At the Heart Failure Society of America’s (HFSA) 17th Annual Scientific Meeting, held this past month in Orlando, FL, researchers presented encouraging results from a Food and Drug Administration (FDA) Phase II study of a neurostimulation device designed to treat central sleep apnea (CSA).
The remedē System, an implantable pacemaker-like device from Respicardia Inc., stimulates the phrenic nerve in the chest to engage the diaphragm and restore normal breathing. Three-month follow-up data on...
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