Evidence map›Paper›PMID 42708226›Full record

Trial reportThe Journal of antimicrobial chemotherapy2026

A prospective pharmacokinetic interaction study between rifampicin and fusidic acid for the treatment of staphylococcal infections.

Callum Maggs, Laurens Manning, Okhee Yoo, Sam Salman, Madhu Page-Sharp, Craig Aboltins

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of antimicrobial chemotherapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Callum MaggsDepartment of Infectious Diseases, St Vincent's Hospital Melbourne, Fitzroy, Melbourne, Vic, Australia.
Laurens ManningDepartment of Infectious Diseases, Fiona Stanley Hospital, Murdoch, WA, Australia.ORCID 0000-0003-4334-5351
Okhee YooWesfarmers Centre for Vaccines and Infectious Diseases, The Kids Research Institute, Nedlands, WA 6009, Australia.
Sam SalmanMedical School, University of Western Australia, Perth, Australia.ORCID 0000-0002-8276-6784
Madhu Page-SharpSchool of Pharmacy, Curtin University, WA, Australia.
Craig AboltinsDepartment of Infectious Diseases, St Vincent's Hospital Melbourne, Fitzroy, Melbourne, Vic, Australia.ORCID 0000-0002-7578-882X

Funding

Infectious Diseases Research Fund-St Vincent's Hospital Melbourne
6 · The paper itself

Abstract

objectiveFusidic acid with rifampicin is used for the treatment of severe staphylococcal infection, particularly prosthetic joint infections. Previous studies using twice daily fusidic acid showed rifampicin increases fusidic acid clearance, potentially causing sub-therapeutic concentrations. It is uncertain whether this occurs with three-times daily dosing. This study sought to re-evaluate this potential drug-drug interaction.

methodsIn this prospective, open-label drug-drug interaction population pharmacokinetic (PK) study, participants were randomized to receive fusidic acid or rifampicin for 24 hours, followed by combination therapy for the duration of treatment. Drug concentration assays used liquid-chromatography mass spectroscopy on dried blood spots. Population PK models were built for fusidic acid, rifampicin and 25-desacetyl rifampicin.

resultsTen participants were recruited. Inter-individual variability for both absorption (98.1%) and clearance (77.8%) were high for fusidic acid. A population pharmacokinetic model for fusidic acid revealed that early autoinhibition dominated over later rifampicin-mediated induction, resulting in a net decrease in fusidic acid clearance. The mean fusidic acid area under the curve during each dosing interval (AUCτ) at steady state was 1.76-fold [0.049, 34.918] higher relative to Day 1, despite high uncertainty.Large inter-individual (110%) variability in absorption was observed for rifampicin. There was no apparent effect on rifampicin metabolism by fusidic acid co-administration, however, fusidic acid decreased clearance of 25-desacetyl rifampicin.

conclusionIn patients treated with fusidic acid three times daily in combination with rifampicin, autoinhibition potentially counteracted rifampicin induction such that fusidic acid concentrations were not reduced. Rifampicin clearance was not affected by fusidic acid, but 25-desacetyl rifampicin clearance was decreased. There was large inter-individual variability in the observed concentrations and final parameter estimates.

Indexed as

Anti-Bacterial AgentsFusidic AcidRifampinStaphylococcal InfectionsAdultAgedChromatography, LiquidDrug InteractionsDrug Therapy, CombinationFemaleHumansMaleMass SpectrometryMiddle AgedProspective StudiesAnti-Bacterial AgentsFusidic AcidRifampin

Identifiers

PMID42708226
PMCPMC13550937

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.