Cargando…

Population pharmacokinetics of piperacillin in febrile children receiving cancer chemotherapy: the impact of body weight and target on an optimal dosing regimen

BACKGROUND: The β-lactam antibiotic piperacillin (in combination with tazobactam) is commonly chosen for empirical treatment of suspected bacterial infections. However, pharmacokinetic variability among patient populations and across ages leads to uncertainty when selecting a dosing regimen to achie...

Descripción completa

Detalles Bibliográficos
Autores principales: Thorsted, Anders, Kristoffersson, Anders N, Maarbjerg, Sabine F, Schrøder, Henrik, Wang, Mikala, Brock, Birgitte, Nielsen, Elisabet I, Friberg, Lena E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6916132/
https://www.ncbi.nlm.nih.gov/pubmed/31273375
http://dx.doi.org/10.1093/jac/dkz270
_version_ 1783480167686995968
author Thorsted, Anders
Kristoffersson, Anders N
Maarbjerg, Sabine F
Schrøder, Henrik
Wang, Mikala
Brock, Birgitte
Nielsen, Elisabet I
Friberg, Lena E
author_facet Thorsted, Anders
Kristoffersson, Anders N
Maarbjerg, Sabine F
Schrøder, Henrik
Wang, Mikala
Brock, Birgitte
Nielsen, Elisabet I
Friberg, Lena E
author_sort Thorsted, Anders
collection PubMed
description BACKGROUND: The β-lactam antibiotic piperacillin (in combination with tazobactam) is commonly chosen for empirical treatment of suspected bacterial infections. However, pharmacokinetic variability among patient populations and across ages leads to uncertainty when selecting a dosing regimen to achieve an appropriate pharmacodynamic target. OBJECTIVES: To guide dosing by establishing a population pharmacokinetic model for unbound piperacillin in febrile children receiving cancer chemotherapy, and to assess pharmacokinetic/pharmacodynamic target attainment (100% fT > 1×MIC and 50% fT > 4×MIC) and resultant exposure, across body weights. METHODS: Forty-three children admitted for 89 febrile episodes contributed 482 samples to the pharmacokinetic analysis. The typical doses required for target attainment were compared for various dosing regimens, in particular prolonged infusions, across MICs and body weights. RESULTS: A two-compartment model with inter-fever-episode variability in CL, and body weight included through allometry, described the data. A high CL of 15.4 L/h (70 kg) combined with high glomerular filtration rate (GFR) values indicated rapid elimination and hyperfiltration. The target of 50% fT > 4×MIC was achieved for an MIC of 4.0 mg/L in a typical patient with extended infusions of 2–3 (q6h) or 3–4 (q8h) h, at or below the standard adult dose (75 and 100 mg/kg/dose for q6h and q8h, respectively). Higher doses or continuous infusion were needed to achieve 100% fT > 1×MIC due to the rapid piperacillin elimination. CONCLUSIONS: The licensed dose for children with febrile neutropenia (80 mg/kg q6h as a 30 min infusion) performs poorly for attainment of fT(>MIC) pharmacokinetic/pharmacodynamic targets. Given the population pharmacokinetic profile, feasible dosing regimens with reasonable exposure are continuous infusion (100% fT > 1×MIC) or prolonged infusions (50% fT > 4×MIC).
format Online
Article
Text
id pubmed-6916132
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-69161322019-12-19 Population pharmacokinetics of piperacillin in febrile children receiving cancer chemotherapy: the impact of body weight and target on an optimal dosing regimen Thorsted, Anders Kristoffersson, Anders N Maarbjerg, Sabine F Schrøder, Henrik Wang, Mikala Brock, Birgitte Nielsen, Elisabet I Friberg, Lena E J Antimicrob Chemother Original Research BACKGROUND: The β-lactam antibiotic piperacillin (in combination with tazobactam) is commonly chosen for empirical treatment of suspected bacterial infections. However, pharmacokinetic variability among patient populations and across ages leads to uncertainty when selecting a dosing regimen to achieve an appropriate pharmacodynamic target. OBJECTIVES: To guide dosing by establishing a population pharmacokinetic model for unbound piperacillin in febrile children receiving cancer chemotherapy, and to assess pharmacokinetic/pharmacodynamic target attainment (100% fT > 1×MIC and 50% fT > 4×MIC) and resultant exposure, across body weights. METHODS: Forty-three children admitted for 89 febrile episodes contributed 482 samples to the pharmacokinetic analysis. The typical doses required for target attainment were compared for various dosing regimens, in particular prolonged infusions, across MICs and body weights. RESULTS: A two-compartment model with inter-fever-episode variability in CL, and body weight included through allometry, described the data. A high CL of 15.4 L/h (70 kg) combined with high glomerular filtration rate (GFR) values indicated rapid elimination and hyperfiltration. The target of 50% fT > 4×MIC was achieved for an MIC of 4.0 mg/L in a typical patient with extended infusions of 2–3 (q6h) or 3–4 (q8h) h, at or below the standard adult dose (75 and 100 mg/kg/dose for q6h and q8h, respectively). Higher doses or continuous infusion were needed to achieve 100% fT > 1×MIC due to the rapid piperacillin elimination. CONCLUSIONS: The licensed dose for children with febrile neutropenia (80 mg/kg q6h as a 30 min infusion) performs poorly for attainment of fT(>MIC) pharmacokinetic/pharmacodynamic targets. Given the population pharmacokinetic profile, feasible dosing regimens with reasonable exposure are continuous infusion (100% fT > 1×MIC) or prolonged infusions (50% fT > 4×MIC). Oxford University Press 2019-10 2019-07-04 /pmc/articles/PMC6916132/ /pubmed/31273375 http://dx.doi.org/10.1093/jac/dkz270 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Research
Thorsted, Anders
Kristoffersson, Anders N
Maarbjerg, Sabine F
Schrøder, Henrik
Wang, Mikala
Brock, Birgitte
Nielsen, Elisabet I
Friberg, Lena E
Population pharmacokinetics of piperacillin in febrile children receiving cancer chemotherapy: the impact of body weight and target on an optimal dosing regimen
title Population pharmacokinetics of piperacillin in febrile children receiving cancer chemotherapy: the impact of body weight and target on an optimal dosing regimen
title_full Population pharmacokinetics of piperacillin in febrile children receiving cancer chemotherapy: the impact of body weight and target on an optimal dosing regimen
title_fullStr Population pharmacokinetics of piperacillin in febrile children receiving cancer chemotherapy: the impact of body weight and target on an optimal dosing regimen
title_full_unstemmed Population pharmacokinetics of piperacillin in febrile children receiving cancer chemotherapy: the impact of body weight and target on an optimal dosing regimen
title_short Population pharmacokinetics of piperacillin in febrile children receiving cancer chemotherapy: the impact of body weight and target on an optimal dosing regimen
title_sort population pharmacokinetics of piperacillin in febrile children receiving cancer chemotherapy: the impact of body weight and target on an optimal dosing regimen
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6916132/
https://www.ncbi.nlm.nih.gov/pubmed/31273375
http://dx.doi.org/10.1093/jac/dkz270
work_keys_str_mv AT thorstedanders populationpharmacokineticsofpiperacillininfebrilechildrenreceivingcancerchemotherapytheimpactofbodyweightandtargetonanoptimaldosingregimen
AT kristofferssonandersn populationpharmacokineticsofpiperacillininfebrilechildrenreceivingcancerchemotherapytheimpactofbodyweightandtargetonanoptimaldosingregimen
AT maarbjergsabinef populationpharmacokineticsofpiperacillininfebrilechildrenreceivingcancerchemotherapytheimpactofbodyweightandtargetonanoptimaldosingregimen
AT schrøderhenrik populationpharmacokineticsofpiperacillininfebrilechildrenreceivingcancerchemotherapytheimpactofbodyweightandtargetonanoptimaldosingregimen
AT wangmikala populationpharmacokineticsofpiperacillininfebrilechildrenreceivingcancerchemotherapytheimpactofbodyweightandtargetonanoptimaldosingregimen
AT brockbirgitte populationpharmacokineticsofpiperacillininfebrilechildrenreceivingcancerchemotherapytheimpactofbodyweightandtargetonanoptimaldosingregimen
AT nielsenelisabeti populationpharmacokineticsofpiperacillininfebrilechildrenreceivingcancerchemotherapytheimpactofbodyweightandtargetonanoptimaldosingregimen
AT friberglenae populationpharmacokineticsofpiperacillininfebrilechildrenreceivingcancerchemotherapytheimpactofbodyweightandtargetonanoptimaldosingregimen