Immediate Treatment for Cerebral Venous Thrombosis (CVT)
Begin anticoagulation immediately with either intravenous unfractionated heparin or subcutaneous low-molecular-weight heparin (LMWH) as soon as CVT is confirmed by imaging, even if intracranial hemorrhage is present. 1, 2
Initial Anticoagulation Strategy
The cornerstone of acute CVT management is prompt anticoagulation, which prevents thrombus propagation, increases recanalization rates, and reduces mortality and severe disability. 3
Choice of anticoagulant:
Low-molecular-weight heparin (LMWH) is preferred as first-line therapy due to superior efficacy 2:
Intravenous unfractionated heparin (UFH) is an appropriate alternative when 2:
- LMWH is contraindicated or unavailable
- Severe renal failure is present (creatinine clearance <30 mL/min)
- Thrombolytic therapy may be needed
- Dosing: Initial bolus of 5000 IU, followed by continuous infusion of approximately 30,000 IU over 24 hours, adjusted to maintain aPTT at 1.5-2.5 times baseline 2
Critical Management Principle: Hemorrhage is NOT a Contraindication
The presence of intracranial hemorrhage related to CVT is explicitly NOT a contraindication to anticoagulation. 4, 1, 2, 3 This is because the hemorrhage results from venous congestion and infarction, not arterial bleeding, and the risk of thrombus propagation outweighs bleeding concerns. 2 Multiple studies confirm that anticoagulation does not increase hemorrhage volume or worsen clinical outcomes in patients with hemorrhagic CVT. 5, 6
Supportive Care and Monitoring
All patients should be admitted to a stroke unit for close monitoring and specialized care. 3 Concurrent management includes:
- Seizure management: Treat acute seizures aggressively with antiepileptic medications, particularly in patients with supratentorial lesions 3, 7
- Elevated intracranial pressure: Consider therapeutic lumbar puncture for severe headache and papilledema 3, 7
- Regular neurological assessment: Monitor for signs of deterioration including worsening consciousness, new focal deficits, or increased mass effect 2
Transition to Oral Anticoagulation
Early initiation of oral anticoagulants should begin during the acute phase 2:
- Continue parenteral anticoagulation for minimum 5 days AND until INR ≥2.0 for at least 24 hours 1, 2
- Target INR range: 2.0-3.0 (target 2.5) for vitamin K antagonists 1, 2
When to Escalate Treatment
Consider endovascular therapy or decompressive hemicraniectomy if 4, 2:
- Neurological deterioration or coma despite medical treatment
- Absolute contraindications to anticoagulation exist
- Failure of initial therapeutic anticoagulation
- Severe mass effect or large intracerebral hemorrhage causing progressive deterioration
Common Pitfalls to Avoid
- Do not delay anticoagulation due to presence of hemorrhage on imaging—this is the most common error 2, 3
- Do not withhold treatment while waiting for thrombophilia workup; anticoagulation should begin immediately upon diagnosis 1
- Do not use prolonged dexamethasone (>3 weeks) as it is associated with significant toxicity 3
- For patients with temporal lobe hemorrhage, enlarging hematomas, or midline shift, exercise greater caution and consider delaying anticoagulation until clinical stability is achieved for at least 24 hours 6