Platelet dysfunction reversal with cold-stored vs room temperature–stored platelet transfusions

Author:

Kogler Valery J.12ORCID,Miles Jeffrey A.13,Özpolat Tahsin14ORCID,Bailey S. Lawrence1,Byrne Daire A.1,Bawcom-Randall Morgan1,Wang Yi1,Larsen Hannah J.1,Reed Franklin1,Fu Xiaoyun15,Stolla Moritz156ORCID

Affiliation:

1. 1Bloodworks Northwest Research Institute, Seattle, WA

2. 2Department of Pathology and Laboratory Medicine, University of Virginia School of Medicine, Charlottesville, VA

3. 3Philadelphia College of Osteopathic Medicine, Philadelphia, PA

4. 4Department of Medicine, Division of Nephrology, University of Arizona, School of Medicine, Tucson, AZ

5. 5Division of Hematology and Oncology, Department of Medicine, University of Washington School of Medicine, Seattle, WA

6. 6Department of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, WA

Abstract

Abstract Platelets are stored at room temperature for 5 to 7 days (room temperature–stored platelets [RSPs]). Because of frequent and severe shortages, the US Food and Drug Administration recently approved up to 14-day cold-stored platelets (CSPs) in plasma. However, the posttransfusion function of CSPs is unknown and it is unclear which donors are best suited to provide either RSPs or CSPs. In this study, we sought to evaluate the posttransfusion platelet function and its predictors for platelets stored for the maximum approved storage times (7-day RSPs and 14-day CSPs) in healthy volunteers on acetylsalicylic acid (ASA). We conducted a randomized crossover study in 10 healthy humans. Individuals donated 1 platelet unit, stored at either 22°C or 4°C based on randomization. Before transfusion, participants ingested ASA to inhibit endogenous platelets. Transfusion recipients were tested for platelet function and lipid mediators. Platelet units were tested for lipid mediators only. A second round of transfusion with the alternative product was followed by an identical testing sequence. RSPs reversed platelet inhibition significantly better in αIIbβ3 integrin activation–dependent assays. In contrast, CSPs in recipients led to significantly more thrombin generation, which was independent of platelet microparticles. Lysophosphatidylcholine-O species levels predicted the procoagulant capacity of CSPs. In contrast, polyunsaturated fatty acid concentrations predicted the aggregation response of RSPs. In summary, we provide, to our knowledge, the first efficacy data of extended-stored CSPs in plasma. Our results suggest that identifying ideal RSP and CSP donors is possible, and pave the way for larger studies in the future. This trial is registered at www.ClinicalTrials.gov as #NCT0511102.

Publisher

American Society of Hematology

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