Publication:
Evaluation of patients with fibrotic interstitial lung disease: Preliminary results from the turk-uip study

dc.contributor.authorBenan, Müsellim
dc.contributor.authorNesrin, Moğulkoç
dc.contributor.authorOğuz, Uzun
dc.contributor.authorFatma, Tokgöz Akyıl
dc.contributor.authorHaluk, Türktaş
dc.contributor.authorÖzlem, Özdemir Kumbasar
dc.contributor.authorGülfer, Okumuş
dc.contributor.authorCandan, Oğus
dc.contributor.authorHülya, Dirol
dc.contributor.authorAdil, Zamani
dc.contributor.authorTülin, Sevim
dc.contributor.authorNihat, Annakkaya Ali
dc.contributor.authorAkıncı, Özyurek Berna
dc.contributor.authorİsmail, Hanta
dc.contributor.authorYusuf, Aydemir
dc.contributor.authorEbru, Çakır Edis
dc.contributor.authorBahar, Kurt
dc.contributor.authorCan, Tertemiz Kemal
dc.contributor.authorLevent, Tabak
dc.contributor.authorOnur, Yazıcı
dc.contributor.authorYurdanur, Erdoğan
dc.contributor.authorGüngör, Ateş
dc.contributor.authorHatice, Türker
dc.contributor.authorBanu, Salepci
dc.contributor.authorArmağan, Hazar
dc.contributor.authorYelda, Niksarlioğlu Elif
dc.contributor.authorBilge, Yılmaz Kara
dc.contributor.authorNurdan, Köktürk
dc.contributor.authorFüsun, Kalpaklıoğlu
dc.contributor.authorIşıl, Uzel
dc.contributor.authorSavaş, Özsu
dc.contributor.authorErsan, Atahan
dc.contributor.authorZeynep, Fendoğlu Türkan
dc.contributor.authorSüreyya, Yılmaz
dc.contributor.authorIlknur, Başyiğit
dc.contributor.authorGüngör, Camsarı
dc.contributor.authorEsin, Tuncay
dc.contributor.authorElif, Uçar Yilmazel
dc.contributor.authorDilek, Kanmaz
dc.contributor.authorAydanur, Ekici
dc.contributor.authorFüsun, Topcu
dc.contributor.authorEsra, Uzaslan
dc.contributor.authorFulsen, Bozkuş
dc.contributor.authorSerap, Argun Barış
dc.contributor.authorSerap, Duru
dc.contributor.authorGöksel, Altınışık
dc.contributor.authorZüleyha, Bingöl
dc.contributor.authorAtadan, Tunacı
dc.contributor.authorRecep, Savaş
dc.contributor.authorFatih, Alper
dc.contributor.authorSelen, Bayraktaroğlu
dc.contributor.authorTuba, Selçuk Can
dc.contributor.authorArslan, Demir Ali
dc.contributor.buuauthorUZASLAN, AYŞE ESRA
dc.contributor.departmentBursa Uludağ Üniversitesi/Tıp Fakültesi/Göğüs Hastalıkları Anabilim Dalı.
dc.contributor.orcid0000-0003-3120-6506
dc.contributor.researcheridCNX-4587-2022
dc.date.accessioned2024-06-07T06:39:21Z
dc.date.available2024-06-07T06:39:21Z
dc.date.issued2021-03-01
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.sponsorshipCompany of Roche
dc.identifier.doi10.5152/TurkThoracJ.2021.20028
dc.identifier.eissn2149-2530
dc.identifier.endpage109
dc.identifier.issue2
dc.identifier.startpage102
dc.identifier.urihttps://doi.org/10.5152/TurkThoracJ.2021.20028
dc.identifier.urihttps://thoracrespract.org/en/evaluation-of-patients-with-fibrotic-interstitial-lung-disease-preliminary-results-from-the-turk-uip-study-131756
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8051299/
dc.identifier.urihttps://hdl.handle.net/11452/41865
dc.identifier.volume22
dc.identifier.wos000659040700001
dc.indexed.wosWOS.ESCI
dc.language.isoen
dc.publisherAves
dc.relation.journalTurkish Thoracic Journal
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectIdiopathic pulmonary-fibrosis
dc.subjectClinical-practice
dc.subjectDiagnosis
dc.subjectEpidemiology
dc.subjectFibrotic interstitial lung diseases
dc.subjectIdiopathic pulmonary fibrosis
dc.subjectUsual interstitial pneumonia
dc.subjectRespiratory system
dc.titleEvaluation of patients with fibrotic interstitial lung disease: Preliminary results from the turk-uip study
dc.typeArticle
dspace.entity.typePublication
relation.isAuthorOfPublication80df98cb-7a8e-4a6c-86c1-65dfe8f4e962
relation.isAuthorOfPublication.latestForDiscovery80df98cb-7a8e-4a6c-86c1-65dfe8f4e962

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