Bacterial screening of platelet components: Experience at a hospital-based blood bank

Arwa Z Al-Riyami1,2, Y Al-Ruzeiqi3, I Al-Omairi1

  • 1Department of Hematology, Sultan Qaboos University Hospital, University Medical City, Muscat, Oman.

Vox Sanguinis
|October 10, 2025
PubMed
Abstract

Insights

Bacterial contamination in platelets is a serious risk. This study found a low rate of positive platelet cultures (0.1%) using the Bactec™ FX system, with Staphylococcus species being the most common contaminant.

Area of Science:

  • Transfusion Medicine
  • Microbiology
  • Infectious Disease

Background:

  • Platelets stored at room temperature carry a high risk of bacterial contamination, leading to severe infections and fatalities.
  • Hospital blood banks routinely screen platelet concentrates (PCs) for bacterial contamination to ensure transfusion safety.

Purpose of the Study:

  • To determine the prevalence of culture-positive platelet concentrates (PCs) in a hospital-based blood bank.
  • To identify the types of microorganisms contaminating PCs and assess their clinical significance.

Main Methods:

  • A retrospective review of bacterial culture records for 5009 platelet units from April 2021 to August 2023.
  • Utilized the Bactec™ FX system for bacterial culture of pooled samples from whole blood-derived and apheresis platelet units.
  • Analyzed positive culture results, identified organisms, and reviewed clinical records for transfusion reactions.

Main Results:

  • An initial positive culture rate of 1.7% (85 out of 5009 PCs) was observed.
  • Staphylococcus species were the most frequently identified organisms (48%).
  • Confirmatory testing revealed a final positivity rate of 0.1% (5 out of 5009 PCs), with Micrococcus luteus and Gram-positive bacilli identified; no clinical sequelae were reported.

Conclusions:

  • The study indicates a low rate of bacterial contamination in platelet concentrates when using the Bactec™ FX system.
  • Staphylococcus species are the predominant contaminants found in platelet cultures.
  • Further research is needed to assess the viability of large-volume, delayed-sampling testing protocols for platelet safety.