›Immediate actions
›Hold anticoagulant
›Document last dose time estimate
›Local hemostatic measures
›Direct pressure
›Topical hemostatic agents when appropriate
›RBC transfusion strategy
›Symptomatic anemia
›Ongoing hemorrhagic shock
›Platelet transfusion strategy
›Platelets < 50 x 10^9/L with major bleeding
›Platelets < 100 x 10^9/L with intracranial bleeding
›Fibrinogen replacement
›Cryoprecipitate for fibrinogen < 1.5 g/L in major bleed
›Tranexamic acid
›1 g IV over 10 minutes for life-threatening bleeding
›1 g IV over 8 hours continuation in selected protocols
›Calcium replacement during massive transfusion
›Ionized calcium guided dosing
Vitamin K antagonist reversal (warfarin)
›Warfarin reversal pathway
›Four-factor PCC plus vitamin K for major bleeding
›PCC dosing per INR and weight
›INR 2-4
›25 IU/kg
›INR 4-6
›35 IU/kg
›INR > 6
›50 IU/kg
›Maximum dose per local protocol
›Vitamin K 10 mg IV for life-threatening bleeding
›Infusion over 20-60 minutes to reduce reaction risk
›Repeat INR reassessment
›30-60 minutes after PCC
›Additional PCC consideration for persistent elevation with ongoing bleeding
›Plasma use considerations
›PCC unavailable
›Volume overload risk acknowledgment
›Evidence and guideline alignment
›Rapid reversal with PCC favored over plasma in many guidelines for warfarin-associated intracranial hemorrhage (Class I recommendation in ICH-focused guidance)
Direct thrombin inhibitor reversal (dabigatran)
›Dabigatran pathway
›Idarucizumab
›5 g IV total
›2.5 g IV x 2 doses
›Back-to-back administration acceptable
›Rebound anticoagulant effect risk
›Consider repeat labs and clinical reassessment
›Activated charcoal
›Recent ingestion window
›Within 2 hours typical consideration
›Airway protected requirement if altered mental status
›Hemodialysis
›Life-threatening bleeding with renal failure or massive exposure
›Significant dabigatran removal compared with factor Xa inhibitors
›Evidence and guideline alignment
›Specific antidote use supported in intracranial hemorrhage guidance (Class I recommendation in ICH-focused guidance)
Factor Xa inhibitor reversal (apixaban, rivaroxaban, edoxaban, betrixaban)
›Factor Xa inhibitor pathway
›Andexanet alfa when available and appropriate
›Dosing per agent and last dose timing per institutional protocol
›Thrombotic risk counseling and monitoring
›Four-factor PCC alternative
›50 IU/kg commonly used in many institutional pathways
›Maximum dose per local protocol
›Activated charcoal
›Recent ingestion window
›Within 2 hours typical consideration
›Airway protected requirement if altered mental status
›Evidence and guideline alignment
›Andexanet alfa supported for factor Xa inhibitor reversal in ICH-focused guidance (Class IIa in many summaries)
›PCC used when andexanet unavailable or unsuitable in many pathways
Unfractionated heparin reversal
›UFH pathway
›Protamine
›1 mg per 100 units heparin given in previous 2-3 hours
›Maximum 50 mg per dose in many protocols
›Slow IV administration to reduce hypotension risk
›Monitoring
›aPTT or anti-Xa reassessment after protamine
›Evidence alignment
›Protamine use suggested for life-threatening bleeding in heparin therapy guidance
Low molecular weight heparin reversal (enoxaparin and similar)
›LMWH pathway
›Protamine partial reversal
›Within 8 hours of LMWH dose
›1 mg protamine per 1 mg enoxaparin equivalent
›8-12 hours after dose
›0.5 mg protamine per 1 mg enoxaparin equivalent
›Second dose consideration
›0.5 mg protamine per 1 mg enoxaparin equivalent if ongoing bleeding
›Anti-Xa monitoring limitations
›Clinical hemostasis as primary endpoint
Fondaparinux-associated bleeding
›Fondaparinux pathway
›No specific antidote widely available
›PCC consideration in life-threatening bleeding per institutional protocol
›Supportive care emphasis
›Source control priority
Adjuncts and special therapies
›Desmopressin consideration
›Suspected uremic platelet dysfunction
›Antiplatelet co-exposure with critical bleeding site
›Antifibrinolytic coordination
›Trauma protocols alignment when trauma suspected
›Thrombosis mitigation after reversal
›Mechanical VTE prophylaxis when safe
›Restart anticoagulant planning after hemostasis
Evidence framework summary
›Guideline concepts
›ACC consensus pathway focus
›Bleeding severity stratification
›Temporary interruption
›Reversal for life-threatening bleeding
›Restart assessment after control