Table 2.
Acute clinically significant respiratory deterioration characterized by evidence of new widespread alveolar abnormality |
Diagnostic criteria |
Previous or concurrent diagnosis of IPF |
Acute worsening of dyspnea (within 1 mo) |
CT evidence of diffuse infiltrates/ground glass/consolidation on a background of UIP pattern |
Deterioration not fully explained by heart failure/fluid overload |
IPF = idiopathic pulmonary fibrosis; UIP = usual interstitial pneumonia.