Evidence map›Paper›PMID 25019039›Full record

ArticleSpringerPlus2014

In vivo interactions of continuous flucloxacillin infusion and high-dose oral rifampicin in the serum of 15 patients with bone and soft tissue infections due to Staphylococcus aureus - a methodological and pilot study.

Christian Garzoni, Ilker Uçkay, Wilson Belaieff, Dominique Breilh, Domizio Suvà, Elzbieta Huggler, Daniel Lew, Pierre Hoffmeyer, Louis Bernard

Open access · diamondAbstract read
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Article in SpringerPlus, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 34% of its field
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

5 citing papers in PubMed, 7 citations in OpenAlex.

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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

9 authors at 2 institutions in 2 countries.

Christian GarzoniDepartment of Infectious Diseases, Geneva University Hospitals and Medical School, 4 Rue Gabrielle Perret-Gentil, 1211 Geneva, Switzerland ; Clinic for Infectious Diseases, University of Berne, Inselspital, Bern Switzerland.
Ilker UçkayDepartment of Infectious Diseases, Geneva University Hospitals and Medical School, 4 Rue Gabrielle Perret-Gentil, 1211 Geneva, Switzerland ; Orthopaedic Surgery Department, Geneva University Hospitals and Medical School, 4 Rue Gabrielle Perret-Gentil, 1211 Geneva, Switzerland.
Wilson BelaieffOrthopaedic Surgery Department, Geneva University Hospitals and Medical School, 4 Rue Gabrielle Perret-Gentil, 1211 Geneva, Switzerland.
Dominique BreilhDepartments of Pharmacokinetics and Clinical Pharmacy, Victor-Segalen University, Bordeaux, France.
Domizio SuvàOrthopaedic Surgery Department, Geneva University Hospitals and Medical School, 4 Rue Gabrielle Perret-Gentil, 1211 Geneva, Switzerland.
Elzbieta HugglerDepartment of Infectious Diseases, Geneva University Hospitals and Medical School, 4 Rue Gabrielle Perret-Gentil, 1211 Geneva, Switzerland.
Daniel LewDepartment of Infectious Diseases, Geneva University Hospitals and Medical School, 4 Rue Gabrielle Perret-Gentil, 1211 Geneva, Switzerland.
Pierre HoffmeyerOrthopaedic Surgery Department, Geneva University Hospitals and Medical School, 4 Rue Gabrielle Perret-Gentil, 1211 Geneva, Switzerland.
Louis BernardOrthopaedic Surgery Department, Geneva University Hospitals and Medical School, 4 Rue Gabrielle Perret-Gentil, 1211 Geneva, Switzerland ; Department of Infectious Diseases, Tours University Hospital, Tours, France.
University Hospital of Geneva · CHGeneva College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIncreased antibiotic resistance against Staphylococcus aureus and low penetration into bone requires regimen optimization of available drugs.

methodsWe evaluate pharmoacokinetic and pharmacodynamic parameters (PK/PD) as well as in vivo interactions of continuous flucloxacillin 12 g/d administration combined with high dose oral rifampicin 600 mg bid in the serum of 15 adult patients with bone and soft tissue infections. We use the patient's own serum directed against his own isolated S. aureus strain to reproduce in vivo conditions as closely as possible.

resultsThe continuous flucloxacillin infusion constantly generated plasma free drug levels largely exceeding the serum minimal inhibitory concentrations (mean 74-fold). Combination with rifampicin significantly increased flucloxacillin levels by 44.5%. Such an increase following rifampicin introduction was documented in 10/15 patients, whereas a decrease was observed in 1/15 patients. Finally, all infections were cured and the combination was well tolerated.

conclusionsIn this in vivo methodological pilot study among adult patients with orthopaedic infections due to S. aureus, we describe a new method and reveal substantial but inconsistent interactions between flucloxacillin and rifampicin, of which the clinical significance remains unclear.

Indexed as

FlucloxacillinPharmacodynamicsRifampicinStaphylococcus aureusSynergism

Identifiers

PMID25019039
PMCPMC4072877
OpenAlexW2123945145

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.