Should we reconsider cefazolin for treating staphylococcal meningitis? A retrospective analysis of cefazolin and cloxacillin cerebrospinal fluid levels in patients treated for staphylococcal meningitis.


Journal

Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases
ISSN: 1469-0691
Titre abrégé: Clin Microbiol Infect
Pays: England
ID NLM: 9516420

Informations de publication

Date de publication:
Oct 2020
Historique:
received: 24 12 2019
revised: 26 04 2020
accepted: 29 04 2020
pubmed: 22 5 2020
medline: 13 5 2021
entrez: 22 5 2020
Statut: ppublish

Résumé

To assess the meningeal penetration of cefazolin and cloxacillin in individuals treated for methicillin-susceptible staphylococcal meningitis. We retrospectively identified individuals treated for Staphylococcus meningitis with measurements of cefazolin or cloxacillin concentrations in cerebrospinal fluid (CSF) using a validated assay of liquid chromatography coupled with mass spectrometry at the Nantes University Hospital between January 2009 and October 2019. Staphylococcus meningitis was defined by a compatible clinical presentation and a microbiological confirmation (positive CSF culture or positive specific PCR). Medical charts were retrospectively reviewed to collect microbiological and clinical data, and to assess therapeutic success. Among the 17 included individuals, eight (47%) were treated with cefazolin and nine (53%) with cloxacillin. Median daily dosages of cefazolin and cloxacillin were 8 g (range 6-12 g) and 12 g (range 10-13 g), respectively. Cefazolin and cloxacillin were mainly administered by continuous infusion. Eleven individuals (65%) were men, median (interquartile range (IQR)) age was 54 years (50; 70), 14 (82%) had postoperative meningitis and 3 (18%) had haematogenous meningitis. Median (IQR) antibiotic CSF concentrations were 2.8 mg/L (2.1; 5.2) and 0.66 mg/L (0.5; 0.9) for cefazolin and cloxacillin groups, respectively. Cloxacillin was discontinued in two individuals for therapeutic failure. Patients with staphylococcal meningitis treated with high-dose continuous intravenous infusion of cefazolin achieved therapeutic concentrations in CSF. Cefazolin appears to be a therapeutic candidate that should be properly evaluated in this indication.

Identifiants

pubmed: 32437956
pii: S1198-743X(20)30274-3
doi: 10.1016/j.cmi.2020.04.046
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Cefazolin IHS69L0Y4T
Cloxacillin O6X5QGC2VB

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1415.e1-1415.e4

Investigateurs

Francois Raffi (F)
David Boutoille (D)
Charlotte Biron (C)
Maeva Lefebvre (M)
Benjamin Jean Gaborit (BJ)
Paul Le Turnier (P)
Colin Deschanvres (C)
Raphael Lecomte (R)
Marie Chauveau (M)
Nathalie Asseray (N)
Matthieu Gregoire (M)
Ronan Bellouard (R)
Guillaume Deslandes (G)
Eric Dailly (E)
Anne-Gaëlle Leroy (AG)
Stéphane Corvec (S)
Pascale Bémer (P)
Jocelyne Caillon (J)
Aurélie Guillouzouic (A)
Karim Lakhal (K)
Raphaël Cinotti (R)
Emmanuel Canet (E)
Cédric Bretonniere (C)
Thomas Guimard (T)
Julia Brochard (J)
Jean Philippe Talarmin (JP)
Lydie Katchatourian (L)

Informations de copyright

Copyright © 2020 European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. All rights reserved.

Auteurs

P Le Turnier (P)

Department of Infectious Diseases, University Hospital of Nantes and CIC 1413, INSERM, Nantes, France.

M Gregoire (M)

Clinical Pharmacology Department, Nantes University Hospital, Nantes, France; UMR INSERM 1235, The Enteric Nervous System in Gut and Brain Disorders, University of Nantes, France.

G Deslandes (G)

Clinical Pharmacology Department, Nantes University Hospital, Nantes, France.

K Lakhal (K)

Department of Anesthesiology and Intensive Care Medicine, University Hospital of Nantes, Nantes, France.

C Deschanvres (C)

Department of Infectious Diseases, University Hospital of Nantes and CIC 1413, INSERM, Nantes, France.

R Lecomte (R)

Department of Infectious Diseases, University Hospital of Nantes and CIC 1413, INSERM, Nantes, France.

J-P Talarmin (JP)

Internal Medicine and Infectious Diseases Department, Centre hospitalier de Cornouaille, Quimper, France.

V Dubée (V)

Department of Infectious Diseases, University Hospital of Angers, Angers, France.

R Bellouard (R)

Clinical Pharmacology Department, Nantes University Hospital, Nantes, France.

D Boutoille (D)

Department of Infectious Diseases, University Hospital of Nantes and CIC 1413, INSERM, Nantes, France; EA 3826, Laboratory of Clinical and Experimental Therapeutics of Infections, IRS2-Nantes Biotech, Nantes, France.

A-G Leroy (AG)

EA 3826, Laboratory of Clinical and Experimental Therapeutics of Infections, IRS2-Nantes Biotech, Nantes, France; Department of Bacteriology, Nantes University Hospital, Nantes, France.

B J Gaborit (BJ)

Department of Infectious Diseases, University Hospital of Nantes and CIC 1413, INSERM, Nantes, France; EA 3826, Laboratory of Clinical and Experimental Therapeutics of Infections, IRS2-Nantes Biotech, Nantes, France. Electronic address: Benjamin.gaborit@chu-nantes.fr.

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