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January 14, 2026Open Forum Infectious Diseases0 citationsOpen Access

P-937. Impact of Rapid Carbapenemase Testing on Time to Active Therapy

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KFKellie FortierCSCamryn SoehnleinJCJared Cvetko

Key Points

  • To evaluate the impact of rapid carbapenemase testing on time to active therapy for patients with carbapenem-resistant Enterobacterales.
  • Descriptive, retrospective analysis of patients with positive Enterobacterales cultures who underwent CARBA5 testing.
  • Included patients admitted between 3/1/24-6/30/24.
  • Primary outcome was time to active therapy prescribed; secondary outcomes included in-hospital mortality and readmission rates.
  • Implemented CARBA5 testing reduced time to active therapy by nearly 2 days compared to previous evaluations.
  • In-hospital mortality decreased from 16% to 10% after testing implementation.
  • 259 patients demonstrated a significant incidence of ICU admissions, with 30.5% requiring intensive care.

Abstract

Abstract Background Antimicrobial resistance continues to be a worldwide threat. Data from the Center for Disease Control (CDC) and our health system shows carbapenem-resistant Enterobacterales (CRE) are a growing problem in the US and in Arizona; within our health system the incidence of CREs have been increasing since 2020. At the end of 2023, rapid carbapenemase testing with NG-TEST® CARBA5 was implemented. This study evaluated if implementation of the NG-TEST® CARBA-5 assay improved time to active therapyPrimary and Secondary Endpoints Methods This descriptive, retrospective analysis included admitted patients with an Enterobacterales positive culture, which exhibited non-susceptibility to a carbapenem and underwent CARBA5 testing between 3/1/24-6/30/24. The primary outcome was time to active therapy prescribed. Other outcomes included time to active therapy administered, in-hospital mortality, readmission for the same infection within 90 days, average length of stay (LOS), and intensive care unit (ICU) admission or transfer. Results A total of 259 patients were included. New Delhi metallo-β-lactamase producing K. pneumoniae from a urinary source was the most common CRE. Time from culture drawn to active treatment ordered was 54.6 hours. In hospital mortality was 10% percent with a readmission rate of 17%. Mean LOS was 13.2 days with 30.5% of patients admitted or transferred to an ICU. Approximately 24% of patients never received active therapy, with 77% of those cultures being from urine. A previous system evaluation showed time to active antimicrobial therapy prescribed was 97.8 hours with an in-hospital mortality of 16%. Conclusion Implementation of CARBA5 testing resulted in a reduction in time to active therapy prescribed by almost 2 days compared to a previous evaluation. In hospital mortality was lower after initiation of CARBA5 testing but could not be statistically compared as groups differed on inclusion and exclusion criteria. A 2-day reduction in time to active therapy is clinically relevant. Further work within the health system is being done to improve time to active therapy. This evaluation serves as a useful source of data for future evaluations or interventions. Disclosures All Authors: No reported disclosures

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Cite This Study

Fortier et al. (2026) studied this question.

synapsesocial.com/papers/6966f33213bf7a6f02c01133https://doi.org/10.1093/ofid/ofaf695.1140
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