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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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