Pulmonary Embolism Work-Up
Begin by assessing clinical probability using a validated scoring system, then proceed with D-dimer testing in low/intermediate probability patients or proceed directly to CT pulmonary angiography (CTPA) in high probability patients, while initiating anticoagulation immediately in intermediate or high probability cases before imaging confirmation. 1
Initial Clinical Assessment
Most patients with PE present with breathlessness and/or tachypnea >20 breaths/min; in the absence of these findings, pleuritic chest pain or hemoptysis is usually due to another cause. 1
Clinical Probability Stratification
Assess clinical probability by asking two key questions: 1
- Is another diagnosis unlikely? (chest radiograph and ECG are helpful for excluding alternatives)
- Is a major risk factor present? (recent immobilization/major surgery, lower limb trauma or surgery, pregnancy/postpartum, major medical illness, previous proven VTE)
Scoring: 1
- Low probability = neither criterion present
- Intermediate probability = either criterion present
- High probability = both criteria present
Alternatively, use the Wells score or revised Geneva score to stratify patients into probability categories. 2
Baseline Testing
Obtain these tests in all patients with suspected PE: 1, 2
- Chest radiograph (abnormal in >80% of PE cases, though findings are non-specific; helps exclude alternative diagnoses) 2
- ECG (may reveal right ventricular strain patterns: T-wave inversion V1-V4, S1Q3T3, right bundle branch block) 2
- Arterial blood gas (does not have sufficient sensitivity/specificity to confirm or exclude PE, but helps assess clinical probability) 3
Critical pitfall: Up to 40% of patients with PE have normal arterial oxygen saturation—normal SaO₂ should never be used to exclude PE. 2
Diagnostic Algorithm for Non-Massive PE
Step 1: D-Dimer Testing (Selective Use)
D-dimer should only be performed after clinical probability assessment and has strict limitations: 1
Do NOT perform D-dimer if: 1
- Alternative diagnosis is highly likely
- Clinical probability is HIGH
- Probable massive PE is present
- Patient is hospitalized with infection, cancer, inflammation, or recent surgery (D-dimer will be elevated in <10% of these cases) 1
Validated D-dimer assays that reliably exclude PE when negative: 1
- SimpliRED (agglutination): for LOW clinical probability only
- Vidas (ELISA): for LOW or INTERMEDIATE clinical probability (cutoff <500 μg/L)
- MDA (latex): for LOW or INTERMEDIATE clinical probability
If D-dimer is negative in appropriate patients, PE is excluded and no further testing is needed. 1, 3
Step 2: Lower Extremity Venous Ultrasound
Leg ultrasound is an alternative to lung imaging in patients with clinical signs of DVT. 1
- If DVT is confirmed, treat for VTE without requiring lung imaging 1
- If ultrasound is normal but D-dimer is elevated, proceed with lung imaging (50% of PE patients have normal leg ultrasound) 1
Step 3: Imaging
CTPA is now the recommended initial lung imaging modality for non-massive PE. 1
- Patients with good quality negative CTPA do not require further investigation or treatment for PE 1
- CTPA allows visualization of pulmonary thromboemboli down to the segmental level and assessment of RV enlargement 4
Isotope lung scanning (V/Q scan) may be considered as initial imaging IF: 1
- Facilities are available on-site, AND
- Chest radiograph is normal, AND
- No significant symptomatic concurrent cardiopulmonary disease, AND
- Standardized reporting criteria are used, AND
- Non-diagnostic results are always followed by further imaging
V/Q scan interpretation: 1
- Normal scan = PE excluded
- Low probability scan + low clinical probability = PE excluded
- High probability scan + high clinical probability = PE present
- Any other combination = requires CTPA or pulmonary angiography
Important caveat: Indeterminate V/Q scans require additional imaging rather than management based solely on clinical features. 2
Step 4: Management of Discordant Results
In patients with high clinical probability and negative CTPA, valid options are: 1
- Conclude PE has been excluded and stop heparin
- Consider further imaging for VTE (leg ultrasound, conventional pulmonary angiography)
- Seek specialist advice
Diagnostic Algorithm for Massive PE
Massive PE is highly likely if: 1
- Collapse/hypotension, AND
- Unexplained hypoxia, AND
- Engorged neck veins, AND
- Right ventricular gallop (often)
The most useful initial test is echocardiography, which shows indirect signs of acute pulmonary hypertension and right ventricular overload. 1
CTPA or echocardiography will reliably diagnose clinically massive PE. 1
- In highly unstable patients, thrombolytic treatment may be initiated based on compatible echocardiographic findings alone 1
- If the patient is stabilized, seek definitive diagnosis with CTPA 1
- A normal lung scan or CTPA should prompt search for another cause of shock 1
Immediate Anticoagulation
Initiate heparin therapy immediately in patients with intermediate or high clinical probability before imaging confirmation. 1, 2
Unfractionated heparin (UFH) should be considered: 1
- As first dose bolus (80 units/kg IV) 1
- In massive PE
- Where rapid reversal of effect may be needed
Low molecular weight heparin (LMWH) is preferable to UFH in non-massive PE, having equal efficacy and safety and being easier to use 1
Common Pitfalls to Avoid
- Never use D-dimer as a routine screening test—it should only be ordered after clinical probability assessment 1
- Do not rely on normal oxygen saturation to rule out PE (occurs in ~40% of cases) 2
- Do not perform D-dimer in high probability patients or hospitalized patients with comorbidities (low yield) 1
- Do not order V/Q scan if chest X-ray is abnormal or patient has chronic cardiopulmonary disease (will likely be non-diagnostic) 1
- Imaging should be performed within 1 hour in massive PE and ideally within 24 hours in non-massive PE 1, 2