Volume 58, Issue 10 pp. 2407-2413
BLOOD COMPONENTS

In vivo viability of extended 4°C-stored autologous apheresis platelets

Moritz Stolla

Corresponding Author

Moritz Stolla

Platelet Transfusion Research Laboratory, Bloodworks Northwest Research Institute, Seattle, Washington

Department of Medicine, Division of Hematology, University of Washington School of Medicine, Seattle, Washington

Address reprint requests to: Moritz Stolla, MD, Bloodworks Northwest, 921 Terry Avenue, Room 408, Seattle, WA 98104; e-mail: [email protected].Search for more papers by this author
Lynda Fitzpatrick

Lynda Fitzpatrick

Platelet Transfusion Research Laboratory, Bloodworks Northwest Research Institute, Seattle, Washington

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Irena Gettinger

Irena Gettinger

Platelet Transfusion Research Laboratory, Bloodworks Northwest Research Institute, Seattle, Washington

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Shawn L. Bailey

Shawn L. Bailey

Platelet Transfusion Research Laboratory, Bloodworks Northwest Research Institute, Seattle, Washington

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Esther Pellham

Esther Pellham

Platelet Transfusion Research Laboratory, Bloodworks Northwest Research Institute, Seattle, Washington

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Todd Christoffel

Todd Christoffel

Platelet Transfusion Research Laboratory, Bloodworks Northwest Research Institute, Seattle, Washington

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Sherrill J. Slichter

Sherrill J. Slichter

Platelet Transfusion Research Laboratory, Bloodworks Northwest Research Institute, Seattle, Washington

Department of Medicine, Division of Hematology, University of Washington School of Medicine, Seattle, Washington

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First published: 10 September 2018
Citations: 34
This work was supported by Department of Defense Award W81XWH-12-1-0441.

Abstract

BACKGROUND

The current 5-day storage time of room temperature (22°C)-stored platelets (RSPs) severely limits platelet (PLT) availability. Extended cold (4°C)-stored PLTs (CSPs) are currently being investigated for actively bleeding patients. However, we currently do not know how to best store PLTs in the cold for extended periods of time. In this study, we investigate how storage in plasma and PLT additive solutions (PASs) affects PLT viability in vivo.

STUDY DESIGN AND METHODS

Twenty normal subjects had a 2-unit hyperconcentrated apheresis PLT collection. One unit was stored at 4°C in plasma for 3 days (“control unit”), and the CSP “test” unit was stored for 10 or 15 days in plasma or 10 days in 35% plasma with either 65% Intersol or Isoplate. After storage, all units were radiolabeled and transfused into their donors.

RESULTS

For 10-day storage, both the plasma and the Intersol units had significantly better PLT recoveries than the Isoplate units (24% ± 8% vs. 11% ± 3% [55% ± 11% vs. 21% ± 8% as percentage of control data], p = 0.002; and 18% ± 4% vs. 11% ± 3% [43% ± 6% vs. 21% ± 8% as percentage of control data], p = 0.004, respectively). There was a trend for lower PLT recoveries with Intersol compared to plasma (p = 0.056). PLT survivals and most in vitro measurements did not differ significantly among the units.

CONCLUSIONS

While the in vitro variables suggest largely comparable results between plasma and PASs, in vivo recoveries were higher with plasma compared with both Intersol and Isoplate (p = 0.057 and p = 0.002, respectively). Whether this difference leads to clinically relevant differences in hemostatic efficacy remains to be determined.

CONFLICT OF INTEREST

The authors have disclosed no conflicts of interest.

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