Connective Tissue Disease, Idiopathic Pulmonary Fibrosis, Interstitial Lung Disease
Conditions
Keywords
Interstitial lung disease, Idiopathic pulmonary fibrosis, Connective tissue disease
Brief summary
We hypothesized that the multi-disciplinary assessment of interstitial lung disease patients would lead to a more accurate diagnosis and consequently alterations in treatment regimens that may lead to improved outcomes.
Interventions
None listed
Sponsors
Study design
Eligibility
Inclusion criteria
* Age above 18 years old * ILD according to ATS/ERS guidelines * Signed inform consent
Exclusion criteria
* Previous lung surgery * Other significant systemic disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The number of patients with collagen related pulmonary fibrosis that are diagnosed by Rheumatologists compared to Pulmonologists. | two years |
Countries
Israel