Efficacy and safety of fixed-combination travoprost 0.004%/timolol 0.5% in patients transitioning from bimatoprost 0.03%/timolol 0.5% combination therapy
Autor: | Douglas A Hubatsch, Dietmar Schnober, Maria-Luise Scherzer |
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Rok vydání: | 2015 |
Předmět: |
medicine.medical_specialty
Intraocular pressure genetic structures Combination therapy Timolol Benzalkonium chloride β-blocker preservative Ophthalmology medicine In patient Original Research integumentary system Bimatoprost business.industry Clinical Ophthalmology prostaglandin analog eye diseases glaucoma Prostaglandin analog sense organs Travoprost business intraocular pressure medicine.drug |
Zdroj: | Clinical Ophthalmology (Auckland, N.Z.) |
ISSN: | 1177-5483 |
Popis: | Dietmar Schnober,1 Douglas A Hubatsch,2 Maria-Luise Scherzer3 1Private Ophthalmology Practice, Werdohl, Germany; 2Alcon Laboratories, Inc., Fort Worth, TX, USA; 3Private Ophthalmology Practice, Regenstauf, Germany Purpose: To determine the efficacy and safety of fixed-combination travoprost 0.004%/timolol 0.5% preserved with polyquaternium-1 in patients with insufficient response to bimatoprost 0.03%/timolol 0.5% preserved with benzalkonium chloride.Patients and methods: In this open-label nonrandomized study conducted at 13 European sites, patients with primary open-angle glaucoma or ocular hypertension with insufficient intraocular pressure (IOP) reduction during bimatoprost/timolol therapy were transitioned to travoprost/timolol (DuoTrav®) administered every evening for 12weeks. Change in IOP from baseline to week 12 was assessed in patients who transitioned from fixed-combination bimatoprost/timolol (n=57, primary endpoint). Secondary assessments included change in IOP at week 4, percentage of patients with IOP ≤18mmHg at weeks 4 and 12, change in Ocular Surface Disease Index and ocular hyperemia scores at week 12, and patient preference. Adverse events were also reported.Results: IOP change (mean ± SD) from baseline to week 12 was –3.8±1.9mmHg (P |
Databáze: | OpenAIRE |
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