Evaluation of Patients with Fibrotic Interstitial Lung Disease: Preliminary results from the Turk-UIP Study.

Benan, Musellim; Nesrin, Mogulkoc; Oguz, Uzun; Fatma, Tokgoz; Haluk, Turktas; Ozlem, Ozdemir; Gulfer, Okumus; Candan, Ogus; Hulya, Dirol; Adil, Zamani; Tulin, Sevim; Nihat, Annakkaya; Akinci, Ozyurek; Ismail, Hanta; Yusuf, Aydemir; Ebru, Cakir; Bahar, Kurt; Can, Tertemiz; Levent, Tabak; Onur, Yazici; Yurdanur, Erdogan; Gungor, Ates; Hatice, Turker; Banu, Salepci; Armagan, Hazar; Yelda, Niksarlioglu; YILMAZ KARA, BİLGE; KÖKTÜRK, NURDAN; Fusun, Kalpaklioglu; Isil, Uzel; Savas, Ozsu; Ersan, Atahan; Zeynep, Fendoglu; Sureyya, Yilmaz; Ilknur, Basyigit; Gungor, Camsari; Esin, Tuncay; Elif, Elif; Dilek, Kanmaz; Aydanur, Ekici; Fusun, Topcu; Esra, Uzaslan; Fulsen, Bozkus; ARGUN BARIŞ, SERAP; Serap, Duru; Goksel, Altinisik; Zuleyha, Bingol; Atadan, Tunaci; SAVAŞ, RECEP; Fatih, Fatih; Selen, Bayraktaroglu; Tuba, Selcuk; Arslan, Demir

doi:10.5152/turkthoracj.2021.20028

Evaluation of Patients with Fibrotic Interstitial Lung Disease: Preliminary results from the Turk-UIP Study.

Atıf İçin Kopyala

Benan M., Nesrin M., Oguz U., Fatma T. A., Haluk T., Ozlem O. K., ...Daha Fazla

Turkish thoracic journal, cilt.22, sa.2, ss.102-109, 2021 (SCI-Expanded)

Yayın Türü: Makale / Tam Makale
Cilt numarası: 22 Sayı: 2
Basım Tarihi: 2021
Doi Numarası: 10.5152/turkthoracj.2021.20028
Dergi Adı: Turkish thoracic journal
Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, TR DİZİN (ULAKBİM)
Sayfa Sayıları: ss.102-109
Anahtar Kelimeler: Fibrotic interstitial lung diseases, idiopathic pulmonary fibrosis, usual interstitial pneumonia, IDIOPATHIC PULMONARY-FIBROSIS, CLINICAL-PRACTICE, DIAGNOSIS, EPIDEMIOLOGY
Atatürk Üniversitesi Adresli: Evet

Özet

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.