Pulmonary Arterial Hypertension
Conditions
Keywords
Pulmonary Arterial Hypertension, Selexipag, Real World Data, Effectiveness
Brief summary
This is an observational, ambrispective study of patients in real world clinical practice, who has pulmonary arterial hypertension in whom a prostacyclin IP receptor agonist (Selexipag) is initiated between 2017 and 2021. The aim of this study answer the following questions: * Changes in the mortality risk profile of these patients after treatment administration. * Baseline characteristics of patients initiating Selexipag. * Parameters used for risk stratification prior to treatment escalation. * Events during follow-up. No comparison group available
Interventions
Real life drug evaluation
Sponsors
Study design
Eligibility
Inclusion criteria
* They agree to participate in the study by signing an informed consent form
Exclusion criteria
* Decline to participate in the study * Patients living 6 months or less in the reference health area * Patients with active malignant tumors
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Clinical improvement (risk profile) | 12 months | Percentage of patients reducing annual mortality risk profile according to ESC/ERS Clinical Practice Guidelines 2015 Risk Stratification. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Risk stratification variables | Basaline | Percentage of clinical tests that have been used to include study treatment. |
| Events | 12 months | Incidence of events in follow-up: admission for worsening pulmonary hypertension; need for systemic prostacyclins; unscheduled admission for any cause; death related to pulmonary hypertension; death from any cause. |
Countries
Spain