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Related Concept Videos

A Porcine Model of Acute Autologous Pulmonary Embolism07:44

A Porcine Model of Acute Autologous Pulmonary Embolism

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This study presents a porcine model of pulmonary embolism (PE) using large autologous emboli that replicate acute intermediate-risk PE. The model is well-suited for the evaluation of both pathophysiology and treatment responses.
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Pulmonary Embolism I: Introduction01:29

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Pulmonary embolism (PE) occurs when a thrombus, fat or air embolus, amniotic fluid, or tumor tissue blocks one or more pulmonary arteries. These blockages originate in the venous system or the right side of the heart.EtiologyPE primarily arises from deep vein thrombosis (DVT) and other hypercoagulable states, such as inherited thrombophilias. Additional etiological factors include venous stasis, commonly seen in obesity, and endothelial injury from surgery and trauma. Less common causes include...
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Establishment of a Minimally Invasive Rat Model of Pulmonary Embolism Using Autologous Blood Clots08:02

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A detailed methodology for establishing a minimally invasive rat model of pulmonary embolism using autologous blood clots is described. Additional methods for quantifying the infarcted area and visualizing the pulmonary arterial tree are also...
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Pulmonary Embolism III: Nursing Management01:27

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A pulmonary embolism occurs when a thrombus, amniotic fluid, tumor tissue, fat, or air embolus blocks one or more pulmonary arteries. Effective nursing management and patient education are crucial for improving outcomes and preventing recurrence.Nursing management starts with obtaining a comprehensive patient history, particularly noting any history of deep vein thrombosis (DVT). Assess for clinical manifestations, including dyspnea, chest pain, crackles, heart murmurs, and signs of right-sided...
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Pulmonary Embolism II: Diagnostic Studies and Interprofessional Care01:29

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Diagnosing Pulmonary EmbolismDiagnosing pulmonary embolism (PE) involves clinical assessment and advanced imaging tests. The preferred diagnostic tool is the spiral (helical) CT scan or CT angiography (CTA), which uses intravenous contrast media to visualize the pulmonary vasculature and identify emboli.A ventilation-perfusion (V/Q) scan is an alternative for patients unable to receive contrast media. This scan includes both perfusion and ventilation scanning. Perfusion scanning involves...
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Related Experiment Video

Updated: Jan 19, 2026

A Porcine Model of Acute Autologous Pulmonary Embolism
07:44

A Porcine Model of Acute Autologous Pulmonary Embolism

Published on: September 6, 2024

772

[Pulmonary Embolism].

Lukas Hobohm, Mareike Lankeit

    Deutsche Medizinische Wochenschrift (1946)
    |September 13, 2019
    PubMed
    Summary
    This summary is machine-generated.

    Pulmonary embolism (PE) is a serious condition. Risk stratification guides treatment, with non-vitamin K-dependent oral anticoagulants (NOACs) often preferred for anticoagulation.

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    Pulmonary Embolism I: Introduction
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    Area of Science:

    • Cardiology
    • Pulmonology
    • Vascular Medicine

    Background:

    • Pulmonary embolism (PE) is a leading cardiovascular cause of death with increasing incidence.
    • Patient risk for PE complications escalates with comorbidities and right ventricular dysfunction.
    • Effective risk stratification is crucial for guiding PE treatment decisions.

    Purpose of the Study:

    • To outline the current understanding and management strategies for pulmonary embolism.
    • To emphasize the importance of risk stratification in tailoring PE therapy.
    • To discuss the role of anticoagulants and specialized teams in PE management.

    Main Methods:

    • Clinical, laboratory, and imaging parameters are used for PE risk stratification into four classes.
    • Treatment decisions, especially for hemodynamically unstable patients, benefit from interdisciplinary Pulmonary Embolism Response Teams (PERT).
    • Anticoagulant therapies, including NOACs and LMWHs, are evaluated for efficacy and safety.

    Main Results:

    • Risk stratification directly influences therapeutic choices, from outpatient management to reperfusion therapy.
    • Non-vitamin K-dependent oral anticoagulants (NOACs) show comparable efficacy and a better safety profile than VKAs for PE.
    • Low molecular weight heparins (LMWHs) are recommended for PE patients with cancer, with factor Xa-inhibitors showing promise.

    Conclusions:

    • PE risk stratification is essential for appropriate and effective treatment selection.
    • NOACs are increasingly favored for anticoagulation in PE due to their safety and efficacy.
    • Prolonged anticoagulation is vital for preventing venous thromboembolism recurrence, particularly in unprovoked events.