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Authordc.contributor.authorSilva, Felipe 
Authordc.contributor.authorNavea, Daniel 
Authordc.contributor.authorSalas, Carolina 
Authordc.contributor.authorTorres, Juan 
Authordc.contributor.authorCatalán, Paula 
Authordc.contributor.authorMorales, Jorge 
Admission datedc.date.accessioned2016-10-12T19:22:01Z
Available datedc.date.available2016-10-12T19:22:01Z
Publication datedc.date.issued2016
Cita de ítemdc.identifier.citationRev Chilena Infectol 2016; 33 (2): 127-134es_ES
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/140738
Abstractdc.description.abstractBackground: Voriconazole (VCZ) serum drug levels (SDL) vary widely and are associated with increased mortality when they are below the therapeutic range for invasive aspergillosis (IA). Aim: To describe VCZ SDL in oncology pediatric patients in order to reach adequate concentrations for prophylaxis (≥ 0.5 mg/L) and treatment (≥ 1.0 y 2.0 mg/L) for IA and their relationship with toxicity. Patients and Methods: Retrospective analysis of VCZ SDL and toxicities recorded in oncology pediatric patients between February 2013 and November 2014. The daily dosage and SDLs were analyzed according to administration route: intravenous (IV) and oral (PO), type of therapy (prophylaxis and treatment) and patient age (< 12 y ≥ 12 years old). Results: 112 through levels from 26 patients were analyzed and the average age was 9.3 years-old. The SDL obtained from the IV route were 43.7%. There were more SDL ≥ 0.5 mg/L and ≥ 1.0 mg/L with the IV route than the PO route (p < 0.05). Patients younger than 12-years-old received a higher dosage than those ≥ 12 years old (median 18.6 and 9.2 mg/kg/d, respectively, p < 0.05). To reach SDL ≥ 0,5 mg/L with the PO route, a dosage of 200 mg every 12 hours showed the best results for all patients (80-100% SDL ≥ 0.5 mg/L). With an IV dosage between 14 and 20 mg/kg/day in patients ≥ 12-yearsold, 80% of the SDL were ≥ 1 mg/L and ≥ 2 mg/L. In patients younger than 12-year-old, dosages between 8-30 mg/ kg/day showed similar results (50-63% of SDL ≥ 1 mg/L and 36-40% of SDL ≥ 2 mg/L). Eight patients (30.8%) presented an adverse drug reaction and no relationship with the SDL was found. Conclusion:A VCZ standard dosage of 200 mg every 12 hours PO showed the best results for IA prophylaxis in all patients. Patients younger than 12-years-old would require higher dosages than the doses used in this study to attain adequate SDL for IA treatment. No relation with SDL and adverse reactions was found. Key words: Voriconazole, serum concentration, pharmacokinetics, adverse drug reactions.es_ES
Lenguagedc.language.isoeses_ES
Publisherdc.publisherSoc Chilena Infectologíaes_ES
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
Sourcedc.sourceRevista Chilena de Infectologíaes_ES
Keywordsdc.subjectVoriconazoles_ES
Keywordsdc.subjectConcentraciones plasmáticases_ES
Keywordsdc.subjectFarmacocinéticaes_ES
Keywordsdc.subjectReacciones adversases_ES
Títulodc.titleAnálisis de concentraciones plasmáticas de voriconazol y su perfil de seguridad en pacientes oncológicos pediátricoses_ES
Title in another languagedc.title.alternativeAnalysis of voriconazole serum concentrations and safety profile in pediatric oncology patientses_ES
Document typedc.typeArtículo de revista
Catalogueruchile.catalogadorlajes_ES
Indexationuchile.indexArtículo de publicación ISIes_ES


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