Conservative Management of Pulmonary Embolism
Immediate Anticoagulation is the Cornerstone
Anticoagulation should be initiated immediately in patients with intermediate or high clinical probability of PE, even before diagnostic imaging is completed, as this approach reduces mortality. 1
Initial Anticoagulant Selection
The choice of initial anticoagulant depends on clinical severity and patient factors:
Low-molecular-weight heparin (LMWH) is preferred over unfractionated heparin (UFH) for most patients with non-massive PE due to equal efficacy, superior safety profile, predictable pharmacokinetics, and ease of administration without laboratory monitoring. 1, 2, 3
- LMWH dosing: Enoxaparin 1 mg/kg subcutaneously twice daily or 1.5 mg/kg once daily 2
- Both once-daily and twice-daily regimens show equivalent efficacy with recurrence rates of 2.9-4.4% 2
Unfractionated heparin should be reserved for specific situations: 1
- Massive PE with hemodynamic instability
- Patients requiring potential rapid reversal (impending procedures)
- Severe renal failure (eGFR <30 mL/min) 1
- Very obese patients 4
UFH dosing when indicated: 1
- Loading dose: 80 U/kg IV bolus (or 5,000-10,000 units) 1
- Maintenance: 18 U/kg/hour continuous infusion 1
- Target aPTT: 1.5-2.5 times control (45-75 seconds) 1
- Monitor aPTT 4-6 hours after bolus, 6-10 hours after dose changes, then daily 1
Transition to Oral Anticoagulation
Warfarin should be started once PE is confirmed, overlapping with parenteral anticoagulation for at least 5 days AND until INR reaches 2.0-3.0 for at least 24 hours. 1
- Initial warfarin dosing: 5-10 mg daily for 2 days 1
- Target INR: 2.0-3.0 1
- Monitor INR every 1-2 days initially 1
- The requirement for overlapping heparin was established by randomized trials showing three-fold higher recurrence rates with warfarin monotherapy 1
Duration of anticoagulation: 1
- 4-6 weeks for temporary/reversible risk factors (surgery, trauma, immobilization) 1
- 3 months minimum for first idiopathic PE 1, 4
- 6-12 months for recurrent PE or persistent risk factors 1, 4
Direct Oral Anticoagulants (DOACs)
Apixaban is not recommended as initial therapy in hemodynamically unstable patients or those requiring thrombolysis/embolectomy—UFH remains the standard. 5
- DOACs should be avoided in triple-positive antiphospholipid syndrome due to increased thrombotic recurrence 5
- Neuraxial procedures require 24-hour delay after last apixaban dose, with 5-hour delay before next dose after catheter removal 5
Supportive Care Measures
Oxygen therapy should be administered to maintain adequate saturation in hypoxemic patients. 1
Fluid resuscitation with colloid is indicated for hypotensive patients, targeting right atrial pressure of 15-20 mm Hg to maximize right ventricular filling. 1
Analgesia for pleuritic pain should avoid opiates in patients with incipient cardiovascular collapse, as opiates cause vasodilation. 1
Diuretics and vasodilators are contraindicated in acute PE. 1
Risk Stratification for Outpatient Management
Selected low-risk patients can be safely managed as outpatients when robust follow-up pathways exist. 1
Use validated risk scores to identify candidates: 1
- PESI class I/II
- Simplified PESI score of 0
- Hestia criteria met
Absolute exclusion criteria for outpatient management: 1
- Hemodynamic instability (HR >110 bpm, SBP <100 mm Hg, shock requiring inotropes)
- Oxygen saturation <90% on room air
- Active bleeding or high bleeding risk
- Already on therapeutic anticoagulation at time of PE
- Severe pain requiring opiates
- Other comorbidities requiring admission
- CKD stage 4-5 (eGFR <30 mL/min) or severe liver disease
- Recent heparin-induced thrombocytopenia
- Social barriers (inability to return home, lack of support, compliance concerns)
RV dilatation on imaging with elevated cardiac biomarkers (BNP, NT-proBNP, troponin) should prompt inpatient observation even in otherwise low-risk patients. 1
Critical Pitfalls to Avoid
Never delay anticoagulation while awaiting imaging in intermediate or high probability patients—the mortality benefit of early treatment outweighs bleeding risk. 1
Do not use fixed-dose UFH—weight-adjusted dosing with aPTT monitoring achieves therapeutic levels faster and reduces fluctuations. 1
Avoid starting warfarin before PE is confirmed—only initiate oral anticoagulation after diagnostic confirmation. 1
Do not discontinue heparin prematurely—continue for minimum 5 days AND until INR therapeutic for 24 hours. 1
Monitor platelet count if UFH continued beyond 5 days due to risk of heparin-induced thrombocytopenia with thrombosis. 1