Latanoprost in the treatment of glaucoma

Albert AlmDepartment of Neuroscience, Ophthalmology, University Hospital, Uppsala, SwedenAbstract: Prostaglandins are approved by the European Glaucoma Society guidelines as first-line treatment for glaucoma. This review focuses on latanoprost, an ester prodrug of prostaglandin (PG) F2α,...

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Main Author: Alm A
Format: Article
Language:English
Published: Dove Medical Press 2014-09-01
Series:Clinical Ophthalmology
Online Access:http://www.dovepress.com/latanoprost-in-the-treatment-of-glaucoma-peer-reviewed-article-OPTH
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spelling doaj-4828795329a441158138cffbf848d3942020-11-24T22:53:49ZengDove Medical PressClinical Ophthalmology1177-54832014-09-012014default1967198518549Latanoprost in the treatment of glaucomaAlm A Albert AlmDepartment of Neuroscience, Ophthalmology, University Hospital, Uppsala, SwedenAbstract: Prostaglandins are approved by the European Glaucoma Society guidelines as first-line treatment for glaucoma. This review focuses on latanoprost, an ester prodrug of prostaglandin (PG) F2α, which was the first of the currently available topical PGF2α analogs to be launched for glaucoma or ocular hypertension and which still accounts for the majority of prescriptions. It is better absorbed than the parent compound through the cornea, and peak concentration of the active drug is in the aqueous humor 1–2 hours after topical dosing (15–30 ng/mL). Metabolism occurs mainly in the liver. Latanoprost (0.005%) has been very well studied in clinical trials and meta-analyses that show it to be generally as effective as the other PG analogs (bimatoprost, travoprost, and tafluprost) and more effective than timolol, dorzolamide, and brimonidine. Latanoprost has good short- and long-term safety and tolerability profiles. In common with other prostaglandins, it lacks systemic effects, but can cause ocular adverse events such as conjunctival hyperemia, pigmentation of the iris, periocular skin or eyelashes, hypertrichosis, and ocular surface effects or irritation. Latanoprost is significantly better tolerated than either bimatoprost or travoprost. Patients treated with latanoprost have better compliance and persist with therapy longer than those that are given other drugs. An improved formulation of latanoprost without the preservative benzalkonium chloride has recently been developed. It is as effective as conventional latanoprost, has a lower incidence of hyperemia, and can be stored at room temperature. In conclusion, latanoprost has the best efficacy–tolerability ratio of the PG analogs available for glaucoma treatment, and has good compliance and persistence. These factors should be improved further by the recent development of preservative-free latanoprost.Keywords: prostaglandin, intraocular pressure, ocular hypertension, hyperemia, glaucoma, latanoprosthttp://www.dovepress.com/latanoprost-in-the-treatment-of-glaucoma-peer-reviewed-article-OPTH
collection DOAJ
language English
format Article
sources DOAJ
author Alm A
spellingShingle Alm A
Latanoprost in the treatment of glaucoma
Clinical Ophthalmology
author_facet Alm A
author_sort Alm A
title Latanoprost in the treatment of glaucoma
title_short Latanoprost in the treatment of glaucoma
title_full Latanoprost in the treatment of glaucoma
title_fullStr Latanoprost in the treatment of glaucoma
title_full_unstemmed Latanoprost in the treatment of glaucoma
title_sort latanoprost in the treatment of glaucoma
publisher Dove Medical Press
series Clinical Ophthalmology
issn 1177-5483
publishDate 2014-09-01
description Albert AlmDepartment of Neuroscience, Ophthalmology, University Hospital, Uppsala, SwedenAbstract: Prostaglandins are approved by the European Glaucoma Society guidelines as first-line treatment for glaucoma. This review focuses on latanoprost, an ester prodrug of prostaglandin (PG) F2α, which was the first of the currently available topical PGF2α analogs to be launched for glaucoma or ocular hypertension and which still accounts for the majority of prescriptions. It is better absorbed than the parent compound through the cornea, and peak concentration of the active drug is in the aqueous humor 1–2 hours after topical dosing (15–30 ng/mL). Metabolism occurs mainly in the liver. Latanoprost (0.005%) has been very well studied in clinical trials and meta-analyses that show it to be generally as effective as the other PG analogs (bimatoprost, travoprost, and tafluprost) and more effective than timolol, dorzolamide, and brimonidine. Latanoprost has good short- and long-term safety and tolerability profiles. In common with other prostaglandins, it lacks systemic effects, but can cause ocular adverse events such as conjunctival hyperemia, pigmentation of the iris, periocular skin or eyelashes, hypertrichosis, and ocular surface effects or irritation. Latanoprost is significantly better tolerated than either bimatoprost or travoprost. Patients treated with latanoprost have better compliance and persist with therapy longer than those that are given other drugs. An improved formulation of latanoprost without the preservative benzalkonium chloride has recently been developed. It is as effective as conventional latanoprost, has a lower incidence of hyperemia, and can be stored at room temperature. In conclusion, latanoprost has the best efficacy–tolerability ratio of the PG analogs available for glaucoma treatment, and has good compliance and persistence. These factors should be improved further by the recent development of preservative-free latanoprost.Keywords: prostaglandin, intraocular pressure, ocular hypertension, hyperemia, glaucoma, latanoprost
url http://www.dovepress.com/latanoprost-in-the-treatment-of-glaucoma-peer-reviewed-article-OPTH
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