Release date: 2013-08-06
On July 15, the US Food and Drug Administration (FDA) approved the launch of the first brain-based medical device to improve the diagnosis of attention deficit hyperactivity disorder in children and adolescents (6 to 17 years old) (ADHD, attention- The accuracy of deficit/hyperactivity disorder).
As part of a complete medical and psychological examination, the device can improve the diagnosis of ADHD or help doctors decide to focus further diagnosis on ADHD and other symptoms similar to ADHD.
The device is an EEG-based neuropsychiatric evaluation aid system (NEBA system, Neuropsychiatric EEG-Based Assessment Aid), which is based on electroencephalography (EEG) technology for recording by the brain. Different types of electrical impulses (waves) emitted by neurons (neural cells) and the frequency of pulses emitted per second. The NEBA system is a 15-20 minute non-invasive test that calculates the ratio of the frequencies of two standard brain waves (theta waves and beta waves). The ratio of θ/β in children and adolescents with ADHD is higher than in normal children, so the NEBA system can help screen out children whose symptoms are more like attention deficit hyperactivity disorder.
Source: China Medical Technology Network
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