IPF, PPF, and non-progressive ILD
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients diagnosed with at least 2 fibrosing ILD codes in different months during the patient identification period Patients aged 20 years or older on the index date Patients for whom data for the 12 months prior to the index date can be extracted as baseline data
Exclusion criteria
Exclusion criteria: None
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To investigate the cumulative incidences of clinically significant outcomes such as mortality (including lung transplantation), all cause hospitalisation, respiratory hospitalisation, and acute exacerbation in patients with fibrosing ILDs in Japan. | — |
Secondary
| Measure | Time frame |
|---|---|
| To describe baseline demographic and clinical characteristics in patients with fibrosing ILDs in Japan. To describe the distribution of PPF progression proxies met in patients with progression to PPF. To describe healthcare resource utilisation (HCRU) and medical cost in patients with fibrosing ILDs in Japan. To describe clinical practice on treatment and management in patients with fibrosing ILDs in Japan. | — |
Countries
Japan
Contacts
Nippon Boehringer Ingelheim Co., Ltd. Medicine Division