SYNCHRONY EAS (Electric Acoustic Stimulation) Hearing Implant System received FDA approval and benefit patients with advanced hearing loss.

‘SYNCHRONY EAS (Electric Acoustic Stimulation) Hearing Implant System approved by the FDA improved hearing in 97% of trial participants.
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“Our clinical trial participants were overwhelmingly receptive to this new technology,” Pillsbury said. “The technology is remarkable and so were the results.”




The implant relies on two auditory technologies – the SYNCHRONY cochlear implant that stimulates the auditory nerve for high-frequency hearing loss and the EAS audio processor, which has a built-in acoustic amplification for low-frequency hearing loss.
The SYNCHRONY EAS implant best assists people whose hearing loss is referred to as “ski-slope” hearing loss, based on the steeply sloping image that appears on an audiogram when a patient has more trouble hearing higher-frequency sounds. Using traditional hearing aids, those patients often have difficulty understanding speech above the din of background noise.
Ninety-seven percent of patients participating in the MED-EL EAS clinical trial reported a benefit from EAS within the first year. Ninety-two percent of participants reported an improvement in their ability to hear even among background noise, one of the most challenging listening environments for people with hearing loss. And 90 percent reported satisfaction with the device overall.
“On average, patients performed more than twice as well on tests of speech understanding with EAS than they did with their hearing aids preoperatively, which speaks to the benefits of this technology,” Pillsbury said.
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The EAS System FDA approval is for candidates who are 18 years old and older who have normal to moderate sensorineural hearing loss in the low frequencies, sloping to a severe-to-profound hearing loss in the high frequencies.
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Source-Newswise