Pulmonary embolism (PE) is a common and often fatal form of venous thromboembolism (VTE)
Clinical presentation of PE is highly variable and non-specific, making diagnosis challenging
Diagnosis of PE requires a high level of suspicion and efficient evaluation for quick therapy administration
Search for risk factors contributing to PE development is essential for treatment and determining optimal therapy duration
Thrombus: A solid or semisolid mass formed from circulating blood constituents within the vascular system
Embolus: Undissolved material carried by the blood stream and impacting part of the vascular tree
Venous Thromboembolism (VTE): Formation of thrombotic material in the systemic venous system with the potential to embolise to distant sites, usually the lungs
PE: Obstruction of the pulmonary artery or its branches by material originating elsewhere in the body
PE can be classified by the type of material embolised, temporal pattern of presentation, haemodynamic stability, anatomic location, and presence of symptoms
PE incidence in the general population has increased with CT pulmonary angiography introduction
PE is slightly more common in males and incidence rises with age
Deaths from confirmed PE have declined, but overall mortality remains high with 30-day and 1-year mortality rates
Thrombus generation involves risk factors classified by Virchow’s Triad: venous stasis, endothelial injury, and hypercoagulable state
Most pulmonary emboli arise from lower extremity proximal veins
PE diagnosis involves clinical suspicion, pretest probability assessment, and definitive testing
Clinical suspicion for PE is determined by the presentation consistency with PE
Clinical features include dyspnoea, pleuritic chest pain, cough, and occasionally haemoptysis
Laboratory investigations for PE include arterial blood gas showing hypoxaemia and hypocapnoea
Assessment of a patient’s pretest probability for PE involves using scoring systems like the Well’s score
High probability patients (Well’s > 4) should undergo definitive diagnostic testing
Low to intermediate probability patients (Well’s 4 or less) may need further assessment before testing
dimers are breakdown products of thrombus and can help rule out PE in low to intermediate probability patients
Elevated D-dimer alone is insufficient for PE diagnosis
Definitive diagnostic testing for PE includes CT pulmonary angiogram (CTPA) or ventilation perfusion (V/Q) scan
CTPA is the imaging modality of choice for PE diagnosis with good sensitivity and specificity
CTPA may assist in discovering alternate diagnoses and is more widely available than V/Q scan
Empiric parenteral anticoagulation is reasonable while awaiting definitive diagnostic testing results to avoid therapeutic delay
V/Q scanning is preferred when CT scanning is contraindicated
V/Q scanning may be preferred over CT scanning when CTPA is indeterminate or negative and suspicion for PE remains high
V/Q scan is highly sensitive but not very specific, good for ruling out pulmonary emboli
V/Q scan is safer than CT as it does not expose the patient to radiation or contrast
V/Q scan is better for visualizing smaller peripheral emboli
V/Q scan requires a normal chest X-ray for positive findings to be interpreted correctly
Doppler ultrasound can be used for DVT evaluation when CTPA or V/Q scan is not available
Echocardiography can be used for visualizing PE in the proximal pulmonary arteries
Patients with massive or high-risk PE are hemodynamically unstable
Supportive therapies for confirmed PE include supplemental oxygen, analgesia, intravenous fluids, and inotropic support
Low-risk patients should be prioritized for early discharge on oral anticoagulation therapy
Intermediate-risk patients require an initial period of parenteral anticoagulation
Anticoagulation strategies include initiation phase, treatment phase, and extended phase