Clinical significance of thromboelastometry parameters: 616‐005.1‐08
Тромбоз, гемостаз и реология

Tromboz, Gemostaz I Reologiya
scientific and practical journal

ISSN 2078–1008 (Print); ISSN 2687-1483 (online)

Keywords

thromboelastometry
TEM parameters
EXTEM
INTEM
FIBTEM

Abstract

Summary. Introduction. Thromboelastometry (TEM) enables comprehensive characterization of all stages of blood clot formation, as well as the assessment of its quality and stability. The TEM system performs tests with activators (EXTEM, INTEM, and FIBTEM), which allow for evaluation of various hemostasis components. TEM parameters are used for point‐of‐care (POC) diagnosis of hemostatic disorders. Аim: to characterize the parameters of tests with activators (EXTEM, INTEM, FIBTEM), determine their relationship with coagulation hemostasis and blood cells, and clarify the TEM scope in clinical practice. Materials and Methods. The cross‐sectional study included 48 blood donors. We studied the parameters of the hemogram, concentration of fibrinogen and plasminogen (PLG), antithrombin activity, proteins C (PrC) and S, coagulation factors (F) VII, VIII and XIII, von Willebrand factor antigen (vWF:Ag) and vWF activity (vWF:RCo), activated partial thromboplastin time (aPTT), thrombin time (TT), prothrombin time (PT), and international normalized ratio (INR), as well as TEM parameters (EXTEM, INTEM, FIBTEM). Results. The time of the СТEXTEM was found to correlate with the PT (r=0.388; р=0.0456), FVIII (r=0,463; р=0,0131), vWF:Ag (r=0.475; р=0.0106), and PrС (r=0.404; р=0.0331). The time of the CTINTEM correlated with аPTT (r=0.425; p=0.0271) and with FVIII (r=–0.530; p=0.0037). Structural parameters (A5, A10, A20, and MCF) and trombodynamic potential index (TPI) of all tests depended on fibrinogen, with the greatest correlation observed in A10 FIBTEM (r = 0.780; p < 0.0001). The platelet count was found to be depend on CFT, angle α, and all structural parameters of the EXTEM and INTEM tests. The RBC count did not affect EXTEM, INTEM, and FIBTEM parameters. The MLINTEM parameter exhibited a correlation with the leukocyte level (r=–0.407; p=0.0351). Conclusion. EXTEM, INTEM, and FIBTEM enable the assessment of the activity of factors related to the external and internal coagulation pathways, fibrinogen concentration, platelet functional activity, and fibrinolysis activity. The rapidly obtained results allow using tests with activators for express diagnosis of hemostasis condition.

For citation: Beznoshchenko O.S., Fedorova T.A., Strelnikova E.V., Gorodnova E.A., Pyregov A.V., Silaev B.V. Clinical significance of thromboelastometry parameters. Tromboz, gemostaz i reologiya. 2024;(3):107–177. (In Russ.).

References

  1. Görlinger K., Pérez-Ferrer A., Dirkmann D. et al. The role of evidence-based algorithms for rotational thromboelastometryguided bleeding management. Korean J Anesthesiol. 2019;72(4):297– 322. DOI: 10.4097/kja.19169.
  2. Katz D., Maher P., Getrajdman C. et al. Monitoring of COVID-19-associated coagulopathy and anticoagulation with thromboelastometry. Transfus Med Hemotherapy. 2021;48(3):168–172. DOI: 10.1159/000514486.
  3. Wang I.J., Park S.W., Bae B.K. et al. FIBTEM improves the sensitivity of hyperfibrinolysis detection in severe trauma patients: a retrospective study using thromboelastometry. Sci Rep. 2020;10(1):6980. DOI: 10.1038/s41598-020-63724-y.
  4. Kanji R., Gue Y.X., Memtsas V., Gorog D.A. Fibrinolysis in platelet thrombi. Int J Mol Sci. 2021;22(10):5135. DOI: 10.3390/ijms22105135.
  5. Hartmann M., Lorenz B., Brenner T., Saner F.H. Elevated preand postoperative ROTEMTM clot lysis indices indicate reduced clot retraction and increased mortality in patients undergoing liver transplantation. Biomedicines. 2022;10(8):1975. DOI: 10.3390/biomedicines10081975.
  6. KatoriN., TanakaK.A., SzlamF., LevyJ.H.The effects of platelet count on clot retraction and tissue plasminogen activator-induced fibrinolysis on thrombelastography. Anesth Analg. 2002;100(6):1781–5. DOI:10.1213/01.ANE.0000149902.73689.64.
  7. Jansen E.E., Hartmann M. Clot retraction: cellular mechanisms and Inhibitors, measuring methods, and clinical implications. Biomedicines. 2021;9(8):1064. DOI: 10.3390/biomedicines9081064.
  8. Tarandovskiy I. D., Surov S. S., Parunov L. A. et al. Investigation of thrombin concentration at the time of clot formation in simultaneous thrombin and fibrin generation assays. Sci Rep.2024;141(1):9225. DOI:10.1038/s41598-023-47694-5.
  9. Jokinen S., Kuitunen A., Uotila J., Yli-Hankala A. et al. Thromboelastometry-guided treatment algorithm in postpartum haemorrhage: a randomised, controlled pilot trial. Br J Anaesth. 2023;130(2):165–74. DOI: 10.1016/j.bja.2022.10.031
  10. Shander A., Hardy J.-F., Ozawa S. et at. A global definition of patient blood management. Anesth Analg. 2022;135(3):476–88.DOI: 10.1213/ANE.0000000000005873.
  11. Muñoz M., Stensballe J., Ducloy-Bouthors A.-S. et al. Patient blood management in obstetrics: prevention and treatment of postpartum haemorrhage. A NATA consensus statement. Blood Transfus. 2019;17(2):112–36. DOI: 10.2450/2019.0245-18.
  12. Görlinger K., Almutawah H., Almutawaa F. et al. The role of rotational thromboelastometry during the COVID-19 pandemic: a narrative review. Korean J Anesthesiol. 2021;74(2):91–102. DOI: 10.4097/ kja.21006.
  13. FrigoM.G.,AgostiniV.,BrizziA.etal.Practicalapproachtotransfusion management of post-partum haemorrhage. Transfus Med. 2021;31(1):11–5. DOI: 10.1111/tme.12755.
  14. Sokou R., Piovani D., Konstantinidi A. et al. A risk score for predicting the incidence of hemorrhage in critically ill neonates: development and validation study. Thromb Haemost. 2021;121(2)131– 9. DOI: 10.1055/s-0040-1715832.
  15. Zipperle J., Schmitt F.C.F., Schöchl H. Point-of-care, goal-directed management of bleeding in trauma patients. Curr Opin Crit Care. 2023;29(6):702–12. DOI: 10.1097/MCC.0000000000001107.
  16. Federal Law dated of July 20, 2012 N 125-FZ (as amended on June 28, 2022) “On the donation of blood and its components”. Moscow, 2022. 25 pp. (In Russ.). Available at: https://gcjs.mos.ru/ npa/federalnoe-zakonodatelstvo/ФЗ20125-ФЗот2020.07.2012.pdf. [Accessed: 10.01.2024].
  17. Dolgov V.V., Vavilova T.V., Svirin P.V. Laboratory diagnosis of hemostasis disorders: educational manual. M. —Tver’: OOO «Izdatel’stvo» Triada, 2019. 400 pp. (In Russ.).
  18. Sahin A.S., Ozkan S., Kaya E. Effect of fibrinogen concentrate on the initial fibrinogen level in trauma and postpartum hemorrhage. Eur Rev Med Pharmacol Sci. 2023;27(18):8531–9. DOI: 10.26355/ eurrev_202309_33778.
  19. Skornova I., Simurda T., Stasko J. et al. Use of fibrinogen determination methods in differential diagnosis of hypofibrinogenemia and dysfibrinogenemia. Clin Lab. 2021;67(4):1028–34. DOI: 10.7754/ Clin.Lab.2020.200820.
  20. Blayney A., McCullough J., Wake E. et al. Substitution of ROTEM FIBTEM A5 for A10 in trauma: an observational study building a case for more rapid analysis of coagulopathy. Eur J Trauma Emerg Surg. 2022;48(2):1077–84. DOI: 10.1007/s00068-021-01652-w.
  21. Scott J. P., Niebler R. A., Stuth E. A.E. et al. Rotational thromboelastometry rapidly predicts thrombocytopenia and hypofibrinogenemia during neonatal cardiopulmonary bypass. World J Pediatr Congenit Heart Surg. 2018;9(4):424–33. DOI: 10.1177/2150135118771318.
  22. Peng H.T., Nascimento B., Beckett A. Thromboelastography and thromboelastometry in aassessment of fibrinogen deficiency and prediction for transfusion requirement: a descriptive review. Biomed Res Int. 2018;2018:7020539. DOI: 10.1155/2018/7020539.
  23. Song J.-G., Jeong S.-M., Jun I.-G. et al. Five-minute parameter of thromboelastometry is sufficient to detect thrombocytopenia and hypofibrinogenaemia in patients undergoing liver transplantation. Br J Anaesth. 2014;112(2):290–7. DOI: 10.1093/bja/aet325.
  24. Moore E.E., Moore H.B., Kornblith L.Z. et al. Trauma-induced coagulopathy. Nat Rev Dis Primers. 2021;7(1):30. DOI: 10.1038/ s41572-021-00264-3.
  25. Hincker A., Feit J., Sladen R.N., Wagener G. Rotational thromboelastometry predicts thromboembolic complications after major non-cardiac surgery. Crit Care.2014;18(5):549. DOI: 10.1186/ S13054-014-0549-2.
  26. Parastatidou S., Sokou R., Tsantes A.G. et al. The role of ROTEM variables based on clot elasticity and platelet component in predicting bleeding risk in thrombocytopenic critically ill neonates. Eur J Haematol. 2021;106(2):175–83. DOI: 10.1111/ejh.13534.
  27. Leyra F., Jofre C., Pena N. et al. Prediction of platelet counts with ROTEM-sigma in cardiac surgery. Minerva Anestesiol. 2022;88(7– 8):573–9. DOI: 10.23736/S0375-9393.22.15912-2.
  28. Nguyen T.H., Tran T.T., Hoang T.H.T., Nguyen T.T.T. Rotational thromboelastometry parameters as predicting factors for bleeding in immune thrombocytopenic purpura. Hematol Oncol Stem Cell Ther. 2021;14(1):27–32. DOI: 10.1016/j.hemonc.2020.05.003.
  29. Karlström C., Gryfelt G., Schmied L. et al. Platelet transfusion improves clot formation and platelet function in severely thrombocytopenic haematology patients. Br J Haematol. 2022;196(1):224– 33. DOI: 10.1111/bjh.17820.
  30. Rossetto A., Vulliamy P., Green L., Davenport R. Platelet transfusion better preserves ROTEM clot strength and thrombin generation: a case-control study. ISTH Congress Abstracts, 2022. PB1227. Available at: https://abstracts.isth.org/abstract/platelet-transfusion-better-preserves-rotem-clot-strength-and-thrombin-generation-a-case-control-study/. [Accessed: 10.01.2024].
  31. Longstaff C. Measuring fibrinolysis: from research to routine diagnostic assays. J Thromb Haemost. 2018;16(4):652–62. DOI: 10.1111/ jth.13957.
  32. Görlinger K., Pérez-Ferrer A., Dirkmann D. et al. The role of evidence-based algorithms for rotational thromboelastometryguided bleeding management. Korean J Anesthesiol. 2019;72(4):297– 322. DOI: 10.4097/kja.19169.
  33. Katz D., Maher P., Getrajdman C. et al. Monitoring of COVID-19-associated coagulopathy and anticoagulation with thromboelastometry. Transfus Med Hemotherapy. 2021;48(3):168–172. DOI: 10.1159/000514486.
  34. Wang I.J., Park S.W., Bae B.K. et al. FIBTEM improves the sensitivity of hyperfibrinolysis detection in severe trauma patients: a retrospective study using thromboelastometry. Sci Rep. 2020;10(1):6980. DOI: 10.1038/s41598-020-63724-y.
  35. Kanji R., Gue Y.X., Memtsas V., Gorog D.A. Fibrinolysis in platelet thrombi. Int J Mol Sci. 2021;22(10):5135. DOI: 10.3390/ijms22105135.
  36. Hartmann M., Lorenz B., Brenner T., Saner F.H. Elevated preand postoperative ROTEMTM clot lysis indices indicate reduced clot retraction and increased mortality in patients undergoing liver transplantation. Biomedicines. 2022;10(8):1975. DOI: 10.3390/biomedicines10081975.
  37. KatoriN., TanakaK.A., SzlamF., LevyJ.H.The effects of platelet count on clot retraction and tissue plasminogen activator-induced fibrinolysis on thrombelastography. Anesth Analg. 2002;100(6):1781–5. DOI:10.1213/01.ANE.0000149902.73689.64.
  38. Jansen E.E., Hartmann M. Clot retraction: cellular mechanisms and Inhibitors, measuring methods, and clinical implications. Biomedicines. 2021;9(8):1064. DOI: 10.3390/biomedicines9081064.
  39. Tarandovskiy I. D., Surov S. S., Parunov L. A. et al. Investigation of thrombin concentration at the time of clot formation in simultaneous thrombin and fibrin generation assays. Sci Rep.2024;141(1):9225. DOI:10.1038/s41598-023-47694-5.
  40. Jokinen S., Kuitunen A., Uotila J., Yli-Hankala A. et al. Thromboelastometry-guided treatment algorithm in postpartum haemorrhage: a randomised, controlled pilot trial. Br J Anaesth. 2023;130(2):165–74. DOI: 10.1016/j.bja.2022.10.031
  41. Shander A., Hardy J.-F., Ozawa S. et at. A global definition of patient blood management. Anesth Analg. 2022;135(3):476–88.DOI: 10.1213/ANE.0000000000005873.
  42. Muñoz M., Stensballe J., Ducloy-Bouthors A.-S. et al. Patient blood management in obstetrics: prevention and treatment of postpartum haemorrhage. A NATA consensus statement. Blood Transfus. 2019;17(2):112–36. DOI: 10.2450/2019.0245-18.