Evidence map›Paper›PMID 37071589›Full record

ArticleThe Journal of antimicrobial chemotherapy2023

A multi-site, international laboratory study to assess the performance of penicillin susceptibility testing of Staphylococcus aureus.

Andrew Henderson, Matthew P Cheng, Ka Lip Chew, Geoffrey W Coombs, Joshua S Davis, Jennifer M Grant, Dan Gregson, Stefano G Giulieri, Benjamin P Howden, Todd C Lee and 7 more

Registry-linked trialAbstract read
In one paragraph

Article in The Journal of antimicrobial chemotherapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05137119 (Staphylococcus Aureus Network Adaptive Platform Trial), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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.

NCT05137119 phase4recruitingnot on this map

Staphylococcus Aureus Network Adaptive Platform Trial

TypeinterventionalSponsorUniversity of MelbourneRan2022 to 2028Enrolled8,000ConditionsStaphylococcus Aureus BacteremiaArmsCefazolin, Penicillin, Clindamycin, Vancomycin, Effectiveness of early switch to oral antibiotics
3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Cefazolin for Methicillin-SusceptibleThe New England journal of medicine · 2026
    Trial
  2. Genomic Characterization and Virulence Determinants ofAntibiotics (Basel, Switzerland) · 2026
    Article
  3. Staphylococcus aureus genotypic penicillin susceptibility using a blaZ qPCR directly on blood cultures shows high concordance with phenotype.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2025
    Article
  4. Article
  5. Measuring beta-lactam minimum inhibitory concentrations inJournal of clinical microbiology · 2024
    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

17 authors.

Andrew HendersonInfection Management Services, Princess Alexandra Hospital, Brisbane, Australia.
Matthew P ChengDepartment of Medicine, and Laboratory Medicine, McGill University Health Centre, Montreal, Canada.ORCID 0000-0002-4867-2063
Ka Lip ChewDepartment of Laboratory Medicine, National University Hospital, Singapore, Singapore.
Geoffrey W CoombsDepartment of Antimicrobial Resistance, and Infectious Diseases Research Laboratory, Murdoch University, Murdoch, Australia.
Joshua S DavisHunter Medical Research Institute, University of Newcastle, Newcastle, Australia.ORCID 0000-0001-9864-5699
Jennifer M GrantDepartment of Medicine, Vancouver Coastal Health, Vancouver, Canada.
Dan GregsonDepartment of Pathology, Laboratory Medicine, and Medicine, Cummings School of Medicine at The University of Calgary, Calgary, Canada.
Stefano G GiulieriDepartment of Microbiology, and Immunology, The University of Melbourne, Melbourne, Australia.
Benjamin P HowdenMicrobiological Diagnostic Unit Public Health Laboratory, The Peter Doherty Institute for Infection and Immunity, Melbourne, Australia.ORCID 0000-0003-0237-1473
Todd C LeeDepartment of Medicine, McGill University, Montreal, Canada.ORCID 0000-0002-2267-4239
Vi NguyenDepartment of Infectious Diseases, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Australia.
Jocelyn M MoraDepartment of Infectious Diseases, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Australia.
Susan C MorpethMicrobiology Laboratory, Middlemore Hospital (Counties Manukau Te Whatu Ora), Otahuhu, New Zealand.
James O RobinsonDepartment of Infectious Diseases, Royal Perth Hospital, Perth, Australia.
Steven Y C TongDepartment of Infectious Diseases, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Australia.ORCID 0000-0002-1368-8356
Sebastiaan J Van HalDepartment of Microbiology, and Infectious Diseases, Royal Prince Alfred Hospital, Missenden Road, Camperdown, NSW 2050, Sydney, Australia.ORCID 0000-0001-5852-4155
Microbiology Working Group of the Staphylococcus aureus Network Adaptive Platform (SNAP) Trial Group

Funding

Department of Health
6 · The paper itself

Abstract

objectivesThere is clinical uncertainty over the optimal treatment for penicillin-susceptible Staphylococcus aureus (PSSA) infections. Furthermore, there is concern that phenotypic penicillin susceptibility testing methods are not reliably able to detect some blaZ-positive S. aureus.

methodsNine S. aureus isolates, including six genetically diverse strains harbouring blaZ, were sent in triplicate to 34 participating laboratories from Australia (n = 14), New Zealand (n = 6), Canada (n = 12), Singapore (n = 1) and Israel (n = 1). We used blaZ PCR as the gold standard to assess susceptibility testing performance of CLSI (P10 disc) and EUCAST (P1 disc) methods. Very major errors (VMEs), major error (MEs) and categorical agreement were calculated.

resultsTwenty-two laboratories reported 593 results according to CLSI methodology (P10 disc). Nineteen laboratories reported 513 results according to the EUCAST (P1 disc) method. For CLSI laboratories, the categorical agreement and calculated VME and ME rates were 85% (508/593), 21% (84/396) and 1.5% (3/198), respectively. For EUCAST laboratories, the categorical agreement and calculated VME and ME rates were 93% (475/513), 11% (84/396) and 1% (3/198), respectively. Seven laboratories reported results for both methods, with VME rates of 24% for CLSI and 12% for EUCAST.

conclusionsThe EUCAST method with a P1 disc resulted in a lower VME rate compared with the CLSI methods with a P10 disc. These results should be considered in the context that among collections of PSSA isolates, as determined by automated MIC testing, less than 10% harbour blaZ. Furthermore, the clinical relevance of phenotypically susceptible, but blaZ-positive S. aureus, remains unclear.

Indexed as

Anti-Bacterial AgentsStaphylococcal InfectionsClinical Decision-MakingHumansMicrobial Sensitivity TestsPenicillinsStaphylococcus aureusUncertaintyAnti-Bacterial AgentsPenicillins

Identifiers

PMID37071589
PMCPMC10232234

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Registered trials

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.