Population pharmacokinetic/pharmacodynamic study suggests continuous infusion of ceftaroline daily dose in ventilated critical care patients with early-onset pneumonia and augmented renal clearance.


Journal

The Journal of antimicrobial chemotherapy
ISSN: 1460-2091
Titre abrégé: J Antimicrob Chemother
Pays: England
ID NLM: 7513617

Informations de publication

Date de publication:
28 10 2022
Historique:
received: 18 03 2022
accepted: 05 08 2022
pubmed: 6 9 2022
medline: 2 11 2022
entrez: 5 9 2022
Statut: ppublish

Résumé

Ceftaroline could be suitable to treat early-onset ventilator-associated pneumonia (VAP) because of its antibacterial spectrum. However, augmented renal clearance (ARC) is frequent in ICU patients and may affect ceftaroline pharmacokinetics and efficacy. The objective of the study was to explore the impact of ARC on ceftaroline pharmacokinetics and evaluate whether the currently recommended dosing regimen (600 mg every 12 h) is appropriate to treat VAP in ICU patients. A population pharmacokinetic model was developed using pharmacokinetic data from 18 patients with measured creatinine clearance (CLCR) ranging between 83 and 309 mL/min. Monte Carlo simulations were conducted to determine the PTA and the cumulative fraction of response (CFR) against Streptococcus pneumoniae and MRSA for five dosing regimens. Study registered at ClinicalTrials.gov (NCT03025841). Ceftaroline clearance increased non-linearly with CLCR, with lower concentrations and lower probability of reaching pharmacokinetic/pharmacodynamic targets when CLCR increases. For the currently recommended dosing regimen, the probability of having unbound ceftaroline concentrations above the MIC over the entire dose range is greater than 90% for MICs below 0.125 mg/L. Considering the distribution of MICs, this regimen would not be effective against MRSA infections (CFR between 21% and 67% depending on CLCR), but would be effective against S. pneumoniae infections (CFR >86%). The recommended dosing regimen of ceftaroline seems sufficient for covering S. pneumoniae in ICU patients with ARC, but not for MRSA. Among the dosing regimens tested it appears that a constant infusion (50 mg/h) after a loading dose of 600 mg could be more appropriate for MRSA infections.

Identifiants

pubmed: 36059138
pii: 6691803
doi: 10.1093/jac/dkac299
pmc: PMC9616540
doi:

Substances chimiques

Anti-Bacterial Agents 0
Cephalosporins 0

Banques de données

ClinicalTrials.gov
['NCT03025841']

Types de publication

Clinical Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3173-3179

Subventions

Organisme : AstraZeneca
Organisme : Pfizer

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of British Society for Antimicrobial Chemotherapy.

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Auteurs

Alexia Chauzy (A)

INSERM U1070, Pharmacologie des Anti-infectieux et Antibiorésistance, Poitiers, France.
Université de Poitiers, UFR de Médecine Pharmacie, Poitiers, France.

Nicolas Gregoire (N)

INSERM U1070, Pharmacologie des Anti-infectieux et Antibiorésistance, Poitiers, France.
Université de Poitiers, UFR de Médecine Pharmacie, Poitiers, France.
CHU de Poitiers, Laboratoire de Toxicologie-Pharmacocinétique, Poitiers, France.

Martine Ferrandière (M)

Groupe ATLANREA, CHU de Nantes, Nantes, France.
CHU de Tours, Service d'Anesthésie-Réanimation, Tours, France.

Sigismond Lasocki (S)

Groupe ATLANREA, CHU de Nantes, Nantes, France.
CHU d'Angers, Service d'Anesthésie-Réanimation, Angers, France.

Karim Ashenoune (K)

Groupe ATLANREA, CHU de Nantes, Nantes, France.
CHU de Nantes, Service d'Anesthésie-Réanimation, Hôtel Dieu - HME, Nantes, France.

Philippe Seguin (P)

Groupe ATLANREA, CHU de Nantes, Nantes, France.
CHU de Rennes, Service d'Anesthésie-Réanimation, Pontchaillou, Rennes, France.

Matthieu Boisson (M)

INSERM U1070, Pharmacologie des Anti-infectieux et Antibiorésistance, Poitiers, France.
Université de Poitiers, UFR de Médecine Pharmacie, Poitiers, France.
Groupe ATLANREA, CHU de Nantes, Nantes, France.
CHU de Poitiers, Service d'Anesthésie-Réanimation et Médecine Périopératoire, Poitiers, France.

William Couet (W)

INSERM U1070, Pharmacologie des Anti-infectieux et Antibiorésistance, Poitiers, France.
Université de Poitiers, UFR de Médecine Pharmacie, Poitiers, France.
CHU de Poitiers, Laboratoire de Toxicologie-Pharmacocinétique, Poitiers, France.

Sandrine Marchand (S)

INSERM U1070, Pharmacologie des Anti-infectieux et Antibiorésistance, Poitiers, France.
Université de Poitiers, UFR de Médecine Pharmacie, Poitiers, France.
CHU de Poitiers, Laboratoire de Toxicologie-Pharmacocinétique, Poitiers, France.

Olivier Mimoz (O)

INSERM U1070, Pharmacologie des Anti-infectieux et Antibiorésistance, Poitiers, France.
Université de Poitiers, UFR de Médecine Pharmacie, Poitiers, France.
Groupe ATLANREA, CHU de Nantes, Nantes, France.
CHU de Poitiers, Service des Urgences & SAMU 86, Poitiers, France.

Claire Dahyot-Fizelier (C)

INSERM U1070, Pharmacologie des Anti-infectieux et Antibiorésistance, Poitiers, France.
Université de Poitiers, UFR de Médecine Pharmacie, Poitiers, France.
Groupe ATLANREA, CHU de Nantes, Nantes, France.
CHU de Poitiers, Service d'Anesthésie-Réanimation et Médecine Périopératoire, Poitiers, France.

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