Prospective assessment of breakthrough infections and neurotoxicity and their association with cefepime trough concentrations in patients with febrile neutropenia.


Journal

International journal of antimicrobial agents
ISSN: 1872-7913
Titre abrégé: Int J Antimicrob Agents
Pays: Netherlands
ID NLM: 9111860

Informations de publication

Date de publication:
Jan 2022
Historique:
received: 20 07 2021
revised: 21 10 2021
accepted: 24 10 2021
pubmed: 11 11 2021
medline: 8 3 2022
entrez: 10 11 2021
Statut: ppublish

Résumé

Cefepime is a first-line antibiotic for the treatment of febrile neutropenia (FN) in haematological cancer patients. Therapeutic drug monitoring (TDM) of cefepime is frequently advocated. However, it remains unclear what range of concentrations should be targeted for maximal efficacy and minimal toxicity. Therefore, we examined the relationship between cefepime exposure and clinical efficacy or neurotoxicity in FN patients. This prospective, observational, single-centre study included all adult hospitalised patients presenting with FN at the haematology ward and treated with cefepime from August 2019 until October 2020. Primary outcomes were incidence of breakthrough infection and neurotoxicity and their relationship with free cefepime serum trough concentrations. A total of 76 patients were included, contributing 96 cefepime treatment courses. The median (interquartile range) estimated glomerular filtration rate according to the Chronic Kidney Disease Epidemiology Collaboration equation (eGFR

Identifiants

pubmed: 34757136
pii: S0924-8579(21)01309-1
doi: 10.1016/j.ijantimicag.2021.106472
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Cefepime 807PW4VQE3

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

106472

Informations de copyright

Copyright © 2021 Elsevier Ltd and International Society of Antimicrobial Chemotherapy. All rights reserved.

Auteurs

Matthias Gijsen (M)

Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium; Pharmacy Department, University Hospitals Leuven, Leuven, Belgium. Electronic address: matthias.gijsen@uzleuven.be.

Britt Bekkers (B)

Pharmacy Department, University Hospitals Leuven, Leuven, Belgium.

Johan Maertens (J)

Department of Hematology, University Hospitals Leuven, Leuven, Belgium; Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.

Katrien Lagrou (K)

Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium; Clinical Department of Laboratory Medicine, University Hospitals Leuven, Leuven, Belgium.

Stefanie Desmet (S)

Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium; Clinical Department of Laboratory Medicine, University Hospitals Leuven, Leuven, Belgium.

Erwin Dreesen (E)

Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium.

Willy E Peetermans (WE)

Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium; Department of Internal Medicine, University Hospitals Leuven, Leuven, Belgium.

Yves Debaveye (Y)

Laboratory for Intensive Care Medicine, Department of Cellular and Molecular Medicine, KU Leuven, Leuven, Belgium.

Isabel Spriet (I)

Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium; Pharmacy Department, University Hospitals Leuven, Leuven, Belgium.

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Classifications MeSH