Survival in interstitial pneumonia with features of autoimmune disease: A comparison of proposed criteria

Abstract Background Some patients with chronic fibrosing interstitial pneumonia (IP) have clinical, serological, and morphological features suggestive of, but not diagnostic for, a connective tissue disease. Several names and diagnostic criteria for this entity have been proposed. The objective of t...

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Veröffentlicht in:	Respiratory medicine 2015-10, Vol.109 (10), p.1326-1331
Hauptverfasser:	Assayag, Deborah, Kim, Eunice J, Elicker, Brett M, Jones, Kirk D, Golden, Jeffrey A, King, Talmadge E, Koth, Laura L, Shum, Anthony K, Wolters, Paul J, Collard, Harold R, Lee, Joyce S
Format:	Artikel
Sprache:	eng
Schlagworte:	Age Aged Autoimmune diseases Autoimmune Diseases - diagnosis Autoimmune Diseases - immunology Autoimmune Diseases - mortality Autoimmune Diseases - pathology Autoimmunity - physiology Cohort Studies Deoxyribonucleic acid Diagnosis, Differential DNA Female Histopathology Humans Idiopathic pulmonary fibrosis Idiopathic Pulmonary Fibrosis - diagnosis Idiopathic Pulmonary Fibrosis - immunology Idiopathic Pulmonary Fibrosis - mortality Idiopathic Pulmonary Fibrosis - pathology Interstitial lung disease Laboratories Longitudinal Studies Lung diseases Male Middle Aged Mortality Physiology Pneumonia Prognosis Prospective Studies Pulmonary/Respiratory Respiratory Function Tests Severity of Illness Index Studies Survival analysis Survival Rate Tomography Scanners, X-Ray Computed Transplants & implants Undifferentiated connective tissue disease
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