Publication:
Evaluation of patients with fibrotic interstitial lung disease: preliminary results from the Turk-UIP study

dc.contributor.coauthorMusellim, Benan
dc.contributor.coauthorMoğulkoç, Nesrin
dc.contributor.coauthorUzun, Oğuz
dc.contributor.coauthorTokgöz Akyıl, Fatma
dc.contributor.coauthorTürktaş, Haluk
dc.contributor.coauthorÖzdemir Kumbasar, Özlem
dc.contributor.coauthorOkumuş, Gülfer
dc.contributor.coauthorÖğüş, Candan
dc.contributor.coauthorDirol, Hülya
dc.contributor.coauthorZamani, Adil
dc.contributor.coauthorSevim, Tülin
dc.contributor.coauthorAnnakkaya, Ali Nihat
dc.contributor.coauthorÖzyürek, Berna Akıncı
dc.contributor.coauthorHanta, İsmail
dc.contributor.coauthorAydemir, Yusuf
dc.contributor.coauthorÇakır Edis, Ebru
dc.contributor.coauthorKurt, Bahar
dc.contributor.coauthorTertemiz, Kemal Can
dc.contributor.coauthorTabak, Levent
dc.contributor.coauthorYazıcı, Onur
dc.contributor.coauthorErdoğan, Yurdanur
dc.contributor.coauthorAteş, Güngör
dc.contributor.coauthorTürker, Hatice
dc.contributor.coauthorSalepçi Banu
dc.contributor.coauthorHazar, Armağan
dc.contributor.coauthorNiksarlıoğlu, Elif Yelda
dc.contributor.coauthorYılmaz Kara, Bilge
dc.contributor.coauthorKöktürk, Nurdan
dc.contributor.coauthorKalpaklıoğlu, Füsun
dc.contributor.coauthorÖzsu, Savaş
dc.contributor.coauthorAtahan, Ersan
dc.contributor.coauthorFendoğlu, Türkan Zeynep
dc.contributor.coauthorYılmaz Süreyya
dc.contributor.coauthorBaşyiğit İlknur
dc.contributor.coauthorÇamsarı, Güngör
dc.contributor.coauthorTunçay, Esin
dc.contributor.coauthorUçar Yılmazel, Elif
dc.contributor.coauthorKanmaz, Dilek
dc.contributor.coauthorEkici, Aydanur
dc.contributor.coauthorTopçu Füsun
dc.contributor.coauthorUzaslan, Esra
dc.contributor.coauthorBozkuş Fulsen
dc.contributor.coauthorArgun Barış, Serap
dc.contributor.coauthorDuru, Serap
dc.contributor.coauthorAltınışık, Göksel
dc.contributor.coauthorBingöl, Züleyha
dc.contributor.coauthorTunacı, Atadan
dc.contributor.coauthorSavaş, Recep
dc.contributor.coauthorAlper, Fatih
dc.contributor.coauthorBayraktaroğlu, Selen
dc.contributor.coauthorSelçuk Can, Tuba
dc.contributor.coauthorDemir, Ali Arslan
dc.contributor.departmentKUH (Koç University Hospital)
dc.contributor.kuauthorUzel, Fatma Işıl
dc.contributor.schoolcollegeinstituteKUH (KOÇ UNIVERSITY HOSPITAL)
dc.date.accessioned2024-11-09T13:23:38Z
dc.date.issued2021
dc.description.abstractObjective: differential diagnosis of idiopathic pulmonary fibrosis (IPF) is important among fibrotic interstitial lung diseases (ILD). This study aimed to evaluate the rate of IPF in patients with fibrotic ILD and to determine the clinical-laboratory features of patients with and without IPF that would provide the differential diagnosis of IPF. Material and methods: the study included the patients with the usual interstitial pneumonia (UIP) pattern or possible UIP pattern on thorax high-resolution computed tomography, and/or UIP pattern, probable UIP or possible UIP pattern at lung biopsy according to the 2011 ATS/ERSARS/ALAT guidelines. Demographics and clinical and radiological data of the patients were recorded. All data recorded by researchers was evaluated by radiology and the clinical decision board. Results: a total of 336 patients (253 men, 83 women, age 65.8 +/- 9.0 years) were evaluated. Of the patients with sufficient data for diag-nosis (n=300), the diagnosis was IPF in 121 (40.3%), unclassified idiopathic interstitial pneumonia in 50 (16.7%), combined pulmonary fibrosis and emphysema (CPFE) in 40 (13.3%), and lung involvement of connective tissue disease (CTD) in 16 (5.3%). When 29 patients with definite IPF features were added to the patients with CPFE, the total number of IPF patients reached 150 (50%). Rate of male sex (p<0.001), smoking history (p<0.001), and the presence of clubbing (p=0.001) were significantly high in patients with IPE None of the women <50 years and none of the men <50 years of age without a smoking history were diagnosed with IPE Presence of at least 1 of the symptoms suggestive of CTD, erythrocyte sedimentation rate (ESR), and antinuclear antibody (FANA) positivity rates were significantly higher in the non-IPF group (p<0.001, p=0.029, p=0.009, respectively). Conclusion: the rate of IPF among patients with fibrotic ILD was 50%. In the differential diagnosis of IPF, sex, smoking habits, and the presence of clubbing are important. The presence of symptoms related to CTD, ESR elevation, and EANA positivity reduce the likelihood of IPF.
dc.description.fulltextYES
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue2
dc.description.openaccessYES
dc.description.publisherscopeNational
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipRoche
dc.description.versionPublisher version
dc.description.volume22
dc.identifier.doi10.5152/TurkThoracJ.2021.20028
dc.identifier.eissn2149-2530
dc.identifier.embargoNO
dc.identifier.filenameinventorynoIR02829
dc.identifier.quartileN/A
dc.identifier.scopus2-s2.0-85103621219
dc.identifier.urihttps://hdl.handle.net/20.500.14288/3379
dc.identifier.wos659040700001
dc.keywordsFibrotic interstitial lung diseases
dc.keywordsIdiopathic pulmonary fibrosis
dc.keywordsUsual interstitial pneumonia
dc.language.isoeng
dc.publisherAves
dc.relation.grantnoNA
dc.relation.ispartofTurkish Thoracic Journal
dc.relation.urihttp://cdm21054.contentdm.oclc.org/cdm/ref/collection/IR/id/9480
dc.subjectRespiratory system
dc.titleEvaluation of patients with fibrotic interstitial lung disease: preliminary results from the Turk-UIP study
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorUzel, Fatma Işıl
local.publication.orgunit1KUH (KOÇ UNIVERSITY HOSPITAL)
local.publication.orgunit2KUH (Koç University Hospital)
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relation.isOrgUnitOfPublication.latestForDiscoveryf91d21f0-6b13-46ce-939a-db68e4c8d2ab
relation.isParentOrgUnitOfPublication055775c9-9efe-43ec-814f-f6d771fa6dee
relation.isParentOrgUnitOfPublication.latestForDiscovery055775c9-9efe-43ec-814f-f6d771fa6dee

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