Clinical, Functional, and Prognostic Evaluation of Idiopathic Pulmonary Fibrosis, Connective Tissue Disease-AssociatedInterstitial Lung Disease, Interstitial Pneumonia with Autoimmune Features: A Single-Center Prospective Study

Öz M., Erol S., Küçükşahin O., Kar İ., Atasoy K. Ç., Özdemir Kumbasar Ö.

Turkish Thoracic Journal, cilt.23, sa.6, ss.395-402, 2022 (ESCI) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 23 Sayı: 6
  • Basım Tarihi: 2022
  • Doi Numarası: 10.5152/turkthoracj.2022.22017
  • Dergi Adı: Turkish Thoracic Journal
  • Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI)
  • Sayfa Sayıları: ss.395-402
  • Anahtar Kelimeler: Interstitial lung diseases, collagen tissue diseases, IPF, IPAF, RHEUMATOLOGY/EUROPEAN LEAGUE, CLASSIFICATION CRITERIA, AMERICAN-COLLEGE, STANDARDIZATION, DIAGNOSIS
  • Ankara Üniversitesi Adresli: Evet

Özet

OBJECTIVE: Our study aimed to evaluate clinical, functional, and prognostic features and to determine the prognosis of idiopathic pulmonary fibrosis, connective tissue disease-associated interstitial lung diseases, and interstitial pneumonia with autoimmune features.