Cargando…

Ciprofloxacin in Patients Undergoing Extracorporeal Membrane Oxygenation (ECMO): A Population Pharmacokinetic Study

Extracorporeal membrane oxygenation (ECMO) is utilized to temporarily sustain respiratory and/or cardiac function in critically ill patients. Ciprofloxacin is used to treat nosocomial infections, but data describing the effect of ECMO on its pharmacokinetics is lacking. Therefore, a prospective, obs...

Descripción completa

Detalles Bibliográficos
Autores principales: Alihodzic, Dzenefa, Wicha, Sebastian G., Frey, Otto R., König, Christina, Baehr, Michael, Jarczak, Dominik, Kluge, Stefan, Langebrake, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9145815/
https://www.ncbi.nlm.nih.gov/pubmed/35631551
http://dx.doi.org/10.3390/pharmaceutics14050965
_version_ 1784716408098127872
author Alihodzic, Dzenefa
Wicha, Sebastian G.
Frey, Otto R.
König, Christina
Baehr, Michael
Jarczak, Dominik
Kluge, Stefan
Langebrake, Claudia
author_facet Alihodzic, Dzenefa
Wicha, Sebastian G.
Frey, Otto R.
König, Christina
Baehr, Michael
Jarczak, Dominik
Kluge, Stefan
Langebrake, Claudia
author_sort Alihodzic, Dzenefa
collection PubMed
description Extracorporeal membrane oxygenation (ECMO) is utilized to temporarily sustain respiratory and/or cardiac function in critically ill patients. Ciprofloxacin is used to treat nosocomial infections, but data describing the effect of ECMO on its pharmacokinetics is lacking. Therefore, a prospective, observational trial including critically ill adults (n = 17), treated with ciprofloxacin (400 mg 8–12 hourly) during ECMO, was performed. Serial blood samples were collected to determine ciprofloxacin concentrations to assess their pharmacokinetics. The pharmacometric modeling was performed (NONMEM(®)) and utilized for simulations to evaluate the probability of target attainment (PTA) to achieve an AUC(0–24)/MIC of 125 mg·h/L for ciprofloxacin. A two-compartment model most adequately described the concentration-time data of ciprofloxacin. Significant covariates on ciprofloxacin clearance (CL) were plasma bicarbonate and the estimated glomerular filtration rate (eGFR). For pathogens with an MIC of ≤0.25 mg/L, a PTA of ≥90% was attained. However, for pathogens with an MIC of ≥0.5 mg/L, plasma bicarbonate ≥ 22 mmol/L or eGFR ≥ 10 mL/min PTA decreased below 90%, steadily declining to 7.3% (plasma bicarbonate 39 mmol/L) and 21.4% (eGFR 150 mL/min), respectively. To reach PTAs of ≥90% for pathogens with MICs ≥ 0.5 mg/L, optimized dosing regimens may be required.
format Online
Article
Text
id pubmed-9145815
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-91458152022-05-29 Ciprofloxacin in Patients Undergoing Extracorporeal Membrane Oxygenation (ECMO): A Population Pharmacokinetic Study Alihodzic, Dzenefa Wicha, Sebastian G. Frey, Otto R. König, Christina Baehr, Michael Jarczak, Dominik Kluge, Stefan Langebrake, Claudia Pharmaceutics Article Extracorporeal membrane oxygenation (ECMO) is utilized to temporarily sustain respiratory and/or cardiac function in critically ill patients. Ciprofloxacin is used to treat nosocomial infections, but data describing the effect of ECMO on its pharmacokinetics is lacking. Therefore, a prospective, observational trial including critically ill adults (n = 17), treated with ciprofloxacin (400 mg 8–12 hourly) during ECMO, was performed. Serial blood samples were collected to determine ciprofloxacin concentrations to assess their pharmacokinetics. The pharmacometric modeling was performed (NONMEM(®)) and utilized for simulations to evaluate the probability of target attainment (PTA) to achieve an AUC(0–24)/MIC of 125 mg·h/L for ciprofloxacin. A two-compartment model most adequately described the concentration-time data of ciprofloxacin. Significant covariates on ciprofloxacin clearance (CL) were plasma bicarbonate and the estimated glomerular filtration rate (eGFR). For pathogens with an MIC of ≤0.25 mg/L, a PTA of ≥90% was attained. However, for pathogens with an MIC of ≥0.5 mg/L, plasma bicarbonate ≥ 22 mmol/L or eGFR ≥ 10 mL/min PTA decreased below 90%, steadily declining to 7.3% (plasma bicarbonate 39 mmol/L) and 21.4% (eGFR 150 mL/min), respectively. To reach PTAs of ≥90% for pathogens with MICs ≥ 0.5 mg/L, optimized dosing regimens may be required. MDPI 2022-04-29 /pmc/articles/PMC9145815/ /pubmed/35631551 http://dx.doi.org/10.3390/pharmaceutics14050965 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Alihodzic, Dzenefa
Wicha, Sebastian G.
Frey, Otto R.
König, Christina
Baehr, Michael
Jarczak, Dominik
Kluge, Stefan
Langebrake, Claudia
Ciprofloxacin in Patients Undergoing Extracorporeal Membrane Oxygenation (ECMO): A Population Pharmacokinetic Study
title Ciprofloxacin in Patients Undergoing Extracorporeal Membrane Oxygenation (ECMO): A Population Pharmacokinetic Study
title_full Ciprofloxacin in Patients Undergoing Extracorporeal Membrane Oxygenation (ECMO): A Population Pharmacokinetic Study
title_fullStr Ciprofloxacin in Patients Undergoing Extracorporeal Membrane Oxygenation (ECMO): A Population Pharmacokinetic Study
title_full_unstemmed Ciprofloxacin in Patients Undergoing Extracorporeal Membrane Oxygenation (ECMO): A Population Pharmacokinetic Study
title_short Ciprofloxacin in Patients Undergoing Extracorporeal Membrane Oxygenation (ECMO): A Population Pharmacokinetic Study
title_sort ciprofloxacin in patients undergoing extracorporeal membrane oxygenation (ecmo): a population pharmacokinetic study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9145815/
https://www.ncbi.nlm.nih.gov/pubmed/35631551
http://dx.doi.org/10.3390/pharmaceutics14050965
work_keys_str_mv AT alihodzicdzenefa ciprofloxacininpatientsundergoingextracorporealmembraneoxygenationecmoapopulationpharmacokineticstudy
AT wichasebastiang ciprofloxacininpatientsundergoingextracorporealmembraneoxygenationecmoapopulationpharmacokineticstudy
AT freyottor ciprofloxacininpatientsundergoingextracorporealmembraneoxygenationecmoapopulationpharmacokineticstudy
AT konigchristina ciprofloxacininpatientsundergoingextracorporealmembraneoxygenationecmoapopulationpharmacokineticstudy
AT baehrmichael ciprofloxacininpatientsundergoingextracorporealmembraneoxygenationecmoapopulationpharmacokineticstudy
AT jarczakdominik ciprofloxacininpatientsundergoingextracorporealmembraneoxygenationecmoapopulationpharmacokineticstudy
AT klugestefan ciprofloxacininpatientsundergoingextracorporealmembraneoxygenationecmoapopulationpharmacokineticstudy
AT langebrakeclaudia ciprofloxacininpatientsundergoingextracorporealmembraneoxygenationecmoapopulationpharmacokineticstudy