Bacterial contamination rate of platelet components by primary culture: a systematic review and meta-analysis
- PMID: 32181889
- DOI: 10.1111/trf.15762
Bacterial contamination rate of platelet components by primary culture: a systematic review and meta-analysis
Erratum in
-
Correction to "Bacterial contamination rate of platelet components by primary culture: a systematic review and meta-analysis".Transfusion. 2024 Jun;64(6):1179. doi: 10.1111/trf.17816. Epub 2024 May 6. Transfusion. 2024. PMID: 38708709 No abstract available.
Abstract
Background: Platelets have the highest bacterial contamination risk of all blood components, and septic transfusion reactions remain a problem. A good estimate of contamination rates could provide information about residual risk and inform optimal testing strategies. We performed a systematic review and meta-analysis of platelet contamination rates by primary culture.
Study design and methods: A literature search in December 2019 identified articles on platelet contamination rates using primary culture. We used meta-analysis to estimate the overall rate of contamination and meta-regression to identify heterogeneity. We studied the following sources of heterogeneity: collection method, sample volume, positivity criteria, and study date. Contamination rate estimates were obtained for apheresis (AP), platelet rich plasma (PRP), and buffy coat (BC) collection methods.
Results: The search identified 6102 studies, and 22 were included for meta-analysis. Among these 22 studies, there were 21 AP cohorts (4,072,022 components), 4 PRP cohorts (138,869 components), and 15 BC cohorts (1,474,679 components). The overall mean contamination rate per 1000 components was 0.51 (95% CI: 0.38-0.67) including AP (0.23, 95% CI: 0.18-0.28), PRP, (0.38, 95% CI: 0.15-0.70), and BC (1.12, 95% CI: 0.51-1.96). There was considerable variability within each collection method. Sample volume, positivity criteria, and publication year were significant sources of heterogeneity.
Conclusion: The bacterial contamination rate of platelets by primary culture is 1 in 1961. AP and PRP components showed a lower contamination rate than BC components. There is clinically significant between-study variability for each method. Larger sample volumes increased sensitivity, and bacterial contamination rates have decreased over time.
© 2020 AABB.
References
REFERENCES
-
- United States Government. Food & Drug Administration (FDA). Fatalities reported to FDA following blood collection and transfusion: annual summary for FY2017.
-
- AABB Donor History Task Force. Full-length donor history questionnaire (DHQ). 2016;v2.0.
-
- Strand CL, Wajsbort RR, Sturmann K. Effect of iodophor vs iodine tincture skin preparation on blood culture contamination rate. JAMA 1993;269:1004-6.
-
- Liumbruno GM, Catalano L, Piccinini V, et al. Reduction of the risk of bacterial contamination of blood components through diversion of the first part of the donation of blood and blood components. Blood Transfus 2009 Apr;7:86-93.
-
- AuBuchon JP, Cooper LK, Leach MF, et al. Experience with universal bacterial culturing to detect contamination of apheresis platelet units in a hospital transfusion service. Transfusion 2002;42:855-61.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
Research Materials