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A multi-site, international laboratory study to assess the performance of penicillin susceptibility testing of Staphylococcus aureus
Journal article   Peer reviewed

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, …
Journal of antimicrobial chemotherapy, Vol.78(6), pp.1499-1504
2023
PMID: 37071589

Abstract

Anti-Bacterial Agents - pharmacology Clinical Decision-Making Humans Microbial Sensitivity Tests Penicillins - pharmacology Staphylococcal Infections Staphylococcus aureus - genetics Uncertainty
Objectives There 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. Methods Nine 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. Results Twenty-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. Conclusions The 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.

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Collaboration types
Domestic collaboration
International collaboration
Citation topics
1 Clinical & Life Sciences
1.23 Antibiotics & Antimicrobials
1.23.173 MRSA and VRE
Web Of Science research areas
Infectious Diseases
Microbiology
Pharmacology & Pharmacy
ESI research areas
Pharmacology & Toxicology
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