Treatment of Pulmonary Embolism
Anticoagulation is the cornerstone of treatment for pulmonary embolism (PE), with treatment approach stratified based on risk classification, with high-risk PE requiring immediate thrombolysis and intermediate/low-risk PE typically managed with anticoagulants alone. 1
Risk Stratification for Treatment Decision
Treatment should be guided by risk classification:
- 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 right ventricular dysfunction)
Acute Treatment Based on Risk Classification
High-Risk PE (with shock/hypotension)
- Immediate anticoagulation with unfractionated heparin (UFH) intravenously without delay (Class I, Level A) 1
- Systemic thrombolytic therapy is strongly recommended (Class I, Level A) 1
- Options include recombinant tissue plasminogen activator (rtPA), streptokinase, or urokinase
- rtPA is often preferred due to lower risk of hypotension and systemic symptoms 1
- Supportive measures (Class I, Level C) 1:
- Oxygen administration for hypoxemia
- Vasopressors for hypotension (norepinephrine and/or dobutamine)
- Avoid aggressive fluid challenge (Class III, Level B)
- If thrombolysis is contraindicated or fails:
Intermediate-Risk PE
- Anticoagulation is the primary treatment (Class I, Level A) 1
- LMWH or fondaparinux preferred over UFH (Class I, Level A)
- NOACs (apixaban, rivaroxaban, edoxaban, dabigatran) preferred over VKA when eligible (Class I, Level A) 1
- Thrombolysis:
Low-Risk PE
- Anticoagulation is the standard treatment (Class I, Level A) 1
- Thrombolysis should not be used (Class III, Level B) 1
- Early discharge and home treatment may be considered for carefully selected patients (Class IIa, Level A) 1
Anticoagulation Specifics
Initial Anticoagulation
- LMWH/fondaparinux: Preferred for most patients with non-high-risk PE (Class I, Level A) 1
- UFH: Preferred for high-risk PE, severe renal dysfunction, or high bleeding risk (Class I, Level C) 1
- Loading dose: 5,000-10,000 units
- Maintenance: 400-600 units/kg/day as continuous infusion
- Target APTT: 1.5-2.5 times control value 1
Oral Anticoagulation
- NOACs (apixaban, rivaroxaban, edoxaban, dabigatran):
- VKA (e.g., warfarin):
Duration of Anticoagulation
- Minimum duration: At least 3 months for all patients 1
- Extended duration:
- First PE with major transient/reversible risk factor: 3 months then discontinue 1
- Unprovoked PE or persistent risk factors: Extended/indefinite treatment should be considered (Class IIa) 1
- Recurrent VTE: Indefinite treatment recommended 1
- Cancer-associated PE: LMWH for at least 6 months, then continue LMWH or switch to VKA while disease active 1
- Antiphospholipid antibody syndrome: Indefinite VKA treatment (Class I) 1
Special Considerations
Inferior Vena Cava (IVC) Filters
- Not recommended for routine use (Class III, Level A) 1
- Consider in patients with:
Pregnancy
- LMWH is the treatment of choice (fixed doses based on early pregnancy weight) 1
- NOACs are contraindicated (Class III, Level C) 1
- Thrombolysis or surgical embolectomy should be considered for high-risk PE (Class IIa) 1
Common Pitfalls and Caveats
- Delay in treatment: Initiate anticoagulation immediately when PE is suspected with intermediate/high probability while awaiting diagnostic confirmation (Class I, Level C) 1
- Inappropriate risk stratification: Ensure proper assessment of hemodynamic status and right ventricular function to guide treatment decisions
- Premature discontinuation of anticoagulation increases thrombotic risk 2
- Neuraxial anesthesia risks: Consider timing of anticoagulant administration relative to spinal procedures to avoid epidural/spinal hematomas 2
- Monitoring requirements: Regular assessment of drug tolerance, adherence, renal/hepatic function, and bleeding risk during extended anticoagulation 1