Key result
Atrial flow regulators in severe PAH show 100% patency, linked to improved symptoms despite oxygen desaturation.
Why the study?
Does Occlutech atrial flow regulator (AFR) implantation improve symptoms and hemodynamics in patients with severe pulmonary arterial hypertension?
Observational
Does Occlutech atrial flow regulator (AFR) implantation improve symptoms and hemodynamics in patients with severe pulmonary arterial hypertension?
Implantation of a novel atrial flow regulator is feasible, safe, and improves symptoms and cardiac index in patients with severe PAH and right heart failure.
May alleviate symptoms in severe PAH despite desaturation; hypothesis-generating, requires prospective trials before adoption.
OBJECTIVES: A novel Occlutech atrial flow regulator (AFR) implantation gives an atrial septal predefined predictable fenestration. BACKGROUND: Atrial septostomy relieves syncope in pulmonary arterial hypertension (PAH) by improving left heart filling, cardiac output and systemic oxygen transport despite hypoxia. Symptoms recur when small fenestrations close spontaneously. METHODS: AFR was implanted after informed consent in patients with severe PAH presenting with syncope and right heart failure. Symptoms, hemodynamics, echocardiographic parameters, brain natriuretic peptide (BNP) levels and device patency were serially documented. RESULTS: ) also showed a significant improvement. Inferior caval vein congestion and pericardial effusion reduced due to improvement in heart failure, but other echocardiographic parameters of right ventricular function did not show significant change. The reduction in BNP levels too did not reach statistical significance. The device was patent in all patients at a median follow-up of 189 days (range 10-296 days) resulting in a significant reduction of oxygen saturations from 98 ± 0.18 to 85.26 ± 2.86% after exercise. CONCLUSIONS: AFR implantation was feasible and safe in all patients with PAH. There was a significant improvement of symptoms, six-minute walk distance, cardiac index and systemic oxygen transport. The device maintained patency in short-term follow-up and the resultant hypoxia was tolerated well.
No takes yet. Share an insight, caveat, or question.
Rajeshkumar et al. (2017) conducted an observational in Severe pulmonary arterial hypertension (PAH). Occlutech atrial flow regulator (AFR) was evaluated on Symptoms, hemodynamics, echocardiographic parameters, brain natriuretic peptide (BNP) levels and device patency. Occlutech atrial flow regulator implantation in severe PAH maintained patency in all patients at a median 189 days, improving symptoms despite exercise oxygen saturation dropping from 98% to 85.26%.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: