Abstract
BackgroundFibrinogen and prothrombin have been suggested to become rate limiting in trauma associated coagulopathy. Administration of fibrinogen is now recommended, however, the importance of prothrombin to patient outcome is unknown.MethodsWe have utilized two trauma patient databases (database 1 n = 358 and database 2 n = 331) to investigate the relationship of plasma prothrombin concentration on clinical outcome and coagulation status. Database 1 has been used to assess the relationship of plasma prothrombin to administered packed red blood cells (PRBC), clinical outcome and coagulation biomarkers (Prothrombin Time (PT), ROTEM EXTEM Coagulation Time (CT) and Maximum Clot Firmness (MCF)). ROC analyses have been performed to investigate the ability of admission coagulation biomarkers to predict low prothrombin concentration (database 1), massive transfusion and 24 h mortality (database 1 and 2). The importance of prothrombin was further investigated in vitro by PT and ROTEM assays in the presence of a prothrombin neutralizing monoclonal antibody and following step-wise dilution.ResultsPatients who survived the first 24 h had higher admission prothrombin levels compared to those who died (94 vs.67 IU/dL). Patients with lower transfusion requirements within the first 24 h (≤10 units of PRBCs) also had higher admission prothrombin levels compared to patients with massive transfusion demands (>10 units of PRBCs) (95 vs.62 IU/dL). Admission PT, in comparison to admission ROTEM EXTEM CT and MCF, was found to be a better predictor of prothrombin concentration <60 IU/dL (AUC 0.94 in database 1), of massive transfusion (AUC 0.92 and 0.81 in database 1 and 2 respectively) and 24 h mortality (AUC 0.90 and 0.78 in database 1 and 2, respectively). In vitro experiments supported a critical role for prothrombin in coagulation and demonstrated that PT and ROTEM EXTEM CT are sensitive methods to measure low prothrombin concentration.DiscussionOur analyses suggest that prothrombin concentration at admission is predictive of mortality and transfusion and indicates that prothrombin and fibrinogen are rate limiting in coagulopathy.ConclusionsAdmission PT is predictive of low prothrombin concentration and clinical outcome. PT could therefore be used as a surrogate for prothrombin concentration and further evaluation of point-of-care devices for faster PT analysis is warranted.
Highlights
Fibrinogen and prothrombin have been suggested to become rate limiting in trauma associated coagulopathy
Admission Prothrombin time (PT) is predictive of low prothrombin concentration and clinical outcome
Association of prothrombin concentration with mortality and transfusion demand in patients Data including survival, administered packed red blood cells (PRBC) and admission PT, EXTEM Coagulation time (CT) and Maximum clot firmness (MCF) were available from 358 patients from London and 331 patients from Innsbruck (Table 1)
Summary
Fibrinogen and prothrombin have been suggested to become rate limiting in trauma associated coagulopathy. Administration of fibrinogen is recommended, the importance of prothrombin to patient outcome is unknown. Fibrinogen and prothrombin have been suggested to be the first coagulation factors to become rate limiting for coagulation in such situations [6]. While the administration of fibrinogen is recommended to restore fibrinogen levels [7,8,9], the importance of prothrombin in trauma-induced coagulopathy and patient outcome is unclear. Administration of prothrombin-containing concentrates may be useful in trauma patients with coagulopathy. Measurement of prothrombin concentration is necessary to identify patients with low levels and address the concern that over supplementation could lead to increased thrombotic risk [12,13,14].
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More From: Scandinavian Journal of Trauma, Resuscitation and Emergency Medicine
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