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ULY CLINIC

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14 Julai 2026, 22:53:45

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Pulmonary embolism (PE)

Pulmonary embolism (PE)

Overview

Pulmonary embolism (PE) is a medical emergency caused by obstruction of pulmonary arterial blood flow, usually by thrombotic material originating from the deep venous system.

PE is a major manifestation of venous thromboembolism (VTE), which includes:

  • Deep vein thrombosis (DVT).

  • Pulmonary embolism (PE).


Approximately 90% of clinically significant PE originates from proximal DVT involving the popliteal, femoral, or iliac veins.


PE causes:

  • Ventilation–perfusion mismatch.

  • Hypoxaemia.

  • Increased pulmonary vascular resistance.

  • Right ventricular strain.

  • Possible cardiovascular collapse.

Severity ranges from incidental/asymptomatic PE to massive PE with haemodynamic instability.


Risk factors

Risk factors are related to Virchow’s triad.


Venous stasis

  • Prolonged immobilization.

  • Bed rest.

  • Long-haul travel.

  • Recent surgery, especially orthopaedic surgery.

  • Stroke with paralysis.

  • Heart failure.


Endothelial injury

  • Major trauma.

  • Surgery.

  • Central venous catheters.


Hypercoagulability

  • Malignancy.

  • Pregnancy and postpartum state.

  • Oral contraceptives or hormone therapy.

  • Inherited thrombophilia:

    • Factor V Leiden.

    • Protein C deficiency.

    • Protein S deficiency.

  • Antiphospholipid syndrome.

  • Obesity.

  • Smoking.

Previous VTE is the strongest predictor of recurrence.


Clinical presentation

Presentation depends on clot size and cardiopulmonary reserve.

Common features include:

  • Transient dyspnoea and tachypnoea without other clinical features.

  • Sudden onset dyspnoea.

  • Pleuritic chest pain.

  • Cough.

  • Haemoptysis.

  • Pleural effusion.

  • Pulmonary infiltrates.

  • Tachycardia.

  • Arrhythmia.

Severe presentations include:

  • Severe dyspnoea and tachypnoea.

  • Right-sided heart failure.

  • Cardiovascular collapse.

  • Hypotension.

  • Syncope.

  • Coma.


Other non-specific presentations:

  • Resistant cardiac failure.

  • Wheezing.

  • Fever.

  • Apprehension.

  • Confusion.


Classification of PE severity


Massive PE

  • Sustained hypotension.

  • Shock.

  • Haemodynamic collapse.


Submassive PE

  • Right ventricular dysfunction without hypotension.

Low-risk PE

  • Haemodynamically stable.

  • No evidence of right ventricular strain.


Investigations

Diagnosis requires clinical assessment and objective confirmation.


Laboratory investigations

  • D-dimer.

  • PT.

  • INR.

  • aPTT.

  • Full blood count.

  • Renal function tests.

  • Arterial blood gases where indicated.

  • Cardiac biomarkers in suspected right ventricular strain.


Imaging

  • CT pulmonary angiography (CTPA):

    • Gold standard imaging test.

Other investigations:

  • Chest X-ray.

  • Compression ultrasonography of lower limbs.

  • Ventilation–perfusion scan if CTPA is contraindicated.

  • Echocardiography for right ventricular dysfunction.


Management

PE is a medical emergency.

Management aims to:

  • Prevent clot extension.

  • Prevent recurrence.

  • Prevent complications.


Non-pharmacological management

  • Oxygen therapy for hypoxia.

  • Haemodynamic support.

  • Cautious IV fluids where required.

  • Vasopressors if hypotensive.

  • Intensive care monitoring in massive PE.

Inferior vena cava (IVC) filter may be considered if:

  • Anticoagulation is contraindicated.


Pharmacological treatment

Treat as Deep Vein Thrombosis (DVT) section.

Long-term anticoagulation is required to prevent:

  • Recurrent VTE.

  • Thrombus extension.


Warfarin-based regimen

  • Warfarin PO 5 mg 24 hourly.

AND

  • Initial unfractionated heparin or low molecular weight heparin therapy overlapping for 5 days.

Continue warfarin according to INR monitoring.

Therapeutic INR range:

  • 2–3 for VTE.

  • 2.5–3.5 for patients with mechanical heart valves.

Monitoring:

  • Monitor INR after 5–7 days of treatment.

  • Continue monitoring as needed throughout treatment duration.


Low molecular weight heparin regimen

  • Low molecular weight heparin SC 1 mg/kg 24 hourly.

Alternative regimen:

  • Enoxaparin SC 1 mg/kg 12 hourly.


Unfractionated heparin regimen

  • Unfractionated heparin IV 75 units/kg loading dose.

AND

  • Continuous infusion 18 units/kg/hour.

Monitoring:

  • Monitor aPTT before and during treatment.


Rivaroxaban regimen

  • Rivaroxaban PO 15 mg 12 hourly for 21 days.

THEN

  • Rivaroxaban PO 20 mg 24 hourly for the remaining duration of treatment.


Adolescents and children

Options include:

  • Unfractionated heparin loading dose 75 units/kg.

THEN

  • 15–25 units/kg/hour by IV infusion.

OR

  • 250 units/kg SC 12 hourly.


Pregnant women

Warfarin is teratogenic and should not be used during pregnancy.

Use:

  • Low molecular weight heparin SC 1 mg/kg 12 hourly for the whole duration of treatment.


Thrombolysis

Consider in:

  • Massive PE with shock.

  • Persistent hypotension.

Example:

  • Alteplase IV 100 mg over 2 hours.


Duration of treatment

For venous thromboembolism:

  • Acquired thromboembolism:

    • Treatment usually lasts 3–6 months.

  • Inherited thrombophilia:

    • Lifelong anticoagulation may be required.

Additional guidance:

  • Provoked PE: 3–6 months.

  • Unprovoked PE: ≥6 months or extended therapy.

  • Recurrent VTE: long-term anticoagulation.


Warfarin precautions

Warfarin interacts with many medicines.

Precautions should be taken when administering warfarin with other drugs.

If warfarin overdose or toxicity occurs:

  • Stop warfarin.

AND

  • Give fresh frozen plasma (FFP) 10–15 ml/kg.

AND

  • Give vitamin K IV 5 mg stat.

Restart warfarin after:

  • Bleeding has stopped.

  • INR is within therapeutic range.

Use a lower dosage when restarting.


VTE prophylaxis in bedridden patients

Options:

  • Enoxaparin SC 40 mg once daily.

OR

  • Rivaroxaban PO 10 mg once daily.

Continue until ambulation resumes.


Complications

  • Recurrent PE.

  • Chronic thromboembolic pulmonary hypertension (CTEPH).

  • Right heart failure.

  • Sudden cardiac death.


Prevention


Primary prevention

  • Early mobilization after surgery.

  • Mechanical prophylaxis using compression devices.

  • Prophylactic LMWH in high-risk hospitalized patients.


Secondary prevention

  • Appropriate duration of anticoagulation.

  • Risk factor modification:

    • Weight reduction.

    • Smoking cessation.


References

  1. Konstantinides SV, Meyer G, Becattini C, et al. 2019 ESC Guidelines for the diagnosis and management of acute pulmonary embolism. Eur Heart J. 2020;41(4):543–603.

  2. Kearon C, Akl EA, Ornelas J, et al. Antithrombotic therapy for VTE disease: CHEST guideline. Chest. 2016;149(2):315–352.

  3. Goldhaber SZ. Pulmonary embolism. N Engl J Med. 1998;339(2):93–104.

  4. Tapson VF. Acute pulmonary embolism. N Engl J Med. 2008;358(10):1037–1052.

  5. World Health Organization. WHO guidelines for management of venous thromboembolism. Geneva: WHO; 2021.

  6. Ministry of Health Tanzania. Standard Treatment Guidelines & National Essential Medicines List. 2021 edition.

  7. Bates SM, Jaeschke R, Stevens SM, et al. Diagnosis of DVT and PE. Chest. 2012;141(2 Suppl):e351S–e418S.

  8. Huisman MV, et al. Venous thromboembolism: clinical practice review. Lancet. 2018;391:1835–1846.



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