Impact of same-day antibiotic susceptibility testing on time to appropriate antibiotic treatment of patients with bacteraemia: a randomised controlled trial

  • J. Beuving
  • P. F. G. Wolffs
  • W. L. J. Hansen
  • E. E. Stobberingh
  • C. A. Bruggeman
  • A. Kessels
  • A. Verbon
Article

Abstract

Inadequate therapy in bloodstream infections is suggested to be associated with higher mortality. We evaluated the reduction in inappropriate antibiotic therapy using rapid identification and antibiotic susceptibility testing (FAST) compared to standard of care (SOC) testing in patients with bloodstream infections. The FAST method used polymerase chain reaction (PCR) for identification and to detect growth in the presence or absence of antibiotics after only 6 h. For SOC testing, the BD Phoenix system was used. Patients with blood cultures growing Staphylococcus, Streptococcus or Enterococcus species or Gram-negative rods were randomised for FAST or SOC tests. A total of 129 patients were randomised for FAST and 121 patients for the SOC group. At the time SOC results became available, 78 patients in the FAST group could have been switched to more appropriate therapy. Although FAST results were highly accurate (agreement with SOC was 94 %), they were only implemented in a minority (16) of patients. However, significantly fewer patients in the FAST group used inappropriate therapy at the time of SOC results (p = 0.025). The time to results in the FAST group was reduced by 15.6 h (p < 0.001). In the patients switched after FAST, this was done after a mean of 42.3 h compared to 61.4 h in those switched after SOC tests (p < 0.001). In bacteraemic patients, FAST resulted in significantly more patients using appropriate antibiotic therapy at the time SOC results were available and 15.6 h earlier than SOC tests. However, the implementation of FAST results was not optimal and no benefit on clinical outcome was shown.

Keywords

Antibiotic Therapy Clavulanic Acid Antibiotic Susceptibility Testing Enterococcus Species Inappropriate Antibiotic Therapy 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Notes

Acknowledgements

The authors would like to thank Su Yan Yue, Rick Thissen, Gertjan Wagenvoort and Charlotte Hakkers for their assistance in the patient inclusion, data collection and laboratory work. This work was supported by the Profileringsfonds azM (grant number PF245). Parts of these results were presented at IDWeek 2012 in San Diego, CA, USA, October 2012.

Ethical standards

The study was approved by the MUMC Medical Ethics Committee. Patients were included after written informed consent was obtained.

Conflict of interest

All authors have contributed significantly to the study. No conflicts of interest were reported by any of the authors. The Profileringsfonds azM had no role in the study design, in the collection or analysis of data, or in the writing or submission of the manuscript.

References

  1. 1.
    Fraser A, Paul M, Almanasreh N et al (2006) Benefit of appropriate empirical antibiotic treatment: thirty-day mortality and duration of hospital stay. Am J Med 119:970–976CrossRefPubMedGoogle Scholar
  2. 2.
    Ibrahim EH, Sherman G, Ward S et al (2000) The influence of inadequate antimicrobial treatment of bloodstream infections on patient outcomes in the ICU setting. Chest 118:146–155CrossRefPubMedGoogle Scholar
  3. 3.
    Kumar A, Roberts D, Wood KE et al (2006) Duration of hypotension before initiation of effective antimicrobial therapy is the critical determinant of survival in human septic shock. Crit Care Med 34:1589–1596CrossRefPubMedGoogle Scholar
  4. 4.
    McGregor JC, Rich SE, Harris AD et al (2007) A systematic review of the methods used to assess the association between appropriate antibiotic therapy and mortality in bacteremic patients. Clin Infect Dis 45:329–337CrossRefPubMedGoogle Scholar
  5. 5.
    Bouza E, Sousa D, Muñoz P et al (2004) Bloodstream infections: a trial of the impact of different methods of reporting positive blood culture results. Clin Infect Dis 39:1161–1169CrossRefPubMedGoogle Scholar
  6. 6.
    Byl B, Clevenbergh P, Jacobs F et al (1999) Impact of infectious diseases specialists and microbiological data on the appropriateness of antimicrobial therapy for bacteremia. Clin Infect Dis 29:60–66CrossRefPubMedGoogle Scholar
  7. 7.
    Garnacho-Montero J, Garcia-Garmendia JL, Barrero-Almodovar A et al (2003) Impact of adequate empirical antibiotic therapy on the outcome of patients admitted to the intensive care unit with sepsis. Crit Care Med 31:2742–2751CrossRefPubMedGoogle Scholar
  8. 8.
    Kerremans JJ, Verboom P, Stijnen T et al (2008) Rapid identification and antimicrobial susceptibility testing reduce antibiotic use and accelerate pathogen-directed antibiotic use. J Antimicrob Chemother 61:428–435CrossRefPubMedGoogle Scholar
  9. 9.
    Livermore DM (2005) Minimising antibiotic resistance. Lancet Infect Dis 5:450–459CrossRefPubMedGoogle Scholar
  10. 10.
    Bruins M, Oord H, Bloembergen P et al (2005) Lack of effect of shorter turnaround time of microbiological procedures on clinical outcomes: a randomised controlled trial among hospitalised patients in the Netherlands. Eur J Clin Microbiol Infect Dis 24:305–313CrossRefPubMedGoogle Scholar
  11. 11.
    Trenholme GM, Kaplan RL, Karakusis PH et al (1989) Clinical impact of rapid identification and susceptibility testing of bacterial blood culture isolates. J Clin Microbiol 27:1342–1345PubMedCentralPubMedGoogle Scholar
  12. 12.
    Doern GV, Vautour R, Gaudet M et al (1994) Clinical impact of rapid in vitro susceptibility testing and bacterial identification. J Clin Microbiol 32:1757–1762PubMedCentralPubMedGoogle Scholar
  13. 13.
    Barenfanger J, Drake C, Kacich G (1999) Clinical and financial benefits of rapid bacterial identification and antimicrobial susceptibility testing. J Clin Microbiol 37:1415–1418PubMedCentralPubMedGoogle Scholar
  14. 14.
    Beuving J, Verbon A, Gronthoud FA et al (2011) Antibiotic susceptibility testing of grown blood cultures by combining culture and real-time polymerase chain reaction is rapid and effective. PLoS One 6:e27689CrossRefPubMedCentralPubMedGoogle Scholar
  15. 15.
    Centers for Disease Control and Prevention (CDC) (2014) CDC/NHSN surveillance definitions for specific types of infections. Available online at: http://www.cdc.gov/nhsn/pdfs/pscmanual/17pscnosinfdef_current.pdf. Accessed 21 July 2014
  16. 16.
    Hansen WL, Beuving J, Bruggeman CA et al (2010) Molecular probes for diagnosis of clinically relevant bacterial infections in blood cultures. J Clin Microbiol 48:4432–4438CrossRefPubMedCentralPubMedGoogle Scholar
  17. 17.
    Donker GA, Deurenberg RH, Driessen C et al (2009) The population structure of Staphylococcus aureus among general practice patients from The Netherlands. Clin Microbiol Infect 15:137–143CrossRefPubMedGoogle Scholar
  18. 18.
    Paterson DL, Ko WC, Von Gottberg A et al (2004) Antibiotic therapy for Klebsiella pneumoniae bacteremia: implications of production of extended-spectrum beta-lactamases. Clin Infect Dis 39:31–37CrossRefPubMedGoogle Scholar
  19. 19.
    de Kraker ME, Davey PG, Grundmann H (2011) Mortality and hospital stay associated with resistant Staphylococcus aureus and Escherichia coli bacteremia: estimating the burden of antibiotic resistance in Europe. PLoS Med 8:e1001104CrossRefPubMedCentralPubMedGoogle Scholar
  20. 20.
    Munson EL, Diekema DJ, Beekmann SE et al (2003) Detection and treatment of bloodstream infection: laboratory reporting and antimicrobial management. J Clin Microbiol 41:495–497CrossRefPubMedCentralPubMedGoogle Scholar
  21. 21.
    Oosterheert JJ, van Loon AM, Schuurman R et al (2005) Impact of rapid detection of viral and atypical bacterial pathogens by real-time polymerase chain reaction for patients with lower respiratory tract infection. Clin Infect Dis 41:1438–1444Google Scholar

Copyright information

© Springer-Verlag Berlin Heidelberg 2014

Authors and Affiliations

  • J. Beuving
    • 1
    • 2
  • P. F. G. Wolffs
    • 1
  • W. L. J. Hansen
    • 1
  • E. E. Stobberingh
    • 1
  • C. A. Bruggeman
    • 1
  • A. Kessels
    • 3
  • A. Verbon
    • 1
    • 4
  1. 1.Department of Medical MicrobiologyMaastricht University Medical Centre (MUMC)MaastrichtThe Netherlands
  2. 2.Department of Medical MicrobiologySt. Elisabeth HospitalTilburgThe Netherlands
  3. 3.Department of Clinical Epidemiology and Medical Technology AssessmentMaastricht University Medical Centre (MUMC)MaastrichtThe Netherlands
  4. 4.Department of Internal MedicineErasmus MCRotterdamThe Netherlands

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