Benefits of Adding a Rapid PCR-Based Blood Culture Identification Panel to an Established Antimicrobial Stewardship

Shawn H MacVane1, Frederick S Nolte2

  • 1Department of Pharmacy, Medical University of South Carolina, Charleston, South Carolina, USA Division of Infectious Diseases, Medical University of South Carolina, Charleston, South Carolina, USA.

Insights

Antimicrobial stewardship programs (ASP) combined with rapid organism identification using multiplex PCR panels (BCID) improve bloodstream infection (BSI) treatment. BCID further shortens time to effective therapy and enhances antimicrobial use compared to ASP alone.

Area of Science:

  • Clinical Microbiology
  • Infectious Diseases
  • Health Services Research

Background:

  • Bloodstream infections (BSI) require timely and appropriate antimicrobial therapy.
  • Antimicrobial stewardship programs (ASP) aim to optimize antimicrobial use.
  • Rapid organism identification methods, such as multiplex PCR-based blood culture identification panels (BCID), may enhance BSI management.

Purpose of the Study:

  • To evaluate the independent and combined effects of ASP and BCID on clinical and economic outcomes in patients with BSI.
  • To determine if BCID adds incremental benefit to an established ASP.

Main Methods:

  • A pre-post quasiexperimental study design was used with three groups: controls (conventional identification), ASP alone, and BCID with ASP.
  • Patients with positive blood cultures were analyzed, comparing time to organism identification, time to effective therapy, antimicrobial de-escalation rates, mortality, readmission, length of stay, and costs.
  • A multiplex PCR panel (BCID) identifying 19 bacterial species, 5 Candida spp., and 4 antimicrobial resistance genes was utilized.

Main Results:

  • The BCID group showed significantly shorter times to organism identification (17 h vs. 57 h/54 h) and effective therapy (5 h vs. 15 h/13 h) compared to control and ASP groups.
  • Both ASP and BCID groups had higher rates of antimicrobial de-escalation than controls, with earlier de-escalation in the BCID group (48 h vs. 61 h/63 h).
  • No significant differences were observed in mortality, 30-day readmission, ICU length of stay, postculture length of stay, or costs across the groups.

Conclusions:

  • ASP alone improves antimicrobial utilization in BSI management.
  • Adding BCID to an established ASP further shortens time to effective therapy and enhances antimicrobial use, even with low resistance rates.
  • BCID provides incremental benefits in optimizing antimicrobial therapy for BSI when integrated with ASP.

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