This is the overview for the medical abbreviations series. This list is far from complete; you can help by expanding it. Comprehensive reference books of medical abbreviations are available in.

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To understand idiopathic pulmonary fibrosis (IPF), it helps to understand how the lungs work. The air that you breathe in through your nose or mouth travels down through your trachea (windpipe) into two tubes in your lungs called bronchial (BRONG-ke-al) tubes or airways.

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Idiopathic pulmonary fibrosis (IPF) belongs to a large group of more than 200 lung diseases known as interstitial lung diseases (ILDs), which are characterized by the involvement of the lung interstitium, the tissue between the air sacs of the lung.

Pulmonary fibrosis — Learn about the symptoms, causes and treatment of this serious lung disease that occurs when lung tissue becomes damaged and scarred.

Pulmonary fibrosis is the scarring of your lung tissues over time. It is also called interstitial lung disease. The air sacs and tissues in your lungs swell, scars form, and the tissues become thick and stiff. This affects how much oxygen you get and makes it hard to breathe. Your healthcare

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Although we don’t have a clear understanding of why some people develop Idiopathic Pulmonary Fibrosis, a growing body of evidence has implicated Gastro-Esophageal Reflux (GER) as a an important co-factor in the development and progression of Idiopathic Pulmonary Fibrosis.

INTRODUCTION. Idiopathic pulmonary fibrosis (IPF, also called cryptogenic fibrosing alveolitis) is specific form of chronic, progressive, fibrosing interstitial pneumonia of unknown cause, occurring in adults and limited to the lungs.

INTRODUCTION. Idiopathic pulmonary fibrosis (IPF), previously known as cryptogenic fibrosing alveolitis (CFA) in Europe, is a chronic, relentlessly progressive fibrotic disorder of the lower respiratory tract that typically affects adults over the age of 40. Idiopathic interstitial pneumonias (IIP) are diffuse parenchymal lung diseases, of.

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Idiopathic pulmonary fibrosis (IPF) is a chronic fibrotic disease of the lung that is marked by progressive decline in pulmonary function and ultimately respiratory failure.

Idiopathic pulmonary fibrosis (IPF) is a disease of unknown cause in which areas of normal lung tissue are replaced by scars. As a result it becomes harder for the lungs to extract oxygen from the air.

NICE | The National Institute for Health and Care. – Guidance, advice and information services for health, public health and social care professionals.

The American Thoracic Society, European Respiratory Society, Japanese Respiratory Society, and Latin American Thoracic Association recently issued joint evidence-based guidelines for the diagnosis and management of idiopathic pulmonary fibrosis (IPF). The Society of Thoracic Radiology and the Pulmonary Pathology Society also endorsed these.

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