Safety Analysis of Extended Platelet Shelf-Life with Large-Volume Delayed Sampling on BACT/ALERT® VIRTUO® in Australia

Author:

Cheng Anthea1ORCID,Das Anindita123ORCID,Chaw Khin14ORCID,Dennington Peta M.5ORCID,Styles Claire E.1ORCID,Gosbell Iain B.16ORCID

Affiliation:

1. Donor and Product Safety Policy Unit, Australian Red Cross Lifeblood, West Melbourne, VIC 3003, Australia

2. Clinical Microbiology, ACT Pathology, Garran, ACT 2606, Australia

3. Faculty of Health, University of Canberra, Bruce, ACT 2617, Australia

4. MetroSouth Public Health Unit, Eight Mile Plains, QLD 4113, Australia

5. Pathology Services, Australian Red Cross Lifeblood, Alexandria, NSW 2015, Australia

6. School of Medicine, Western Sydney University, Penrith, NSW 2747, Australia

Abstract

Transfusion-transmitted bacterial infection (TTBI) is the leading cause of transfusion-transmitted infections. Platelet components are more likely to be associated with bacterial contamination due to their storage requirements. Australian Red Cross Lifeblood introduced the bacterial contamination screening (BCS) of all platelet components in 2008. The process was recently updated with the use of BACT/ALERT® VIRTUO®, a large-volume delayed sampling (LVDS) protocol and extending platelet shelf-life to seven days. This article describes the results from the routine BCS of platelet components in Australia. Use of VIRTUO has resulted in lower false-positive rates, reducing wastage and improving platelet inventory. Our findings show that the combination of LVDS and VIRTUO improves the safety of platelet transfusions through earlier time to detection, especially for pathogenic bacterial species. Pathogenic bacteria grew within 24 h of incubation with a clear delineation between pathogenic and non-pathogenic species. The data show this protocol is very safe, with no TTBI cases during this time. There were no TTBI reports in recipients of platelet components that subsequently had a positive culture with Cutibacterium species, probably due to the low pathogenic potential of these organisms and slow replication in aerobic platelet bags. We conclude there is no advantage in incubating culture bottles beyond five days.

Publisher

MDPI AG

Subject

Virology,Microbiology (medical),Microbiology

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