ESCRS - P181 - EFFICACY, AND SAFETY OF AB-INTERNO CANALOPLASTY USING ITRACK ADVANCE IN PRIMARY OPEN-ANGLE GLAUCOMA

EFFICACY, AND SAFETY OF AB-INTERNO CANALOPLASTY USING ITRACK ADVANCE IN PRIMARY OPEN-ANGLE GLAUCOMA

Published 2024 - 28th ESCRS Winter Meeting

Reference: P181 | Type: Submission | DOI: 10.82333/vghh-3b46

Authors: Simon Ondrejka* 1 , Norbert Koerber 1

1Augencentrum Köln,Köln,Germany

Purpose

To assess the safety and efficacy of ab-interno canaloplasty using iTrack Advance (Nova Eye, Inc., Fremont, USA) in reducing intraocular pressure (IOP) and glaucoma medications in patients with open-angle glaucoma (OAG).

Setting

Augencentrum Köln, Germany.

Methods

A retrospective, single-center, consecutive case series. Patients with open angle glaucoma, and no previous glaucoma surgery except for selective laser trabeculoplasty (SLT) were treated with ab-interno canaloplasty performed using the iTrack Advance microcatheter combined with phacoemulsification and followed for up to 12 months (no medications washout). The iTrack Advance was used to circumferentially catheterize and viscodilate 360° Schlemm’s canal in one single procedure. Primary efficacy endpoints included IOP and number of glaucoma medications at 6 and 12 months postoperatively.

Results

Fifty-seven eyes of 34 patients (mean age of 73.4±6.7-year-old; 47% females) were recruited. Four eyes had previous SLT. Mean IOP (mmHg) significantly decreased from 18.28±4.24 (n=57) at baseline to 13.82±2.80, and 13.38±2.63 at 6 (n=46; p<0.001), and 12 months (n=36; p<0.001), respectively. The number of glaucoma medications was significantly reduced from 1.54±0.75 (n=57) at baseline to 0.08±0.55, and 0.10±0.63 at 6 (n=49; p<0.001), and 12 months (n=36; p<0.001), respectively. At 12 months, 97% eyes were medication-free Vs 3,5% at baseline; all eyes that reached 12 months of follow up were  ≤18mmHg and 30/36 eyes (83.3%) had an IOP  ≤15mmHg. No serious complications were recorded.

Conclusion

Ab interno canaloplasty performed with the iTrack Advance proved to be safe and effective in reducing intraocular pressure (IOP) and the need for medications in OAG patients up to 12 months postoperatively. Moreover, the majority of patients were glaucoma controlled (≤15mmHg) and medication-free 1 year following the procedure.