Begitek Clínica Oftalmológica - Miranza, Pz. Teresa de Calcuta, 7, 20012, Donostia-San Sebastian, Spain.
Hospital Universitario Araba, Vitoria-Gasteiz, Spain.
Int Ophthalmol. 2023 Oct;43(10):3695-3705. doi: 10.1007/s10792-023-02779-y. Epub 2023 Jul 6.
To evaluate the effectiveness of ab-externo canaloplasty using the iTrack canaloplasty microcatheter (Nova Eye Inc, Fremont, California), with or without suture, in glaucoma patients with high myopia.
This was a prospective, single-center, single-surgeon, observational study comparing the outcomes of ab-externo canaloplasty performed with a tensioning suture (suture group) and without a tensioning suture (no-suture group) in mild to severe glaucoma patients with high myopia. Twenty-three eyes received canaloplasty as a standalone procedure, 5 in combination with phacoemulsification. Primary efficacy endpoints included intraocular pressure (IOP) and the number of glaucoma medications. Safety was assessed based on reported complications and adverse events.
Twenty-nine eyes of 29 patients with a mean age of 61.2 ± 12.3 years; 19 eyes in the no-suture group and 10 eyes in the suture group. All eyes demonstrated a significant reduction in IOP 24 months postoperatively, from 21.9 ± 7.22 to 15.4 ± 4.86 mmHg in the suture group and from 23.8 ± 7.58 to 19.7 ± 3.68 mmHg in the no-suture group. The mean number of anti-glaucoma medications reduced from 3.1 ± 0.6 to 0.4 ± 0.7 in the suture group and 3.3 ± 0.9 to and 0.2 ± 0.6 in the no-suture group at 24 months. IOP was not significantly different at baseline between the 2 groups, but it was statistically different at 12 and 24 months. There was no statistically significant difference in the number of medications between the groups at baseline, 12 and 24 months. No serious complications were reported.
Ab-externo canaloplasty performed either with or without a tensioning suture demonstrated good effectiveness in highly myopic eyes with a significant reduction in IOP and number of anti-glaucoma medications. The suture group achieved a lower postoperative IOP. However, the no-suture modification provides a similar reduction in medications with reduced tissue handling.
评估使用 iTrack 经外路房水引流管(Nova Eye Inc,加利福尼亚州弗里蒙特)进行房水引流管成形术的有效性,包括带或不带缝线的术式,用于治疗伴有高度近视的青光眼患者。
这是一项前瞻性、单中心、单医师、观察性研究,比较了伴有(缝线组)或不伴有(无缝线组)缝线张力的经外路房水引流管成形术在伴有轻至重度青光眼的高度近视患者中的疗效。23 只眼单独行房水引流管成形术,5 只眼联合超声乳化术。主要疗效终点包括眼压(IOP)和降眼压药物的数量。安全性基于报告的并发症和不良事件进行评估。
29 例患者的 29 只眼,平均年龄 61.2±12.3 岁;无缝线组 19 只眼,缝线组 10 只眼。所有眼术后 24 个月时 IOP 均显著降低,缝线组从 21.9±7.22mmHg 降至 15.4±4.86mmHg,无缝线组从 23.8±7.58mmHg 降至 19.7±3.68mmHg。缝线组降眼压药物的平均数量从 3.1±0.6 降至 0.4±0.7,无缝线组从 3.3±0.9 降至 0.2±0.6。两组在基线时的 IOP 无显著差异,但在 12 个月和 24 个月时存在统计学差异。两组在基线、12 个月和 24 个月时的药物数量均无统计学差异。未报告严重并发症。
经外路房水引流管成形术无论是否带缝线,对高度近视眼均具有良好的疗效,可显著降低眼压和降眼压药物的数量。缝线组术后眼压更低。然而,无缝线改良术式可减少组织处理,同时提供类似的药物减少。