Eye Unit and Eye Bank, Queen Victoria Hospital NHS Foundation Trust, East Grinstead, UK.
Ophthalmology, "St. Spiridon" University Hospital, Iasi, Romania.
Br J Ophthalmol. 2020 Oct;104(10):1378-1383. doi: 10.1136/bjophthalmol-2019-315434. Epub 2020 Jan 24.
Comparing outcomes after combined phacoemulsification, two iStents insertion and endocyclophotocoagulation (ECP) versus phacoemulsification-iStents alone.
This is a longitudinal retrospective 12 months study in eyes with ocular hypertension or early-to-moderate open angle glaucoma. Level of disease, intraocular pressure (IOP) and tolerance of glaucoma medication were considered before planning surgery. Best-corrected visual acuity (BCVA-logMAR), IOP (mm Hg), number of medications were assessed at baseline, week 1, week 5, month 3, 6, 12 postop.
percentage (%) in IOP reduction at 12 months vs medicated baseline.
absolute values of IOP/medication reduction, BCVA and postop complications.
The ICE2 (two iStents-cataract extraction-ECP) group included 63 eyes and Phaco-iStent group included 46 eyes. Baseline IOP was higher in the ICE2 than phaco-iStent group (19.97±4.31 mm Hg vs 17.63±3.86 mm Hg, p=0.004) and mean deviation was lower (-7.20±2.58 dB vs -4.94±4.51 dB, p=0.037). Number of medications were comparable at baseline: 2.22±1.06 (ICE2) vs 2.07±1.02 (phaco-iStent), p=0.442. At month 12 postop, IOP in the ICE2 group decreased 35% from baseline vs 21% in the phaco-iStent group (p=0.03); absolute IOP reduction was significantly lower than baseline in each group (p<0.001), yet final IOP was lower in the ICE2 group than phaco-iStent group (13.05±2.18 mm Hg vs 14.09±1.86 mm Hg, p=0.01). Similar results were found for glaucoma medication (1.24±1.05 in ICE2 group vs 1.39±1.03 in phaco-iStent group, p=0.01). Final BCVA was 0.11±0.18 (phaco-iStent group) vs 0.08±0.08 (ICE2 group), p=0.309. Safety outcomes were comparable between groups.
ICE2 procedure offers better results in IOP/medication reduction at 12 months than phacoemulsification-iStents alone.
比较白内障超声乳化联合植入 2 枚 iStent 及内路激光睫状体光凝术(ECP)与单纯白内障超声乳化联合植入 iStent 的疗效。
这是一项为期 12 个月的回顾性纵向研究,纳入对象为患有眼压升高或早期至中期开角型青光眼的患者。在计划手术前,根据疾病程度、眼内压(IOP)和青光眼药物耐受情况进行评估。在基线、术后第 1 周、第 5 周、第 3 个月、第 6 个月和第 12 个月时评估最佳矫正视力(BCVA-logMAR)、IOP(mmHg)和用药数量。
与基线用药时相比,12 个月时 IOP 降低的百分比。
IOP/药物降低的绝对值、BCVA 和术后并发症。
ICE2(2 枚 iStent-白内障超声乳化-ECP)组纳入 63 只眼,Phaco-iStent 组纳入 46 只眼。与 Phaco-iStent 组相比,ICE2 组的基线 IOP 更高(19.97±4.31mmHg 比 17.63±3.86mmHg,p=0.004),平均偏差更低(-7.20±2.58dB 比-4.94±4.51dB,p=0.037)。基线时两组药物使用数量相当:2.22±1.06(ICE2 组)比 2.07±1.02(Phaco-iStent 组),p=0.442。术后 12 个月时,ICE2 组的 IOP 较基线降低 35%,而 Phaco-iStent 组降低 21%(p=0.03);两组的 IOP 绝对值均较基线显著降低(p<0.001),但 ICE2 组的终末 IOP 低于 Phaco-iStent 组(13.05±2.18mmHg 比 14.09±1.86mmHg,p=0.01)。在青光眼药物使用方面也观察到了类似的结果(ICE2 组 1.24±1.05,Phaco-iStent 组 1.39±1.03,p=0.01)。最终 BCVA 为 0.11±0.18(Phaco-iStent 组)和 0.08±0.08(ICE2 组),p=0.309。两组的安全性结局相当。
与单纯白内障超声乳化联合植入 iStent 相比,ICE2 手术在 12 个月时的 IOP/药物降低效果更好。