Ramirez-Arcos Sandra, Kou Yuntong, Kumaran Dilini, Culibrk Brankica, Stewart Tamiko, Schubert Peter, McTaggart Ken
Medical Affairs and Innovation, Canadian Blood Services, Ottawa, Ontario, Canada.
Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, Ontario, Canada.
Vox Sang. 2022 May;117(5):678-684. doi: 10.1111/vox.13246. Epub 2022 Jan 11.
Whole blood (WB) transfusion has regained attention to treat trauma patients. We reported no significant changes in in vitro quality through 21 days of cold storage for leukoreduced WB (LCWB) when time to filtration was extended from 8 to 24 h from collection. This study evaluated the impact of extended WB-hold at room temperature (RT) prior to leukoreduction on proliferation of transfusion-relevant bacteria.
WB units were spiked with suspensions of Klebsiella pneumoniae, Streptococcus pyogenes, Staphylococcus aureus and Listeria monocytogenes prepared in saline solution (SS) or trypticase soy broth (TSB) to a concentration of ~0.2 CFU/ml (N = 6). Spiked units were held at RT for 18-24 h before leukoreduction and cold-stored for 21 days. Bacterial growth was determined on days 2, 7, 14 and 21. In vitro quality of WB inoculated with unspiked diluents was assessed.
K. pneumoniae and S. pyogenes proliferated in WB prior to leukoreduction reaching concentrations ≤10 CFU/ml. These bacteria, however, did not proliferate during the subsequent cold storage. S. aureus did not survive in WB while L. monocytogenes reached a concentration of ~10 CFU/ml by day 21. LCWB in vitro quality was not affected by SS or TSB.
Extended WB-hold prior to leukoreduction allowed proliferation of bacteria able to resist immune clearance, although they did not grow to clinically significant levels. While L. monocytogenes proliferated in LCWB, clinically relevant concentrations were not reached by day 21. These data suggest that transfusing LCWB may not pose a significant bacterial contamination safety risk to transfusion patients.
全血(WB)输注在创伤患者治疗中重新受到关注。我们报告称,当从采集到过滤的时间从8小时延长至24小时时,白细胞滤除全血(LCWB)在冷藏21天的体外质量没有显著变化。本研究评估了白细胞滤除前在室温(RT)下延长WB保存时间对与输血相关细菌增殖的影响。
将肺炎克雷伯菌、化脓性链球菌、金黄色葡萄球菌和产单核细胞李斯特菌的悬浮液加入到WB单位中,这些悬浮液用盐溶液(SS)或胰蛋白胨大豆肉汤(TSB)制备,浓度约为0.2 CFU/ml(N = 6)。加样后的单位在白细胞滤除前于室温下保存18 - 24小时,然后冷藏21天。在第2、7、14和21天测定细菌生长情况。评估接种未加样稀释剂的WB的体外质量。
肺炎克雷伯菌和化脓性链球菌在白细胞滤除前在WB中增殖,浓度≤10 CFU/ml。然而,这些细菌在随后的冷藏过程中没有增殖。金黄色葡萄球菌在WB中无法存活,而产单核细胞李斯特菌到第21天达到约10 CFU/ml的浓度。SS或TSB对LCWB的体外质量没有影响。
白细胞滤除前延长WB保存时间会使能够抵抗免疫清除的细菌增殖,尽管它们没有生长到具有临床意义的水平。虽然产单核细胞李斯特菌在LCWB中增殖,但到第21天未达到临床相关浓度。这些数据表明,输注LCWB可能不会给输血患者带来重大的细菌污染安全风险。