Approach to Pulmonary Embolism
Start anticoagulation immediately when PE is suspected based on clinical probability, even before diagnostic confirmation is complete, unless the patient has active bleeding or absolute contraindications. 1
Initial Assessment and Risk Stratification
Hemodynamic Status Evaluation
- Perform bedside transthoracic echocardiography (TTE) immediately in patients presenting with hemodynamic instability to differentiate high-risk PE from other acute life-threatening conditions 1
- Identify high-risk PE by presence of systemic hypotension (systolic BP <90 mmHg), cardiogenic shock, or sudden collapse with elevated jugular venous pressure 1
- Recognize that most PE patients present with breathlessness and/or tachypnea (respiratory rate >20/min) 1, 2
Clinical Probability Assessment
- Use validated diagnostic algorithms incorporating standardized clinical probability assessment and D-dimer testing to avoid unnecessary imaging and radiation exposure 1
- Score major risk factors including: recent immobilization or major surgery, recent lower limb trauma/surgery, clinical deep vein thrombosis, previous proven DVT/PE, pregnancy/postpartum, or major medical illness 1, 2
- Consider classic presentations: sudden collapse with raised JVP, pulmonary hemorrhage syndrome (pleuritic pain/hemoptysis), or isolated dyspnea 1, 2
- Note that PE is rare in patients under age 40 without risk factors 1, 2
Diagnostic Testing
- Normal D-dimer levels exclude PE in patients with low to intermediate clinical probability 1
- Proceed to CT pulmonary angiography (CTPA) for patients with high clinical probability or elevated D-dimer 1
- If CTPA reports single subsegmental PE, consider false-positive findings and discuss with radiology for second opinion before committing to anticoagulation 1
Immediate Anticoagulation Management
Hemodynamically Stable Patients
Prefer novel oral anticoagulants (NOACs) over traditional LMWH-warfarin regimen unless contraindications exist 1
NOAC Therapy (First-Line)
- Rivaroxaban 15 mg twice daily for 21 days, then 20 mg once daily for treatment of acute PE 3
- Administer with food to ensure optimal absorption 3
- Avoid rivaroxaban in hemodynamically unstable patients who may require thrombolysis or pulmonary embolectomy 3
- Do not use in patients with CrCl <30 mL/min, moderate-to-severe hepatic impairment (Child-Pugh B or C), or triple-positive antiphospholipid syndrome 3
Alternative: Weight-Adjusted Heparin
- Initial bolus: 80 IU/kg IV, followed by continuous infusion of 18 IU/kg/hour 1, 2
- Target aPTT 1.5-2.5 times control (45-75 seconds) 1, 2
- Check aPTT 4-6 hours after initial bolus, then daily once therapeutic 1, 2
- Failure to achieve adequate anticoagulation (aPTT >1.5 times control) within 24 hours is associated with 25% risk of recurrent VTE 4
- Continue heparin for 7-10 days while overlapping with warfarin during last 4-5 days 1, 4
Warfarin Transition
- Target INR 2.0-3.0 (therapeutic range 2.0-3.0) 1, 5
- Continue heparin until INR therapeutic for 2 consecutive days 1
Hemodynamically Unstable Patients (High-Risk PE)
Systemic thrombolysis is indicated for patients with systemic hypotension or cardiogenic shock 1, 2
Thrombolytic Regimens
- rtPA: 100 mg IV over 2 hours (first-line) 1, 2
- Streptokinase: 250,000 units over 20 minutes, then 100,000 units/hour for 24 hours (plus hydrocortisone to prevent circulatory instability) 1
- Urokinase: 4,400 IU/kg over 10 minutes, then 4,400 IU/kg/hour for 12 hours 1
- Stop heparin before thrombolysis; resume maintenance dose after completion 1
Rescue Interventions
- Consider surgical embolectomy if thrombolysis is contraindicated or fails to produce clinical improvement within one hour 1
- Catheter-directed treatment is an alternative reperfusion option when surgical expertise is available 1
Intermediate-High Risk PE
- Reperfusion is not first-line treatment 1
- Prospectively plan management strategy with contingency plan ready if clinical deterioration occurs 1
- Monitor closely for signs of hemodynamic decompensation requiring escalation to thrombolysis 1
Special Populations
Cancer Patients
- Low molecular weight heparin (LMWH) is superior to NOACs and should be continued indefinitely while cancer is active 6
- The optimal anticoagulant regimen after the first 6 months requires further study 1
Pregnant Patients
- Consider diagnostic pathways including CTPA or V/Q scan, which can be used safely during pregnancy 1
- Anticoagulation dosing in pregnancy has not been well-studied; promptly evaluate any signs of blood loss 3
Antiphospholipid Syndrome
- Test for antiphospholipid antibodies in unprovoked or recurrent PE 6
- NOACs are contraindicated in triple-positive APS; use warfarin (INR 2.0-3.0) instead 6, 3
Duration of Anticoagulation
Initial Treatment Phase
- Minimum 3 months anticoagulation for all confirmed PE 1, 5
- Continue for 3 months if PE provoked by major transient/reversible risk factor 1, 6
Extended Therapy Decision (After 3-6 Months)
Re-examine patient after initial 3-6 months to weigh benefits versus bleeding risks for extended anticoagulation 1
- Discontinue after 3 months: First episode with strong transient/reversible risk factor 1, 6
- Continue indefinitely: Unprovoked PE, recurrent VTE, or active cancer 1, 6
- Consider reduced-dose anticoagulation for extended therapy to minimize bleeding risk 1
Contraindications and Filters
IVC Filter Indications
Place IVC filter only in patients with: 1
- Absolute contraindication to anticoagulation, OR
- Recurrent PE despite adequate anticoagulation 1
Follow-Up and Long-Term Monitoring
Structured Follow-Up Schedule
- Initial follow-up within 1-2 weeks of discharge 7
- Comprehensive assessment at 6-12 weeks 7
- Yearly examinations for patients on extended anticoagulation 1
Surveillance for Complications
- Ask about persistent or new-onset dyspnea or functional limitation at every visit 1
- If symptomatic after 3 months, implement staged diagnostic workup to exclude chronic thromboembolic pulmonary hypertension (CTEPH) 1, 7
- Screen for VTE recurrence, occult malignancy, and bleeding complications 1
- Routine follow-up imaging is not recommended in asymptomatic patients 1
Critical Pitfalls to Avoid
- Never delay anticoagulation while awaiting diagnostic confirmation in high or intermediate probability cases 1
- Do not use rivaroxaban as initial therapy in hemodynamically unstable PE requiring potential thrombolysis 3
- Avoid premature discontinuation of anticoagulation, as this increases thrombotic risk 3
- Do not lose patients to follow-up after acute treatment; lifelong VTE recurrence risk exists except when provoked by strong transient factors 1
- Ensure adequate initial anticoagulation intensity to prevent the 25% recurrence rate associated with subtherapeutic dosing 4