4.0 Article

Retention of Coagulation Factors and Storage of Freeze-Dried Plasma

Journal

MILITARY MEDICINE
Volume 186, Issue -, Pages 400-407

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/milmed/usaa347

Keywords

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Funding

  1. U.S. government [H92222-16-C-0081]

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The study demonstrated that Terumo BCT's TFDP has no negative impact on coagulation factor activity, remains stable for up to 24 months at room and refrigerated temperatures, and has coagulation factor activity comparable to PF24/FFP, with residual moisture content below 2%.
Introduction: Terumo BCT is developing a system to produce a freeze-dried plasma product, Terumo's freeze-dried plasma (TFDP), that is stored in a rugged, light-weight plastic package suitable for field use, which retains a stable level of specific coagulation factors and proteins within clinical range, when stored for up to 2 years at room temperature and 4 degrees C. Materials and Methods: Plasma frozen within 24 hours of phlebotomy (PF24) were thawed, sampled, and individually lyophilized to produce a corresponding TFDP unit. Fresh frozen plasma (FFP) units were thawed, sampled, pooled in groups of 10 units (also sampled) and lyophilized to produce 2 lots of TFDP. Each TFDP unit was reconstituted with water for injection (WFI) and tested for pH, prothrombin time, activated partial thromboplastin time, factors V and VIII, fibrinogen, protein C, and protein S. Results were compared with PF24/FFP. Additional FFP units were thawed, sampled, pooled, divided to generate 2 TFDP units for each time point (1, 2, 3, 6, 12, 18, and 24 months, one each stored at 4 degrees C and 25 degrees C) and lyophilized. Postlyophilization, TFDP units were stored at 4 degrees C or 25 degrees C, reconstituted with WFI, and tested for the factors listed above. Residual moisture content of the lyophilized plasma was also tested. Results: Coagulation factor activity of TFDP was +/- 20% of PF24/FFP. Pooling standardized variation in TFDP coagulation factor activities, which were within clinical ranges postlyophilization. The pH of TFDP and PF24/FFP were within required range. Residual moisture content of TFDP was <2%. Conclusions: The TFDP process had no negative impact on coagulation factor activity. Input plasma and anticoagulant type did not affect TFDP quality. Pooling FFP normalized factor variability in TFDP and did not negatively impact product quality. The TFDP is stable for up to 24 months at room and refrigerated temperatures. Terumo's freeze-dried plasma is comparable to PF24/FFP. It does not require complex logistics or time-consuming thawing. Terumo's freeze-dried plasma may be suitable for rapid treatment of coagulopathies with logistical advantages over PF24/FFP.

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