Blood culture contamination: a randomized trial evaluating the comparative effectiveness of 3 skin antiseptic

Laraine L Washer1, Carol Chenoweth, Hae-Won Kim

  • 1Department of Internal Medicine, Division of Infectious Diseases, University of Michigan Health System, Ann Arbor, Michigan 48109, USA. laraine@med.umich.edu

Abstract

Insights

When phlebotomy teams collect blood cultures, skin antiseptic choice (povidone-iodine or chlorhexidine) does not affect contamination rates. Cost or preference should guide antiseptic selection for these procedures.

Area of Science:

  • Infectious Diseases
  • Clinical Microbiology
  • Patient Safety

Background:

  • Blood culture contamination is a significant issue impacting patient care and healthcare costs.
  • Standardizing skin antisepsis protocols is crucial for accurate diagnostic results.
  • Dedicated phlebotomy teams may influence the effectiveness of different antiseptic agents.

Purpose of the Study:

  • To compare the blood culture contamination rates associated with three skin antisepsis agents: 10% povidone-iodine aqueous solution (PI), 2% iodine tincture (IT), and 2% chlorhexidine gluconate in 70% isopropyl alcohol (CHG).
  • To evaluate these agents when used by specialized phlebotomy teams for peripheral blood culture collection.

Main Methods:

  • A randomized crossover trial design was employed, with hospital floors serving as the unit of randomization.
  • The study included adult patients undergoing peripheral blood culture collection across three medical-surgical floors over a five-month period.
  • Phlebotomy teams administered each antisepsis intervention sequentially, with blinded adjudication of positive blood cultures to determine contamination.

Main Results:

  • A total of 12,904 peripheral blood culture sets were analyzed, with an overall contamination rate of 0.76%.
  • Contamination rates did not significantly differ among the three antiseptics: PI at 0.58%, IT at 0.76%, and CHG at 0.93%.
  • These findings indicate no statistically significant impact of the antiseptic agent on blood culture contamination when collected by phlebotomy teams.

Conclusions:

  • The choice of skin antiseptic agent does not appear to influence blood culture contamination rates when collections are performed by dedicated phlebotomy teams.
  • Antiseptic selection for blood cultures should be based on factors such as cost-effectiveness and clinician preference.
  • These results support flexibility in antiseptic choice for phlebotomy teams, potentially optimizing resource allocation.

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