Safety and Efficacy of the Rho-Kinase Inhibitor (Ripasudil) in Bleb Needling after Trabeculectomy: A Prospective Multicenter Study

Author:

Mizuno Yu1ORCID,Komatsu Kaori1,Tokumo Kana1,Okada Naoki1ORCID,Onoe Hiromitsu1ORCID,Okumichi Hideaki1ORCID,Hirooka Kazuyuki1,Aoki Gaku2,Miura Yukiko3,Kiuchi Yoshiaki1ORCID

Affiliation:

1. Department of Ophthalmology and Visual Science, Hiroshima University, 1-2-3 Kasumi Minamiku, Hiroshima 734-8551, Japan

2. Department of Biostatistics, Clinical Research Center, Hiroshima University Hospital, 1-2-3 Kasumi Minamiku, Hiroshima 734-8551, Japan

3. Hiroshima Eye Clinic, 13-4, Noborimachi Nakaku, Hiroshima 730-0016, Japan

Abstract

Ripasudil, a rho-associated protein kinase inhibitor ophthalmic solution, shows a protective effect in preventing excessive scarring in vitro. This study aims to evaluate the safety and efficacy of ripasudil for glaucoma patients submitted to the needling procedure. In this prospective, multicenter, single-arm study, we included 20 eyes of 20 patients with glaucoma who underwent the needling procedure without antimetabolites. All patients administered ripasudil after needling for three months. The primary endpoint of this study was the safety of ripasudil in patients, and the secondary endpoint was the change in IOP at 12 weeks after the needling procedure. No serious complications were found in the patients. One eye experienced pruritus and conjunctival follicle, while another eye had conjunctival follicle. These complications were transient and resolved quickly after discontinuation of ripasudil. The mean preoperative IOP was 14.6 ± 4.6 mmHg, which decreased to 11.0 ± 4.7 mmHg (p = 0.0062) at 1 week postoperatively. The IOP reduction effect continued to 12 weeks (11.8 ± 3.1 mmHg; p = 0.0448). The administration of the ROCK inhibitor, ripasudil, after the needling procedure is safe and effective in maintaining IOP for 12 weeks.

Funder

Hiroshima University Hospital

Publisher

MDPI AG

Subject

General Medicine

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