Análisis de concentraciones plasmáticas de voriconazol y su perfil de seguridad en pacientes oncológicos pediátricos
Author
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Silva, Felipe
Author
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Navea, Daniel
Author
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Salas, Carolina
Author
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Torres, Juan
Author
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Catalán, Paula
Author
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Morales, Jorge
Admission date
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2016-10-12T19:22:01Z
Available date
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2016-10-12T19:22:01Z
Publication date
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2016
Cita de ítem
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Rev Chilena Infectol 2016; 33 (2): 127-134
es_ES
Identifier
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https://repositorio.uchile.cl/handle/2250/140738
Abstract
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Background: 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.