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2025 PACUPrep BCCCP Preparatory Course

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  1. Pulmonary

    ARDS
    4 Topics
    |
    1 Quiz
  2. Asthma Exacerbation
    4 Topics
    |
    1 Quiz
  3. COPD Exacerbation
    4 Topics
    |
    1 Quiz
  4. Cystic Fibrosis
    6 Topics
    |
    1 Quiz
  5. Drug-Induced Pulmonary Diseases
    3 Topics
    |
    1 Quiz
  6. Mechanical Ventilation Pharmacotherapy
    5 Topics
    |
    1 Quiz
  7. Pleural Disorders
    5 Topics
    |
    1 Quiz
  8. Pulmonary Hypertension (Acute and Chronic severe pulmonary hypertension)
    5 Topics
    |
    1 Quiz
  9. Cardiology
    Acute Coronary Syndromes
    6 Topics
    |
    1 Quiz
  10. Atrial Fibrillation and Flutter
    6 Topics
    |
    1 Quiz
  11. Cardiogenic Shock
    4 Topics
    |
    1 Quiz
  12. Heart Failure
    7 Topics
    |
    1 Quiz
  13. Hypertensive Crises
    5 Topics
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    1 Quiz
  14. Ventricular Arrhythmias and Sudden Cardiac Death Prevention
    5 Topics
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    1 Quiz
  15. NEPHROLOGY
    Acute Kidney Injury (AKI)
    5 Topics
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    1 Quiz
  16. Contrast‐Induced Nephropathy
    5 Topics
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    1 Quiz
  17. Drug‐Induced Kidney Diseases
    5 Topics
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    1 Quiz
  18. Rhabdomyolysis
    5 Topics
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    1 Quiz
  19. Syndrome of Inappropriate Antidiuretic Hormone (SIADH)
    5 Topics
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    1 Quiz
  20. Renal Replacement Therapies (RRT)
    5 Topics
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    1 Quiz
  21. Neurology
    Status Epilepticus
    5 Topics
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    1 Quiz
  22. Acute Ischemic Stroke
    5 Topics
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    1 Quiz
  23. Subarachnoid Hemorrhage
    5 Topics
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    1 Quiz
  24. Spontaneous Intracerebral Hemorrhage
    5 Topics
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    1 Quiz
  25. Neuromonitoring Techniques
    5 Topics
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    1 Quiz
  26. Gastroenterology
    Acute Upper Gastrointestinal Bleeding
    5 Topics
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    1 Quiz
  27. Acute Lower Gastrointestinal Bleeding
    5 Topics
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    1 Quiz
  28. Acute Pancreatitis
    5 Topics
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    1 Quiz
  29. Enterocutaneous and Enteroatmospheric Fistulas
    5 Topics
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    1 Quiz
  30. Ileus and Acute Intestinal Pseudo-obstruction
    5 Topics
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    1 Quiz
  31. Abdominal Compartment Syndrome
    5 Topics
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    1 Quiz
  32. Hepatology
    Acute Liver Failure
    5 Topics
    |
    1 Quiz
  33. Portal Hypertension & Variceal Hemorrhage
    5 Topics
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    1 Quiz
  34. Hepatic Encephalopathy
    5 Topics
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    1 Quiz
  35. Ascites & Spontaneous Bacterial Peritonitis
    5 Topics
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    1 Quiz
  36. Hepatorenal Syndrome
    5 Topics
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    1 Quiz
  37. Drug-Induced Liver Injury
    5 Topics
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    1 Quiz
  38. Dermatology
    Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis
    5 Topics
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    1 Quiz
  39. Erythema multiforme
    5 Topics
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    1 Quiz
  40. Drug Reaction (or Rash) with Eosinophilia and Systemic Symptoms (DRESS)
    5 Topics
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    1 Quiz
  41. Immunology
    Transplant Immunology & Acute Rejection
    5 Topics
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    1 Quiz
  42. Solid Organ & Hematopoietic Transplant Pharmacotherapy
    5 Topics
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    1 Quiz
  43. Graft-Versus-Host Disease (GVHD)
    5 Topics
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    1 Quiz
  44. Hypersensitivity Reactions & Desensitization
    5 Topics
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    1 Quiz
  45. Biologic Immunotherapies & Cytokine Release Syndrome
    5 Topics
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    1 Quiz
  46. Endocrinology
    Relative Adrenal Insufficiency and Stress-Dose Steroid Therapy
    5 Topics
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    1 Quiz
  47. Hyperglycemic Crisis (DKA & HHS)
    5 Topics
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    1 Quiz
  48. Glycemic Control in the ICU
    5 Topics
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    1 Quiz
  49. Thyroid Emergencies: Thyroid Storm & Myxedema Coma
    5 Topics
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    1 Quiz
  50. Hematology
    Acute Venous Thromboembolism
    5 Topics
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    1 Quiz
  51. Drug-Induced Thrombocytopenia
    5 Topics
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    1 Quiz
  52. Anemia of Critical Illness
    5 Topics
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    1 Quiz
  53. Drug-Induced Hematologic Disorders
    5 Topics
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    1 Quiz
  54. Sickle Cell Crisis in the ICU
    5 Topics
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    1 Quiz
  55. Methemoglobinemia & Dyshemoglobinemias
    5 Topics
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    1 Quiz
  56. Toxicology
    Toxidrome Recognition and Initial Management
    5 Topics
    |
    1 Quiz
  57. Management of Acute Overdoses – Non-Cardiovascular Agents
    5 Topics
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    1 Quiz
  58. Management of Acute Overdoses – Cardiovascular Agents
    5 Topics
    |
    1 Quiz
  59. Toxic Alcohols and Small-Molecule Poisons
    5 Topics
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    1 Quiz
  60. Antidotes and Gastrointestinal Decontamination
    5 Topics
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    1 Quiz
  61. Extracorporeal Removal Techniques
    5 Topics
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    1 Quiz
  62. Withdrawal Syndromes in the ICU
    5 Topics
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    1 Quiz
  63. Infectious Diseases
    Sepsis and Septic Shock
    5 Topics
    |
    1 Quiz
  64. Pneumonia (CAP, HAP, VAP)
    5 Topics
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    1 Quiz
  65. Endocarditis
    5 Topics
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    1 Quiz
  66. CNS Infections
    5 Topics
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    1 Quiz
  67. Complicated Intra-abdominal Infections
    5 Topics
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    1 Quiz
  68. Antibiotic Stewardship & PK/PD
    5 Topics
    |
    1 Quiz
  69. Clostridioides difficile Infection
    5 Topics
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    1 Quiz
  70. Febrile Neutropenia & Immunocompromised Hosts
    5 Topics
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    1 Quiz
  71. Skin & Soft-Tissue Infections / Acute Osteomyelitis
    5 Topics
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    1 Quiz
  72. Urinary Tract and Catheter-related Infections
    5 Topics
    |
    1 Quiz
  73. Pandemic & Emerging Viral Infections
    5 Topics
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    1 Quiz
  74. Supportive Care (Pain, Agitation, Delirium, Immobility, Sleep)
    Pain Assessment and Analgesic Management
    5 Topics
    |
    1 Quiz
  75. Sedation and Agitation Management
    5 Topics
    |
    1 Quiz
  76. Delirium Prevention and Treatment
    5 Topics
    |
    1 Quiz
  77. Sleep Disturbance Management
    5 Topics
    |
    1 Quiz
  78. Immobility and Early Mobilization
    5 Topics
    |
    1 Quiz
  79. Oncologic Emergencies
    5 Topics
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    1 Quiz
  80. End-of-Life Care & Palliative Care
    Goals of Care & Advance Care Planning
    5 Topics
    |
    1 Quiz
  81. Pain Management & Opioid Therapy
    5 Topics
    |
    1 Quiz
  82. Dyspnea & Respiratory Symptom Management
    5 Topics
    |
    1 Quiz
  83. Sedation & Palliative Sedation
    5 Topics
    |
    1 Quiz
  84. Delirium Agitation & Anxiety
    5 Topics
    |
    1 Quiz
  85. Nausea, Vomiting & Gastrointestinal Symptoms
    5 Topics
    |
    1 Quiz
  86. Management of Secretions (Death Rattle)
    5 Topics
    |
    1 Quiz
  87. Fluids, Electrolytes, and Nutrition Management
    Intravenous Fluid Therapy and Resuscitation
    5 Topics
    |
    1 Quiz
  88. Acid–Base Disorders
    5 Topics
    |
    1 Quiz
  89. Sodium Homeostasis and Dysnatremias
    5 Topics
    |
    1 Quiz
  90. Potassium Disorders
    5 Topics
    |
    1 Quiz
  91. Calcium and Magnesium Abnormalities
    5 Topics
    |
    1 Quiz
  92. Phosphate and Trace Electrolyte Management
    5 Topics
    |
    1 Quiz
  93. Enteral Nutrition Support
    5 Topics
    |
    1 Quiz
  94. Parenteral Nutrition Support
    5 Topics
    |
    1 Quiz
  95. Refeeding Syndrome and Specialized Nutrition
    5 Topics
    |
    1 Quiz
  96. Trauma and Burns
    Initial Resuscitation and Fluid Management in Trauma
    5 Topics
    |
    1 Quiz
  97. Hemorrhagic Shock, Massive Transfusion, and Trauma‐Induced Coagulopathy
    5 Topics
    |
    1 Quiz
  98. Burns Pharmacotherapy
    5 Topics
    |
    1 Quiz
  99. Burn Wound Care
    5 Topics
    |
    1 Quiz
  100. Open Fracture Antibiotics
    5 Topics
    |
    1 Quiz

Participants 432

  • Allison Clemens
  • April
  • ababaabhay
  • achoi2392
  • adhoward1
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Diagnostics and Classification in Hemorrhagic Shock and Trauma-Induced Coagulopathy

Diagnostics and Classification in Hemorrhagic Shock and Trauma-Induced Coagulopathy

Objectives Icon A crosshair target, symbolizing a specific objective.

Learning Objective

Apply diagnostic criteria, laboratory markers, viscoelastic testing, and clinical scoring to stratify bleeding severity and guide activation of massive transfusion protocols.

1. Clinical Classification of Shock

Early bedside assessment using ATLS shock classes and the Shock Index expedites recognition of hemodynamic compromise. These tools provide a rapid, physiology-based framework for initial triage before laboratory data are available.

ATLS Classes of Hemorrhagic Shock

Advanced Trauma Life Support (ATLS) Classification of Hemorrhagic Shock
Class Blood Loss (%) Heart Rate (bpm) Blood Pressure Resp. Rate Mental Status
I <15% (<750 mL) <100 Normal 14–20 Normal / Slight Anxiety
II 15–30% (750–1500 mL) 100–120 Normal / Postural Drop 20–30 Mildly Anxious
III 30–40% (1500–2000 mL) 120–140 Hypotensive (SBP <90) 30–40 Anxious / Confused
IV >40% (>2000 mL) >140 Profound Hypotension >35 Confused / Lethargic

Limitations: It’s crucial to recognize that elderly patients, those on beta-blockers, or well-conditioned athletes may not manifest classic tachycardic responses. Compensatory mechanisms vary widely among individuals.

Shock Index (SI)

The Shock Index (SI), calculated as Heart Rate divided by Systolic Blood Pressure (HR/SBP), is a more sensitive marker of early shock than vital signs alone. An SI >0.9 suggests significant hemodynamic decompensation and correlates with higher transfusion requirements and mortality. Variants like the Modified SI (HR/MAP) and Age-Shock Index (Age x SI) further refine risk stratification.

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A rising Shock Index in a patient who appears to be in ATLS Class II often precedes overt hypotension (progression to Class III). Monitoring the trend of the SI is a powerful tool for anticipating clinical deterioration.

2. Traditional Laboratory Markers

While clinical assessment is primary, laboratory markers quantify the extent of coagulopathy and shock. However, their turnaround time can delay targeted therapy, highlighting the need for faster point-of-care alternatives.

  • PT/INR & aPTT: An INR >1.5 or aPTT >60 seconds signals significant coagulation factor deficiency. A major limitation is the 30–45 minute turnaround time and their inability to assess platelet function or fibrinolysis.
  • Fibrinogen & Platelets: These are the critical substrates for clot formation. A fibrinogen level <150 mg/dL is a hallmark of acute trauma-induced coagulopathy (TIC). A platelet count <100×10⁹/L increases bleeding risk, and transfusion is typically indicated for counts <50×10⁹/L in the setting of active hemorrhage.
  • Lactate & Base Deficit: These are markers of global tissue hypoperfusion. A lactate >4 mmol/L or a base deficit more negative than –6 mEq/L are strongly correlated with shock severity and mortality.
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Lactate clearance (the rate at which lactate levels decrease with resuscitation) is a key therapeutic endpoint. A rapid decline in lactate often precedes the normalization of vital signs and indicates successful restoration of tissue perfusion.

3. Point-of-Care Viscoelastic Testing (TEG/ROTEM)

Viscoelastic tests like Thromboelastography (TEG) and Rotational Thromboelastometry (ROTEM) provide a rapid, holistic assessment of the entire clotting cascade. They analyze clot kinetics, strength, and fibrinolysis in whole blood, enabling real-time, goal-directed component therapy.

Core Parameters and Actions

Interpretation of Common Viscoelastic Test Parameters
Parameter (TEG) Measures Indicated Therapy if Abnormal
R-Time Time to initial fibrin formation (clot initiation) Prolonged (>8-10 min) → Give Fresh Frozen Plasma (FFP)
K-Time / Angle Speed of clot strengthening (fibrin cross-linking) Prolonged K / Low Angle → Give Cryoprecipitate (Fibrinogen)
MA (Maximum Amplitude) Maximum clot strength (platelet contribution) Low (<50 mm) → Give Platelets
LY30 Percent lysis at 30 minutes (fibrinolysis) High (>7.5%) → Give Antifibrinolytic (e.g., TXA)

Indications & Controversies: These tests are most valuable in patients with active, uncontrolled hemorrhage where coagulopathy is suspected. Their use in massive transfusion protocols (MTPs) has been shown to reduce the administration of unnecessary blood products. However, variability between devices, a lack of universally accepted thresholds, and the need for operator training remain limitations.

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A prolonged R-Time on a TEG/ROTEM can predict significant factor depletion up to 30 minutes before the traditional INR value becomes critically elevated. This “head start” is crucial for timely plasma administration.

4. Clinical Scoring Tools

Simple, validated bedside scores like the ABC score are designed to rapidly identify patients who are likely to require massive transfusion, allowing for protocol activation before definitive lab results are back.

The ABC Score

The Assessment of Blood Consumption (ABC) score assigns one point for each of the following four criteria present on arrival:

  • Assessment: Penetrating mechanism of injury
  • Blood Pressure: Systolic BP ≤90 mmHg
  • Cardiac Rate: Heart Rate ≥120 bpm
  • FAST Exam: Positive Focused Assessment with Sonography for Trauma

A score of 2 or more is highly predictive of the need for massive transfusion, with a reported sensitivity of ~75% and specificity of ~85%. However, its performance may be reduced in patients with bradycardia or in geriatric populations. Therefore, it should be supplemented with clinical judgment and physiologic trends.

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Combine the ABC score with the Shock Index for earlier and more accurate detection of exsanguination risk. For example, a patient with an ABC score of 1 but a Shock Index >1.0 should be viewed with a very high degree of suspicion for impending massive hemorrhage.

5. Triggers for Massive Transfusion Protocol (MTP) Activation

The decision to activate an MTP should be based on a harmonized assessment of clinical scores, laboratory values, and viscoelastic findings to avoid both over- and under-transfusion.

Massive Transfusion Protocol (MTP) Activation Flowchart A flowchart showing three categories of triggers (Clinical, Laboratory, Viscoelastic) that lead to the decision to activate an MTP. A feedback loop indicates reassessment after transfusion. MTP Activation Algorithm Clinical Triggers • ABC Score ≥2 • Shock Index >0.9 • Persistent Hypotension • Uncontrolled Bleeding Laboratory Triggers • Lactate >4 mmol/L • Base Deficit < -6 • INR >1.5 • Fibrinogen <150 mg/dL Viscoelastic Triggers • R-Time Prolonged • MA <50 mm • LY30 >7.5% • Low Alpha Angle ACTIVATE MTP Reassess after each cycle
Figure 1: Integrated MTP Activation Triggers. The decision to activate a massive transfusion protocol should be based on a combination of clinical, laboratory, and viscoelastic data. Any single strong trigger or a combination of weaker triggers should prompt activation, followed by systematic reassessment.
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Just as important as activating an MTP is deactivating it. Incorporate a mandatory “MTP deactivation review” or huddle after every 4-6 units of red blood cells are transfused. This scheduled check-in prevents iatrogenic fluid overload and transfusion-related complications once hemostasis is achieved.

6. Integration of Data to Guide Initial Management

Effective management of hemorrhagic shock relies on a seamless integration of rapid triage, point-of-care diagnostics, and evolving laboratory data to guide a balanced resuscitation strategy.

The Resuscitation Workflow

The initial approach should follow a rapid, tiered sequence: use the ABC score and Shock Index to make an initial decision on MTP activation and empirical 1:1:1 component therapy. Simultaneously, obtain point-of-care (POC) lactate and viscoelastic tests. The results of these POC tests should guide the first hour of resuscitation, allowing for a shift from empirical to goal-directed therapy. Central laboratory results are then used to refine targets and guide ongoing management after initial hemostasis is achieved.

Future Directions

The field is moving towards greater standardization of viscoelastic thresholds and the development of machine-learning models that can predict coagulopathy and transfusion needs even earlier. Research into novel biomarkers of endothelial injury and coagulation is ongoing, promising a more personalized approach to trauma resuscitation in the future.

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Early, targeted component therapy guided by point-of-care testing is superior to “shotgun” resuscitation. By precisely correcting the specific deficits (e.g., factors vs. fibrinogen vs. platelets), this approach has been shown to reduce total blood product utilization, decrease costs, and may improve patient survival.

References

  1. American College of Surgeons. ATLS Advanced Trauma Life Support Student Manual. 10th ed. 2018.
  2. Cotton BA, et al. Assessment of Blood Consumption: a new approach to identify massive transfusion need. J Trauma. 2010;68(2):346–350.
  3. Brohi K, Cohen MJ, Davenport RA. Acute coagulopathy of trauma: mechanism, identification and effect. Curr Opin Crit Care. 2007;13(6):680–685.
  4. Maegele M, et al. Update on acute trauma hemorrhage and coagulopathy based on viscoelastic testing. Clin Exp Emerg Med. 2024;11(1):1–12.
  5. Johansson PI, Stensballe J. Effect of hemostatic control resuscitation on mortality in massively bleeding patients: a before and after study. Vox Sang. 2009;96(2):111–118.
  6. Holcomb JB, et al. 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(5):471–482.
  7. CRASH-2 trial collaborators. Effects of tranexamic acid on death, vascular occlusive events, and blood transfusion in trauma patients with significant hemorrhage. Lancet. 2010;376(9734):23–32.
  8. Wray JP, et al. The diamond of death: Hypocalcemia in trauma and resuscitation. Am J Emerg Med. 2021;41:104–109.
  9. Ganter MT, Hofer CK. Coagulation monitoring: current techniques and clinical use of viscoelastic point-of-care coagulation devices. Anesth Analg. 2008;106(5):1366–1375.
  10. Hayter MA, et al. Massive transfusion in the trauma patient: continuing professional development. Can J Anesth. 2012;59:1130–1145.