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Related Concept Videos

Chronic Obstructive Pulmonary Disease-II: Pathophysiology01:20

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Chronic Obstructive Pulmonary Disease (COPD) pathophysiology is intricate and multifaceted, involving a complex interplay of physiological processes. Understanding these mechanisms is crucial for effectively managing and treating COPD. Here is an in-depth look at the critical elements in the pathophysiology of COPD:
Chronic Inflammation
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Chronic Obstructive Pulmonary Disease-I: Introduction01:20

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Chronic Obstructive Pulmonary Disease (COPD) is a long-lasting respiratory condition requiring continuous attention and care. It is a progressive lung disease that leads to breathing challenges due to airflow obstruction. It manifests as persistent respiratory symptoms and restricted airflow resulting from abnormalities in the airways and alveoli, usually due to long-term exposure to harmful particles or gases. COPD mainly consists of two primary conditions: emphysema and chronic bronchitis.
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Pulmonary Hypertension: Classification and Pathogenesis01:30

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Pulmonary hypertension (PH) is a severe health condition in which the mean pulmonary arterial pressure increases to 25 mmHg or more, even when the body is at rest. This high pressure in the blood vessels that transport blood from the heart to the lungs can cause various symptoms, including shortness of breath, can lead to right heart failure, and significantly affect the overall quality of life.
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Chronic Obstructive Pulmonary Disease01:22

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COPD is defined as a heterogeneous lung condition marked by persistent respiratory symptoms such as dyspnea, cough, and sputum production, caused by abnormalities in the airways that cause airflow obstruction.
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Updated: Jan 8, 2026

Refined Murine Model of Idiopathic Pulmonary Fibrosis
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Refined Murine Model of Idiopathic Pulmonary Fibrosis

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Progressive pulmonary fibrosis.

Ramey Bajwa1, Drew Lancaster2, Sujal R Desai3,4

  • 1Department of Interstitial Lung Disease, Royal Brompton Hospital, London, UK. rameybajwa@gmail.com.

European Radiology
|December 19, 2025
PubMed
Summary
This summary is machine-generated.

Progressive pulmonary fibrosis (PPF) mimics idiopathic pulmonary fibrosis (IPF) and increases mortality. Identifying radiological progression on CT scans is crucial for timely antifibrotic treatment and slowing lung function decline.

Keywords:
AntifibroticsComputed tomographyNintedanibProgressive pulmonary fibrosisRadiological progression of fibrosis

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Area of Science:

  • Pulmonology
  • Radiology
  • Medical Imaging

Background:

  • A subset of non-idiopathic pulmonary fibrosis (IPF) cases exhibit a progressive pulmonary fibrosis (PPF) trajectory.
  • PPF is linked to heightened patient mortality and mimics IPF clinically.
  • Identifying PPF is critical for patient management and prognosis.

Purpose of the Study:

  • To define radiological progression criteria for identifying PPF.
  • To highlight the role of radiologists in managing PPF patients.
  • To underscore the importance of early detection for antifibrotic therapy.

Main Methods:

  • Analysis of serial high-resolution computed tomography (CT) scans.
  • Evaluation of fibrosis extent and severity changes over time.
  • Radiological assessment for progression in non-IPF cases.

Main Results:

  • Radiological progression in PPF is characterized by increased overall fibrosis extent.
  • Progression can also manifest as increased fibrosis severity with unchanged overall extent.
  • Accurate radiological identification enables timely intervention.

Conclusions:

  • Radiologists are pivotal in diagnosing PPF through CT assessment.
  • Identifying radiological progression allows for initiation of antifibrotic drugs.
  • Early antifibrotic treatment can significantly mitigate lung function decline in PPF.