Connective Tissue Disease-associated Interstitial Lung Diseases (CTD-ILD) Epidemiology Non-interventional Study (NIS)

Más betegség

• Patient with a biopsy definition of usual interstitial pneumonitis, related to any other non-CTD.
• Patient with post-chemotherapy or post-radiotherapy pneumonitis.

Egyéb

• Medical Records of patients without full diagnostic of ILD (clinically and by biopsy or high-resolution computed tomography).

• For newly data collection:
• Male and female Patients.
• Patients over 18 years old.
• Patient who gives his/her signed informed consent to be able to use information about their condition.
• Patient who has the diagnosis of: rheumatoid arthritis, connective tissue disease (CTD) (systemic sclerosis or scleroderma; inflammatory myopathy: antisynthetase, dermatomyositis, polymyositis, mixed connective tissue disease; systemic lupus erythematosus; primary Sjögren syndrome; pulmonary fibrosis associated with non-specific autoimmunity; primary systemic vasculitis; psoriasis, anchylosing spondylitis, reactive arthritis) Spondyloarthritis (SpA) or sarcoidosis, (accordingly with the updated clinical criteria for each pathology).
  • Patient with any interstitial lung diseases (ILD) diagnosed clinically and by a high-resolution computed tomography study with an interstitial pattern (supervised by an expert radiologist).
  • For existing data collection:
• Medical Records from patients with whom contact was permanently lost for any reason since 2012 till the study start date.
• Medical Records from male and female Patients.
• Medical Records from patients over 18 years old.
• Medical Records of patients that have at least: patient initials, date of birth, gender, date of diagnosis, full diagnosis of:
  • Patient who has the diagnosis of: rheumatoid arthritis, CTD (systemic sclerosis or scleroderma; inflammatory myopathy: antisynthetase, dermatomyositis, polymyositis, mixed connective tissue disease; Systemic lupus erythematosus; primary Sjögren syndrome; pulmonary fibrosis associated with non-specific autoimmunity; primary systemic vasculitis; psoriasis, anchylosing spondylitis, reactive arthritis) SpA or Sarcoidosis, (accordingly with the updated clinical criteria for each pathology).
  • Patient with any ILD diagnosed clinically and by a high-resolution computed tomography study with an interstitial pattern (supervised by an expert radiologist).