Idiopathic pulmonary fibrosis : What primary care physicians need to know
Copyright © 2018 Cleveland Clinic..
Idiopathic pulmonary fibrosis (IPF) is a specific type of fibrosing interstitial pneumonia of unknown cause. It is usually chronic and progressive, tends to affect mainly adults over age 60, has a predilection for men, and is often fatal. The condition is still underappreciated by pulmonologists and primary care physicians. This article attempts to close that information gap by reviewing the natural course of IPF and presenting an algorithmic approach to diagnosis and treatment based on evidence-based international guidelines. New treatment options are briefly discussed, to raise awareness of new medications that target pulmonary fibrosis.
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CommentIn: Cleve Clin J Med. 2018 May;85(5):387-389. - PMID 29733780 |
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Medienart: |
E-Artikel |
Erscheinungsjahr: |
2018 |
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Erschienen: |
2018 |
Enthalten in: |
Zur Gesamtaufnahme - volume:85 |
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Enthalten in: |
Cleveland Clinic journal of medicine - 85(2018), 5 vom: 20. Mai, Seite 377-386 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Tolle, Leslie B [VerfasserIn] |
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Date Completed 20.11.2018 Date Revised 20.11.2018 published: Print CommentIn: Cleve Clin J Med. 2018 May;85(5):387-389. - PMID 29733780 Citation Status MEDLINE |
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doi: |
10.3949/ccjm.85a.17018 |
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520 | |a Idiopathic pulmonary fibrosis (IPF) is a specific type of fibrosing interstitial pneumonia of unknown cause. It is usually chronic and progressive, tends to affect mainly adults over age 60, has a predilection for men, and is often fatal. The condition is still underappreciated by pulmonologists and primary care physicians. This article attempts to close that information gap by reviewing the natural course of IPF and presenting an algorithmic approach to diagnosis and treatment based on evidence-based international guidelines. New treatment options are briefly discussed, to raise awareness of new medications that target pulmonary fibrosis | ||
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