Risk assessment validation in patients with pulmonary arterial hypertension: Data from a Southern Brazil registry (RESPHIRAR study)

• Published in: Pulmonary circulation 2023-01, Vol.13 (1), p.e12193-n/a
• Main Authors: Spilimbergo, Fernanda Brum, Pirath Rodrigues, Roger, Credidio Dias‐Pinto, Marcelo, Blanco, Daniela Cavalet, Barbieri, Gláucia Maria, Andrade‐Lima, Marina, Leal Fagundes, Ariovaldo, Gazzana, Marcelo Basso, Roncato, Gabriela, Mello, Marcelo Martins, Watte, Guilherme, Assmann, Taís Silveira, Caurio, Cássia Ferreira Braz, Souza, Rogerio, Meyer, Gisela Martina Bohns
• Format: Article
• Language: English
• Subjects: Mortality; pulmonary arterial hypertension; Pulmonary hypertension; Risk assessment; Southern Brazil registry
• ISSN: 2045-8940; 2045-8932; 2045-8940
• DOI: 10.1002/pul2.12193

Pulmonary arterial hypertension (PAH) is a severe and progressive disease characterized by increased pulmonary vascular resistance, ultimately leading to right heart failure and death. Registries are a valuable tool in the research of rare conditions such as PAH. Moreover, the risk assessment strategy has been validated in European and North American registries and has been reported to provide an accurate prediction of mortality and the clinical advantage of reaching low‐risk status. However, there is no available data from Brazil. Thus, the aim of the present study was to describe the characteristics of a sample of PAH from Southern Brazil and to retrospectively validate the risk assessment at our population. The RESPHIRAR is a retrospective and multicentric registry on pulmonary hypertension. With a join collaboration from nine centers in Southern Brazil, demographics, clinical presentation, and hemodynamics data of PAH were collected between 2007 and 2017. Moreover, the REVEAL 2.0 and REVEAL 2.0 Lite risk assessments were validated in our population. Overall, 370 PAH patients were included in the present study. Patients were predominantly female (78.5%) and had a mean age of 41.8 ± 18.8 years. Most patients (33.4%) had idiopathic PAH, 30.2% had PAH associated with congenital heart disease, and 23.5% had PAH associated with connective tissue disease. The low‐risk group showed significantly lower mortality than the intermediated‐ or high‐risk group at diagnosis (p