Functional characteristics and clinical effectiveness of platelet concentrates treated with riboflavin and ultraviolet light in plasma and in platelet additive solution
Background and ObjectivesPathogen reduction technologies may affect platelet quality during storage. We studied functional characteristics and clinical effectiveness of platelet concentrates (PCs) treated with Mirasol in plasma and in platelet-additive solution SSP+. Materials and MethodsMirasol-treated, gamma-irradiated and untreated apheresis PCs were examined on days 0, 1, 3 and 5 of storage. Phosphatidylserine, P-selectin and active glycoprotein IIb/IIIa were analysed using flow cytometry before and after platelet stimulation. Platelet count increments, the numbers of inefficient transfusions and post-transfusion reactions were analysed to estimate clinical effectiveness. ResultsA significant increase in all platelet activation markers occurred during storage in all PC groups. Activation markers in Mirasol-treated samples were already significantly higher compared with the control ones on the day of harvesting, and continued to grow during the storage. Mirasol treatment increased the number of platelets with a mitochondrial membrane potential loss. On the 3rd day of storage, 50% of Mirasol-treated platelets did not respond to activation; on the 5th day, none did. This agreed well with a decrease (approximately twofold) in the effectiveness of Mirasol-treated PC transfusions. Transfusions of PCs stored in SSP+ were accompanied by fewer inefficient transfusions and post-transfusion reactions than of PCs stored in plasma. ConclusionTreatment with Mirasol decreased platelet function, particularly profoundly on the 5th day of storage, and led to a decrease in the effectiveness of transfusions. SSP+ did not affect laboratory parameters significantly compared with plasma, but decreased the percentage of transfusion complications.
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Univ British Columbia, Canadian Blood Serv, Vancouver, BC V5Z 1M9, Canada
Univ British Columbia, Ctr Blood Res, Vancouver, BC V5Z 1M9, CanadaUniv British Columbia, Canadian Blood Serv, Vancouver, BC V5Z 1M9, Canada
Chen, Zhongming
Schubert, Peter
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Univ British Columbia, Canadian Blood Serv, Vancouver, BC V5Z 1M9, Canada
Univ British Columbia, Ctr Blood Res, Vancouver, BC V5Z 1M9, Canada
Univ British Columbia, Dept Pathol & Lab Med, Vancouver, BC V5Z 1M9, CanadaUniv British Columbia, Canadian Blood Serv, Vancouver, BC V5Z 1M9, Canada
Schubert, Peter
Culibrk, Brankica
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Univ British Columbia, Canadian Blood Serv, Vancouver, BC V5Z 1M9, Canada
Univ British Columbia, Ctr Blood Res, Vancouver, BC V5Z 1M9, CanadaUniv British Columbia, Canadian Blood Serv, Vancouver, BC V5Z 1M9, Canada
Culibrk, Brankica
Devine, Dana V.
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Univ British Columbia, Canadian Blood Serv, Vancouver, BC V5Z 1M9, Canada
Univ British Columbia, Ctr Blood Res, Vancouver, BC V5Z 1M9, Canada
Univ British Columbia, Dept Pathol & Lab Med, Vancouver, BC V5Z 1M9, CanadaUniv British Columbia, Canadian Blood Serv, Vancouver, BC V5Z 1M9, Canada
机构:Univ British Columbia, Canadian Blood Serv, UBC Ctr Blood Res, Vancouver, BC V6T 1Z3, Canada
Schubert, Peter
Culibrk, Brankica
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机构:Univ British Columbia, Canadian Blood Serv, UBC Ctr Blood Res, Vancouver, BC V6T 1Z3, Canada
Culibrk, Brankica
Coupland, Danielle
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机构:Univ British Columbia, Canadian Blood Serv, UBC Ctr Blood Res, Vancouver, BC V6T 1Z3, Canada
Coupland, Danielle
Scammell, Ken
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机构:Univ British Columbia, Canadian Blood Serv, UBC Ctr Blood Res, Vancouver, BC V6T 1Z3, Canada
Scammell, Ken
Gyongyossy-Issa, Maria
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机构:Univ British Columbia, Canadian Blood Serv, UBC Ctr Blood Res, Vancouver, BC V6T 1Z3, Canada
Gyongyossy-Issa, Maria
Devine, Dana V.
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Univ British Columbia, Canadian Blood Serv, UBC Ctr Blood Res, Vancouver, BC V6T 1Z3, CanadaUniv British Columbia, Canadian Blood Serv, UBC Ctr Blood Res, Vancouver, BC V6T 1Z3, Canada