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Pharmacokinetics of Intravenous Posaconazole in Critically Ill Patients
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ABSTRACT
To date, there is no information on the intravenous (i.v.) posaconazole pharmacokinetics for intensive care unit (ICU) patients. This prospective observational study aimed to describe the pharmacokinetics of a single dose of i.v. posaconazole in critically ill patients. Patients with no history of allergy to triazole antifungals and requiring systemic antifungal therapy were enrolled if they were aged ≥18 years, central venous access was available, they were not pregnant, and they had not received prior posaconazole or drugs interacting with posaconazole. A single dose of 300 mg posaconazole was administered over 90 min. Total plasma concentrations were measured from serial plasma samples collected over 48 h, using a validated chromatographic method. The pharmacokinetic data set was analyzed by noncompartmental methods. Eight patients (7 male) were enrolled with the following characteristics: median age, 46 years (interquartile range [IQR], 40 to 51 years); median weight, 68 kg (IQR, 65 to 82 kg); and median albumin concentration, 20 g/liter (IQR, 18 to 24 g/liter). Median (IQR) pharmacokinetic parameter estimates were as follows: observed maximum concentration during sampling period (
C
max
), 1,702 ng/ml (1,352 to 2,141 ng/ml); area under the concentration-time curve from zero to infinity (AUC
0–∞
), 17,932 ng · h/ml (13,823 to 27,905 ng · h/ml); clearance (CL), 16.8 liters/h (11.1 to 21.7 liters/h); and volume of distribution (
V
), 529.1 liters (352.2 to 720.6 liters). The
V
and CL were greater than 2-fold and the AUC
0–∞
was 39% of the values reported for heathy volunteers. The AUC
0–∞
was only 52% of the steady-state AUC
0–24
reported for hematology patients. The median of estimated average steady-state concentrations was 747 ng/ml (IQR, 576 to 1,163 ng/ml), which is within but close to the lower end of the previously recommended therapeutic range of 500 to 2,500 ng/ml. In conclusion, we observed different pharmacokinetics of i.v. posaconazole in this cohort of critically ill patients compared to those in healthy volunteers and hematology patients.
American Society for Microbiology
Title: Pharmacokinetics of Intravenous Posaconazole in Critically Ill Patients
Description:
ABSTRACT
To date, there is no information on the intravenous (i.
v.
) posaconazole pharmacokinetics for intensive care unit (ICU) patients.
This prospective observational study aimed to describe the pharmacokinetics of a single dose of i.
v.
posaconazole in critically ill patients.
Patients with no history of allergy to triazole antifungals and requiring systemic antifungal therapy were enrolled if they were aged ≥18 years, central venous access was available, they were not pregnant, and they had not received prior posaconazole or drugs interacting with posaconazole.
A single dose of 300 mg posaconazole was administered over 90 min.
Total plasma concentrations were measured from serial plasma samples collected over 48 h, using a validated chromatographic method.
The pharmacokinetic data set was analyzed by noncompartmental methods.
Eight patients (7 male) were enrolled with the following characteristics: median age, 46 years (interquartile range [IQR], 40 to 51 years); median weight, 68 kg (IQR, 65 to 82 kg); and median albumin concentration, 20 g/liter (IQR, 18 to 24 g/liter).
Median (IQR) pharmacokinetic parameter estimates were as follows: observed maximum concentration during sampling period (
C
max
), 1,702 ng/ml (1,352 to 2,141 ng/ml); area under the concentration-time curve from zero to infinity (AUC
0–∞
), 17,932 ng · h/ml (13,823 to 27,905 ng · h/ml); clearance (CL), 16.
8 liters/h (11.
1 to 21.
7 liters/h); and volume of distribution (
V
), 529.
1 liters (352.
2 to 720.
6 liters).
The
V
and CL were greater than 2-fold and the AUC
0–∞
was 39% of the values reported for heathy volunteers.
The AUC
0–∞
was only 52% of the steady-state AUC
0–24
reported for hematology patients.
The median of estimated average steady-state concentrations was 747 ng/ml (IQR, 576 to 1,163 ng/ml), which is within but close to the lower end of the previously recommended therapeutic range of 500 to 2,500 ng/ml.
In conclusion, we observed different pharmacokinetics of i.
v.
posaconazole in this cohort of critically ill patients compared to those in healthy volunteers and hematology patients.
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