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Authordc.contributor.authorCuchacovich Turteltaub, Miguel 
Authordc.contributor.authorPacheco, Patricio es_CL
Authordc.contributor.authorDíaz Vilches, Gonzalo es_CL
Authordc.contributor.authorRojas, Basilio es_CL
Authordc.contributor.authorStoppel, Juan es_CL
Authordc.contributor.authorMerino, Guillermo es_CL
Authordc.contributor.authorVerdaguer, Juan Ignacio es_CL
Authordc.contributor.authorVerdaguer, Juan es_CL
Authordc.contributor.authorVillarroel, Francisco es_CL
Admission datedc.date.accessioned2014-08-29T16:33:48Z
Available datedc.date.available2014-08-29T16:33:48Z
Publication datedc.date.issued2007
Cita de ítemdc.identifier.citationRev Méd Chile 2007; 135: 702-707en_US
Identifierdc.identifier.issn0034-9887
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/129318
General notedc.descriptionArtículo de publicación SciELOen_US
Abstractdc.description.abstractBackground: Topical and systemic steroids are the first line of treatment of non infectious inflammatory ocular disease. Immunosuppresants are reserved as a second line treatment. Aim: To evaluate the role of Azathioprine (AZA) as a coadyuvant immunosuppressive treatment for non infectious ocular inflammatory diseases (OIDs) resistant to systemic steroid therapy in a retrospective, noncomparative interventional case series. Patients and methods: Patients using oral Prednisone due to an active or recurrent OID, without clinical response, and not receiving any other immunosuppressive treatment were studied. A standard protocol of oral Prednisone (0.5 mg/kg/ day) and oral AZA (2-3 mg/kg/day) during one year was used. Ocular and systemic monthly evaluations were done including relapse rate, steroid dosage, inflammatory score and visual acuity. Results: Thirty patients (10 male) aged 18-75 years (mean 44 years) were studied. Three had bilateral anterior uveitis, one had pars planitis, four had diffuse uveitis, eight Vogt-Koyanahi-Harada syndrome, three Behçet’s disease, three necrotizing scleritis and eight had retinochoroidopathy. A complete initial response was observed in 26 patients (87%). The time of response was between 1 to 6 months (mean 2.65 months). Seventeen percent of these had a relapse 6 to 12 months after AZA was started. In 61%, visual acuity improved. The ocular inflammatory score decreased in 86.5%. Eleven patients had mild controlled side effects that did not require discontinuation of AZA. Conclusions: Combined systemic steroid and oral AZA therapy is safe and effective in controlling steroid resistant non infectious inflammatory ocular diseasesen_US
Lenguagedc.language.isoesen_US
Publisherdc.publisherSociedad Médica de Santiagoen_US
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
Keywordsdc.subjectAzathioprineen_US
Títulodc.titleEficacia de la azatioprina en la enfermedad ocular inflamatoria no infecciosa resistente a tratamiento esteroidal sistémicoen_US
Title in another languagedc.title.alternativeRole of Azathioprine in steroid resistant non infectious ocular inflammatory diseasesen_US
Document typedc.typeArtículo de revista


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Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile