Treatment for Deep Vein Thrombosis (DVT)
The recommended treatment for DVT is initial anticoagulation with low-molecular-weight heparin (LMWH) followed by oral anticoagulants, with duration determined by whether the DVT was provoked (3 months) or unprovoked (6-12 months or indefinite therapy). 1
Initial Anticoagulation Therapy
First-Line Treatment
- LMWH is the preferred initial anticoagulant for most patients with DVT 1
- Enoxaparin: 1 mg/kg twice daily or 1.5 mg/kg once daily
- Dalteparin: 200 U/kg once daily
- Tinzaparin: 175 U/kg once daily
- LMWH advantages over unfractionated heparin:
Special Considerations
- For patients with renal failure: Unfractionated heparin is preferred 1
- For patients with active cancer: LMWH is preferred over vitamin K antagonists for long-term therapy, with dose reduction to 75-80% of initial dose after the first month 1
Transition to Oral Anticoagulation
Vitamin K Antagonists (e.g., Warfarin)
- Target INR: 2.0-3.0 3, 1, 4
- Continue parenteral anticoagulation until INR ≥2.0 for at least 24 hours 1
Direct Oral Anticoagulants (DOACs)
- Standard-dose or lower-dose DOACs can be used for secondary prevention 3, 1
- Lower-dose options for secondary prevention:
- Rivaroxaban: 10 mg daily
- Apixaban: 2.5 mg twice daily 3
Duration of Anticoagulation
Provoked DVT (by temporary risk factors such as surgery, trauma, infection)
Unprovoked DVT
- 6-12 months of anticoagulation is recommended 1, 4
- The American Society of Hematology (ASH) suggests indefinite antithrombotic therapy over stopping anticoagulation (conditional recommendation) 3
Special Situations
- Cancer-associated DVT: Continue anticoagulation as long as cancer is active 1
- Recurrent DVT or high-risk thrombophilia: Consider indefinite anticoagulation 1, 4
- For patients with two or more documented episodes of DVT, indefinite treatment with anticoagulation is suggested 4
Management of Complications and Special Populations
Breakthrough DVT During Treatment
- For breakthrough DVT during therapeutic VKA treatment, ASH suggests using LMWH over DOAC therapy 3
Pregnancy
- Avoid vitamin K antagonists due to teratogenicity
- Use LMWH or unfractionated heparin throughout pregnancy 1
Monitoring and Follow-up
- Regular monitoring of renal function for patients on LMWH
- Monitor anti-Xa levels for patients on LMWH with renal impairment 1
- Consider compression stockings for prevention of post-thrombotic syndrome 1
Treatment Approach Based on Risk Stratification
Low-risk patients (provoked DVT with transient risk factor):
- Initial LMWH followed by oral anticoagulation for 3 months
- Can often be managed as outpatients
Intermediate-risk patients (unprovoked DVT):
- Initial LMWH followed by oral anticoagulation for 6-12 months
- Consider indefinite therapy based on bleeding risk assessment
High-risk patients (recurrent DVT, active cancer, high-risk thrombophilia):
- Initial LMWH (particularly for cancer patients)
- Extended or indefinite anticoagulation
- Closer monitoring for complications
The evidence strongly supports LMWH as initial therapy for most patients with DVT, with transition to oral anticoagulants for continued treatment. The duration of therapy should be tailored based on whether the DVT was provoked by temporary risk factors or unprovoked, with longer or indefinite therapy recommended for unprovoked events and patients with ongoing risk factors.