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March 25, 2026Microorganisms0 citationsOpen Access

A Proof-of-Concept of a 2-Hours Direct Antimicrobial Susceptibility Test from Inoculated Urine Samples

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MSMariana Sousa-PinheiroIMInês Martins-OliveiraDADavid Brusaca Abreu

Key Points

  • This research aims to evaluate a rapid method for antimicrobial susceptibility testing directly from urine samples.
  • Analyzed 154 inoculated urine samples using FASTinov® panels for Gram-negative and Gram-positive bacteria.
  • Employed flow cytometry for rapid phenotypic antimicrobial susceptibility testing.
  • Evaluated performance against conventional methods based on EUCAST guidelines.
  • Achieved 97.5% agreement for Gram-negative and 95.0% for Gram-positive bacteria compared to conventional methods.
  • Identified all resistance mechanisms correctly without false positives.
  • Showed 95.2% essential agreement for vancomycin's MIC with a BIAS of +14.3%.
  • Demonstrated reproducibility rates of 99.5% for FASTgramneg and 95.0% for FASTgrampos.

Abstract

Urinary tract infections (UTIs) are the most frequent infections in hospitalized and outpatient settings, where Escherichia coli is the predominant pathogen. Conventional diagnostic and antimicrobial susceptibility testing (AST) methods are time-consuming, often requiring 48 h, leading to empirical antibiotic therapy and contributing to antimicrobial resistance (AMR). FASTinov® developed a rapid phenotypic method that enables AST directly from urine samples within two hours using flow cytometry. In this study, 154 inoculated urine samples were analyzed to evaluate the performance of two diagnostic panels: FASTgramneg for Gram-negative bacteria and FASTgrampos for Gram-positive bacteria. Data analysis was performed using bioFAST® software (version 3.0), providing results in accordance with EUCAST guidelines. The FASTgramneg panel allows detection of resistance mechanisms, including extended-spectrum β-lactamases (ESBLs), and screening of AmpC β-lactamases and carbapenemases; the FASTgrampos panel additionally determines the minimal inhibitory concentration (MIC) of vancomycin for Staphylococcus aureus. Overall agreement with conventional AST methods was 97.5% for Gram-negative bacteria and 95.0% for Gram-positive bacteria. All resistance mechanisms were correctly identified with no false positives. The essential agreement for vancomycin’s MIC was 95.2%, with a BIAS of +14.3%. Reproducibility was 99.5% for FASTgramneg and 95.0% for FASTgrampos. These results demonstrate that the FASTinov® kit significantly reduces turnaround time while maintaining high accuracy, supporting improved UTI management and antimicrobial stewardship.

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Cite This Study

Sousa-Pinheiro et al. (2026) studied this question.

synapsesocial.com/papers/69c37b74b34aaaeb1a67de94https://doi.org/10.3390/microorganisms14030711
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1A multisite validation of a two hours antibiotic susceptibility flow cytometry assay directly from positive blood cultures2024 · 7 citations
  2. 2Towards enhanced selection of antibiotics in a hospital laboratory – development of a rapid electrochemical-based antimicrobial sensitivity test for Urinary Tract Infections.2025
  3. 3Toward Enhanced Selection of Antibiotics in a Hospital Laboratory—Development of a Rapid Electrochemical Antimicrobial Sensitivity Test for Urinary Tract Infections2026
  4. 4Multisite clinical evaluation of the iFAST rapid antimicrobial susceptibility test direct from positive blood cultures containing gram-negative organisms2026
  5. 5Sedimentation field-flow fractionation for rapid phenotypic antimicrobial susceptibility testing: a pilot study2024