Management of Acute Pulmonary Embolism
The management of acute pulmonary embolism should be stratified based on risk assessment, with high-risk PE requiring immediate thrombolysis, intermediate-risk PE requiring anticoagulation with close monitoring, and low-risk PE treated with direct oral anticoagulants as first-line therapy. 1
Risk Stratification
Risk stratification is essential for determining the appropriate treatment approach:
- High-risk PE (hemodynamically unstable with shock/hypotension)
- Intermediate-risk PE (hemodynamically stable with right ventricular dysfunction and/or myocardial injury)
- Low-risk PE (hemodynamically stable without RV dysfunction)
Initial Management
High-Risk PE (with shock or hypotension)
Anticoagulation: Initiate unfractionated heparin without delay 2
- IV bolus of 80 U/kg followed by infusion at 18 U/kg/h
- Adjust dose based on aPTT (target 1.5-2.5 times control)
Hemodynamic support:
Thrombolytic therapy:
When thrombolysis is contraindicated or fails:
Intermediate-Risk PE (hemodynamically stable with RV dysfunction)
Anticoagulation: Primary treatment approach 1
Thrombolysis:
Low-Risk PE (hemodynamically stable without RV dysfunction)
- Anticoagulation:
Anticoagulation Therapy Details
Initial Anticoagulation
- NOACs (preferred): Apixaban, rivaroxaban, edoxaban, or dabigatran 1
- LMWH (e.g., enoxaparin): 1 mg/kg twice daily subcutaneously 3
- Fondaparinux: Weight-based dosing
- Unfractionated heparin: Reserved for patients with severe renal impairment (CrCl <30 mL/min) or high bleeding risk 2
Duration of Anticoagulation
Minimum 3 months for all patients 1
Consider extended/indefinite anticoagulation for:
- Recurrent PE not related to transient risk factors
- Unprovoked PE
- Persistent risk factors
- Antiphospholipid syndrome 1
After 6 months of extended anticoagulation, reduced doses of apixaban or rivaroxaban may be considered 1
Special Populations
Cancer Patients
- Edoxaban or rivaroxaban should be considered as alternatives to LMWH, except in patients with gastrointestinal cancer 1
Pregnancy
- NOACs not recommended during pregnancy or lactation 1
- LMWH is the anticoagulant of choice
- Thrombolysis or surgical embolectomy should be considered for pregnant women with high-risk PE 1
Renal Impairment
- For severe renal impairment (CrCl <30 mL/min), use unfractionated heparin with aPTT monitoring 2
- Avoid rivaroxaban in patients with CrCl <15 mL/min 4
Contraindications to Anticoagulation
When anticoagulation is contraindicated (e.g., active major bleeding, recent intracranial hemorrhage):
- Consider inferior vena cava filter placement as a temporary measure 5
- Resume anticoagulation as soon as contraindication resolves
Follow-up
- Routine clinical evaluation 3-6 months after acute PE 1
- Assessment should include:
- Persistent symptoms
- Medication adherence
- Complications
- Need for extended anticoagulation
- Refer to specialized center for chronic thromboembolic pulmonary hypertension (CTEPH) evaluation if persistent symptoms and perfusion defects 1
Common Pitfalls and Caveats
- Avoid delaying anticoagulation while awaiting diagnostic confirmation in patients with high clinical suspicion 2
- Do not initiate NOACs in hemodynamically unstable patients with PE 4
- Avoid routine thrombolysis in non-high-risk PE patients 2
- Do not use NOACs in patients with triple-positive antiphospholipid syndrome due to increased risk of recurrent thrombosis 4
- Avoid NOACs in patients with mechanical heart valves 4
- Monitor closely for bleeding complications, especially in elderly patients, those with renal impairment, or low body weight 3, 4