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
Study Type
OBSERVATIONAL
Enrollment
60
Real life drug evaluation
Hospital de Poniente
El Ejido, Almería, Spain
RECRUITINGHospital San Juan de la Cruz
Úbeda, Jaén, Spain
RECRUITINGHospital Costa del Sol
Clinical improvement (risk profile)
Percentage of patients reducing annual mortality risk profile according to ESC/ERS Clinical Practice Guidelines 2015 Risk Stratification.
Time frame: 12 months
Risk stratification variables
Percentage of clinical tests that have been used to include study treatment.
Time frame: Basaline
Events
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.
Time frame: 12 months
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Marbella, Málaga, Spain
Hospital Clinico Universitario San Cecilio
Granada, Spain
RECRUITINGHospital Juan Ramón Jiménez
Huelva, Spain
RECRUITINGHospital Regional de Malaga
Málaga, Spain
RECRUITINGHospital Universitario Virgen de la Victoria
Málaga, Spain
RECRUITINGHospital Universitario de Valme
Seville, Spain
RECRUITINGHospital Universitario Virgen del Rocío
Seville, Spain
RECRUITINGHospital Universitario Virgen Macarena
Seville, Spain
RECRUITING