OVERALL: Uncontrolled hemorrhage is the major cause of death in adults exposed to severe trauma. Trauma-induced coagulopathy (TIC) occurs after injury and shock, accompanied by a ?storm? of inflammatory and coagulation events leading to incapacitation of the hemostatic process. TIC compromises the hemostatic system because of dysregulated processes occurring on a systemic basis in which proteolytic systems destroy essential coagulation components. Previous studies have identified activated protein C-mediated destruction of the cofactor factor Va and implicated systemic fibrinolytic activity in which unregulated proteolysis destroys fibrinogen and parts of the plasma coagulation system. These terminal events observed in phlebotomy blood of TIC patients are caused by in vivo processes involving the proteins, cells and cytokines in blood and vascular tissues and tissue damage material entering the blood. The causes and breadth of TIC are not understood. This TACTIC project provides a comprehensive evaluation of the contributions of plasma proteins, blood cells, the vascular endothelium, the blood vessel, and extravascular tissue to TIC, making use of a unique infrastructure that includes already-funded DoD sites involved in trauma trials and Systems Biology. A comprehensive team approach by leading investigators in coagulation and inflammation research addresses the problem using a composite of in vitro and in vivo approaches to identify candidates responsible for TlC. Early translation of laboratory results into useful technology will be enabled by a set of 5 TACTIC trauma centers. Simultaneous with these studies, interactions with clinical centers engaged in DoD clinical trials will be developed in which research personnel at each center will be responsible for point-of-care studies and processing of blood samples. Collection techniques will utilize inhibitory cocktails to block ex vivo, post- phlebotomy artifacts. Blood/plasma samples will be shipped to a secure repository and analyzed utilizing new technology to identify the natural history of TIC events. Continuation of TACTIC research projects will be dependent upon their potential utility for diagnosis and selection of therapy for trauma patients. Summaries for the Coagulation, Inflammation and Coordinating Center remain unchanged from the original submission.

Public Health Relevance

Although uncontrolled bleeding is the major cause of death in people with severe traumatic injuries, the reasons for this bleeding are not completely understood. We plan to comprehensively describe the causes of trauma-related clotting and bleeding, and propose methods to diagnose the different causes and ultimately therapeutic interventions to prevent morbidity and mortality in traumatic settings. Project Narratives for the Coagulation, Inflammation and Coordinating Center Components remain unchanged from the original submission.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project with Complex Structure Cooperative Agreement (UM1)
Project #
3UM1HL120877-05S1
Application #
9986376
Study Section
Program Officer
Kindzelski, Andrei L
Project Start
2018-06-01
Project End
2020-05-31
Budget Start
2019-09-01
Budget End
2020-05-31
Support Year
5
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Biochemistry
Type
Schools of Medicine
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Banerjee, Anirban; Silliman, Christopher C; Moore, Ernest E et al. (2018) Systemic hyperfibrinolysis after trauma: a pilot study of targeted proteomic analysis of superposed mechanisms in patient plasma. J Trauma Acute Care Surg 84:929-938
Moore, Ernest E; Moore, Hunter B; Chapman, Michael P et al. (2018) Goal-directed hemostatic resuscitation for trauma induced coagulopathy: Maintaining homeostasis. J Trauma Acute Care Surg 84:S35-S40
Bouchard, Beth A; Orfeo, Thomas; Keith, Hollis N et al. (2018) Microparticles formed during storage of red blood cell units support thrombin generation. J Trauma Acute Care Surg 84:598-605
Reisz, Julie A; Wither, Matthew J; Moore, Ernest E et al. (2018) All animals are equal but some animals are more equal than others: Plasma lactate and succinate in hemorrhagic shock-A comparison in rodents, swine, nonhuman primates, and injured patients. J Trauma Acute Care Surg 84:537-541
Matusik, Pawe? T; Prior, Shannon M; Butenas, Saulius et al. (2018) Association of cardiac troponin I with prothrombotic alterations in atrial fibrillation. Kardiol Pol 76:1106-1109
Stettler, Gregory R; Moore, Ernest E; Nunns, Geoffrey R et al. (2018) Rotational thromboelastometry thresholds for patients at risk for massive transfusion. J Surg Res 228:154-159
Morris, Alan H (2018) Human Cognitive Limitations. Broad, Consistent, Clinical Application of Physiological Principles Will Require Decision Support. Ann Am Thorac Soc 15:S53-S56
Pinsky, Michael R (2018) Cardiopulmonary Interactions: Physiologic Basis and Clinical Applications. Ann Am Thorac Soc 15:S45-S48
Lawson, Peter J; Moore, Hunter B; Moore, Ernest E et al. (2018) Microfluidics contrasted to thrombelastography: perplexities in defining hypercoagulability. J Surg Res 231:54-61
Dyer, Mitchell R; Hickman, DaShawn; Luc, Norman et al. (2018) Intravenous administration of synthetic platelets (SynthoPlate) in a mouse liver injury model of uncontrolled hemorrhage improves hemostasis. J Trauma Acute Care Surg 84:917-923

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