Department of Ophthalmology, National Healthcare Group Eye Institute, Tan Tock Seng Hospital.
Yong Loo Lin School of Medicine, National University of Singapore.
J Glaucoma. 2024 Nov 1;33(11):855-861. doi: 10.1097/IJG.0000000000002475. Epub 2024 Aug 1.
This study reports 12-month outcomes of combined phacoemulsification and Hydrus Microstent implantation in Asian eyes with moderate-to-severe normal tension glaucoma (NTG), demonstrating a significant reduction in glaucoma medications with an excellent intra and postoperative safety profile.
To evaluate the 12-month safety and efficacy outcomes of combined phacoemulsification and Hydrus Microstent (Ivantis Inc.) implantation in Asian eyes with moderate to severe NTG.
Retrospective study of consecutive surgeries performed from August 2019 to August 2021 in a single tertiary eye centre in Singapore. Outcome measures included a reduction in intraocular pressure (IOP), number of glaucoma medications, and intra and postoperative complications.
Data from 21 eyes of 21 subjects were analyzed. All subjects were ethnic Chinese, and the majority were males (14, 66.7%). At baseline, the mean IOP was 13.3 (2.3) mm Hg, all eyes had a Humphrey visual field mean deviation of ≥-6 dB [mean: -13.9 (4.3) dB], and all eyes were on at least one glaucoma medication. There was no statistically significant reduction in IOP at all time points compared with baseline (all P > 0.05). However, the median number of medications was reduced from 2 to 0 at all time points, up to postoperative month (POM) 12 (all P < 0.001). There were no intraoperative complications. No eyes underwent secondary glaucoma procedures nor lost any Snellen line of visual acuity by POM12. One (4.8%) eye experienced numerical hypotony at postoperative day 1, which resolved conservatively. Two (9.5%) eyes underwent laser iridoplasty for stent occlusion by iris. There was no deterioration in Humphrey visual field mean deviation at POM12 compared with baseline (n = 20, P > 0.05).
Combined phacoemulsification and Hydrus Microstent implantation were effective in reducing medication burden in Asian eyes with moderate to severe NTG, up to 12 months postoperatively.
本研究报告了在亚洲中度至重度正常眼压性青光眼(NTG)患者中联合施行超声乳化白内障吸除术和 Hydrus Microstent 植入术的 12 个月结果,表明该治疗方案可显著减少青光眼药物的使用,并具有良好的围手术期安全性。
评估在亚洲中度至重度 NTG 患者中施行超声乳化白内障吸除术联合 Hydrus Microstent(Ivantis Inc.)植入术的 12 个月安全性和疗效。
这是一项回顾性研究,纳入了 2019 年 8 月至 2021 年 8 月在新加坡一家三级眼科中心连续施行的手术。主要观察指标包括眼压(IOP)降低情况、青光眼药物使用数量以及围手术期并发症。
共纳入 21 例(21 只眼)患者,所有患者均为华裔,大多数为男性(14 例,66.7%)。基线时,平均 IOP 为 13.3(2.3)mmHg,所有患者的 Humphrey 视野平均缺损值均≥-6 dB[平均:-13.9(4.3)dB],所有患者均至少使用一种青光眼药物。与基线相比,所有时间点的 IOP 均无统计学显著降低(均 P > 0.05)。然而,药物使用数量中位数从基线时的 2 种降至 0 种,直至术后 12 个月(所有 P < 0.001)。术中无并发症发生。截至术后 12 个月时,无眼行二次青光眼手术,也无眼视力丧失超过 1 行(Snellen 视力表)。术后第 1 天有 1 只眼(4.8%)发生数值性低眼压,经保守治疗后缓解。2 只眼(9.5%)因虹膜支架阻塞行激光虹膜切开术。与基线相比,术后 12 个月时 Humphrey 视野平均缺损值无恶化(n = 20,P > 0.05)。
在亚洲中度至重度 NTG 患者中施行超声乳化白内障吸除术联合 Hydrus Microstent 植入术可有效减少药物负担,疗效可维持至术后 12 个月。