Rifampicin does not reduce moxifloxacin concentrations at the site of infection and may not improve treatment outcome of a one-stage exchange surgery protocol of implant-associated osteomyelitis lesions in a porcine model

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

We aimed to evaluate moxifloxacin steady-state concentrations in infected bone and soft tissue and to explore the additive microbiological and pathological treatment effect of rifampicin to standard moxifloxacin treatment of implant-associated osteomyelitis (IAO). 16 pigs were included. On Day 0, IAO was induced in the proximal tibia using a susceptible Staphylococcus aureus strain. On Day 7, the pigs underwent one-stage exchange surgery of the IAO lesions and were randomized to receive seven days of intravenous antibiotic treatment of either rifampicin combined with moxifloxacin or moxifloxacin monotherapy. On Day 14, microdialysis was applied for continuous sampling (8 h) of moxifloxacin concentrations. Microbiological, macroscopical pathology, and histopathological analyses were performed postmortem. Steady-state moxifloxacin area under the concentration–time curve was lower in the combination therapy group in plasma (total) and subcutaneous tissue compartments (infected and noninfected) (p < 0.04), while no differences were found in bone compartments. No additional treatment effect of rifampicin to moxifloxacin treatment was found (p = 0.57). Conclusive, additive rifampicin treatment does not reduce moxifloxacin concentrations at the infection site. Rifampicin treatment may not be necessary in a one-stage exchange treatment of IAO. However, our sample size and treatment period may have been too small and short to reveal true clinical differences.

OriginalsprogEngelsk
TidsskriftAPMIS
Vol/bind132
Udgave nummer3
Sider (fra-til)198-209
Antal sider12
ISSN0903-4641
DOI
StatusUdgivet - 2024

Bibliografisk note

Funding Information:
This work was supported by A.P. Møller Fonden, Oda og Hans Svenningsens Fond, Kai Lange og Gunhild Kai Langes Fond, Aarhus Universitets Forskningsfond, Frimodt‐Heineke Fonden, Direktør Emil C Hertz og Inger Hertz' Fond, Gigtforeningen, Grosserer A.V. Lykfeldt og Hustrus Fond, Riisfort Fonden. The funding sources had no involvement in study design; in the collection, analysis and interpretation of data; in the writing of the report; or in the decision to submit the article for publication.

Publisher Copyright:
© 2023 Scandinavian Societies for Pathology, Medical Microbiology and Immunology.

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