Management of Embolism and Thrombosis
For confirmed venous thromboembolism (deep vein thrombosis or pulmonary embolism), immediately initiate anticoagulation with low-molecular-weight heparin (LMWH) or unfractionated heparin (UFH), followed by transition to oral anticoagulation for a minimum of 3 months. 1, 2
Immediate Assessment and Risk Stratification
Hemodynamic Status Evaluation
- Assess for massive PE immediately: Look for hypotension (systolic BP <90 mmHg), persistent hypotension requiring vasopressors, cardiogenic shock, collapse, unexplained hypoxia, engorged neck veins, and right ventricular gallop. 1, 2
- Check vital signs: Tachycardia, tachypnea (respiratory rate >20/min), hypoxia (O2 saturation <90%), and altered mental status indicate higher mortality risk. 1
- Calculate PESI score to stratify 30-day mortality risk: Class I-II (≤85 points) have <3.5% mortality; Class III-V (>85 points) have 7-24% mortality. 1
Imaging Strategy
- For massive PE with hemodynamic instability: Obtain CTPA or bedside echocardiography within 1 hour to confirm diagnosis and assess right ventricular dysfunction. 1, 2
- For non-massive PE: Imaging should ideally occur within 24 hours. 1
- McConnell sign on echocardiography (RV free wall hypokinesis with apical sparing) is highly specific for acute PE and justifies emergency treatment when CT is not immediately available. 2
Anticoagulation Protocol
Initial Parenteral Therapy
For hemodynamically stable patients (most cases):
- Start LMWH immediately without waiting for imaging confirmation if clinical suspicion is high. 1, 3
- LMWH is preferred over UFH for stable patients due to equal efficacy, lower bleeding risk, and feasibility of outpatient management. 1, 3
- Continue parenteral anticoagulation for minimum 5 days before transitioning to oral agents. 1, 4
For hemodynamically unstable patients or specific contraindications:
- Use UFH instead of LMWH if the patient has severe renal insufficiency (CrCl <30 mL/min), hemodynamic instability, high bleeding risk, or morbid obesity. 3
- UFH dosing: 5,000-10,000 units IV bolus, followed by continuous infusion at 1,300 units/hour (or weight-adjusted 80 units/kg bolus, then 18 units/kg/hour). 1, 2
- Monitor APTT: Check 4-6 hours after starting, then 6-10 hours after each dose adjustment, maintaining APTT at 1.5-2.5 times control (45-75 seconds). 1
Transition to Oral Anticoagulation
Direct oral anticoagulants (DOACs) - Preferred option:
- Dabigatran 150 mg twice daily after 5-10 days of parenteral anticoagulation (reduce to 75 mg twice daily if CrCl 15-30 mL/min). 4
- Rivaroxaban or apixaban can be started immediately without parenteral overlap in stable patients. 3, 5
- DOACs have equal efficacy to warfarin with lower bleeding risk, particularly lower intracranial hemorrhage. 3, 5
Warfarin - Alternative option:
- Start warfarin 5-10 mg daily while continuing heparin. 1
- Continue heparin for minimum 5 days AND until INR is 2.0-3.0 for 24 hours. 1
- Target INR 2.0-3.0 throughout treatment course. 1
- Monitor INR every 1-2 days initially, then adjust frequency based on stability. 1
Thrombolytic Therapy Decision
Indications for Thrombolysis
Administer thrombolytic therapy immediately if:
- Hemodynamic instability (hypotension, cardiogenic shock) with confirmed or highly suspected PE. 1, 2
- Cardiac arrest due to massive PE. 2
- In life-threatening massive PE with obstructive shock, ignore relative contraindications to thrombolysis as mortality risk exceeds bleeding risk. 2
Thrombolytic Dosing Regimens
- Alteplase 100 mg IV over 2 hours (standard regimen). 1, 2
- Alteplase 50 mg IV bolus for cardiac arrest, reassess at 30 minutes. 2
- Alternative accelerated regimen: 0.6 mg/kg over 15 minutes (maximum 50 mg) - equally effective with similar bleeding risk. 2
- Streptokinase: 250,000 units over 20 minutes, then 100,000 units/hour for 24 hours (plus hydrocortisone to prevent circulatory instability). 1
Absolute Contraindications to Thrombolysis
- Active or recent hemorrhage (within 3 weeks). 2
- Recent stroke (within 3 months). 2
- Current gastrointestinal bleeding. 2
- Recent major surgery or trauma. 1
However, in truly life-threatening PE with obstructive shock, these contraindications should be overridden. 2
Duration of Anticoagulation
Minimum Treatment Duration
Extended Anticoagulation Decision Algorithm
Provoked VTE with transient risk factors (surgery, trauma, immobilization):
Unprovoked VTE (no identifiable trigger):
- Continue anticoagulation beyond 3 months, consider indefinite therapy - recurrence risk is 10% per year off anticoagulation. 2, 3
- Reassess bleeding risk annually. 3
Active cancer:
- Use LMWH indefinitely (preferred over warfarin or DOACs due to superior efficacy). 3
Recurrent VTE:
- Indefinite anticoagulation required. 2
Special Populations and Situations
Pregnancy
- LMWH throughout pregnancy and 6 weeks postpartum - warfarin and DOACs are contraindicated. 3
Severe Renal Insufficiency (CrCl <30 mL/min)
- Use UFH or warfarin - most DOACs are contraindicated except dabigatran 75 mg twice daily (if CrCl 15-30 mL/min). 4, 3
Outpatient vs. Inpatient Management
- Up to 50% of PE patients can be managed as outpatients if hemodynamically stable, low PESI score (Class I-II), adequate home support, and no high bleeding risk. 1, 3
- All DVT patients without PE can be managed outpatient with LMWH or DOACs. 3
Common Pitfalls to Avoid
- Never delay anticoagulation while awaiting imaging if clinical suspicion is moderate-to-high - start heparin immediately. 1
- Do not use inferior vena cava filters as primary treatment when anticoagulation is feasible - filters do not reduce mortality and increase DVT risk. 3
- Do not give thrombolytics to hemodynamically stable patients - bleeding risk outweighs benefit in this population. 1
- Do not stop heparin prematurely when transitioning to warfarin - continue until INR therapeutic for 24 hours. 1
- Do not use DOACs in patients with mechanical heart valves - they are contraindicated and increase thrombotic risk. 4