Evidence map›Paper›PMID 33448872›Full record

ArticleBone & joint research2021

Flucloxacillin bone and soft tissue concentrations assessed by microdialysis in pigs after intravenous and oral administration.

Mathias A F Bendtsen, Mats Bue, Pelle Hanberg, Josefine Slater, Maja B Thomassen, Jakob Hansen, Kjeld Søballe, Kristina Öbrink-Hansen, Maiken Stilling

Open access · goldAbstract read
In one paragraph

Article in Bone & joint research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
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 1 institution in 1 country.

Mathias A F BendtsenDepartment of Clinical Medicine, Faculty of Health, Aarhus University, Aarhus, Denmark.
Mats BueDepartment of Clinical Medicine, Faculty of Health, Aarhus University, Aarhus, Denmark.ORCID https://orcid.org/0000-0001-7215-8323
Pelle HanbergDepartment of Clinical Medicine, Faculty of Health, Aarhus University, Aarhus, Denmark.
Josefine SlaterDepartment of Clinical Medicine, Faculty of Health, Aarhus University, Aarhus, Denmark.
Maja B ThomassenDepartment of Clinical Medicine, Faculty of Health, Aarhus University, Aarhus, Denmark.
Jakob HansenDepartment of Clinical Medicine, Faculty of Health, Aarhus University, Aarhus, Denmark.ORCID https://orcid.org/0000-0002-4115-2858
Kjeld SøballeDepartment of Clinical Medicine, Faculty of Health, Aarhus University, Aarhus, Denmark.
Kristina Öbrink-HansenDepartment of Clinical Medicine, Faculty of Health, Aarhus University, Aarhus, Denmark.
Maiken StillingDepartment of Clinical Medicine, Faculty of Health, Aarhus University, Aarhus, Denmark.ORCID https://orcid.org/0000-0002-4530-2075
Aarhus University · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsFlucloxacillin is commonly administered intravenously for perioperative antimicrobial prophylaxis, while oral administration is typical for prophylaxis following smaller traumatic wounds. We assessed the time, for which the free flucloxacillin concentration was maintained above the minimum inhibitory concentration (

methodsA total of 16 pigs were randomly allocated to either intravenous (Group IV) or oral (Group PO) flucloxacillin 1 g every six hours during a 24-hour period. Microdialysis was used for sampling in cancellous and cortical bone, subcutaneous tissue, and the knee joint. In addition, plasma was sampled. The flucloxacillin

resultsIntravenous administration resulted in longer

conclusionAlthough intravenous administration of flucloxacillin 1 g provided higher fT > MIC for the low MIC target compared to oral administration, concentrations were surprisingly low, particularly for bone tissue. Achievement of sufficient bone and soft tissue flucloxacillin concentrations may require a dose increase or continuous administration. Cite this article:

Indexed as

Animal modelBoneFlucloxacillinInfectionOsteomyelitis

Identifiers

PMID33448872
PMCPMC7845458
OpenAlexW3120014243

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.