Treatment of Pulmonary Artery Thrombosis
For acute pulmonary artery thrombosis (pulmonary embolism), initiate immediate anticoagulation with unfractionated heparin (5,000-10,000 units bolus followed by continuous infusion) if the patient is hemodynamically unstable, or low-molecular-weight heparin/fondaparinux for stable patients, followed by transition to oral anticoagulation for a minimum of 3 months. 1, 2, 3
Immediate Management Based on Hemodynamic Status
High-Risk (Hemodynamically Unstable) Pulmonary Embolism
For patients with hypotension (systolic BP <90 mmHg) or cardiogenic shock:
- Initiate unfractionated heparin immediately with a bolus of 5,000-10,000 units followed by continuous infusion of 400-600 units/kg/day (or 30,000-40,000 units/24 hours), targeting aPTT 1.5-2.5 times control 1, 2, 3
- Unfractionated heparin is preferred over LMWH in this setting due to its short half-life and immediate reversibility 1
- Administer systemic thrombolysis immediately unless absolute contraindications exist (hemorrhagic stroke, recent major surgery/trauma, active bleeding, CNS neoplasm) 1, 2
- Alteplase (rtPA) is the preferred thrombolytic: 0.6 mg/kg over 15 minutes (maximum 50 mg) or 100 mg over 2 hours 1
Supportive measures for hemodynamically unstable patients:
- Administer high-flow supplemental oxygen to correct hypoxemia 1
- Administer colloids while monitoring central venous pressure, maintaining high right atrial pressure (15-20 mmHg) to ensure maximum right ventricular filling 1
- Correct systemic hypotension with vasopressors (phenylephrine preferred) to prevent right ventricular failure progression 1, 2
- Avoid diuretics, vasodilators, and opioids as they may worsen cardiovascular collapse 1
If thrombolysis fails or is contraindicated:
- Consider surgical pulmonary embolectomy as the primary alternative 1, 2, 3
- Catheter-based embolectomy or fragmentation may be considered if surgical expertise is unavailable 1, 2, 3
- ECMO may be necessary in extreme cases for stabilization 1
Intermediate and Low-Risk (Hemodynamically Stable) Pulmonary Embolism
For stable patients without hypotension:
- Initiate low-molecular-weight heparin (LMWH) or fondaparinux as preferred initial anticoagulation over unfractionated heparin 4, 2, 3
- LMWH dosing: typically 1 mg/kg subcutaneously twice daily 5
- Continue parenteral anticoagulation for at least 5 days before transitioning to oral therapy 3
- Reserve unfractionated heparin for patients with severe renal dysfunction (CrCl <30 mL/min) or high bleeding risk 3
Transition to Long-Term Oral Anticoagulation
Direct oral anticoagulants (DOACs) are preferred over warfarin for long-term therapy:
- Rivaroxaban: 15 mg twice daily with food for 21 days, then 20 mg once daily with food 6, 3
- Apixaban, dabigatran, or edoxaban are acceptable alternatives 2, 3
- DOACs offer predictable anticoagulant response without required monitoring 7
If DOACs are contraindicated, use vitamin K antagonists (warfarin):
- Target INR 2.0-3.0 4, 3
- Overlap with parenteral anticoagulation until INR ≥2.0 for at least 2 consecutive days 3
- Warfarin can be initiated as soon as diagnosis is confirmed 1
Duration of Anticoagulation
Minimum treatment duration is 3 months for all patients 4, 1, 2, 3
Extended anticoagulation beyond 3 months should be considered for:
- Unprovoked pulmonary embolism with low or moderate bleeding risk 4, 1, 2, 3
- Active cancer: use LMWH over warfarin for at least 6 months (edoxaban and rivaroxaban may be acceptable alternatives) 3
- Persistent risk factors such as antiphospholipid antibodies 8
For patients requiring extended anticoagulation, consider reduced-dose rivaroxaban (10 mg daily) or apixaban to balance efficacy and bleeding risk 3
Discontinue after 3 months for:
- Pulmonary embolism provoked by surgery or transient nonsurgical risk factor 4
- High bleeding risk patients 4
Special Considerations
In Situ Pulmonary Artery Thrombosis (Not Embolic)
Warfarin anticoagulation should be considered unless active uncontrolled hemoptysis is present:
- Target INR in the lower range of 2.0-2.5 due to higher bleeding risk in patients with pulmonary hypertension 4
- No controlled trials are available for this specific scenario, so management is based on expert consensus 4
Pediatric and Congenital Heart Disease Patients
For pulmonary embolism in patients with congenital heart disease:
- Target INR 2.0-3.0 for PE arising from right atrium or venous circulation 4
- Indefinite anticoagulation with warfarin should be considered in most patients with CHD 4
- Risk of paradoxical embolization is higher in patients with atrial-level shunts 4
Pregnancy
- Use LMWH as the anticoagulant of choice throughout pregnancy 3
- DOACs and warfarin are contraindicated in pregnancy 3
Follow-Up Care
Routine clinical evaluation 3-6 months after acute PE is mandatory 2, 3
Assessment should include:
- Evaluation for persistent dyspnea or functional limitation (screening for chronic thromboembolic pulmonary hypertension) 2, 3, 8
- Assessment of bleeding complications 3
- Screening for occult malignancy 3
- Risk-benefit assessment for anticoagulation duration 2, 3
- Measurement of D-dimer levels after discontinuation of therapy (elevated levels indicate higher recurrence risk) 8
Critical Pitfalls to Avoid
- Never delay anticoagulation while awaiting diagnostic confirmation in hemodynamically unstable patients 3
- Do not prematurely discontinue anticoagulation without considering coverage with another anticoagulant, as this increases thrombotic risk 6
- Avoid using DOACs in patients with severe renal impairment (CrCl <30 mL/min); use adjusted-dose LMWH or unfractionated heparin instead 3
- Do not use rivaroxaban or other DOACs in patients with prosthetic heart valves or triple-positive antiphospholipid syndrome 6
- Recognize that warfarin patients transitioning from XARELTO require adequate bridging to avoid periods of inadequate anticoagulation 6