Rapid detection of carbapenemase-producing organisms directly from blood cultures positive for Gram-negative bacilli

Eur J Clin Microbiol Infect Dis. 2021 Feb;40(2):381-384. doi: 10.1007/s10096-020-04005-4. Epub 2020 Aug 11.

Abstract

Introduction: The rapid detection of carbapenemase-producing organisms (CPOs) directly from blood cultures (BCs) positive for Gram-negative bacilli (GNB) may accelerate the appropriate treatment of at-risk patients.

Objective: To evaluate the performance of two commercial assays in the rapid detection of CPOs directly from BC positive for GNB.

Methods: BC positive for GNB were tested for the presence of CPOs with β CARBA® and NG-Test® CARBA 5. A subset of sterile BC samples was seeded with multidrug-resistant (MDR) GNB. Positive BCs from clinical and seeded samples were tested directly with β CARBA and CARBA 5 from BC pellets.

Results: Sixty-five samples were tested (30 clinical, 35 seeded). β CARBA had a sensitivity, specificity, NPV, and PPV of 100%, 65.7%, 100%, and 71.4%, respectively. CARBA 5 had a sensitivity, specificity, NPV, and PPV of 90.0%, 100%, 92.1%, and 100%. False negatives for CARBA 5 occurred with 1 GES, 1 VIM-1, and 1 IMP-14.

Conclusions: This study demonstrates that the detection of CPOs directly from positive BC can be accurately achieved. β CARBA had excellent sensitivity but suffered from poor specificity. CARBA 5 had good sensitivity and specificity but is unable to detect certain CPOs.

Keywords: Bacteremia; CARBA 5; Carbapenemase-producing organisms; Rapid diagnostics; β CARBA.

Publication types

  • Evaluation Study

MeSH terms

  • Bacteremia / microbiology*
  • Bacterial Proteins
  • Bacteriological Techniques / methods
  • Blood Culture / methods*
  • Gram-Negative Bacteria / enzymology
  • Gram-Negative Bacteria / isolation & purification*
  • Gram-Negative Bacterial Infections / diagnosis*
  • Humans
  • Point-of-Care Testing*
  • Sensitivity and Specificity
  • beta-Lactamases

Substances

  • Bacterial Proteins
  • beta-Lactamases
  • carbapenemase