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Nathalie Jeanne Magioli Bravo-Valenzuela1, Flavia Navarro2, Socrates Pereira Silva3
1 Department of Pediatrics, Federal University of Rio de Janeiro, Rio de Janeiro, RJ; PEDICOR-Pediatric and Perinatal Cardiology Center, Sao Jose dos Campos, SP, Brazil
2 Pulmonary Hypertension Center, Faculty of Medical Sciences, Santa Casa de Sao Paulo, Sao Paulo, SP, Brazil
3 PEDICOR-Pediatric and Perinatal Cardiology Center, Sao Jose dos Campos, SP, Brazil
Correspondence Address:
Prof. Nathalie Jeanne Magioli Bravo-Valenzuela
Av. Andromeda, 693, s. 601-603, Zip Code: 12230-000, São José dos Campos- SP
Brazil
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/apc.APC_63_19
Pulmonary arterial hypertension (PAH) is a chronic, progressive, multifactorial disease. Currently, combination therapy is an attractive option for PAH management because three pathways (endothelin, nitric oxide, and prostacyclin) are involved in this disease. Selexipag is a novel oral prostacyclin pathway drug and is a highly selective IP prostacyclin receptor agonist with vasodilatory and antiproliferative effects. We report the case of a teenage patient with idiopathic PAH who presented in World Health Organization functional Class IV and showed no clinical improvement with dual therapy. We added oral selexipag to the treatment regimen and observed substantial improvement in her quality of life at the short-time follow-up. Despite the lack of childhood data regarding the use of selexipag in pediatric patients with PAH, the use of this drug in the current teenage patient improved her quality of life and exercise capacity.
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