Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/46311
Title: Evaluation of Patients with Fibrotic Interstitial Lung Disease: Preliminary results from the Turk-UIP Study
Authors: Benan, Musellim
Nesrin, Mogulkoc
Oguz, Uzun
Fatma, Tokgoz Akyil
Haluk, Turktas
Ozlem, Ozdemir Kumbasar
Gulfer, Okumus
Candan, Ogus
Hulya, Dirol
Adil, Zamani
Tulin, Sevim
Nihat, Annakkaya Ali
Akinci, Ozyurek Berna
Ismail, Hanta
Yusuf, Aydemir
Ebru, Cakir Edis
Bahar, Kurt
Can, Tertemiz Kemal
Levent, Tabak
Onur, Yazici
Yurdanur, Erdogan
Gungor, Ates
Hatice, Turker
Banu, Salepci
Armagan, Hazar
Yelda, Niksarlioglu Elif
Bilge, Yilmaz Kara
Nurdan, Kokturk
Fusun, Kalpaklioglu
Isil, Uzel
Savas, Ozsu
Ersan, Atahan
Zeynep, Fendoglu Turkan
Sureyya, Yilmaz
Ilknur, Basyigit
Gungor, Camsari
Esin, Tuncay
Elif, Ucar Yilmazel
Dilek, Kanmaz
Aydanur, Ekici
Fusun, Topcu
Esra, Uzaslan
Fulsen, Bozkus
Serap, Argun Baris
Serap, Duru
Goksel, Altinisik
Zuleyha, Bingol
Atadan, Tunaci
Recep, Savas
Fatih, Alper
Selen, Bayraktaroglu
Tuba, Selcuk Can
Arslan, Demir Ali
Keywords: Fibrotic interstitial lung diseases
idiopathic pulmonary fibrosis
usual interstitial pneumonia
Idiopathic Pulmonary-Fibrosis
Clinical-Practice
Diagnosis
Epidemiology
Publisher: Aves
Abstract: OBJECTIVE: 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.
URI: https://doi.org/10.5152/TurkThoracJ.2021.20028
https://hdl.handle.net/11499/46311
ISSN: 2149-2530
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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