Effect of achieving bone sterilisation on bone architecture and bone marrow, in an experimental rabbit model of osteomyelitis caused by carbapenemase-producing Enterobacterales.


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:
Dec 2023
Historique:
received: 14 06 2023
revised: 05 09 2023
accepted: 29 09 2023
medline: 4 12 2023
pubmed: 16 10 2023
entrez: 15 10 2023
Statut: ppublish

Résumé

Natural history and treatment of bone infections caused by carbapenemase-producing Enterobacterales (CPE) are poorly defined. We evaluated the effect of treatment on the progression of subacute osteomyelitis in a rabbit model. Two isolates were used: a KPC-producing Klebsiella pneumoniae and an Escherichia coli harbouring bla Bone marrow modifications induced by local infection were similar between prematurely deceased animals and non-sterilised animals (P = 0.14) but differed significantly from animals that achieved bone sterilisation after treatment (P = 0.04). Conversely, when comparing bone deformity, rabbits who died early (n = 13) had similar bone architecture as those achieving bone sterilisation (P = 0.12), as opposed to those not sterilised after treatment (P = 0.04). After a multivariate logistic regression, bone marrow scale ≤2 was associated with bone sterilisation (P < 0.001), and bone architecture scale ≤2 was associated with bone sterilisation (adjusted odds ratio = 2.7; 95% confidence interval 1.14-6.37) and KPC infection (adjusted odds ratio = 5.1; 95% confidence interval 2.17-12.13). Effective antibacterial treatment reduces bone architecture distortion and bone marrow changes. These variables may be used as proxy for bone sterilisation.

Identifiants

pubmed: 37839717
pii: S0924-8579(23)00277-7
doi: 10.1016/j.ijantimicag.2023.107003
pii:
doi:

Substances chimiques

carbapenemase EC 3.5.2.6
Ceftazidime 9M416Z9QNR
Anti-Bacterial Agents 0
Bacterial Proteins 0
beta-Lactamases EC 3.5.2.6
Azabicyclo Compounds 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

107003

Informations de copyright

Copyright © 2023 Elsevier Ltd and International Society of Antimicrobial Chemotherapy. All rights reserved.

Auteurs

B Davido (B)

UMR 1173, Versailles Saint-Quentin University, Versailles, France; Infectious Diseases Department, Raymond Poincaré Paris Saclay University Hospital, Garches, France. Electronic address: benjamin.davido@aphp.fr.

A C Crémieux (AC)

UMR 1173, Versailles Saint-Quentin University, Versailles, France; FHU PROTHEE, St Louis-Lariboisière Hospital, Paris-Cité University, Paris, France.

C Nich (C)

Orthopaedic Surgery Unit, Nantes University Hospital, Nantes, France; INSERM, UMRS 1229, Nantes University, Regenerative Medicine and Skeleton, ONIRIS, Nantes, France.

P De Truchis (P)

UMR 1173, Versailles Saint-Quentin University, Versailles, France.

I Vaugier (I)

CIC, Raymond Poincaré Paris Saclay University Hospital, Garches, France.

L Gatin (L)

Neuro-orthopedy Unit, Raymond Poincaré Paris Saclay University Hospital, Garches, France.

P Tattevin (P)

INSERM, CIC 1414, Rennes, France; Infectious diseases department, CHU Ponchaillou, Rennes, France.

A Saleh-Mghir (A)

UMR 1173, Versailles Saint-Quentin University, Versailles, France; Infectious Diseases Department, Raymond Poincaré Paris Saclay University Hospital, Garches, France.

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Classifications MeSH