Evidence map›Paper›PMID 35884197›Full record

ArticleAntibiotics (Basel, Switzerland)2022

Causative Pathogens Do Not Differ between Early, Delayed or Late Fracture-Related Infections.

Ruth A Corrigan, Jonathan Sliepen, Maria Dudareva, Frank F A IJpma, Geertje Govaert, Bridget L Atkins, Rob Rentenaar, Marjan Wouthuyzen-Bakker, Martin McNally

Abstract read
In one paragraph

Article in Antibiotics (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–field-weighted citation impact
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

23 citing papers in PubMed.

  1. Article
  2. MRSA-dominant colonization and synergistic pathogenicity withJournal of orthopaedic translation · 2026
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  16. Review
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  18. Article
  19. Article
  20. Current Concepts of Fracture-Related Infection.International journal of clinical practice · 2023
    Review
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.

Ruth A CorriganBone Infection Unit, Nuffield Orthopaedic Centre, Oxford University Hospitals, Oxford OX3 7HE, UK.
Jonathan SliepenDepartment of Trauma Surgery, University Medical Centre Groningen, University of Groningen, 9712 CP Groningen, The Netherlands.ORCID 0000-0003-0176-112X
Maria DudarevaBone Infection Unit, Nuffield Orthopaedic Centre, Oxford University Hospitals, Oxford OX3 7HE, UK.
Frank F A IJpmaDepartment of Trauma Surgery, University Medical Centre Groningen, University of Groningen, 9712 CP Groningen, The Netherlands.ORCID 0000-0002-9420-2732
Geertje GovaertDepartment of Trauma Surgery, University Medical Centre Utrecht, 3584 CX Utrecht, The Netherlands.
Bridget L AtkinsBone Infection Unit, Nuffield Orthopaedic Centre, Oxford University Hospitals, Oxford OX3 7HE, UK.
Rob RentenaarDepartment of Medical Microbiology and Infection Prevention, University Medical Centre Groningen, University of Groningen, 9713 GZ Groningen, The Netherlands.
Marjan Wouthuyzen-BakkerDepartment of Medical Microbiology, University Medical Centre Utrecht, 3584 CX Utrecht, The Netherlands.
Martin McNallyBone Infection Unit, Nuffield Orthopaedic Centre, Oxford University Hospitals, Oxford OX3 7HE, UK.ORCID 0000-0003-2003-9044

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fracture-related infections (FRIs) are classically considered to be early (0−2 weeks), delayed (3−10 weeks) or late (>10 weeks) based on hypothesized differences in causative pathogens and biofilm formation. Treatment strategies often reflect this classification, with debridement, antimicrobial therapy and implant retention (DAIR) preferentially reserved for early FRI. This study examined pathogens isolated from FRI to confirm or refute these hypothesized differences in causative pathogens over time. Cases of FRI managed surgically at three centres between 2015−2019 and followed up for at least one year were included. Data were analysed regarding patient demographics, time from injury and pathogens isolated. Patients who underwent DAIR were also analysed separately. In total, 433 FRIs were studied, including 51 early cases (median time from injury of 2 weeks, interquartile range (IQR) of 1−2 weeks), 82 delayed cases (median time from injury of 5 weeks, IQR of 4−8 weeks) and 300 late cases (median time from injury of 112 weeks, IQR of 40−737 weeks). The type of infection was associated with time since injury; early or delayed FRI are most likely to be polymicrobial, whereas late FRIs are more likely to be culture-negative, or monomicrobial. Staphylococcus aureus was the most commonly isolated pathogen at all time points; however, we found no evidence that the type of pathogens isolated in early, delayed or late infections were different (p = 0.2). More specifically, we found no evidence for more virulent pathogens (S. aureus, Gram-negative aerobic bacilli) in early infections and less virulent pathogens (such as coagulase negative staphylococci) in late infections. In summary, decisions on FRI treatment should not assume microbiological differences related to time since injury. From a microbiological perspective, the relevance of classifying FRI by time since injury remains unclear.

Indexed as

early delayed or late fracture-related infectionfracturefracture-related infectioninfectionmicrobiologypathogen

Identifiers

PMID35884197
PMCPMC9312187

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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.