Vol. 35 No. 1 (2018): February
Original Article

Pharmacokinetics of posaconazol in the prophylaxis and treatment of invasive fungal infection in immunocompromised children in a pediatric hospital

Romina Valenzuela
Universidad de Chile; Hospital Dr. Luis Calvo Mackenna
Patricio García
Hospital Dr. Luis Calvo Mackenna
Marlon Barraza
Hospital Dr. Luis Calvo Mackenna
Julia Palma
Hospital Dr. Luis Calvo Mackenna
Paula Catalán
Hospital Dr. Luis Calvo Mackenna
M. Elena Santolaya
Universidad de Chile; Hospital Dr. Luis Calvo Mackenna
J. Pablo Torres
Universidad de Chile; Hospital Dr. Luis Calvo Mackenna
Jorge Morales
Hospital Dr. Luis Calvo Mackenna

Published 2018-02-28

How to Cite

1.
Valenzuela R, García P, Barraza M, Palma J, Catalán P, Santolaya ME, Torres JP, Morales J. Pharmacokinetics of posaconazol in the prophylaxis and treatment of invasive fungal infection in immunocompromised children in a pediatric hospital. Rev. Chilena. Infectol. [Internet]. 2018 Feb. 28 [cited 2025 Nov. 13];35(1). Available from: https://revinf.cl/index.php/revinf/article/view/17

Abstract

Background: There is no consensus on the optimal dosage use of posaconazole (PSC) for invasive fungal infection (IFI) in pediatric patients and normally it is adjusted with drug levels (DLs) ≥ 0.7 μg/ml and ≥ 1.25 μg/ml for prophylaxis and treatment, respectively. Objective: To describe the experience of monitoring DLs of PSC in immunocompromised pediatric patients with IFI and to determine if the recommended doses reach CP effective in prophylaxis (≥ 0.7 μg/mL) and treatment (≥ 1.25 μg/mL). Method: A retrospective analysis in children who received PSC from January 2012 to October 2016, in the Oncology and Bone Marrow Transplant units at Hospital Calvo Mackenna was done. Results: Six patients with 78 DLs were reviewed (4 prophylaxis and 4 treatment). Median PSC dose was 12.5 and 18.8 mg/kg/d for prophylaxis and treatment, resulting in mean DLs of 0.97 and 1.8 μg/ mL respectively. In prophylaxis 40/67 (60%) were recorded with DLs ≥ 0.70 μg/mL receiving a median dose of 12.5 mg/kg/d. While for treatment: 5/11 (46%) presented DLs ≥ 1.25 μg/mL, receiving a median dose of 18 mg/ kg/d. Conclusion: Our results are in line with the recommended for PSC dosage, but individualized monitoring is required to maintain adequate DLs.