Improving the performance of culture-based bacterial screening by increasing the sample volume from 4 mL to 8 mL in aerobic culture bottles

Transfusion. 2012 Jul;52(7):1576-82. doi: 10.1111/j.1537-2995.2011.03489.x. Epub 2011 Dec 29.

Abstract

Background: In the setting of bacterial detection of apheresis platelets (PLTs), the manufacturer recommended PLT inoculation volume for BacT/ALERT culture bottles (bioMérieux) ranges from 4 to 10 mL. This study compares the rate of capture of true-positive (TP) contaminations between aerobic culture bottles inoculated with either 4 or 8 mL of sample and assesses if a larger sample volume reduces time to detection.

Study design and methods: Detection of TP samples and mean time to detection were compared for 4- and 8-mL samples collected between September 1, 2003, and May 2, 2011.

Results: A total of 180,263 and 283,114 PLT collections were tested with an 8- and 4-mL sample, respectively. Analysis of TP rates by volume sampled show an increase in the rate of detection of TP with the 8-mL sample relative to the 4-mL sample (139 vs. 106 per million events; odds ratio, 1.31; 95% confidence interval, 0.77-2.23). Comparison of mean time to detection for TP shows a decrease in mean time to detection using 8 mL compared with 4 mL (12.36 ± 3.7 hr to 15.97 ± 6.3 hr, p = 0.012).

Conclusion: Doubling the sample volume to 8 mL showed a trend in improvement for the rate of detection of TP and shortened the mean time of detection for TP by 23% when compared to a sample volume of 4 mL. The decrease in mean time to detection using a larger sample volume suggests that a shorter release time after inoculation could be achieved without significantly increasing patient risk.

Publication types

  • Comparative Study

MeSH terms

  • Aerobiosis
  • Bacteria* / growth & development
  • Bacteria* / isolation & purification
  • Bacterial Infections / prevention & control
  • Bacterial Infections / transmission
  • Bacteriological Techniques / instrumentation
  • Bacteriological Techniques / methods
  • Blood Platelets / microbiology*
  • Humans
  • Sensitivity and Specificity
  • Time Factors