Musellim Benan, Mogulkoc Nesrin, Uzun Oguz, Tokgoz Akyil Fatma, Turktas Haluk, Ozdemir Kumbasar Ozlem, Okumus Gulfer, Ogus Candan, Dirol Hulya, Zamani Adil, Sevim Tulin, Annakkaya Ali Nihat, Ozyurek Berna Akinci, Hanta Ismail, Aydemir Yusuf, Cakir Edis Ebru, Kurt Bahar, Tertemiz Kemal Can, Tabak Levent, Yazici Onur, Erdogan Yurdanur, Ates Gungor, Turker Hatice, Salepci Banu, Hazar Armagan, Niksarlioglu Elif Yelda, Yılmaz Kara Bilge, Kokturk Nurdan, Kalpaklioglu Fusun, Uzel Isil, Ozsu Savas, Atahan Ersan, Fendoglu Turkan Zeynep, Yilmaz Sureyya, Basyigit Ilknur, Camsari Gungor, Tuncay Esin, Ucar Yilmazel Elif, Kanmaz Dilek, Ekici Aydanur, Topcu Fusun, Uzaslan Esra, Bozkus Fulsen, Argun Baris Serap, Duru Serap, Altinisik Goksel, Bingol Zuleyha, Tunaci Atadan, Savas Recep, Alper Fatih, Bayraktaroglu Selen, Selcuk Can Tuba, Demir Ali Arslan
{"title":"Evaluation of Patients with Fibrotic Interstitial Lung Disease: Preliminary results from the Turk-UIP Study.","authors":"Musellim Benan, Mogulkoc Nesrin, Uzun Oguz, Tokgoz Akyil Fatma, Turktas Haluk, Ozdemir Kumbasar Ozlem, Okumus Gulfer, Ogus Candan, Dirol Hulya, Zamani Adil, Sevim Tulin, Annakkaya Ali Nihat, Ozyurek Berna Akinci, Hanta Ismail, Aydemir Yusuf, Cakir Edis Ebru, Kurt Bahar, Tertemiz Kemal Can, Tabak Levent, Yazici Onur, Erdogan Yurdanur, Ates Gungor, Turker Hatice, Salepci Banu, Hazar Armagan, Niksarlioglu Elif Yelda, Yılmaz Kara Bilge, Kokturk Nurdan, Kalpaklioglu Fusun, Uzel Isil, Ozsu Savas, Atahan Ersan, Fendoglu Turkan Zeynep, Yilmaz Sureyya, Basyigit Ilknur, Camsari Gungor, Tuncay Esin, Ucar Yilmazel Elif, Kanmaz Dilek, Ekici Aydanur, Topcu Fusun, Uzaslan Esra, Bozkus Fulsen, Argun Baris Serap, Duru Serap, Altinisik Goksel, Bingol Zuleyha, Tunaci Atadan, Savas Recep, Alper Fatih, Bayraktaroglu Selen, Selcuk Can Tuba, Demir Ali Arslan","doi":"10.5152/TurkThoracJ.2021.20028","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>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.</p><p><strong>Material and methods: </strong>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/ERS/JRS/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.</p><p><strong>Results: </strong>A total of 336 patients (253 men, 83 women, age 65.8±9.0 years) were evaluated. Of the patients with sufficient data for diagnosis (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 IPF. None of the women <50 years and none of the men <50 years of age without a smoking history were diagnosed with IPF. 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).</p><p><strong>Conclusion: </strong>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 FANA positivity reduce the likelihood of IPF.</p>","PeriodicalId":37452,"journal":{"name":"Turkish Thoracic Journal","volume":"22 2","pages":"102-109"},"PeriodicalIF":0.8000,"publicationDate":"2021-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8051299/pdf/ttj-22-2-102.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Turkish Thoracic Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5152/TurkThoracJ.2021.20028","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"RESPIRATORY SYSTEM","Score":null,"Total":0}
引用次数: 0
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/ERS/JRS/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 diagnosis (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 IPF. None of the women <50 years and none of the men <50 years of age without a smoking history were diagnosed with IPF. 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 FANA positivity reduce the likelihood of IPF.
期刊介绍:
Turkish Thoracic Journal (Turk Thorac J) is the double-blind, peer-reviewed, open access, international publication organ of Turkish Thoracic Society. The journal is a quarterly publication, published on January, April, July, and October and its publication language is English. Turkish Thoracic Journal started its publication life following the merger of two journals which were published under the titles “Turkish Respiratory Journal” and “Toraks Journal” until 2007. Archives of both journals were passed on to the Turkish Thoracic Journal. The aim of the journal is to convey scientific developments and to create a dynamic discussion platform about pulmonary diseases. With this intent, the journal accepts articles from all related scientific areas that address adult and pediatric pulmonary diseases, as well as thoracic imaging, environmental and occupational disorders, intensive care, sleep disorders and thoracic surgery. Clinical and research articles, reviews, statements of agreement or disagreement on controversial issues, national and international consensus reports, abstracts and comments of important international articles, interesting case reports, writings related to clinical and practical applications, letters to the editor, and editorials are accepted.