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Gerinnungsmanagement beim Polytrauma

Management of coagulation after multiple trauma

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Zusammenfassung

Große Blutverluste bei schweren Verletzungen verursachen durch den Verlust an Gerinnungsfaktoren und Thrombozyten eine Gerinnungsstörung. Verdünnung von Gerinnungsfaktoren durch Kristalloide und Kolloide, gesteigertes fibrinolytisches Potenzial, Hypothermie, metabolische Veränderungen und Anämie beeinträchtigen ebenfalls das Hämostasegleichgewicht. Für die Therapie ist ein engmaschiges Monitoring des aktuellen Gerinnungsstatus unerlässlich. „Point-of-care-taugliche“ Geräte können Zeitintervalle bis zum Vorliegen des aktuellen Gerinnungsstatus verkürzen. Therapiert wird v. a. mit Frischplasmen (FFP), Thrombozytenkonzentraten und Antifibrinolytika. Gerinnungsfaktorenkonzentrate sind indiziert, wenn ein Faktorenmangel isoliert besteht, FFP nicht zur Verfügung stehen oder die Gerinnungsstörung bereits so ausgeprägt ist, dass mit Transfusion von FFP allein keine Besserung eintritt. Der rekombinate Faktor VIIa (NovoSeven®) wurde bereits bei vielen schweren Blutungen, die konventionell nicht sanierbar waren, eingesetzt. Die Ergebnisse großer klinischer Studien sind jedoch noch ausständig.

Abstract

Hemorrhage after traumatic injury results in coagulopathy which only worsens the situation. This coagulopathy is caused by depletion and dilution of clotting factors and platelets, increased fibrinolytic activity, hypothermia, metabolic changes and anemia. The effect of synthetic colloids used for compensating the blood loss, further aggravates the situation through their specific action on the hemostatic system. Bedside coagulation monitoring permits relevant impairment of the coagulation system to be detected very early and the efficacy of the hemostatic therapy to be controlled directly. Administration of fresh frozen plasma (FFP), platelet concentrates and antifibrinolytic agents is essential for restoring the impaired coagulation system in trauma patients. Clotting factor concentrates should be administered if coagulopathy is based on diagnosed depletion of clotting factors, if FFP is not available and if transfusion of FFP is insufficient to treat the coagulopathy. Recombined FVIIa is frequently employed during severe bleeding which could not be treated by conventional methods but the results of on-going clinical trials are not yet available.

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Literatur

  1. American Society of Anesthesiologists Task Force on Blood Component Therapy (1996) Practical guidelines for blood component therapy. Anesthesiology 84:732–747

    PubMed  Google Scholar 

  2. Bernabei A, Levison M, Bender J (1992) The effects of hypothermia and injury severity on blood loss during trauma laparotomy. J Trauma 33:835–839

    CAS  PubMed  Google Scholar 

  3. Calatzis A, Haas S, Gödje O et al. (2000) Thrombelastographic coagulation monitoring during cardiovascular surgery with the ROTEG Coagulation Analyzer. In: Pifarre R (ed) Management of bleeding in cardiovascular surgery. Hanley & Belfus, Philadelphia, pp 215–226

  4. Chowdhury P, Saayman AG, Paulus U, Findlay GP, Collins PW (2004) Efficacy of standard dose and 30 ml/kg fresh frozen plasma in correcting laboratory parameters of haemostasis in critically ill patients. Br J Haematol 125:69–73

    PubMed  Google Scholar 

  5. Cochraine Injuries Group Albumin Reviewers (1998) Human albumin administration in critically ill patients. Systemic review of randomised controlled trials. BMJ 317:235–240

    PubMed  Google Scholar 

  6. Cosgrif N, Moore EE, Sauaia A et al. (1997) Predicting life-threatening coagulopathy in the massively transfused trauma patient: hypothermia and acidosis revisited. J Trauma 42:857–862

    PubMed  Google Scholar 

  7. Despotis GJ, Santoro SA, Spitznagel E et al. (1994) Prospective evaluation and clinical utility of on-site monitoring of coagulation in patients undergoing cardiac operations. J Thorac Cardiovasc Surg 107:271–279

    CAS  PubMed  Google Scholar 

  8. Dunn CJ, Goa KL (1999) Tranexamic acid, a review of its use in surgery and other indications. Drugs 57:1005–1032

    CAS  PubMed  Google Scholar 

  9. Enderson BL, Chen JP, Robinson R, Maul KI (1991) Fibrinolysis in multisystem trauma patients. J Trauma 31:1240–1246

    CAS  PubMed  Google Scholar 

  10. Engelman DT, Gabram SG, Allen L, Ens GE, Jacobs LM (1996) Hypercoagulability following multiple trauma. World J Surg 20:5–10

    Article  CAS  PubMed  Google Scholar 

  11. Entholzner EK, Mielke LL, Calatzis AN et al. (2000) Coagulation effects of a recently developed hydroxyethyl starch (HES 130/0.4) compared to hydroxyethyl starches with higher molecular weight. Acta Anaesthesiol Scand 44:1116–1121

    Article  CAS  PubMed  Google Scholar 

  12. Favaloro EJ (2001) Appropriate laboratory assessment as a critical facet in the proper diagnosis and classification of von Willebrand disorder. Best Pract Res Clin Haematol 14:299–319

    Article  CAS  PubMed  Google Scholar 

  13. Fries D, Krismer A, Schobersberger A et al. (2003) The effect of fibrinogen on dilutional coagulopathy—a porcine model. Intensive Care Med 29 [Suppl 1]:527

  14. Gando S, Tedo I, Kubota M (1992) Post-traumatic coagulation and fibrinolysis. Crit Care Med 20:594–600

    CAS  PubMed  Google Scholar 

  15. Gentilello LM, Pierson DJ (2001) Trauma critical care. Am J Respir Crit Care Med 163:604–607

    CAS  PubMed  Google Scholar 

  16. Gibbs NM, Weightman WM, Thackray NM et al. (2001) The effects of recent aspirin ingestion on platelet function in cardiac surgical patients. J Cardiothorac Vasc Anesth 15:55–59

    Article  CAS  PubMed  Google Scholar 

  17. Haisch G, Boldt J, Krebs C et al. (2001) The influence of intravascular therapy with a new hydroxyethyl starch preparation (6% HES 130/0.4) on coagulation in patients undergoing major abdominal surgery. Anesth Analg 92:565–571

    CAS  PubMed  Google Scholar 

  18. Henry DA, Moxey AJ, Carless PA et al. (2001) Anti-fibrinolytic use for minimising allogenic blood transfusion. Cochrane Database Syst Rev 1:CD0011866

    Google Scholar 

  19. Hippala S (1998) Replacement of massive blood loss. Vox Sang 74 [Suppl 2]:399–407

  20. Innerhofer P, Fries D, Margreiter J et al. (2002) The effect of perioperatively administered colloids and crystalloids on primary hemostasis and clot formation. Anesth Analg 95:858–865

    Article  PubMed  Google Scholar 

  21. Johnston T, Chen Y, Reed R (1994) Functional equivalence of hypothermia to specific clotting factor deficiencies. J Trauma 37:413–417

    CAS  PubMed  Google Scholar 

  22. Jonge E de, Levi M (2001) Effects of different plasma substitutes on blood coagulation. Crit Care Med 29:1261–1267

    Article  PubMed  Google Scholar 

  23. Köhler M, Hellstern P, Lechler E, Überfuhr P, Müller-Berghaus G (1998) Thromboembolic complications associated with the use of prothrombin complex and factor IX concentrates. Thromb Haemost 80:399–402

    PubMed  Google Scholar 

  24. Lundberg GD, Task Force of the College of American Pathologists (1994) Practice parameters for the use of fresh frozen plasma, cryoprecipitate, and platelets. JAMA 271:777–781

    PubMed  Google Scholar 

  25. Mardel SN, Saunders FM, Allen H et al. (1998) Reduced quality of clot formation with gelatin-based plasma substitutes. Br J Anaesth 80:204–207

    CAS  PubMed  Google Scholar 

  26. Martinowitz U, Kenet G, Segal E et al. (2001) Recombinant activated factor VII for adjunctive hemorrhage control in trauma. J Trauma 51:431–439

    CAS  PubMed  Google Scholar 

  27. McLeod J, Lynn M, McKenney M, Cohn S, Murtha M (2003) Early coagulopathy predicts mortality in trauma. J Trauma 55:39–44

    PubMed  Google Scholar 

  28. Menache D (1981) Prothrombin complex concentrates: clinical use. Ann N Y Acad Sci 370:747–756

    CAS  PubMed  Google Scholar 

  29. Nuttall GA, Oliver WC, Beynen FM et al. (1993) Intraoperative measurement of activated partial thromboplastin time and prothrombin time by a portable laser photometer in patients following cardiopulmonary bypass. J Cardiothorac Vasc Anesth 7:402–409

    Article  CAS  PubMed  Google Scholar 

  30. Sauaia A, Moore FA, Moore EE et al. (1995) Epidemiology of trauma deaths: reassessment. J Trauma 38:185–193

    CAS  PubMed  Google Scholar 

  31. Schierhout G, Roberts I (1998) Fluid resuscitation with colloid or crystalloid solution in critically ill patients: a systemic review of randomized trials. BMJ 316:961–964

    CAS  PubMed  Google Scholar 

  32. Singbartl K, Innerhofer P, Radvan J et al. (2003) Hemostasis and hemodilution: a quantitative mathematical guide for clinical practice. Anesth Analg 96:929–935

    Article  PubMed  Google Scholar 

  33. Staudinger T, Frass M, Rintelen C et al. (1999) Influence of prothrombin complex concentrates on plasma coagulation in critically ill patients. Intensive Care Med 25:1105–1110

    Article  CAS  PubMed  Google Scholar 

  34. Valeri C, Cassidy G, Kuhri S, Hollace F, Ragino G, Altschule M (1986) Hypothermia induced platelet dysfunction. Ann Surg 205:175–181

    Google Scholar 

  35. Vorstand und wissenschaftlicher Beirat der Bundesärztekammer (2001) Leitlinien zur Therapie mit Blutkomponenten und Plasmaderivaten. Deutscher Arzteverlag, Köln

  36. White B, McHale J, Ravi N et al. (1999) Successful use of recombinant FVIIa [NovoSeven] in the management of intractable post-surgical intra-abdominal hemorrhage. Br J Haematol 107:677–678

    Article  CAS  PubMed  Google Scholar 

  37. Wolberg A, Meng ZH, Monroe DM, Hoffman M (2004) A systemic evaluation of the effect of temperature on coagulation enzyme activity and platelet function. J Trauma 56:1221–1228

    CAS  PubMed  Google Scholar 

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Correspondence to D. Fries.

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Internetlinks und Kontaktadressen

Arbeitsgruppe für perioperative Gerinnungstherapie der Österreichischen Gesellschaft für Anaesthesiologie, Reanimation und Intensivmedizin (ÖGARI)

  • Ansprechpartner:

  • Univ. Doz. Dr. Thomas Pernerstorfer

  • Wels, Österreich

  • e-mail: thomas.pernerstorfer@univie.at

  • Network of Advancement of Transfusion Alternatives (NATA).

  • Homepage: http://www.nataonline.org

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Fries, D., Haas, T., Salchner, V. et al. Gerinnungsmanagement beim Polytrauma. Anaesthesist 54, 137–144 (2005). https://doi.org/10.1007/s00101-004-0760-7

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  • DOI: https://doi.org/10.1007/s00101-004-0760-7

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