Initial Management of Hemorrhagic Diathesis
The immediate priority is to control active bleeding through direct pressure, tourniquets, or hemostatic dressings while simultaneously securing large-bore IV access and initiating resuscitation with warmed blood products rather than crystalloid. 1
Immediate Actions (First 15 Minutes)
Hemorrhage Control and Airway Management
- Apply direct pressure, tourniquets, or hemostatic dressings to all visible bleeding sites 1
- Secure airway and administer high FiO2, particularly if the patient has altered consciousness 1, 2
- Establish the largest bore IV access possible, ideally including central venous access 1, 2
Rapid Clinical Assessment
- If the patient is conscious, talking, and has a palpable peripheral pulse, blood pressure is adequate for the moment 1
- Assess for obvious blood loss (on clothing, floor, drains) and signs of internal bleeding 1
- Evaluate physiology: skin color, heart rate, capillary refill, and conscious level 1
Initial Laboratory Evaluation
- Draw baseline labs immediately: complete blood count, PT, aPTT, Clauss fibrinogen (not derived fibrinogen), and cross-match 1, 2
- Obtain near-patient testing with thromboelastography (TEG) or thromboelastometry (ROTEM) if available 1
- Measure serum lactate and base deficit to estimate bleeding severity 1
Resuscitation Strategy
Blood Product Administration
Begin fluid resuscitation with warmed blood and blood components, not crystalloid 1. The most recent European trauma guidelines (2023) recommend two initial strategies 1:
- Option 1: Fibrinogen concentrate or cryoprecipitate plus packed red blood cells
- Option 2: Fresh frozen plasma (FFP) with packed red blood cells in a ratio of at least 1:2 (FFP:pRBC)
Use blood group O initially for fastest availability, followed by group-specific, then cross-matched blood 1
Temperature Management
- Actively warm the patient and all transfused fluids to prevent hypothermia-induced coagulopathy 1, 2
Blood Pressure Targets
- Target systolic blood pressure of 80-100 mmHg until bleeding is controlled in patients without brain injury 1
- Avoid vasopressors during active bleeding 1
- Restore organ perfusion without achieving normal blood pressure initially 1
Goal-Directed Coagulation Management
Fibrinogen Replacement
Administer initial fibrinogen supplementation of 3-4 g fibrinogen concentrate or 15-20 single donor units of cryoprecipitate 1. Repeat doses should be guided by viscoelastic monitoring and laboratory fibrinogen levels 1.
Fresh Frozen Plasma
- Use FFP for PT/aPTT >1.5 times normal or viscoelastic evidence of coagulation factor deficiency 1, 2
- Avoid FFP solely for hypofibrinogenemia correction 1
Platelet Transfusion
- Maintain platelet count above 50 × 10⁹/L in ongoing bleeding 1
- Maintain platelet count above 75-100 × 10⁹/L in traumatic brain injury 1, 2
- Administer 4-8 single platelet units or one apheresis pack initially 1
Antifibrinolytic Therapy
Administer tranexamic acid 1 g over 10 minutes as soon as possible (ideally en route to hospital), followed by 1 g infused over 8 hours, within 3 hours of injury 1. Do not await viscoelastic assessment results before administration 1.
Calcium Supplementation
Monitor and maintain ionized calcium levels within normal range; administer calcium chloride to correct hypocalcemia 1
Definitive Bleeding Control
Surgical Intervention
- Consider damage-control surgery early in patients with hemorrhagic shock, ongoing bleeding, or coagulopathy 1
- Surgery may need to be interrupted and limited to damage control until bleeding is controlled 1
Imaging and Interventional Procedures
- Obtain rapid imaging (ultrasound, CT) when patient is sufficiently stable 1
- For pelvic fractures with hemorrhagic shock, perform immediate pelvic ring closure and stabilization 1
- Consider angioembolization or temporary extra-peritoneal packing if bleeding persists 1
Post-Resuscitation Care
Critical Care Monitoring
Admit to critical care for continuous monitoring of coagulation parameters, hemoglobin, blood gases, and wound drains 1, 2
Thromboprophylaxis
Commence standard venous thromboprophylaxis as soon as bleeding is controlled, as patients rapidly develop a prothrombotic state 1, 2
Common Pitfalls
- Avoid using derived fibrinogen levels—they are misleading; use Clauss fibrinogen only 1
- Do not delay tranexamic acid administration for laboratory confirmation 1
- Prevent dilutional coagulopathy by early FFP infusion rather than relying on crystalloid or colloid resuscitation 1
- Recognize that some patients compensate well despite significant blood loss; clinical assessment is paramount 1