TY - JOUR
T1 - The ocular hypotensive efficacy of topical fasudil, a rho-associated protein kinase inhibitor, in patients with end-stage glaucoma
AU - Pakravan, Mohammad
AU - Beni, Afsaneh Naderi
AU - Ghahari, Elham
AU - Varshochian, Reyhaneh
AU - Yazdani, Shahin
AU - Esfandiari, Hamed
AU - Ahmadieh, Hamid
N1 - Publisher Copyright:
© 2016 Wolters Kluwer Health, Inc.
PY - 2016/1/28
Y1 - 2016/1/28
N2 - To investigate the effects of topical administration of a selective Rho-associated kinase (ROCK) inhibitor, fasudil 0.5% and 1.2% in glaucomatous patients. In this interventional case series study, 4 eyes of 4 patients with unilateral end-stage primary open-angle glaucoma and no light perception vision were assigned to receive topical fasudil 0.5% (in 3 eyes) or 1.2% (in 1 eye) ophthalmic solution twice daily for 8 weeks. At weeks 1, 2, 3, 4, and 8, intraocular pressure (IOP) and adverse events were evaluated. Baseline mean IOP was 53.5 6 3.4 mm Hg and mean IOP reductions of the last visit were 28.25 6 1.2 mm Hg at 2 hours and 28.75 6 2.2 mm Hg at 4 hours. Mean IOP reductions were clinically and statistically significant with 0.5% and 1.2% fasudil and peak effects occurred 2-4 hours after application (P = 0.0002). The largest IOP reductions were produced by 1.2% fasudil (up to 212 mm Hg). Conjunctival hyperemia was found in 1 patient with 1.2% fasudil. Topical administration of fasudil in end-stage primary open-angle glaucoma patients, caused reduction in IOP and was well tolerated. ROCK inhibitors could be considered as a candidate for glaucoma therapy in future.
AB - To investigate the effects of topical administration of a selective Rho-associated kinase (ROCK) inhibitor, fasudil 0.5% and 1.2% in glaucomatous patients. In this interventional case series study, 4 eyes of 4 patients with unilateral end-stage primary open-angle glaucoma and no light perception vision were assigned to receive topical fasudil 0.5% (in 3 eyes) or 1.2% (in 1 eye) ophthalmic solution twice daily for 8 weeks. At weeks 1, 2, 3, 4, and 8, intraocular pressure (IOP) and adverse events were evaluated. Baseline mean IOP was 53.5 6 3.4 mm Hg and mean IOP reductions of the last visit were 28.25 6 1.2 mm Hg at 2 hours and 28.75 6 2.2 mm Hg at 4 hours. Mean IOP reductions were clinically and statistically significant with 0.5% and 1.2% fasudil and peak effects occurred 2-4 hours after application (P = 0.0002). The largest IOP reductions were produced by 1.2% fasudil (up to 212 mm Hg). Conjunctival hyperemia was found in 1 patient with 1.2% fasudil. Topical administration of fasudil in end-stage primary open-angle glaucoma patients, caused reduction in IOP and was well tolerated. ROCK inhibitors could be considered as a candidate for glaucoma therapy in future.
KW - Glaucoma
KW - Intraocular pressure
KW - ROCK inhibitors
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U2 - 10.1097/MJT.0000000000000362
DO - 10.1097/MJT.0000000000000362
M3 - Article
C2 - 26825486
AN - SCOPUS:84955619852
SN - 1075-2765
VL - 24
SP - E676-E680
JO - American Journal of Therapeutics
JF - American Journal of Therapeutics
IS - 6
ER -