Platelet Component False Positive Detection Rate in Aerobic and Anaerobic Primary Culture: A Systematic Review and

Jessica Corean1, Sandra K White1, Robert L Schmidt2

  • 1Department of Pathology, University of Utah, Salt Lake City, UT, USA.

Insights

False positive rates in platelet transfusion bacterial cultures are high, potentially misleading safety efforts. This systematic review analyzes culture methods to improve accuracy and patient safety.

Area of Science:

  • Hematology
  • Microbiology
  • Public Health

Background:

  • Septic reactions from platelet transfusions are a significant cause of transfusion-associated mortality.
  • Current FDA guidelines mandate aerobic and anaerobic bacterial cultures for platelet safety.
  • Previous studies reported false positive rates (FPR) but lacked comprehensive summarization and analysis of influencing factors.

Purpose of the Study:

  • To systematically review and meta-analyze existing data on the false positive rate (FPR) of bacterial cultures in platelet transfusions.
  • To identify and analyze factors influencing the FPR in platelet bacterial risk control.

Main Methods:

  • A systematic review and meta-analysis were conducted following established guidelines.
  • Eighteen studies, encompassing nearly 5 million tested units, were included in the analysis.
  • FPR was assessed for combined aerobic/anaerobic, aerobic-only, and anaerobic-only culture methods.

Main Results:

  • The combined aerobic/anaerobic FPR was 2.4 events per thousand (EPT) (prediction interval: 0.5-5.7).
  • Aerobic-only cultures showed an FPR of 1.0 EPT (0.2-2.2), while anaerobic-only cultures had an FPR of 1.8 EPT.
  • Instrument error contributed 0.5-1.7 EPT false positives, and sampling contamination contributed 0.3-1.0 EPT.

Conclusions:

  • The overall FPR of platelet bacterial cultures is significantly higher than the true positive rate, potentially impacting transfusion safety protocols.
  • Understanding the sources of false positives, such as instrument error and contamination, is crucial for refining bacterial detection methods.
  • The findings highlight the need for improved strategies to reduce false positives and enhance the reliability of bacterial screening in platelet products.

Related Concept Videos