were intraocular pressure (IOP), topical hypotensive medications required, and best-corrected visual acuity (BCVA). . 20 patients were enrolled. Mean follow-up was 47.4 ± 18.46 months. Mean baseline IOP was 19.95 ± 3.71 mmHg with medication and 26 ± 3.11 mmHg after washout. Mean end-follow-up IOP was 16.25 ± 1.99 mmHg, representing an IOP decrease of 36.92%, 9.74 ± 3.14 mmHg ( < 0.001), from baseline washout IOP. The mean number of medications was significantly reduced from 1.3 ± 0.66 to 0.75 ± 0.79 ( = 0.017). 45% of patients were medication-free by the end of follow-up. Mean log⁡MAR BCVA improved significantly from 0.42 ± 0.16 to 0.18 ± 0.16 ( < 0.001). No complications of surgery were observed. . The iStent device combined with cataract surgery served to significantly reduce both IOP and medication use in the long term in patients with coexistent open-angle glaucoma or ocular hypertension (OHT) and cataract.

摘要

评估iStent装置(Glaukos公司,加利福尼亚州拉古纳希尔斯)联合超声乳化术治疗合并白内障和开角型青光眼或高眼压症(OHT)患者的长期疗效和安全性。对合并轻度或中度开角型青光眼或OHT及白内障的患者进行了一项前瞻性、非对照、非随机的干预性病例系列研究。患者接受白内障手术并植入两枚iStent装置。观察指标为眼压(IOP)、所需局部降压药物及最佳矫正视力(BCVA)。共纳入20例患者。平均随访时间为47.4±18.46个月。用药时平均基线眼压为19.95±3.71 mmHg,停药后为26±3.11 mmHg。末次随访时平均眼压为16.25±1.99 mmHg,较基线停药眼压降低了36.92%,即9.74±3.14 mmHg(P<0.001)。平均用药数量从1.3±0.66显著减少至0.75±0.79(P=0.017)。45%的患者在随访结束时无需用药。平均log⁡MAR BCVA从0.42±0.16显著改善至0.18±0.16(P<0.001)。未观察到手术并发症。iStent装置联合白内障手术可长期显著降低合并开角型青光眼或高眼压症(OHT)及白内障患者的眼压和药物使用量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81f0/5108856/f23f2fe49dda/JOPH2016-1056573.001.jpg

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