USE OF BIFEMELANE HYDROCHLORIDE IN IMPROVING AND MAINTAINING THE VISUAL-FIELD OF PATIENTS WITH GLAUCOMA

Citation
T. Shigemitsu et Y. Majima, USE OF BIFEMELANE HYDROCHLORIDE IN IMPROVING AND MAINTAINING THE VISUAL-FIELD OF PATIENTS WITH GLAUCOMA, Clinical therapeutics, 18(1), 1996, pp. 106-113
Citations number
30
Categorie Soggetti
Pharmacology & Pharmacy
Journal title
ISSN journal
01492918
Volume
18
Issue
1
Year of publication
1996
Pages
106 - 113
Database
ISI
SICI code
0149-2918(1996)18:1<106:UOBHII>2.0.ZU;2-S
Abstract
We investigated the change of visual fields in 40 patients with primar y or secondary glaucoma. No limitations were placed on the type of ang ular glaucoma tie, open or closed). The intraocular pressure of the pa tients had been controlled at <20 mm Hg for 2 years before the study, and patients with normal-tension glaucoma also were included. We evalu ated the effect of 48 months of treatment with bifemelane hydrochlorid e, 150 mg/d in three divided doses, on 20 patients with glaucoma. The control group included 20 glaucoma patients whose intraocular pressure had been controlled at <20 mm Hg for 2 years before the study by the instillation or oral administration of an intraocular hypotensive agen t. They had not received any oral agent, such as a cerebral circulatio n metabolism activator. Results showed that the visual field was impro ved in 14 (70%) of 20 patients who received bifemelane hydrochloride, whereas the visual field was improved in 4 (20%) of 20 patients in the control group. More patients in the bifemelane hydrochloride group ha d improved visual fields than in the control group; differences betwee n groups were significant. In addition, an evaluation of the visual fi eld with the use of the Kosaki and Inoue classification showed improve ment in all patients in stages IIa to V. We conclude that this drug is useful for maintaining and improving the disturbed visual field of pa tients in whom the intraocular pressure can be maintained at <20 mm Hg and in patients who can tolerate 150 mg/d in three separate doses.