Management of Pulmonary Embolism
Immediate risk stratification and appropriate anticoagulation therapy are the cornerstones of pulmonary embolism management, with thrombolysis reserved for hemodynamically unstable patients with high-risk PE. 1
Risk Stratification
Risk stratification is essential for determining the appropriate management approach:
High-risk (massive) PE
- Characterized by hemodynamic instability, shock, or hypotension
- Systolic BP <90 mmHg or drop of ≥40 mmHg for >15 minutes
- Requires immediate intervention
Intermediate-risk (submassive) PE
- Hemodynamically stable with right ventricular dysfunction
- Evidence of myocardial injury (elevated troponin)
- Higher risk of decompensation than low-risk PE
Low-risk PE
- Hemodynamically stable without right ventricular dysfunction
- No evidence of myocardial injury
Diagnostic Approach
Clinical Probability Assessment
- Assess risk factors: recent immobilization, surgery, trauma, DVT, previous PE, pregnancy, malignancy
- Evaluate symptoms: sudden dyspnea, chest pain, hemoptysis, syncope
Laboratory Testing
- D-dimer: Useful for excluding PE in patients with low/intermediate clinical probability
- For patients >50 years, use age-adjusted D-dimer cutoff (age × 10 ng/mL) 1
- Negative D-dimer safely excludes PE in appropriate clinical context
Imaging
- CT pulmonary angiography (CTPA): First-line imaging test for most patients
- Immediate bedside echocardiography: For suspected high-risk PE to assess RV dysfunction
- Leg ultrasound: Alternative when lung imaging is contraindicated or unavailable
Treatment Algorithm
1. High-Risk PE (Hemodynamically Unstable)
Immediate Actions:
- Oxygen supplementation
- Hemodynamic support (vasopressors if needed)
- Systemic thrombolysis (Class I recommendation) 1
- Alteplase 100 mg over 2 hours or 0.6 mg/kg over 15 min (max 50 mg)
- Streptokinase 250,000 IU loading dose over 30 min, then 100,000 IU/h for 24h
- Urokinase 4,400 IU/kg loading dose, then 4,400 IU/kg/h for 12-24h
If thrombolysis contraindicated or fails:
2. Intermediate-Risk PE
Anticoagulation therapy:
Close monitoring for signs of hemodynamic deterioration
- Consider rescue thrombolysis if decompensation occurs
3. Low-Risk PE
- Anticoagulation therapy:
Anticoagulation Regimens
Direct Oral Anticoagulants (Preferred)
Rivaroxaban 3
- 15 mg twice daily for 21 days
- Then 20 mg once daily for at least 3 months
Apixaban 4
- 10 mg twice daily for 7 days
- Then 5 mg twice daily for at least 3 months
Traditional Anticoagulation
Initial therapy:
- LMWH (preferred over unfractionated heparin)
- Unfractionated heparin: 80 IU/kg bolus, then 18 IU/kg/hour
- Adjust to maintain APTT 1.5-2.5 times control
Long-term therapy:
- Warfarin (target INR 2-3)
- Start simultaneously with parenteral anticoagulation
- Continue parenteral anticoagulation for at least 5 days and until INR ≥2.0 for 24 hours
Duration of Anticoagulation
- Minimum 3 months for all patients 1
- Extended anticoagulation considered for:
- Unprovoked PE
- Persistent risk factors
- Recurrent VTE
Special Considerations
IVC Filter Placement
- Consider only in patients with:
Follow-up
- Clinical evaluation at 3-6 months after acute PE
- Assess for persistent symptoms, signs of recurrence, bleeding complications
- Evaluate for chronic thromboembolic pulmonary hypertension (CTEPH) if persistent symptoms
Common Pitfalls to Avoid
- Delaying anticoagulation while awaiting diagnostic confirmation in patients with high clinical suspicion
- Inappropriate use of thrombolysis in hemodynamically stable patients without evidence of clinical deterioration
- Failure to consider PE in patients with unexplained dyspnea, tachycardia, or hypoxemia
- Inadequate risk stratification leading to inappropriate treatment intensity
- Premature discontinuation of anticoagulation therapy, which increases risk of recurrent VTE
By following this structured approach to PE management, clinicians can effectively reduce mortality and morbidity associated with this potentially life-threatening condition.