Management of Haematuria Post Stroke Thrombolysis
Immediately discontinue the thrombolytic infusion if haematuria develops, as this represents a bleeding complication requiring urgent intervention. 1
Immediate Actions and Assessment
Stop thrombolysis immediately upon recognition of haematuria, as continued infusion will worsen bleeding. 1, 2
Obtain urgent laboratory work including:
- Complete blood count with platelets 1, 2
- PT/INR and aPTT to assess coagulation status 1, 2
- Type and cross-match blood products in preparation for potential transfusion 1, 2
Monitor vital signs closely with particular attention to blood pressure and heart rate to detect hemodynamic compromise. 1, 2
Pharmacological Reversal
Administer tranexamic acid 1000 mg IV infused over 10 minutes as the first-line antifibrinolytic agent for active bleeding. 1, 2
Alternative antifibrinolytic therapy includes ε-aminocaproic acid at 4-5 g IV over 1 hour, followed by 1 g IV until bleeding is controlled. 1, 2 Tranexamic acid competitively inhibits the activation of plasminogen and can reverse thrombolysis in the setting of hemorrhage after IV thrombolytic therapy. 3
If the patient was receiving vitamin K antagonists concurrently, administer vitamin K 5-10 mg by slow IV injection. 1, 2
For severe bleeding with hemodynamic compromise, consider administration of 6-8 units of cryoprecipitate containing factor VIII or 6-8 units of platelets. 2
Supportive Care and Monitoring
Maintain adequate hydration to promote urinary flow and prevent clot formation in the urinary tract. 1, 2
Consider urinary catheterization with gentle irrigation if clots are causing obstruction, but use caution as this may exacerbate bleeding. 2
Avoid unnecessary invasive procedures for at least 24 hours after thrombolysis to prevent additional bleeding sites. 1, 2
Volume replacement with colloids should be administered if needed, along with RBC transfusion if hemoglobin drops significantly. 1
Transfusion Thresholds
Transfuse packed red blood cells to maintain adequate oxygen-carrying capacity based on clinical assessment and hemoglobin levels. 1
Platelet transfusion should be considered if thrombocytopenia ≤60 × 10⁹/L or thrombopathy is present. 1
Resuming Anticoagulation After Bleeding Resolution
Do not restart heparin until aPTT has decreased to less than twice the normal control value. 1, 2
When restarting anticoagulation is necessary after bleeding resolution, initiate heparin without a loading dose when aPTT falls below 2× the upper limit of normal. 1, 2
Target aPTT should be 1.5 to 2 times normal (55 to 80 seconds) with initial dosing typically around 1,300 U/hour. 1, 2
Monitor aPTT closely: check four times every 6 hours for the first 24 hours, then three times every 8 hours, then daily due to rapidly changing levels of fibrinogen and heparin binding proteins. 4
For long-term anticoagulation in high-risk patients, consider low molecular weight heparin at 75-80% of the initial dose rather than vitamin K antagonists. 1, 2
Investigation of Underlying Pathology
Once the patient is stabilized, investigate for underlying urological pathology, as up to 25% of patients with gross haematuria while on anticoagulant therapy may have underlying neoplastic disease. 1, 2
Consider urological evaluation with cystoscopy after stabilization if haematuria persists beyond the acute bleeding episode. 1, 2
Special Considerations
Elderly patients (>75 years) have a higher risk of bleeding complications with thrombolytic therapy and require more aggressive monitoring and management. 1, 2 However, renal dysfunction itself does not increase the risk of bleeding complications or poor outcomes after thrombolysis. 5, 6
Patients with renal dysfunction may have prolonged heparin effect and altered clearance of tranexamic acid, requiring dose adjustments. 1
Critical Pitfalls to Avoid
Never restart thrombolytic therapy after a significant bleeding episode. 1, 2
Do not use automatic blood pressure cuffs on the same arm as venous access to prevent hematoma formation. 1, 2
Do not overlook the possibility of underlying urological pathology as the cause or contributor to haematuria. 2
Avoid invasive procedures such as arterial punctures or insertion of catheters for at least 24 hours after thrombolytic therapy. 2