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DOI: 10.1055/s-0042-1756305
Advances in the Management of Coagulopathy in Trauma: The Role of Viscoelastic Hemostatic Assays across All Phases of Trauma Care
Abstract
Uncontrolled bleeding is the leading cause of preventable death following injury. Trauma-induced coagulopathy can manifest as diverse phenotypes ranging from hypocoagulability to hypercoagulability, which can change quickly during the acute phase of trauma care. The major advances in understanding coagulation over the past 25 years have resulted from the cell-based concept, emphasizing the key role of platelets and their interaction with the damaged endothelium. Consequently, conventional plasma-based coagulation testing is not accurate in predicting bleeding and does not provide an assessment of which blood products are indicated. Viscoelastic hemostatic assays (VHA), conducted in whole blood, have emerged as a superior method to guide goal-directed transfusion. The major change in resuscitation has been the shift from unbridled crystalloid loading to judicious balanced blood product administration. Furthermore, the recognition of the rapid changes from hypocoagulability to hypercoagulability has underscored the importance of ongoing surveillance beyond emergent surgery. While the benefits of VHA testing are maximized when used as early as possible, current technology limits use in the pre-hospital setting and the time to results compromises its utility in the emergency department. Thus, most of the reported experience with VHA in trauma is in the operating room and intensive care unit, where there is compelling data to support its value. This overview will address the current and potential role of VHA in the seriously injured patient, throughout the continuum of trauma management.
Keywords
viscoelastic assay - thrombelastography - rotational thromboelastometry - trauma - hemorrhage - coagulopathy* Co–first authors.
Publication History
Article published online:
16 September 2022
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References
- 1 Centers for Disease Control and Prevention, . National Center for Injury Prevention and Control. Web-based Injury Statistics Query and Reporting System (WISQARS) [online]. Accessed February 14, 2017, at: https://www.cdc.gov/injury/wisqars/leadingcauses.html
- 2 Kauvar DS, Lefering R, Wade CE. Impact of hemorrhage on trauma outcome: an overview of epidemiology, clinical presentations, and therapeutic considerations. J Trauma 2006; 60 (6, Suppl): S3-S11
- 3 Brohi K, Singh J, Heron M, Coats T. Acute traumatic coagulopathy. J Trauma 2003; 54 (06) 1127-1130
- 4 Moore EE, Moore HB, Kornblith LZ. et al. Trauma-induced coagulopathy. Nat Rev Dis Primers 2021; 7 (01) 30
- 5 Kornblith LZ, Moore HB, Cohen MJ. Trauma-induced coagulopathy: the past, present, and future. J Thromb Haemost 2019; 17 (06) 852-862
- 6 Hoffman M, Monroe III DM. A cell-based model of hemostasis. Thromb Haemost 2001; 85 (06) 958-965
- 7 Moore HB, Moore EE, Liras IN. et al. Targeting resuscitation to normalization of coagulating status: hyper and hypocoagulability after severe injury are both associated with increased mortality. Am J Surg 2017; 214 (06) 1041-1045
- 8 Sumislawski JJ, Christie SA, Kornblith LZ. et al. Discrepancies between conventional and viscoelastic assays in identifying trauma-induced coagulopathy. Am J Surg 2019; 217 (06) 1037-1041
- 9 Chin TL, Moore EE, Moore HB. et al. A principal component analysis of postinjury viscoelastic assays: clotting factor depletion versus fibrinolysis. Surgery 2014; 156 (03) 570-577
- 10 Kutcher ME, Ferguson AR, Cohen MJ. A principal component analysis of coagulation after trauma. J Trauma Acute Care Surg 2013; 74 (05) 1223-1229 , discussion 1229–1230
- 11 White NJ, Contaifer Jr D, Martin EJ. et al. Early hemostatic responses to trauma identified with hierarchical clustering analysis. J Thromb Haemost 2015; 13 (06) 978-988
- 12 Gonzalez E, Moore EE, Moore HB. et al. Goal-directed hemostatic resuscitation of trauma-induced coagulopathy: a pragmatic randomized clinical trial comparing a viscoelastic assay to conventional coagulation assays. Ann Surg 2016; 263 (06) 1051-1059
- 13 Baksaas-Aasen K, Gall LS, Stensballe J. et al. Viscoelastic haemostatic assay augmented protocols for major trauma haemorrhage (ITACTIC): a randomized, controlled trial. Intensive Care Med 2021; 47 (01) 49-59
- 14 Park MS, Spears GM, Bailey KR. et al. Thrombin generation profiles as predictors of symptomatic venous thromboembolism after trauma: a prospective cohort study. J Trauma Acute Care Surg 2017; 83 (03) 381-387
- 15 Cotton BA, Minei KM, Radwan ZA. et al. Admission rapid thrombelastography predicts development of pulmonary embolism in trauma patients. J Trauma Acute Care Surg 2012; 72 (06) 1470-1475 , discussion 1475–1477
- 16 Sumislawski JJ, Moore HB, Moore EE. et al. Not all in your head (and neck): Stroke after blunt cerebrovascular injury is associated with systemic hypercoagulability. J Trauma Acute Care Surg 2019; 87 (05) 1082-1087
- 17 Hagemo JS. Prehospital detection of traumatic coagulopathy. Transfusion 2013; 53 (Suppl. 01) 48S-51S
- 18 Robinson S, Kirton J. Tools to predict acute traumatic coagulopathy in the pre-hospital setting: a review of the literature. Br Paramed J 2020; 5 (03) 23-30
- 19 Tonglet ML, Minon JM, Seidel L, Poplavsky JL, Vergnion M. Prehospital identification of trauma patients with early acute coagulopathy and massive bleeding: results of a prospective non-interventional clinical trial evaluating the Trauma Induced Coagulopathy Clinical Score (TICCS). Crit Care 2014; 18 (06) 648
- 20 Beynon C, Erk AG, Potzy A, Mohr S, Popp E. Point of care coagulometry in prehospital emergency care: an observational study. Scand J Trauma Resusc Emerg Med 2015; 23: 58
- 21 Dhara S, Moore EE, Yaffe MB, Moore HB, Barrett CD. Modern management of bleeding, clotting, and coagulopathy in trauma patients: What is the role of viscoelastic assays?. Curr Trauma Rep 2020; 6 (01) 69-81
- 22 Boyé M, Boissin J, Poyat C, Pasquier P, Martinaud C. Evaluation of the altitude impact on a point-of-care thromboelastography analyzer measurement: prerequisites for use in airborne medical evacuation courses. Eur J Trauma Emerg Surg 2022; 48 (01) 489-495
- 23 Scott R, Burns B, Ware S, Oud F, Miller M. The reliability of thromboelastography in a simulated rotary wing environment. Emerg Med J 2018; 35 (12) 739-742
- 24 Roberts TR, Jones JA, Choi JH. et al. Thromboelastography on-the-go: evaluation of the TEG 6s device during ground and high-altitude aeromedical evacuation with extracorporeal life support. J Trauma Acute Care Surg 2019; 87 (1S, Suppl 1): S119-S127
- 25 Meledeo MA, Peltier GC, McIntosh CS, Voelker CR, Bynum JA, Cap AP. Functional stability of the TEG 6s hemostasis analyzer under stress. J Trauma Acute Care Surg 2018; 84 (6S Suppl 1): S83-S88
- 26 Bates A, Donohue A, McCullough J, Winearls J. Viscoelastic haemostatic assays in aeromedical transport. Emerg Med Australas 2020; 32 (05) 786-792
- 27 Doran CM, Woolley T, Midwinter MJ. Feasibility of using rotational thromboelastometry to assess coagulation status of combat casualties in a deployed setting. J Trauma 2010; 69 (Suppl. 01) S40-S48
- 28 Modesti PA, Rapi S, Paniccia R. et al. Index measured at an intermediate altitude to predict impending acute mountain sickness. Med Sci Sports Exerc 2011; 43 (10) 1811-1818
- 29 Lammers DT, Marenco CW, Morte KR, Bingham JR, Martin MJ, Eckert MJ. Viscoelastic testing in combat resuscitation: Is it time for a new standard?. J Trauma Acute Care Surg 2020; 89 (01) 145-152
- 30 Prat NJ, Meyer AD, Ingalls NK, Trichereau J, DuBose JJ, Cap AP. Rotational thromboelastometry significantly optimizes transfusion practices for damage control resuscitation in combat casualties. J Trauma Acute Care Surg 2017; 83 (03) 373-380
- 31 Duchesne J, Slaughter K, Puente I. et al. Impact of time to surgery on mortality in hypotensive patients with noncompressible torso hemorrhage: an AAST multicenter, prospective study. J Trauma Acute Care Surg 2022; 92 (05) 801-811
- 32 Douglas M, Obaid O, Castanon L. et al. After 9,000 laparotomies for blunt trauma, resuscitation is becoming more balanced and time to intervention shorter: evidence in action. J Trauma Acute Care Surg 2022; DOI: 10.1097/TA.0000000000003574. (online ahead of print)
- 33 Schroll R, Smith A, Alabaster K. et al. AAST multicenter prospective analysis of prehospital tourniquet use for extremity trauma. J Trauma Acute Care Surg 2022; 92 (06) 997-1004
- 34 Muldowney M, Aichholz P, Nathwani R, Stansbury LG, Hess JR, Vavilala MS. Advances in hemorrhage control resuscitation. Curr Opin Anaesthesiol 2022; 35 (02) 176-181
- 35 Henry R, Matsushima K, Ghafil C. et al. Increased use of prehospital tourniquet and patient survival: Los Angeles countywide study. J Am Coll Surg 2021; 233 (02) 233-239.e2
- 36 Ordoñez CA, Parra MW, Serna JJ. et al. Damage control resuscitation: REBOA as the new fourth pillar. Colomb Med (Cali) 2020; 51 (04) e4014353
- 37 Granieri S, Frassini S, Cimbanassi S. et al. Impact of resuscitative endovascular balloon occlusion of the aorta (REBOA) in traumatic abdominal and pelvic exsanguination: a systematic review and meta-analysis. Eur J Trauma Emerg Surg 2022; DOI: 10.1007/s00068-022-01955-6. (online ahead of print)
- 38 Palacios-Rodríguez HE, Hiroe N, Guzmán-Rodríguez M. et al. Hybrid trauma service: on the leading edge of damage control. Colomb Med (Cali) 2021; 52 (02) e4014686
- 39 D'Amours SK, Rastogi P, Ball CG. Utility of simultaneous interventional radiology and operative surgery in a dedicated suite for seriously injured patients. Curr Opin Crit Care 2013; 19 (06) 587-593
- 40 Johnson A, Rott M, Kuchler A. et al. Direct to operating room trauma resuscitation: optimizing patient selection and time-critical outcomes when minutes count. J Trauma Acute Care Surg 2020; 89 (01) 160-166
- 41 Meizoso JP, Ray JJ, Karcutskie IV CA. et al. Effect of time to operation on mortality for hypotensive patients with gunshot wounds to the torso: the golden 10 minutes. J Trauma Acute Care Surg 2016; 81 (04) 685-691
- 42 Beekley AC. Damage control resuscitation: a sensible approach to the exsanguinating surgical patient. Crit Care Med 2008; 36 (7, Suppl): S267-S274
- 43 Ball CG. Damage control resuscitation: history, theory and technique. Can J Surg 2014; 57 (01) 55-60
- 44 Holcomb JB, Tilley BC, Baraniuk S. et al; PROPPR Study Group. Transfusion of plasma, platelets, and red blood cells in a 1:1:1 vs a 1:1:2 ratio and mortality in patients with severe trauma: the PROPPR randomized clinical trial. JAMA 2015; 313 (05) 471-482
- 45 Walsh M, Moore EE, Moore HB. et al. Whole blood, fixed ratio, or goal-directed blood component therapy for the initial resuscitation of severely hemorrhaging trauma patients: a narrative review. J Clin Med 2021; 10 (02) 320
- 46 Walsh M, Fries D, Moore E. et al. Whole blood for civilian urban trauma resuscitation: historical, present, and future considerations. Semin Thromb Hemost 2020; 46 (02) 221-234
- 47 Kashuk JL, Moore EE, Millikan JS, Moore JB. Major abdominal vascular trauma–a unified approach. J Trauma 1982; 22 (08) 672-679
- 48 Volod O, Bunch CM, Zackariya N. et al. Viscoelastic hemostatic assays: a primer on legacy and new generation devices. J Clin Med 2022; 11 (03) 860
- 49 Lantry JH, Mason P, Logsdon MG. et al. Hemorrhagic resuscitation guided by viscoelastography in far-forward combat and austere civilian environments: goal-directed whole-blood and blood-component therapy far from the trauma center. J Clin Med 2022; 11 (02) 356
- 50 Blaine KP, Dudaryk R. Pro-con debate: viscoelastic hemostatic assays should replace fixed ratio massive transfusion protocols in trauma. Anesth Analg 2022; 134 (01) 21-31
- 51 Brill JB, Brenner M, Duchesne J. et al. The role of TEG and ROTEM in damage control resuscitation. Shock 2021; 56 (1S): 52-61
- 52 Sperry JL, Guyette FX, Brown JB. et al; PAMPer Study Group. Prehospital plasma during air medical transport in trauma patients at risk for hemorrhagic shock. N Engl J Med 2018; 379 (04) 315-326
- 53 Moore HB, Moore EE, Chapman MP. et al. Plasma-first resuscitation to treat haemorrhagic shock during emergency ground transportation in an urban area: a randomised trial. Lancet 2018; 392 (10144): 283-291
- 54 Schroll R, Swift D, Tatum D. et al. Accuracy of shock index versus ABC score to predict need for massive transfusion in trauma patients. Injury 2018; 49 (01) 15-19
- 55 Zhu CS, Cobb D, Jonas RB. et al. Shock index and pulse pressure as triggers for massive transfusion. J Trauma Acute Care Surg 2019; 87 (1S, Suppl 01): S159-S164
- 56 Schreiber MA, Perkins J, Kiraly L, Underwood S, Wade C, Holcomb JB. Early predictors of massive transfusion in combat casualties. J Am Coll Surg 2007; 205 (04) 541-545
- 57 Rozycki GS, Ballard RB, Feliciano DV, Schmidt JA, Pennington SD. Surgeon-performed ultrasound for the assessment of truncal injuries: lessons learned from 1540 patients. Ann Surg 1998; 228 (04) 557-567
- 58 Rozycki GS, Ochsner MG, Schmidt JA. et al. A prospective study of surgeon-performed ultrasound as the primary adjuvant modality for injured patient assessment. J Trauma 1995; 39 (03) 492-498 , discussion 498–500
- 59 Callcut RA, Johannigman JA, Kadon KS, Hanseman DJ, Robinson BR. All massive transfusion criteria are not created equal: defining the predictive value of individual transfusion triggers to better determine who benefits from blood. J Trauma 2011; 70 (04) 794-801
- 60 McLaughlin DF, Niles SE, Salinas J. et al. A predictive model for massive transfusion in combat casualty patients. J Trauma 2008;64(2, Suppl):S57–S63, discussion S63
- 61 Zhang J, Jiang R, Liu L, Watkins T, Zhang F, Dong JF. Traumatic brain injury-associated coagulopathy. J Neurotrauma 2012; 29 (17) 2597-2605
- 62 Maegele M. Coagulopathy after traumatic brain injury: incidence, pathogenesis, and treatment options. Transfusion 2013; 53 (Suppl. 01) 28S-37S
- 63 Laroche M, Kutcher ME, Huang MC, Cohen MJ, Manley GT. Coagulopathy after traumatic brain injury. Neurosurgery 2012; 70 (06) 1334-1345
- 64 Meizoso JP, Moore HB, Moore EE. et al. Traumatic brain injury provokes low fibrinolytic activity in severely injured patients. J Trauma Acute Care Surg 2022; 93 (01) 8-12
- 65 Samuels JM, Moore EE, Silliman CC. et al. Severe traumatic brain injury is associated with a unique coagulopathy phenotype. J Trauma Acute Care Surg 2019; 86 (04) 686-693
- 66 Maegele M, Schöchl H, Menovsky T. et al. Coagulopathy and haemorrhagic progression in traumatic brain injury: advances in mechanisms, diagnosis, and management. Lancet Neurol 2017; 16 (08) 630-647
- 67 Maegele M, Aversa J, Marsee MK. et al. Changes in coagulation following brain injury. Semin Thromb Hemost 2020; 46 (02) 155-166
- 68 Cannon JW, Dias JD, Kumar MA. et al. Use of thromboelastography in the evaluation and management of patients with traumatic brain injury: a systematic review and meta-analysis. Crit Care Explor 2021; 3 (09) e0526
- 69 Bradbury JL, Thomas SG, Sorg NR. et al. Viscoelastic testing and coagulopathy of traumatic brain injury. J Clin Med 2021; 10 (21) 5039
- 70 Fletcher-Sandersjöö A, Thelin EP, Maegele M, Svensson M, Bellander BM. Time course of hemostatic disruptions after traumatic brain injury: a systematic review of the literature. Neurocrit Care 2021; 34 (02) 635-656
- 71 Maegele M. Coagulopathy and progression of intracranial hemorrhage in traumatic brain injury: mechanisms, impact, and therapeutic considerations. Neurosurgery 2021; 89 (06) 954-966
- 72 Webb AJ, Brown CS, Naylor RM, Rabinstein AA, Mara KC, Nei AM. Thromboelastography is a marker for clinically significant progressive hemorrhagic injury in severe traumatic brain injury. Neurocrit Care 2021; 35 (03) 738-746
- 73 Riojas CM, Ekaney ML, Ross SW. et al. Platelet dysfunction after traumatic brain injury: a review. J Neurotrauma 2021; 38 (07) 819-829
- 74 Xu X, Kozar R, Zhang J, Dong JF. Diverse activities of von Willebrand factor in traumatic brain injury and associated coagulopathy. J Thromb Haemost 2020; 18 (12) 3154-3162
- 75 Palta S, Saroa R, Palta A. Overview of the coagulation system. Indian J Anaesth 2014; 58 (05) 515-523
- 76 Raum D, Marcus D, Alper CA, Levey R, Taylor PD, Starzl TE. Synthesis of human plasminogen by the liver. Science 1980; 208 (4447): 1036-1037
- 77 Georgiou C, Inaba K, Teixeira PG. et al. Cirrhosis and trauma are a lethal combination. World J Surg 2009; 33 (05) 1087-1092
- 78 Christmas AB, Wilson AK, Franklin GA, Miller FB, Richardson JD, Rodriguez JL. Cirrhosis and trauma: a deadly duo. Am Surg 2005; 71 (12) 996-1000
- 79 Demetriades D, Constantinou C, Salim A, Velmahos G, Rhee P, Chan L. Liver cirrhosis in patients undergoing laparotomy for trauma: effect on outcomes. J Am Coll Surg 2004; 199 (04) 538-542
- 80 Wahlstrom K, Ney AL, Jacobson S. et al. Trauma in cirrhotics: survival and hospital sequelae in patients requiring abdominal exploration. Am Surg 2000; 66 (11) 1071-1076
- 81 Rezende-Neto JB, Rodrigues GP, Lisboa TA. et al. Fresh frozen plasma: red blood cells (1:2) coagulation effect is equivalent to 1:1 and whole blood. J Surg Res 2015; 199 (02) 608-614
- 82 Spinella PC, Cap AP. Whole blood: back to the future. Curr Opin Hematol 2016; 23 (06) 536-542
- 83 Spinella PC, Pidcoke HF, Strandenes G. et al. Whole blood for hemostatic resuscitation of major bleeding. Transfusion 2016; 56 (Suppl. 02) S190-S202
- 84 Yazer MH, Jackson B, Sperry JL, Alarcon L, Triulzi DJ, Murdock AD. Initial safety and feasibility of cold-stored uncrossmatched whole blood transfusion in civilian trauma patients. J Trauma Acute Care Surg 2016; 81 (01) 21-26
- 85 Einersen PM, Moore EE, Chapman MP. et al. Rapid thrombelastography thresholds for goal-directed resuscitation of patients at risk for massive transfusion. J Trauma Acute Care Surg 2017; 82 (01) 114-119
- 86 Paige JT, Garbee DD, Bonanno LS, Kerdolff KE. Qualitative analysis of effective teamwork in the operating room (OR). J Surg Educ 2021; 78 (03) 967-979
- 87 Alexandrino H, Baptista S, Vale L. et al. Improving intraoperative communication in trauma: the educational effect of the joint DSTC™-DATC™ courses. World J Surg 2020; 44 (06) 1856-1862
- 88 Neal MD, Moore HB, Moore EE. et al; TACTIC Investigators. Clinical assessment of trauma-induced coagulopathy and its contribution to postinjury mortality: a TACTIC proposal. J Trauma Acute Care Surg 2015; 79 (03) 490-492
- 89 Schreiber MA, Differding J, Thorborg P, Mayberry JC, Mullins RJ. Hypercoagulability is most prevalent early after injury and in female patients. J Trauma 2005; 58 (03) 475-480 , discussion 480–481
- 90 Sumislawski JJ, Kornblith LZ, Conroy AS, Callcut RA, Cohen MJ. Dynamic coagulability after injury: Is delaying venous thromboembolism chemoprophylaxis worth the wait?. J Trauma Acute Care Surg 2018; 85 (05) 907-914
- 91 Moore HB, Moore EE, Gonzalez E. et al. Hyperfibrinolysis, physiologic fibrinolysis, and fibrinolysis shutdown: the spectrum of postinjury fibrinolysis and relevance to antifibrinolytic therapy. J Trauma Acute Care Surg 2014; 77 (06) 811-817 , discussion 817
- 92 Stettler GR, Moore EE, Moore HB. et al. Redefining post injury fibrinolysis phenotypes using two viscoelastic assays. J Trauma Acute Care Surg 2019; 86 (04) 679-685
- 93 Innes D, Sevitt S. Coagulation and fibrinolysis in injured patients. J Clin Pathol 1964; 17: 1-13
- 94 Gall LS, Vulliamy P, Gillespie S. et al. The S100A10 pathway mediates an occult hyperfibrinolytic subtype in trauma patients. Ann Surg 2019; 269 (06) 1184-1191
- 95 Cardenas JC, Wade CE, Cotton BA. et al; PROPPR Study Group. TEG lysis shutdown represents coagulopathy in bleeding trauma patients: analysis of the PROPPR cohort. Shock 2019; 51 (03) 273-283
- 96 Gomez-Builes JC, Acuna SA, Nascimento B, Madotto F, Rizoli SB. Harmful or physiologic: diagnosing fibrinolysis shutdown in a trauma cohort with rotational thromboelastometry. Anesth Analg 2018; 127 (04) 840-849
- 97 Moore HB, Moore EE, Chapman MP. et al. Does tranexamic acid improve clot strength in severely injured patients who have elevated fibrin degradation products and low fibrinolytic activity, measured by thrombelastography?. J Am Coll Surg 2019; 229 (01) 92-101
- 98 Meizoso JP, Dudaryk R, Mulder MB. et al. Increased risk of fibrinolysis shutdown among severely injured trauma patients receiving tranexamic acid. J Trauma Acute Care Surg 2018; 84 (03) 426-432
- 99 Coleman JR, Moore EE, Moore HB. et al. Tranexamic acid disturbs the dynamics of postinjury fibrinolysis. ANZ J Surg 2020; 90 (04) 420-422
- 100 Moore HB, Moore EE, Liras IN. et al. Acute fibrinolysis shutdown after injury occurs frequently and increases mortality: a multicenter evaluation of 2,540 severely injured patients. J Am Coll Surg 2016; 222 (04) 347-355
- 101 Hayes HV, Droege ME, Furnish CJ, Goodman MD, Ernst NE, Droege CA. Admission thrombelastography does not guide dose adjustment of enoxaparin in trauma patients. Surg Open Sci 2020; 2 (04) 41-44
- 102 Coleman JR, Kay AB, Moore EE. et al. It's sooner than you think: Blunt solid organ injury patients are already hypercoagulable upon hospital admission - Results of a bi-institutional, prospective study. Am J Surg 2019; 218 (06) 1065-1073
- 103 Harr JN, Moore EE, Chin TL. et al. Postinjury hyperfibrinogenemia compromises efficacy of heparin-based venous thromboembolism prophylaxis. Shock 2014; 41 (01) 33-39
- 104 Yakovlev S, Gorlatov S, Ingham K, Medved L. Interaction of fibrin(ogen) with heparin: further characterization and localization of the heparin-binding site. Biochemistry 2003; 42 (25) 7709-7716
- 105 Louis SG, Van PY, Riha GM. et al. Thromboelastogram-guided enoxaparin dosing does not confer protection from deep venous thrombosis: a randomized controlled pilot trial. J Trauma Acute Care Surg 2014; 76 (04) 937-942 , discussion 942–943
- 106 Bugaev N, Como JJ, Golani G. et al. Thromboelastography and rotational thromboelastometry in bleeding patients with coagulopathy: practice management guideline from the Eastern Association for the Surgery of Trauma. J Trauma Acute Care Surg 2020; 89 (06) 999-1017
- 107 Geerts WH, Code KI, Jay RM, Chen E, Szalai JP. A prospective study of venous thromboembolism after major trauma. N Engl J Med 1994; 331 (24) 1601-1606
- 108 Park MS, Perkins SE, Spears GM. et al. Risk factors for venous thromboembolism after acute trauma: a population-based case-cohort study. Thromb Res 2016; 144: 40-45
- 109 Hardaway III RM. The significance of coagulative and thrombotic changes after injury. J Trauma 1970; 10 (04) 354-357
- 110 Schmitt FCF, Manolov V, Morgenstern J. et al. Acute fibrinolysis shutdown occurs early in septic shock and is associated with increased morbidity and mortality: results of an observational pilot study. Ann Intensive Care 2019; 9 (01) 19
- 111 Park MS, Martini WZ, Dubick MA. et al. Thromboelastography as a better indicator of hypercoagulable state after injury than prothrombin time or activated partial thromboplastin time. J Trauma 2009; 67 (02) 266-275 , discussion 275–276
- 112 Harr JN, Moore EE, Chin TL. et al. Platelets are dominant contributors to hypercoagulability after injury. J Trauma Acute Care Surg 2013; 74 (03) 756-762 , discussion 762–765
- 113 Connelly CR, Van PY, Hart KD. et al. Thrombelastography-based dosing of enoxaparin for thromboprophylaxis in trauma and surgical patients: a randomized clinical trial. JAMA Surg 2016; 151 (10) e162069
- 114 You D, Skeith L, Korley R. et al. Identification of hypercoagulability with thrombelastography in patients with hip fracture receiving thromboprophylaxis. Can J Surg 2021; 64 (03) E324-E329
- 115 Wu XD, Chen Y, Tian M. et al. Application of thrombelastography (TEG) for safety evaluation of tranexamic acid in primary total joint arthroplasty. J Orthop Surg Res 2019; 14 (01) 214
- 116 Barrera LM, Perel P, Ker K, Cirocchi R, Farinella E, Morales Uribe CH. Thromboprophylaxis for trauma patients. Cochrane Database Syst Rev 2013; (03) CD008303
- 117 Louis SG, Sato M, Geraci T. et al. Correlation of missed doses of enoxaparin with increased incidence of deep vein thrombosis in trauma and general surgery patients. JAMA Surg 2014; 149 (04) 365-370
- 118 Knudson MM, Moore EE, Kornblith LZ. et al. Challenging traditional paradigms in posttraumatic pulmonary thromboembolism. JAMA Surg 2022; 157 (02) e216356
- 119 Brill JB, Calvo RY, Wallace JD. et al. Aspirin as added prophylaxis for deep vein thrombosis in trauma: a retrospective case-control study. J Trauma Acute Care Surg 2016; 80 (04) 625-630
- 120 Kashuk JL, Moore EE, Johnson JL. et al. Progressive postinjury thrombocytosis is associated with thromboembolic complications. Surgery 2010; 148 (04) 667-674 , discussion 674–675
- 121 Matthay ZA, Hellmann ZJ, Nunez-Garcia B. et al. Post-injury platelet aggregation and venous thromboembolism. J Trauma Acute Care Surg 2022; DOI: 10.1097/TA.0000000000003655. (online ahead of print)
- 122 Vulliamy P, Kornblith LZ, Kutcher ME, Cohen MJ, Brohi K, Neal MD. Alterations in platelet behavior after major trauma: adaptive or maladaptive?. Platelets 2021; 32 (03) 295-304
- 123 Ley EJ, Brown CVR, Moore EE. et al. Updated guidelines to reduce venous thromboembolism in trauma patients: a Western Trauma Association critical decisions algorithm. J Trauma Acute Care Surg 2020; 89 (05) 971-981
- 124 Rappold JF, Sheppard FR, Carmichael Ii SP. et al. Venous thromboembolism prophylaxis in the trauma intensive care unit: an American Association for the Surgery of Trauma Critical Care Committee Clinical Consensus Document. Trauma Surg Acute Care Open 2021; 6 (01) e000643
- 125 Wright FL, Vogler TO, Moore EE. et al. Fibrinolysis shutdown correlates to thromboembolic events in severe COVID-19 infection. J Am Coll Surg 2020; 231 (02) 193-203.e1
- 126 Brown W, Lunati M, Maceroli M. et al. Ability of thromboelastography to detect hypercoagulability: a systematic review and meta-analysis. J Orthop Trauma 2020; 34 (06) 278-286
- 127 Barrett CD, Moore HB, Moore EE. et al. STudy of Alteplase for Respiratory failure in SARS-Cov2 COVID-19 (STARS): a vanguard multicenter, rapidly adaptive, pragmatic, randomized, controlled trial. Chest 2022; 161 (03) 710-727
- 128 Mohammadi Aria M, Erten A, Yalcin O. Technology advancements in blood coagulation measurements for point-of-care diagnostic testing. Front Bioeng Biotechnol 2019; 7: 395
- 129 Gill M. The TEG®6s on Shaky Ground? A novel assessment of the TEG®6s performance under a challenging condition. J Extra Corpor Technol 2017; 49 (01) 26-29
- 130 Gurbel PA, Bliden KP, Tantry US. et al. First report of the point-of-care TEG: a technical validation study of the TEG-6S system. Platelets 2016; 27 (07) 642-649
- 131 Ferrante EA, Blasier KR, Givens TB, Lloyd CA, Fischer TJ, Viola F. A novel device for the evaluation of hemostatic function in critical care settings. Anesth Analg 2016; 123 (06) 1372-1379
- 132 Cotton BA, Faz G, Hatch QM. et al. Rapid thrombelastography delivers real-time results that predict transfusion within 1 hour of admission. J Trauma 2011; 71 (02) 407-414 , discussion 414–417
- 133 Barrett CD, Moore HB, Vigneshwar N. et al. Plasmin thrombelastography rapidly identifies trauma patients at risk for massive transfusion, mortality, and hyperfibrinolysis: a diagnostic tool to resolve an international debate on tranexamic acid?. J Trauma Acute Care Surg 2020; 89 (06) 991-998
- 134 Moore EE, Moore HB, Gonzalez E. et al. Postinjury fibrinolysis shutdown: Rationale for selective tranexamic acid. J Trauma Acute Care Surg 2015; 78 (6, Suppl 1): S65-S69
- 135 Moore HB, Moore EE, Chapman MP. et al. Viscoelastic tissue plasminogen activator challenge predicts massive transfusion in 15 minutes. J Am Coll Surg 2017; 225 (01) 138-147
- 136 Walker CB, Moore EE, Kam A. et al. Clot activators do not expedite the time to predict massive transfusion in trauma patients analyzed with tissue plasminogen activator thrombelastography. Surgery 2019; 166 (03) 408-415
- 137 Cardenas JC, Matijevic N, Baer LA, Holcomb JB, Cotton BA, Wade CE. Elevated tissue plasminogen activator and reduced plasminogen activator inhibitor promote hyperfibrinolysis in trauma patients. Shock 2014; 41 (06) 514-521
- 138 Hayakawa M, Tsuchida T, Honma Y. et al. Fibrinolytic system activation immediately following trauma was quickly and intensely suppressed in a rat model of severe blunt trauma. Sci Rep 2021; 11 (01) 20283
- 139 Yamashita M, Darlington DN, Weeks EJ, Jones RO, Gann DS. Plasminogen activator inhibitor-1 rises after hemorrhage in rats. Am J Physiol 1995; 268 (6, Pt 1): E1065-E1069
- 140 Chapman MP, Moore EE, Moore HB. et al. Overwhelming tPA release, not PAI-1 degradation, is responsible for hyperfibrinolysis in severely injured trauma patients. J Trauma Acute Care Surg 2016; 80 (01) 16-23 , discussion 23–25
- 141 Hoshino K, Nakashio M, Maruyama J, Irie Y, Kawano Y, Ishikura H. Validating plasminogen activator inhibitor-1 as a poor prognostic factor in sepsis. Acute Med Surg 2020; 7 (01) e581
- 142 Stillson JE, Bunch CM, Gillespie L. et al. Thromboelastography-guided management of anticoagulated COVID-19 patients to prevent hemorrhage. Semin Thromb Hemost 2021; 47 (04) 442-446
- 143 Bunch CM, Thomas AV, Stillson JE. et al. Preventing thrombohemorrhagic complications of heparinized COVID-19 patients using adjunctive thromboelastography: a retrospective study. J Clin Med 2021; 10 (14) 3097
- 144 Kashuk JL, Moore EE, Sabel A. et al. Rapid thrombelastography (r-TEG) identifies hypercoagulability and predicts thromboembolic events in surgical patients. Surgery 2009; 146 (04) 764-772 , discussion 772–774
- 145 Gary JL, Schneider PS, Galpin M. et al. Can thrombelastography predict venous thromboembolic events in patients with severe extremity trauma?. J Orthop Trauma 2016; 30 (06) 294-298
- 146 Brill JB, Badiee J, Zander AL. et al. The rate of deep vein thrombosis doubles in trauma patients with hypercoagulable thromboelastography. J Trauma Acute Care Surg 2017; 83 (03) 413-419
- 147 Tsantes AG, Papadopoulos DV, Trikoupis IG. et al. Rotational thromboelastometry findings are associated with symptomatic venous thromboembolic complications after hip fracture surgery. Clin Orthop Relat Res 2021; 479 (11) 2457-2467