Eficacia de la azatioprina en la enfermedad ocular inflamatoria no infecciosa resistente a tratamiento esteroidal sistémico
Author
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Cuchacovich Turteltaub, Miguel
Author
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Pacheco, Patricio
es_CL
Author
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Díaz Vilches, Gonzalo
es_CL
Author
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Rojas, Basilio
es_CL
Author
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Stoppel, Juan
es_CL
Author
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Merino, Guillermo
es_CL
Author
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Verdaguer, Juan Ignacio
es_CL
Author
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Verdaguer, Juan
es_CL
Author
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Villarroel, Francisco
es_CL
Admission date
dc.date.accessioned
2014-08-29T16:33:48Z
Available date
dc.date.available
2014-08-29T16:33:48Z
Publication date
dc.date.issued
2007
Cita de ítem
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Rev Méd Chile 2007; 135: 702-707
en_US
Identifier
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0034-9887
Identifier
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https://repositorio.uchile.cl/handle/2250/129318
General note
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Artículo de publicación SciELO
en_US
Abstract
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Background: 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 diseases