fibrosis

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fibrosis

the formation of an abnormal amount of fibrous tissue in an organ or part as the result of inflammation, irritation, or healing

fibrosis

[fī′brō·səs]
(medicine)
Growth of fibrous connective tissue in an organ or part in excess of that naturally present.
References in periodicals archive ?
The statistically and clinically significant increase FEV-1, SaO2, PEF, FVC, especially the improved FEV1/FVC ratio from 52% to 86%, was clinically significant since these patients remained on their current therapies (steroids) while using the non-steroidal nasal spray, demonstrating that current therapies in use are inadequate to treat patient with idiopathic pulmonary fibrosis, EmphyCorp said.
The Global Idiopathic Pulmonary Fibrosis Treatment Market is expected to register a CAGR of 12.3% during the forecast period of 2019 to 2025, with a market value of USD 2,237 million in 2018.
Diagnosis of idiopathic pulmonary fibrosis: an official ATS/ERS/JRS/ALAT Clinical Practice Guideline.
Idiopathic Pulmonary Fibrosis. Animal studies have reported on the promising effects of a number of botanicals.
[2.] Raghu G, Collard HR, Egan JJ, Martinez FJ; ATS/ERS/JRS/ALAT Committee on Idiopathic Pulmonary Fibrosis. An official ATS/ERS/JRS/ALAT statement: Idiopathic pulmonary fibrosis: Evidence-based guidelines for diagnosis and management.
Idiopathic pulmonary fibrosis: relationship between histopathologic features and mortality.
Phelix Therapeutics, LLC is dedicated to saving the lives of people diagnosed with Idiopathic Pulmonary Fibrosis, and other Fibrotic Diseases, by developing innovative treatments for these fatal conditions.
King Jr, "Clinical course and prediction of survival in idiopathic pulmonary fibrosis," American Journal of Respiratory and Critical Care Medicine, vol.
Idiopathic pulmonary fibrosis (IPF) is a chronic, devastating, and ultimately fatal disease characterized by a progressive decline in lung function.
A study on patients of idiopathic pulmonary fibrosis concluded that investigation by HRCT can lead to earlier detection and treatment as compared to conventional radiography13.
Conclusion: Idiopathic pulmonary fibrosis was found to be the most common interstitial lung disease subtype followed by non-specific interstitial pneumonia, sarcoidosis and connective tissue disease-related-interstitial lung disease.

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