Department of Ophthalmology, Military Institute of Medicine, Warsaw, Poland,
Department of Ophthalmology, Medical University of Białystok, Białystok, Poland.
Ophthalmic Res. 2021;64(2):327-336. doi: 10.1159/000511456. Epub 2020 Sep 9.
To assess the effect of iStent trabecular microbypass implantation combined with phacoemulsification on intraocular pressure (IOP) and glaucoma medications and to compare this to outcomes of phacoemulsification alone in patients with mild to moderate primary open-angle glaucoma (POAG) depending on initial IOP.
Eighty subjects with cataract and POAG were randomized 1:1 into either iStent implantation and cataract surgery (iStent group) (n = 44) or cataract surgery alone (control group) (n = 36). Groups were divided according to initial IOP (after washout period) into IOP <26 mm Hg and IOP ≥26 mm Hg. Patients were assessed preoperatively and at postoperative day 1, week 1, and months 1, 3, 6, 12, and 24. Outcome measures included best-corrected visual acuity, IOP, and glaucoma medications.
Postoperatively at 24 months, mean IOP decreased from 20.93 ± 1.28 to 17.79 ± 2.50 mm Hg in the IOP subgroup <26 mm Hg and from 26.00 ± 0.00 to 19.86 ± 2.19 in the subgroup ≥26 mm Hg in the control group. In the iStent group <26 mm Hg, IOP decreased from 22.04 ± 1.64 to 15.57 ± 2.13 mm Hg and from 26.6 ± 1.09 to 17.06 ± 2.43 mm Hg in the iStent group ≥26 mm Hg.
In patients with open-angle glaucoma and cataract, iStent implantation combined with cataract surgery reduced IOP significantly through 2 years, with greater reductions achieved versus phacoemulsification alone. In patients with baseline IOP <26 mm Hg, surgery reduced IOP and medication use significantly declined through 2 years, with greater reductions achieved versus patients with baseline IOP ≥26 mm Hg. The study was registered at ClinicalTrials.gov under the number NCT03807869.
评估 iStent 小梁微旁路植入联合超声乳化术对眼压(IOP)和青光眼药物的影响,并根据初始 IOP 将其与单纯超声乳化术治疗轻度至中度原发性开角型青光眼(POAG)患者的结果进行比较。
80 名白内障合并 POAG 患者随机分为 iStent 植入和白内障手术(iStent 组)(n = 44)或单纯白内障手术(对照组)(n = 36)。根据初始 IOP(冲洗期后)分为 IOP<26mmHg 和 IOP≥26mmHg 两组。患者术前和术后第 1、1 周、第 1、3、6、12 和 24 个月进行评估。主要评估指标包括最佳矫正视力、眼压和青光眼药物。
在 24 个月的随访中,IOP<26mmHg 的亚组中,iStent 组术后 24 个月时的平均眼压从 20.93±1.28mmHg 降至 17.79±2.50mmHg,对照组从 26.00±0.00mmHg 降至 19.86±2.19mmHg。在 iStent 组<26mmHg 的亚组中,iStent 组的 IOP 从 22.04±1.64mmHg 降至 15.57±2.13mmHg,从 26.6±1.09mmHg 降至 17.06±2.43mmHg。
在开角型青光眼合并白内障患者中,iStent 植入联合白内障手术可显著降低眼压,2 年内的降幅大于单纯超声乳化术。在基线 IOP<26mmHg 的患者中,2 年内手术降低眼压和减少药物使用的效果显著,基线 IOP≥26mmHg 的患者降幅更大。该研究在 ClinicalTrials.gov 上注册,编号为 NCT03807869。