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

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dc.authorid0000-0001-7570-2339en_US
dc.contributor.authorMusellim, 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.authorÖzyurek, 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.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.accessioned2021-07-05T13:06:30Z
dc.date.available2021-07-05T13:06:30Z
dc.date.issued2021en_US
dc.departmentDicle Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Göğüs Hastalıkları Ana Bilim Dalıen_US
dc.descriptionWOS:000659040700001
dc.descriptionPMID: 33871332
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.identifier.citationMusellim, B., Uzun, O., Tokgöz, Akyıl, F., Türktaş, H., Kumbasar, Ö.Ö., Okumuş, G. ve diğerleri. (2021). Evaluation of patients with fibrotic interstitial lung disease: Preliminary results from the Turk-UIP study. Turkish Thoracic Journal, 22(2), 102-109.en_US
dc.identifier.doi10.5152/TurkThoracJ.2021.20028
dc.identifier.endpage109en_US
dc.identifier.issn2149-2530
dc.identifier.issue2en_US
dc.identifier.pmid33871332
dc.identifier.scopus2-s2.0-85103621219
dc.identifier.scopusqualityQ4
dc.identifier.startpage102en_US
dc.identifier.trdizinid468008
dc.identifier.urihttps://turkthoracj.org/en/evaluation-of-patients-with-fibrotic-interstitial-lung-disease-preliminary-results-from-the-turk-uip-study-131756
dc.identifier.urihttps://hdl.handle.net/11468/7208
dc.identifier.volume22en_US
dc.identifier.wosWOS:000659040700001
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.indekslendigikaynakTR-Dizin
dc.institutionauthorTopçu, Füsun
dc.language.isoenen_US
dc.publisherAvesen_US
dc.relation.ispartofTurkish Thoracic Journal
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_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.titleEvaluation of patients with fibrotic interstitial lung disease: Preliminary results from the Turk-UIP study
dc.typeArticleen_US

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