Massive Transfusion Protocol
Activate your institutional massive transfusion protocol immediately when massive hemorrhage is anticipated or confirmed, and begin resuscitation with blood products in a 1:1:1 ratio of RBC:FFP:platelets while simultaneously controlling the bleeding source. 1, 2
Immediate Protocol Activation
Declare the massive transfusion situation immediately when you anticipate 1-1.5 blood volumes may need infusion acutely or within 24 hours—do not wait for laboratory confirmation or formal thresholds to be met. 3, 2 The nature of the injury pattern itself should trigger activation. 1
Critical Initial Actions (First 5 Minutes)
- Control obvious bleeding through direct pressure, tourniquets, or hemostatic dressings as the paramount priority. 1, 4
- Secure large-bore IV access: 8-Fr central access is ideal in adults; use intra-osseous or surgical venous access if peripheral fails. 3, 4
- Administer high FiO₂ to ensure adequate oxygenation. 1, 4
- Send baseline laboratory tests: FBC, PT, aPTT, Clauss fibrinogen (not derived), and cross-match. 3, 1 Use near-patient testing (TEG or ROTEM) if available for rapid coagulation assessment. 3, 4
Blood Product Resuscitation Strategy
The 1:1:1 Ratio Protocol
Administer blood products in a 1:1:1 ratio of RBC:FFP:platelets for severely injured patients with massive bleeding—this military-derived approach has shown improved survival in observational studies. 1, 2, 5 This balanced ratio prevents dilutional coagulopathy and approximates whole blood. 6, 7
Specific Product Administration
- Begin early FFP at 10-15 ml/kg to prevent dilutional coagulopathy before it develops—do not wait for coagulation test results. 1, 2
- Use warmed blood products exclusively: Start with O-negative blood if needed immediately, transition to group-specific (which can be issued without antibody screen in massive hemorrhage), then cross-matched blood. 3, 4, 2
- Maintain platelet count ≥75 × 10⁹/L throughout resuscitation. 3, 1, 2
Critical Pitfall to Avoid
Do not administer excessive crystalloid—this causes dilutional coagulopathy and worsens outcomes. 4 Fluid resuscitation in massive hemorrhage means warmed blood and blood components, not crystalloid. 3
Management of Coagulopathy
Fibrinogen Replacement
Target fibrinogen levels >1 g/L using fibrinogen concentrate or cryoprecipitate—fibrinogen <1 g/L represents established hemostatic failure and predicts microvascular bleeding. 1, 4, 2 Established coagulopathy requires more than 15 ml/kg of FFP to correct. 3, 1
Coagulation Monitoring
- Use Clauss fibrinogen (not derived fibrinogen, which is misleading). 3
- Monitor PT/aPTT: Values >1.5 times normal represent established hemostatic failure. 4
- Utilize TEG or ROTEM if available for real-time coagulation assessment and goal-directed therapy. 3, 5
Active Warming and Physiologic Optimization
Actively warm the patient and all transfused fluids using approved blood warming devices with visible thermometers and audible warnings—hypothermia exacerbates coagulopathy. 3, 4 Warming devices must be available in all emergency rooms and theatre suites, allowing adequate warming at high infusion rates. 3
Permissive Hypotension Until Bleeding Controlled
Restore organ perfusion but do not attempt to achieve normal blood pressure initially—aggressive normalization before bleeding control worsens outcomes. 3, 4 Once bleeding is controlled, aggressively normalize blood pressure, acid-base status, and temperature, but avoid vasopressors. 3, 4
Definitive Hemorrhage Control
Surgical Intervention
Consider surgery early—damage control surgery may be necessary, limited to controlling bleeding before complete physiologic normalization. 3, 4 Surgery may need to be interrupted and limited to "damage control" until bleeding is controlled and abnormal physiology can be corrected. 3
Imaging and Diagnostics
- Obtain rapid imaging (ultrasound, radiography, CT) or focused assessment with sonography for trauma if the patient is sufficiently stable. 3, 4
- Alert the theatre team about the need for cell salvage autotransfusion. 3, 4
Organizational Structure
Team Roles
Designate a team leader (usually the most senior physician) who declares the massive hemorrhage situation and coordinates management. 3, 2 Appoint a communications lead whose sole role is communicating with laboratories and other departments. 3
Allocate a dedicated member to convey blood samples and products between laboratory and clinical area—this person should be in constant radio communication. 3
Post-Resuscitation Management
Critical Care Admission
Admit to critical care for ongoing monitoring of coagulation, hemoglobin, blood gases, and wound drain assessment to identify overt or covert bleeding. 3, 1
Venous Thromboprophylaxis
Commence standard venous thromboprophylaxis as soon as hemostasis is secured—patients rapidly develop a prothrombotic state following massive hemorrhage. 3, 1, 4, 2 Temporary inferior vena cava filtration may be necessary. 3
Electrolyte Monitoring
Monitor and correct electrolyte abnormalities, particularly hypocalcemia from citrate toxicity, which can cause cardiac dysfunction. 1, 4
Common Pitfalls
- Delaying protocol activation increases mortality—activate immediately when massive hemorrhage is anticipated, not after formal thresholds are met. 1, 4
- Waiting for laboratory results before administering blood products in obvious massive hemorrhage increases mortality—begin transfusion based on clinical assessment. 1, 4
- Using hemoglobin level as the sole trigger for transfusion fails to account for the dynamic nature of hemorrhagic shock. 4
- Attempting to achieve normal blood pressure before bleeding control worsens outcomes—use permissive hypotension until hemorrhage is controlled. 3, 4