Management of Suspected Hematoma in Patients on Apixaban (Eliquis)
Apixaban (Eliquis) should be held immediately if a hematoma is suspected, as continued anticoagulation could lead to expansion of the hematoma and increased morbidity and mortality.
Assessment of Hematoma
When a hematoma is suspected in a patient on apixaban, the following steps should be taken:
Evaluate the hematoma location and severity:
- Determine if the hematoma is in a critical location (intracranial, spinal, retroperitoneal)
- Assess for signs of hemodynamic instability or compartment syndrome
- Evaluate for mass effect or functional impairment
Laboratory assessment:
- Complete blood count to assess for anemia
- Renal function (as apixaban clearance is affected by renal function)
- Coagulation parameters (though standard tests may not accurately reflect apixaban activity)
Management Algorithm
Immediate Actions:
- Hold apixaban immediately regardless of hematoma location 1
- Monitor for expansion of the hematoma with appropriate imaging
For Life-Threatening Bleeding:
- Consider reversal with andexanet alfa for apixaban-related life-threatening bleeding, especially with intracranial hemorrhage 2
- If andexanet alfa is unavailable, administer prothrombin complex concentrate (PCC) at 25-50 U/kg 2
For Non-Life-Threatening Bleeding:
- Hold apixaban and monitor the hematoma
- Provide supportive care including local measures to control bleeding if accessible
- Monitor hemoglobin levels and provide blood products if necessary
Resumption of Anticoagulation
Resumption of apixaban should be considered only when:
- Adequate hemostasis is established (typically at least 24 hours after the bleeding has stopped) 1
- The risk of thrombosis outweighs the risk of recurrent bleeding
For patients with high thrombotic risk but ongoing concerns about bleeding:
- Consider starting with prophylactic doses of heparin or LMWH first
- Transition back to apixaban when bleeding risk is acceptably low 1
Special Considerations
Renal Function
- Apixaban has prolonged clearance in patients with renal impairment:
- Normal/mild impairment (CrCl ≥50 mL/min): 3-4 days to clear
- Moderate impairment (CrCl 30-50 mL/min): 4-5 days to clear
- Severe impairment (CrCl 15-29 mL/min): 5+ days to clear 1
Procedure Planning After Hematoma Resolution
If procedures are needed after hematoma resolution, consider the following discontinuation timeline:
- Normal/mild renal impairment: Stop 3 days before procedure
- Moderate renal impairment: Stop 4 days before procedure
- Severe renal impairment: Stop 5 days before procedure 1
Potential Complications
Apixaban-related hematomas can occur in various locations with serious consequences:
- Intracranial hemorrhage 3, 4
- Rectus sheath hematoma 5
- Intramural bowel hematoma leading to intussusception 6
- Other soft tissue hematomas
Key Pitfalls to Avoid
- Do not delay holding apixaban when a hematoma is suspected
- Do not restart anticoagulation prematurely before adequate hemostasis is achieved
- Do not underestimate the severity of anticoagulant-related bleeding complications
- Do not rely on standard coagulation tests to assess apixaban activity
- Do not bridge with heparin when stopping apixaban for procedures after hematoma resolution 1
By following this approach, you can minimize morbidity and mortality associated with apixaban-related hematomas while maintaining appropriate anticoagulation when it becomes safe to resume.