Respicardia Announces Results Of The remede® System Pilot Study For The Treatment Of Central Sleep Apnea
RESULTS PRESENTED DURING LATE BREAKING SCIENTIFIC SESSION AT HFSA 2013
ORLANDO, Fla., Sept. 23, 2013 /PRNewswire/ -- Respicardia®, a developer of implantable therapies to improve respiratory and cardiovascular health, announced results from the remede System Pilot Study during the Heart Failure Society of America (HFSA) Late Breaking Scientific Session in Orlando. Dr. William T. Abraham of The Ohio State University Wexner Medical Center in Columbus presented the results for the first and only implantable device for respiratory rhythm management to treat central sleep apnea (CSA).
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The remede System Pilot Study represents the first prospective, multi-center, global trial to treat CSA. Implanted by electrophysiologists using a procedure similar to the implantation of intracardiac devices, the remede System is designed to restore normal sleep and breathing to improve respiratory and cardiovascular health in patients with CSA. A total of 44 CSA patients were implanted with the system and completed 6 months of follow-up. Patients experienced a greater than 50% decrease in apnea-hypopnea index (AHI), improved oxygenation by over 50%, decreased arousals and improved quality of life.
"I am impressed by the clinically meaningful results of the remede System," says Dr. William Abraham, Co-Principal Investigator of the remede System Pilot Study. "The remede System which provides a safe and innovative therapy shows promise for the treatment of CSA and is being studied further in the Pivotal Trial."
CSA is associated with increased mortality and hospitalization in heart failure (HF) patients. Studies show that CSA affects up to 40% of HF patients and 30% atrial fibrillation patients.
"We are pleased with the 6 month results from the Pilot Study. These findings reaffirm our belief that the remede System will improve patients' quality of life and will become a standard of care for treating Central Sleep Apnea," remarked Bonnie Labosky, President and CEO of Respicardia.
About the remedeSystem:
The remede System is an implantable pacemaker-like device that was designed for improved respiratory rhythm management. The remede System delivers electrical pulses via an implantable lead to one of the body's two phrenic nerves. The diaphragm responds by restoring a more natural, less disrupted, breathing pattern.
About Central Sleep Apnea:
Central sleep apnea is a type of sleep disordered breathing that disturbs the normal breathing pattern during sleep and adversely affects overall cardiovascular health. The disease occurs when the brain does not send the correct signals to the diaphragm and can lead to excessive daytime sleepiness, reduced exercise capacity, and irregular or very fast heart rhythms (arrhythmia). CSA affects up to 40% of heart failure patients and 30% of atrial fibrillation patients and is associated with the worsening of heart failure and an increased risk of death.
About Respicardia:
Founded in late 2006 and headquartered near Minneapolis, Minnesota, Respicardia is developing implantable therapies designed to improve respiratory and cardiovascular health. The company's initial product, the remede System, is an implantable stimulation device designed to restore a more regular breathing pattern during sleep for central sleep apnea patients.
For more information please visit www.respicardia.com.
SOURCE Respicardia
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