![]() They can be caused by any number of things, including stress at home or work, a sudden disturbance in the amount of sleep a person gets, a change in daily schedule or other physical factors. Sleep disorders are conditions that can disrupt the amount and quality of sleep a person receives. Many of these same people suffer from common problems known as sleep disorders. Learn more about how to tell if you have a sleeping disorder, how to improve your sleep conditions and general information about sleep disorders in adults. ![]() As such, the procedure is less invasive and should result in a shorter recovery time.Some people simply find it difficult to relax after a hard day at work or at home, while others struggle to understand why they can't fall asleep. In contrast to other surgical options to treat sleep apnea, Inspire therapy does not require removal or permanent alteration of facial or airway anatomy. When activated, Inspire therapy senses breathing patterns and delivers mild stimulation to key airway muscles, which keeps the airway open during sleep. The single external component is a small handheld Inspire sleep remote used to turn the therapy on before bed and off upon waking. Sleep apnea controller Inspire therapy is a fully implanted system consisting of three components: a small generator, a sensing lead and a stimulation lead. People who suffer from sleep apnea lose important deep sleep time which can put them at higher risk for accidents, heart attack and stroke. One of the main causes of sleep apnea is that the tongue and throat muscles relax too much during sleep and can block breathing and wake the patient. Inspire therapy is the first kind of device that keeps airways open by sending a mild electrical shock that prevents the tongue from relaxing and obstructing the airway. Inspire therapy is a pacemaker-like device for sleep apnea patients unable to use continuous positive airway pressure (CPAP). Inspire Therapy: Implantable Device for Sleep Apnea Tampa General Hospital recently performed the 250th implant of the new FDA-approved device, a landmark milestone
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