Please use this identifier to cite or link to this item: http://repositorio.unifesp.br/handle/11600/34847
Title: Safety and Efficacy of Moxifloxacin-Dexamethasone Eyedrops as Treatment for Bacterial Ocular Infection Associated with Bacterial Blepharitis
Authors: Belfort, Rubens [UNIFESP]
Gabriel, Luis [UNIFESP]
Martins Bispo, Paulo Jose [UNIFESP]
Muccioli, Cristina [UNIFESP]
Zacharias Serapicos, Patricia Cabral [UNIFESP]
Clark, Linda
Bell, Belinda
Bartell, John
Stroman, David W.
Hoefling-Lima, Ana Luisa [UNIFESP]
Universidade Federal de São Paulo (UNIFESP)
Alcon Res Ltd
Keywords: Blepharitis
Conjunctivitis
Dexamethasone
Keratitis
Moxifloxacin
Issue Date: 1-May-2012
Publisher: Springer
Citation: Advances in Therapy. New York: Springer, v. 29, n. 5, p. 416-426, 2012.
Abstract: Treatments that offer two medications in a fixed combination have the potential to offer efficacious and safe treatment with advantages such as a regimen that is simpler than administering two separate solutions. This study evaluated the safety and efficacy of fixed-combination versus concomitant moxifloxacin 0.5% and dexamethasone 0.1% ocular solutions for the treatment of bacterial ocular inflammation and infection.The clinical study design was a randomized, double-masked, active-controlled, parallel-group trial of 102 subjects with bacterial blepharitis in which two patients also had bacterial conjunctivitis. All subjects received two bottles of study medication: either a fixed combination of moxifloxacin 0.5%/dexamethasone 0.1% ophthalmic solution and placebo eye drops (fixed-dose group), or moxifloxacin 0.5% ophthalmic solution and dexamethasone 0.1% (concomitant group). One drop of each study medication was instilled bilaterally four times per day for 7 days. Clinical resolution, signs, symptoms, and safety were assessed. Microbiological specimens were collected from the eyelid margin and conjunctivae of each eye from each patient at the time of enrollment and at the exit visit.Clinical resolution occurred similarly in both groups (81.6% of eyes, fixed-dose group; 82.3% of eyes, concomitant group). Moreover, the microbiological efficacy of the treatment was also similar for both the fixed-dose group (84%) and the concomitant group (83%). Ocular symptoms and signs improved over time, with no significant differences between groups after 7 days of treatment, except the fixed-dose group had significantly more eyes with clinical resolution in eyelid erythema (100%, n = 98/98, fixed-dose group; 92.7%, n = 89/96, concomitant group; P = 0.0194) and eyelid scaling/crusting (98%, n = 96/98, fixed-dose group; 89.6%; n = 86/96 eyes, concomitant group; P = 0.0337). Both regimens were safe and well tolerated.The fixed-dose combination of moxifloxacin, 0.5% and dexamethasone, 0.1% was therapeutically equivalent and as well tolerated as the concomitant dosage.
URI: http://repositorio.unifesp.br/handle/11600/34847
ISSN: 0741-238X
Other Identifiers: http://dx.doi.org/10.1007/s12325-012-0018-8
Appears in Collections:Em verificação - Geral

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.