scholarly journals Atrial septostomy in the treatment of severe pulmonary arterial hypertension

Heart ◽  
2004 ◽  
Vol 90 (1) ◽  
pp. 69-69
Author(s):  
F Reichenberger
2020 ◽  
Vol 10 (3) ◽  
pp. 004947552095973
Author(s):  
Samantha L. Brackett ◽  
Nina Deutsch ◽  
Chinwe Unegbu

Pulmonary arterial hypertension is a pernicious disease with a diverse etiology in the pediatric population. Despite the increased availability of drug therapies, pulmonary arterial hypertension continues to cause significant morbidity and mortality. In pediatric patients with severe pulmonary arterial hypertension who have failed medical therapy, a few studies have demonstrated the role of balloon atrial septostomy as a bridge to lung transplantation or a means of improving symptomatology. However, no data exists on the utilization of balloon atrial septostomy as a palliative intervention to wean from extracorporeal membrane oxygenation (ECMO) when all other therapies are exhausted. Here we describe a case series of two pediatric patients with severe pulmonary arterial hypertension, requiring ECMO support, who were successfully weaned from ECMO following balloon atrial septostomy.


2016 ◽  
Vol 69 (1) ◽  
pp. 78-81 ◽  
Author(s):  
Maite Velázquez Martín ◽  
Agustín Albarrán González-Trevilla ◽  
Carmen Jiménez López-Guarch ◽  
Julio García Tejada ◽  
Roberto Martín Asenjo ◽  
...  

2016 ◽  
Vol 15 (1) ◽  
pp. 19-25 ◽  
Author(s):  
Julio Sandoval ◽  
Tomás Pulido ◽  
Juan Pablo Sandoval ◽  
Nayeli Zayas ◽  
Jorge Gaspar

Despite advances in pharmacologic treatment, pulmonary arterial hypertension (PAH) remains a fatal disease. In recent years, surgical/interventional approaches including balloon dilation atrial septostomy and Potts anastomosis have been applied to improve the hemodynamic variables associated with right ventricular failure in the setting of PAH. These interventions may improve quality of life and prolong survival in this population. In this review, we will discuss the role of these 2 therapeutic alternatives in the management of PAH.


2015 ◽  
Vol 26 (2) ◽  
pp. 378-381 ◽  
Author(s):  
Saul Flores ◽  
Joshua Daily ◽  
Jayant “Nick” Pratap ◽  
Michelle C. Cash ◽  
Russel Hirsch

AbstractWe describe the course and management of a 12-year-old girl with severe pulmonary arterial hypertension who initially presented with severe systemic hypertension. Successful therapy included pulmonary vasodilators and an atrial septostomy, while ensuring adequate maintenance of her systemic vascular resistance to maintain cardiac output. Clear understanding of the physiology and judicious medical management in patients with severe pulmonary arterial hypertension using extreme compensatory mechanisms is vitally important.


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