Evidence map›Paper›PMID 32199450›Full record

ArticleAnnals of clinical microbiology and antimicrobials2020

Ceftobiprole: a potential empirical post-operative monotherapy in prosthetic joint infections.

Claire Duployez, Frédéric Wallet, Henri Migaud, Eric Senneville, Caroline Loiez

Open access · goldAbstract read
In one paragraph

Article in Annals of clinical microbiology and antimicrobials, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

2 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Low prevalence of tissue detection of cefepime and daptomycin used as empirical treatment during revision for periprosthetic joint infections: results of a prospective multicenter study.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2021
    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

5 authors at 2 institutions in 1 country.

Claire DuployezInstitute of Microbiology, Lille University Hospital, 59037, Lille, France.
Frédéric WalletInstitute of Microbiology, Lille University Hospital, 59037, Lille, France.
Henri MigaudOrthopaedic Department, Lille University Hospital, 59037, Lille, France.
Eric SennevilleInfectious Diseases Department, Gustave Dron Hospital, 59200, Tourcoing, France.
Caroline LoiezInstitute of Microbiology, Lille University Hospital, 59037, Lille, France. caroline.loiez@chru-lille.fr.
Centre Hospitalier de Tourcoing · FRLille’s Cardiology Hospital · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study aimed to evaluate in vitro susceptibility to ceftobiprole of clinical strains identified from prosthetic joint infections (PJIs) compared to that of the associations currently recommended for post-operative empirical antibiotic therapy (PEAT) (vancomycin with either cefepime, third-generation cephalosporin or piperacillin-tazobactam).

methodsWe performed a 1-year retrospective study on all the surgical procedures performed in our hospital for PJI. Susceptibility profiles of all the strains cultured from surgical samples were reviewed to compare ceftobiprole to current used associations.

resultsDuring the study period (from January 2018 to December 2018), we identified 106 patients managed for PJI and a total of 216 surgical interventions. One hundred-fifty strains were identified from intraoperative samples, excluding redundant strains. Staphylococcus spp. represented 52.7% of all strains and Enterobacteriales 13.3%. Twenty-three patients had polymicrobial infection (22%). Among 149 surgical procedures with positive culture results, ceftobiprole covered the bacterial strains in 138 (92.6%) cases. In comparison, this percentage was 94.6% for vancomycin plus cefepime (p = 0.64), 92.6% for vancomycin plus a third-generation cephalosporin in 138 cases (p = 1) and 94.6% for vancomycin plus piperacillin-tazobactam) (p = 0.64).

conclusionBased on antimicrobial susceptibility testing, our results suggest that ceftobiprole could be an interesting option for PEAT in PJIs, allowing the use of a single agent.

Indexed as

Anti-Bacterial AgentsCephalosporinsCoinfectionEnterobacteriaceae InfectionsFemaleHumansMaleMicrobial Sensitivity TestsProsthesis-Related InfectionsRetrospective StudiesStaphylococcal InfectionsAnti-Bacterial AgentsceftobiproleCephalosporinsBacterial resistanceCeftobiproleEmpirical antibiotic therapyProsthetic joint infection

Identifiers

PMID32199450
PMCPMC7085185
OpenAlexW3012609896

What OpenQuestion holds

Textmetadata
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.