Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/7854
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dc.contributor.authorMusellim, B.-
dc.contributor.authorOkumus, G.-
dc.contributor.authorUzaslan, E.-
dc.contributor.authorAkgün, M.-
dc.contributor.authorCetinkaya, E.-
dc.contributor.authorTuran, O.-
dc.contributor.authorAkkoclu, A.-
dc.date.accessioned2019-08-16T12:32:54Z-
dc.date.available2019-08-16T12:32:54Z-
dc.date.issued2014-
dc.identifier.issn1752-6981-
dc.identifier.urihttps://hdl.handle.net/11499/7854-
dc.identifier.urihttps://doi.org/10.1111/crj.12035-
dc.description.abstractIntroduction: There is very few data on the epidemiological features of interstitial lung diseases (ILD) in the literature. These studies on this subject suffer from limited number of patients. Objective: The goal of this study was to evaluate the epidemiological features of ILD in Turkey. Methods: Fifty-four investigators, 31 centres in 19 cities from six regions of Turkey, participated in the study. Two thousand two hundred forty-five newly diagnosed patients (51.8% females), led by Turkish Thoracic Society Clinical Problems Study Group, enrolled in this prospective study. Results: The mean age was 51.8±16.7 years. The mean age among males was 50.5±18.6 years and 53.0±14.6 years among females (P<0.001). 23.8% of the cases had ILD with known causes, while 39.4% were in granulomatous group, 23.7% were idiopathic, and 4.4% were in the unclassified group. Overall, histopathologically confirmed diagnosis rate was 40.4%. Sarcoidosis was the most common disease (37%), whereas cases with idiopathic pulmonary fibrosis (IPF) constituted 19,9% of patients. 53% of the sarcoidosis patients were females, and the ratio reaches to 75% under 50 years of age (for this group, IPF ratio is %3). In contrast, sarcoidosis and IPF ratios were equal in males (25%). Sarcoidosis was 8% in men over 50, while IPF was %45. Conclusion: The overall incidence of ILD in Turkey was computed to be 25.8/100000. © 2013 John Wiley & Sons Ltd.en_US
dc.language.isoenen_US
dc.relation.ispartofClinical Respiratory Journalen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectDistributionen_US
dc.subjectEpidemiologyen_US
dc.subjectIncidenceen_US
dc.subjectInterstitial lung diseasesen_US
dc.subjectadulten_US
dc.subjectageen_US
dc.subjectarticleen_US
dc.subjectdisease classificationen_US
dc.subjectfemaleen_US
dc.subjectgranulomatosisen_US
dc.subjecthistopathologyen_US
dc.subjecthumanen_US
dc.subjectinterstitial lung diseaseen_US
dc.subjectmajor clinical studyen_US
dc.subjectmaleen_US
dc.subjectmiddle ageden_US
dc.subjectpriority journalen_US
dc.subjectprospective studyen_US
dc.subjectsarcoidosisen_US
dc.subjectTurkey (republic)en_US
dc.subjectdistributionen_US
dc.subjectepidemiologyen_US
dc.subjectincidenceen_US
dc.subjectinterstitial lung diseasesen_US
dc.subjectAdulten_US
dc.subjectAgeden_US
dc.subjectFemaleen_US
dc.subjectHumansen_US
dc.subjectIdiopathic Pulmonary Fibrosisen_US
dc.subjectLung Diseases, Interstitialen_US
dc.subjectMaleen_US
dc.subjectMiddle Ageden_US
dc.subjectProspective Studiesen_US
dc.subjectSarcoidosis, Pulmonaryen_US
dc.subjectTurkeyen_US
dc.titleEpidemiology and distribution of interstitial lung diseases in Turkeyen_US
dc.typeArticleen_US
dc.identifier.volume8en_US
dc.identifier.issue1en_US
dc.identifier.startpage55
dc.identifier.startpage55en_US
dc.identifier.endpage62en_US
dc.identifier.doi10.1111/crj.12035-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.scopus2-s2.0-84891830034en_US
dc.identifier.wosWOS:000333527800007en_US
dc.identifier.scopusqualityQ2-
dc.ownerPamukkale University-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.languageiso639-1en-
item.grantfulltextnone-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
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WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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