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The role of Brimonidine in the treatment of open-angle glaucoma
At present, medical therapy is the first line of attack against primary open-angle glaucoma. β-blockers, miotics, sympathomimetics, carbonic anhydrase inhibitors, and prostaglandins have been used with varying degrees of success. The α 2-agonists, clonidine, apraclonidine, and now brimonidine are po...
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Published in: | Survey of ophthalmology 1996-11, Vol.41, p.S3-S7 |
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Main Author: | |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | At present, medical therapy is the first line of attack against primary open-angle glaucoma. β-blockers, miotics, sympathomimetics, carbonic anhydrase inhibitors, and prostaglandins have been used with varying degrees of success. The α
2-agonists, clonidine, apraclonidine, and now brimonidine are powerful inhibitors of aqueous humor production, thereby lowering intraocular pressure (IOP) in these patients. Brimonidine is emerging as a potential first-line therapy for primary open-angle glaucoma, with a peak IOP-lowering efficacy comparable to that of timolol, but without timolol's adverse cardiopulmonary side effects. Brimonidine promises to be an important new drug to help meet the therapeutic challenges faced by ophthalmologists in treating glaucoma. |
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ISSN: | 0039-6257 1879-3304 |
DOI: | 10.1016/S0039-6257(96)82026-1 |