HemostaticIn VitroProperties of Novel Plasma Supernatants Produced from Late-storage Low-titer Type O Whole Blood

Author:

Mihalko Emily P.1ORCID,Srinivasan Amudan J.2,Rahn Katelin C.3,Seheult Jansen N.4,Spinella Philip C.5,Cap Andrew P.6,Triulzi Darrell J.7,Yazer Mark H.8,Neal Matthew D.9,Shea Susan M.10ORCID

Affiliation:

1. 1Trauma and Transfusion Medicine Research Center, Department of Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania.

2. 2Trauma and Transfusion Medicine Research Center, Department of Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania.

3. 3Trauma and Transfusion Medicine Research Center, Department of Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania.

4. 4Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.

5. 5Trauma and Transfusion Medicine Research Center, Department of Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania; Department of Critical Care, University of Pittsburgh, Pittsburgh, Pennsylvania.

6. 6United States Army Institute of Surgical Research, JBSA-Fort Sam Houston, Texas.

7. 7Department of Pathology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.

8. 8Department of Pathology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.

9. 9Trauma and Transfusion Medicine Research Center, Department of Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania; Department of Critical Care, University of Pittsburgh, Pittsburgh, Pennsylvania.

10. 10Trauma and Transfusion Medicine Research Center, Department of Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania.

Abstract

BackgroundThe use of low-titer group O whole blood is increasing. To reduce wastage, unused units can be converted to packed red blood cells. Supernatant is currently discarded post-conversion; however, it could be a valuable transfusable product. The aim of this study was to evaluate supernatant prepared from late-storage low-titer group O whole blood being converted to red blood cells, hypothesizing it will have higher hemostatic activity compared to fresh never-frozen liquid plasma.MethodsLow-titer group O whole blood supernatant (n = 12) prepared on storage day 15 was tested on days 15, 21, and 26 and liquid plasma (n = 12) on 3, 15, 21, and 26. Same-day assays included cell counts, rotational thromboelastometry, and thrombin generation. Centrifuged plasma from units was banked for microparticle characterization, conventional coagulation, clot structure, hemoglobin, and additional thrombin generation assays.ResultsLow-titer group O whole blood supernatant contained more residual platelets and microparticles compared to liquid plasma. At day 15, low-titer group O whole blood supernatant elicited a faster intrinsic clotting time compared to liquid plasma (257 ± 41 vs. 299 ± 36 s, P = 0.044), and increased clot firmness (49 ± 9 vs. 28 ± 5 mm, P < 0.0001). Low-titer group O whole blood supernatant showed more significant thrombin generation compared to liquid plasma (day 15 endogenous thrombin potential 1,071 ± 315 vs. 285 ± 221 nM·min, P < 0.0001). Flow cytometry demonstrated low-titer group O whole blood supernatant contained significantly more phosphatidylserine and CD41+ microparticles. However, thrombin generation in isolated plasma suggested residual platelets in low-titer group O whole blood supernatant were a greater contributor than microparticles. Additionally, low-titer group O whole blood supernatant and liquid plasma showed no difference in clot structure, despite higher CD61+ microparticle presence.ConclusionsPlasma supernatant produced from late-storage low-titer group O whole blood shows comparable, if not enhanced, in vitro hemostatic efficacy to liquid plasma.Editor’s PerspectiveWhat We Already Know about This TopicWhat This Article Tells Us That Is New

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Anesthesiology and Pain Medicine

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