Comparison of haemostatic function of PAS-C-platelets vs. plasma-platelets in reconstituted whole blood using impedance aggregometry and thromboelastography

Vox Sang. 2017 Aug;112(6):549-556. doi: 10.1111/vox.12534. Epub 2017 Jun 9.

Abstract

Background and objectives: There are concerns about the haemostatic function of platelets stored in platelet additive solution (PAS). Aim of this study was to compare the haemostatic function of PAS-C-platelets to plasma-platelets in reconstituted whole blood.

Materials and methods: In our experiment, whole blood was reconstituted with red blood cells, solvent-detergent (SD) plasma and either PAS-C-platelets or plasma-platelets (n = 7) in a physiological ratio. On storage days 2, 5, 8 and 13, the agonist-induced aggregation (multiple electrode aggregometry), clot formation (thromboelastography) and agonist-induced CD62P responsiveness (flow cytometry) were measured.

Results: Samples with PAS-C-platelets showed significantly lower aggregation than plasma-platelets when induced with adenosine diphosphate, -6 U (95% confidence interval: -8; -4) or thrombin receptor-activating protein, -15 U (-19; -10). Also when activated with collagen and ristocetin, the PAS-C-platelets showed less aggregation, although not statistically significant. All samples with PAS-C-platelets showed significantly lower agonist-induced CD62P responsiveness than samples with plasma-platelets. However, there was no difference regarding all TEG parameters.

Conclusion: Our findings demonstrate that the function - aggregation and CD62P responsiveness - of PAS-C-platelets in reconstituted whole blood is inferior to that of plasma-platelets, which may have implications in the setting of massive transfusions.

Keywords: CD62P expression; haemostatic function; multiple electrode aggregometry; platelet additive solution; thromboelastography.

Publication types

  • Comparative Study

MeSH terms

  • Adenosine Diphosphate / pharmacology
  • Blood Platelets / drug effects
  • Blood Platelets / physiology*
  • Blood Preservation*
  • Collagen / pharmacology
  • Electric Impedance
  • Erythrocytes
  • Hemostasis / physiology*
  • Humans
  • P-Selectin / pharmacology
  • Platelet Aggregation / drug effects
  • Platelet Aggregation / physiology
  • Platelet Function Tests
  • Ristocetin / pharmacology
  • Thrombelastography

Substances

  • P-Selectin
  • SELP protein, human
  • Ristocetin
  • Adenosine Diphosphate
  • Collagen