TY - JOUR
T1 - Population pharmacokinetics of four β-lactams in critically ill septic patients comedicated with amikacin
AU - Delattre, Isabelle K.
AU - Musuamba Tshinanu, Flora
AU - Jacqmin, Philippe
AU - Taccone, Fabio S.
AU - Laterre, Pierre François
AU - Verbeeck, Roger K.
AU - Jacobs, Frédérique
AU - Wallemacq, Pierre
N1 - Funding Information:
The study was supported by AstraZeneca , Wyeth Pharmaceuticals , GlaxoSmithKline Pharmaceuticals and Bristol-Myers Squibb .
PY - 2012/7
Y1 - 2012/7
N2 - Objectives: The study aimed to characterize the pharmacokinetics (PK) of four β-lactams (piperacillin, ceftazidime, cefepime, and meropenem) in patients comedicated with amikacin (AMK), and to confirm the predictive performance of AMK data, obtained from therapeutic drug monitoring (TDM), on these PK, using a population modeling approach. Design and methods: Serum samples were collected in 88 critically ill septic patients. For each β-lactam, the covariate model was optimized using renal function. Furthermore, predictive performance of AMK concentrations and PK parameters was assessed on β-lactam PK. Results: A two-compartment model with first-order elimination best fitted the β-lactam data. Results supported the superiority of AMK concentrations, over renal function and AMK PK parameters, to assess the β-lactam PK. Conclusion: The study confirmed the significant link between the exposure to AMK and to β-lactams, and presented population models able to guide β-lactam dosage adjustments using renal biomarkers or TDM-related aminoglycoside data.
AB - Objectives: The study aimed to characterize the pharmacokinetics (PK) of four β-lactams (piperacillin, ceftazidime, cefepime, and meropenem) in patients comedicated with amikacin (AMK), and to confirm the predictive performance of AMK data, obtained from therapeutic drug monitoring (TDM), on these PK, using a population modeling approach. Design and methods: Serum samples were collected in 88 critically ill septic patients. For each β-lactam, the covariate model was optimized using renal function. Furthermore, predictive performance of AMK concentrations and PK parameters was assessed on β-lactam PK. Results: A two-compartment model with first-order elimination best fitted the β-lactam data. Results supported the superiority of AMK concentrations, over renal function and AMK PK parameters, to assess the β-lactam PK. Conclusion: The study confirmed the significant link between the exposure to AMK and to β-lactams, and presented population models able to guide β-lactam dosage adjustments using renal biomarkers or TDM-related aminoglycoside data.
KW - β-lactams
KW - Population pharmacokinetics
KW - Severe sepsis
KW - Therapeutic drug monitoring
UR - http://www.scopus.com/inward/record.url?scp=84862534688&partnerID=8YFLogxK
U2 - 10.1016/j.clinbiochem.2012.03.030
DO - 10.1016/j.clinbiochem.2012.03.030
M3 - Article
C2 - 22503878
AN - SCOPUS:84862534688
SN - 0009-9120
VL - 45
SP - 780
EP - 786
JO - Clinical biochemistry
JF - Clinical biochemistry
IS - 10-11
ER -