Idiopathic pulmonary fibrosis (IPF) and evidence-based guidelines

dc.authorscopusid56444283800
dc.contributor.authorComez, Mehmet Selim
dc.date.accessioned2024-09-19T15:49:54Z
dc.date.available2024-09-19T15:49:54Z
dc.date.issued2020
dc.departmentHatay Mustafa Kemal Üniversitesien_US
dc.description.abstractIdiopathic pulmonary fibrosis (IPF) is defined as a specific form of chronic, progressive fibrosing interstitial pneumonia of unknown cause. The first guideline on IPF management, published in 2000, is based on the consensus of an international group of experts in the field. The guideline, created by hard work by the American Thoracic Society (ATS), European Respiratory Society (ERS), Japanese Respiratory Society (JRS), and Latin American Thoracic Society (ALAT) in 2011, reviewed all available evidence, clarified the definition of IPF, provided precise diagnostic criteria, described the natural course of the disease, and provided evidence-based recommendations for treatment. In 2015, recommendations for the treatment of IPF were updated on the basis of new scientific evidence. No pharmacological intervention has received strong recommendations for treatment. Clinicians should make individualized decisions based on conditional recommendations in the treatment of patients with IPF. © 2020 Nova Science Publishers, Inc.en_US
dc.identifier.endpage405en_US
dc.identifier.isbn978-153617848-7
dc.identifier.isbn978-153617847-0
dc.identifier.scopus2-s2.0-85144501267en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage395en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12483/15486
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherNova Science Publishers, Inc.en_US
dc.relation.ispartofRespiratory Ventilatory Strategies in Acute and Chronic Respiratory Failure in Idiopathic Pulmonary Diseases: A Practical Approachen_US
dc.relation.publicationcategoryKitap Bölümü - Uluslararasıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleIdiopathic pulmonary fibrosis (IPF) and evidence-based guidelinesen_US
dc.typeBook Chapteren_US

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