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dc.contributor.authorMüsellim, Benan
dc.contributor.authorMoğulkoç, Nesrin
dc.contributor.authorUzun, Oğuz
dc.contributor.authorAkyıl, Fatma Tokgöz
dc.contributor.authorTürktaş, Haluk
dc.contributor.authorKumbasar, Özlem Özdemir
dc.contributor.authorOkumuş, Gülfer
dc.contributor.authorOğuş, Candan
dc.contributor.authorDirol, Hülya
dc.contributor.authorZamani, Adil
dc.contributor.authorSevim, Tülin
dc.contributor.authorAnnakkaya Ali Nihat
dc.contributor.authorÖzyürek, Berna Akıncı
dc.contributor.authorHanta, İsmail
dc.contributor.authorAydemir, Yusuf
dc.contributor.authorEdis, Ebru Çakır
dc.contributor.authorKurt, Bahar
dc.contributor.authorTertemiz, Kemal Can
dc.contributor.authorTabak, Levent
dc.contributor.authorYazıcı, Onur
dc.contributor.authorErdoğan, Yurdanur
dc.contributor.authorAteş, Güngör
dc.contributor.authorTürker, Hatice
dc.contributor.authorSalepçi, Banu
dc.contributor.authorHazar, Armağan
dc.contributor.authorNiksarlıoğu, Elif Yelda
dc.contributor.authorKara, Bilge Yılmaz
dc.contributor.authorKöktürk, Nurdan
dc.contributor.authorKalpaklıoğlu, Füsun
dc.contributor.authorUzel, Işıl
dc.contributor.authorÖzsu, Savaş
dc.contributor.authorAtahan, Ersan
dc.contributor.authorFendoğlu, Türkan Zeynep
dc.contributor.authorSüreyya, Yılmaz
dc.contributor.authorBaşyiğit, İlknur
dc.contributor.authorÇamsarı, Güngör
dc.contributor.authorTuncay, Esin
dc.contributor.authorYılmazel, Elif Uçar
dc.contributor.authorKanmaz, Dilek
dc.contributor.authorKanmaz, Dilek
dc.contributor.authorEkici, Aydanur
dc.contributor.authorTopçu, Füsun
dc.contributor.authorUzaslan, Esra
dc.contributor.authorBozkuş, Fülsen
dc.contributor.authorBarış, Serap Argun
dc.contributor.authorDuru, Serap
dc.contributor.authorAltınışık, Göksel
dc.contributor.authorBingöl, Züleyha
dc.contributor.authorTunacı, Atadan
dc.contributor.authorSavaş, Recep
dc.contributor.authorAlper, Fatih
dc.contributor.authorBayraktaroğlu, Selen
dc.contributor.authorCan, Tuba Selçuk
dc.contributor.authorDemir, Ali Arslan
dc.date.accessioned2022-09-13T08:16:27Z
dc.date.available2022-09-13T08:16:27Z
dc.date.issued2021en_US
dc.identifier.citationBenan, M., Nesrin, M., Oguz, U., Fatma, T. A., Haluk, T., Ozlem, O. K., Gulfer, O., Candan, O., Hulya, D., Adil, Z., Tulin, S., Nihat, A. A., Akinci, O. B., Ismail, H., Yusuf, A., Ebru, C. E., Bahar, K., Can, T. K., Levent, T., Onur, Y., … Arslan, D. A. (2021). Evaluation of Patients with Fibrotic Interstitial Lung Disease: Preliminary results from the Turk-UIP Study. Turkish thoracic journal, 22(2), 102–109. https://doi.org/10.5152/TurkThoracJ.2021.20028en_US
dc.identifier.issn2149-2530
dc.identifier.urihttps://doi.org/10.5152/TurkThoracJ.2021.20028
dc.identifier.urihttps://hdl.handle.net/11436/6455
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.en_US
dc.language.isoengen_US
dc.publisherAVESen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectFibrotic interstitial lung diseasesen_US
dc.subjectIdiopathic pulmonary fibrosisen_US
dc.subjectUsual interstitial pneumoniaen_US
dc.titleEvaluation of patients with fibrotic interstitial lung disease: Preliminary results from the Turk-UIP studyen_US
dc.typearticleen_US
dc.contributor.departmentRTEÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümüen_US
dc.contributor.institutionauthorKara, Bilge Yılmaz
dc.identifier.doi10.5152/TurkThoracJ.2021.20028en_US
dc.identifier.volume22en_US
dc.identifier.issue2en_US
dc.identifier.startpage102en_US
dc.identifier.endpage109en_US
dc.relation.journalTurkish Thoracic Journalen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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