Management of Pulmonary Embolism Based on PE Score
Low-risk PE patients (PESI Class I/II or sPESI=0) should be managed as outpatients with direct oral anticoagulants (apixaban or rivaroxaban), while intermediate-risk patients (PESI Class III or higher) require inpatient management with standard anticoagulation and close monitoring, and high-risk patients (hemodynamically unstable) need immediate inpatient management with consideration of thrombolytic therapy. 1, 2
Risk Stratification Framework
The PESI score stratifies patients into five classes (I-V) based on 11 clinical variables including age, vital signs, comorbidities, and clinical findings. 3, 2 The score demonstrates excellent discriminatory power with area under the ROC curve of 0.77-0.87 for predicting 30-day mortality. 3, 2
Key mortality rates by PESI class:
- Class I (very low risk): ≤1.6% 30-day mortality 3, 2
- Class II (low risk): 3.6% 30-day mortality 3, 2
- Classes III-V (intermediate to high risk): 7.1% to 23.9% 30-day mortality 3
The simplified PESI (sPESI) uses six binary variables (age >80, cancer, chronic cardiopulmonary disease, pulse ≥110, systolic BP <100, oxygen saturation <90%), with a score of 0 identifying low-risk patients with 30-day mortality of 1.0-1.1%. 3, 1
Management Algorithm by Risk Category
Low-Risk Patients (PESI I/II or sPESI=0)
Outpatient management is appropriate when exclusion criteria are absent. 1, 2 Mandatory exclusion criteria include: physiologic instability, active bleeding or recent major bleeding risk, severe renal impairment, and social factors precluding safe discharge. 1
Anticoagulation options for outpatient management:
- Single-drug regimens: apixaban or rivaroxaban (preferred, no LMWH lead-in required) 1, 2
- LMWH bridge regimens: LMWH plus dabigatran or LMWH plus edoxaban 2
Critical implementation requirements:
- Same-day anticoagulation initiation before discharge 1
- Consultant or senior clinician review before discharge 2
- Robust pathway for follow-up and monitoring 3, 2
- Same-day investigation ideally completed 2
Intermediate-Risk Patients (PESI III or Higher with sPESI ≥1)
Inpatient management with standard anticoagulation and close monitoring is required. 1, 4 These patients need further stratification based on right ventricular dysfunction and cardiac biomarkers. 1
Initial anticoagulation strategy:
- Start anticoagulation immediately without waiting for complete diagnostic confirmation 4
- Use LMWH or fondaparinux for most intermediate-risk patients 4
- Reserve unfractionated heparin for high bleeding risk or severe renal dysfunction 4
Transition to oral anticoagulation:
- DOACs (apixaban, dabigatran, edoxaban, rivaroxaban) strongly preferred over vitamin K antagonists 4
- Apixaban and rivaroxaban offer single-drug regimens without LMWH lead-in 4
- Dabigatran and edoxaban require initial parenteral anticoagulation before transitioning 4
Monitoring and escalation:
- Close monitoring for clinical deterioration with assessment of RV function by imaging or biomarkers 4
- Routine primary thrombolysis is NOT recommended for stable intermediate-risk PE 4
- Rescue thrombolytic therapy is strongly recommended if hemodynamic deterioration develops despite anticoagulation 4
- Recalculate PESI at 48 hours (PESI-48) to identify candidates for early discharge 4
Hemodynamic support if needed:
- Supplemental oxygen for hypoxemia (SaO2 <90%), but avoid aggressive fluid challenges which may worsen RV failure 4
- Vasopressor support with norepinephrine and/or dobutamine if hemodynamic compromise develops, signaling need for rescue thrombolysis 4
High-Risk Patients (Hemodynamically Unstable)
Immediate inpatient management with consideration of thrombolytic therapy is required. 3, 1 Overwhelming consensus supports treating hemodynamically unstable patients with confirmed PE when benefits outweigh risks. 3
Critical Exceptions and Nuances
Right heart thrombus represents a critical exception where anatomic location significantly impacts prognosis, with mortality of 21% versus 11% without right heart thrombi. 1 Thrombolytic therapy is the only treatment independently associated with decreased mortality in this subset. 1
Concomitant DVT is an adverse prognostic factor independently associated with 30-day all-cause mortality (OR 1.9,95% CI 1.5-2.4). 1
Additional biomarkers for risk refinement:
- High-sensitivity troponin and sPESI combination may identify extremely low-risk patients (0% complicated outcomes when both sPESI=0 and hsTnT <14 pg/mL) 3
- However, sPESI alone had 100% negative predictive value in some cohorts, so adding hsTnT may not improve identification of very low-risk patients 3
Common Pitfalls to Avoid
Do not rely solely on RV dilation on imaging to exclude patients from outpatient management. 1 If RV dilation is present, measure cardiac biomarkers (BNP/troponin) for additional risk stratification. 1
Do not use routine bleeding risk scores beyond the exclusion criteria already outlined for patients deemed low-risk by PESI/sPESI. 1
Do not discharge patients without same-day anticoagulation. 1
Do not delay anticoagulation while awaiting complete diagnostic confirmation in intermediate-risk patients. 4
Do not prescribe DOACs to patients with severe renal impairment, pregnancy, or antiphospholipid syndrome. 4
Do not use routine thrombolysis in stable intermediate-risk patients, as bleeding risk outweighs benefit. 4