4.7 Article

Intrapulmonary pharmacokinetics of high doses of tigecycline in patients with ventilator-associated pneumonia

Journal

Publisher

ELSEVIER
DOI: 10.1016/j.ijantimicag.2021.106487

Keywords

Ventilator-associated pneumonia; VAP; Tigecycline; Intrapulmonary pharmacokinetics

Ask authors/readers for more resources

This study aimed to evaluate the pharmacokinetics of off-label high-dose tigecycline in patients with ventilator-associated pneumonia (VAP). The results showed that a daily dose of 200 mg tigecycline can increase drug concentrations in plasma and epithelial lining fluid (ELF), and the high ELF penetration supports the effectiveness of tigecycline in VAP.
Tigecycline is commonly used for infections by multidrug-resistant bacteria. However, it is not approved for ventilator-associated pneumonia (VAP) as increased mortality has been reported in VAP patients treated with conventional doses. The purpose of this study was to prospectively evaluate the intrapulmonary pharmacokinetics of off-label high-dose tigecycline in patients with VAP. Nine mechanically ventilated patients received tigecycline intravenously (loading dose 200 mg followed by 100 mg every 12 h). After = 5 doses, two bronchoscopies were performed in each patient on consecutive days and eight blood samples were collected. Tigecycline concentrations in plasma and bronchoalveolar lavage fluid were determined by liquid chromatography. The urea dilution method was used to calculate epithelial lining fluid (ELF) concentrations. A two-compartmental pharmacokinetic (PK) model with linear elimination was used to estimate PK parameters. Mean patient age was 69 +/- 11.86 years and mean APACHE II score was 21. The estimated population mean PK parameters (relative standard error) were: clearance, 11.64 L/h (54%); volume of distribution in central compartment, 79.01 L (37%); volume of distribution in peripheral compartment, 92.95 L (17%); intercompartmental clearance, 62.81 L/h (34%); and ELF penetration ratio, 2.41 (40%). C-max, C-min, plasma AUC(0-12), plasma fAUC(0-12) and ELF AUC(0-12) were 1.99 +/- 1.82 mu g/mL, 0.81 +/- 1.27 mu g/mL, 12.89 +/- 17.25 mu g.h/mL, 3.24 +/- 3.09 mu g.h/mL and 7.13 +/- 2.61 mu g.h/mL, respectively. The increased plasma and ELF AUC(0-12) achieved with a 200 mg daily tigecycline dose, combined with high ELF penetration, support the effectiveness of off-label high-dose tigecycline in VAP. (c) 2021 Elsevier Ltd and International Society of Antimicrobial Chemotherapy. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available