Pulmonary Hypertension, Sarcoidosis
Conditions
Keywords
ambrisentan, Bosentan, Iloprost
Brief summary
Registry to follow patients with sarcoidosis associated pulmonary hypertension
Detailed description
This is a multi center registry of sarcoidosis associated pulmonary hypertension (SAPH). With this registry, the investigators will characterize the demographics, clinical course, hemodynamics, pulmonary physiology, and disease management of sarcoidosis associated pulmonary hypertension on the United States. The investigators will also compare these features to non-US sites.
Interventions
Observe patients
Sponsors
Study design
Eligibility
Inclusion criteria
* Patients with sarcoidosis as defined by the ATS/WASOG statement * Patients with pulmonary hypertension as confirmed by right heart catheterization * Patients willing to provide written informed consent
Exclusion criteria
* Unwillingness to provide assurance that they will complete the follow up visits for the study
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Survival | 4 years | Mortality during time of study |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Disease management | 4 years | Examine initial and follow up management |
Countries
United States