| Literature DB >> 28702718 |
Roberto Gallotti1, Diana E Drogalis-Kim1, Gary Satou1,2, Juan Alejos3,4.
Abstract
Pulmonary arterial hypertension (PAH) is a rare and progressive disorder. Current treatment in the pediatric population includes phosphodiesterase 5 inhibitors (PDE-5i), endothelin receptor antagonists (ERA), and both inhaled and intravenous prostacyclin pathway agonists. As of December 22, 2015 the first oral prostacyclin pathway agonist, selexipag (Uptravi®), was FDA approved in the US. In this case series, we discuss our single-center experience using selexipag in a pediatric population, composed of both patients with idiopathic PAH, and patients with congenital heart disease and PAH.Entities:
Keywords: Pediatrics; Pulmonary hypertension; Remodulin®; Selexipag; Treprostinil; Uptravi®
Mesh:
Substances:
Year: 2017 PMID: 28702718 DOI: 10.1007/s00246-017-1677-7
Source DB: PubMed Journal: Pediatr Cardiol ISSN: 0172-0643 Impact factor: 1.655