by emma
28. October 2011 14:41
A neurostimulation device that offers sufferers from obstructive sleep apnoea (OSA) an alternative to continuous positive airway pressure (CPAP) therapy has gained CE Mark approval.
The Hypoglossal Nerve Stimulation (HGNS) system from US company Apnex Medical has been approved for sale in Europe based on the results of clinical studies in the US and Australia that showed the device to reduce the symptoms of OSA.
OSA – an inability to breathe during sleep – is estimated to affect 100 million people worldwide. It causes excessive daytime fatigue and increases the risk of stroke, heart disease and death.
CPAP therapy is the current standard for OSA, but many patients cannot tolerate it or comply poorly with it. The HGNS system offers a radically different approach: an implantable therapy that activates the muscles in the upper airway.
Implanted in the shoulder, the HGNS system measures the patient’s breathing during sleep and delivers mild electrical pulses to the hypoglossal nerve (which controls the tongue) to keep the airway open.
The system can be programmed to operate only when the patient is asleep, or be turned on and off with a hand-held switch.
The Apnex Clinical Study, a randomised clinical trial, is ongoing in the USA, Europe and Australia. It is designed to test the safety and effectiveness of the HGNS therapy in patients with OSA in whom CPAP therapy has not been effective.
“CE Mark approval is an important confirmation of the substantial benefits that patients receive from our HGNS therapy for obstructive sleep apnoea and is a key milestone for our company,” said Chas McKhann, President and CEO of Apnex Medical. “We are excited to bring this innovative new therapy to Europe.”
Based in Minnesota, USA, Apnex Medical specialises in innovative therapies for sleep-disordered breathing.
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Tags: sleep apnea, sleep apnoea, treatment, CE Mark approval, CE Mark, neurostimulation device, medical devices, medtech, med tech, medical technologies, obstructive sleep apnoea, OSA, CPAP, continuous positive airway pressure, therapy, hypoglossal nerve stimulation, HGNS, US, USA, company, Apnex medical, sales, Europe, clinical studies, Australia, symptoms, CPAP therapy, implant, HGNS system, Chas McKhann, President, CEO, innovation, new therapy, Minnesota, innovative therapies, sleep disorders, breathing
Medtech News
by emma
26. October 2011 17:10
A video clip of a young American woman enabled by the first fully implantable hearing aid to hear her own voice clearly for the first time has become famous online.
Sarah Churman, aged 29, from Texas, was born profoundly deaf and has grown up using external auditory devices to provide partial hearing ability.
The surgical implantation of an Esteem device from Envoy Medical behind each ear resulted in her experiencing much clearer hearing.
Churman’s emotional reaction to her greatly improved hearing was filmed and uploaded to YouTube, where it became a massive hit despite user comments that showed ignorance about her condition.
The Esteem device is the first fully implantable hearing aid, with no microphone or speaker. Based on pacemaker technology, it is implanted under the skin behind the ear. Two leads extend into the middle ear from the device to sense the vibrations of the eardrum and auditory ossicles.
Churman commented that conventional hearing aids had never given her good discrimination of sounds or a sense of their distance: “With my hearing aids everything is jumbled, just white noise.”
Now, she added, voices were clear for the first time: “I could hear my two daughters’ words rather than having to read their lips.” In addition, she said, she was able to hear the sounds of rain, thunder and birdsong.
Each medical device and its implantation would cost nearly £20,000 in the UK, and is not available from the NHS.
Envoy Medical is based in Minnesota, USA.
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Medtech News