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Diagnostic Device Approved by FDA for Evaluating ADHD

The Federal Drug Administration recently approved a new device for assessing ADHD. This is the first medical device approved for the diagnosis of this common condition of childhood.

 
The technique, called the Neuropsychiatric EEG-Based Assessment Aid (NEBA) System, relies on deciphering encephalogram (EEG) waves. Taking 15 to 20 minutes, this non-invasive test uses computer functions to calculate the ratio of beta and theta brain wave frequencies. Previous research has shown that theta and beta ratios are higher in children and adolescents with ADHD compared to non-ADHD subjects.

 
Although officially approved, significant uncertainty exists among experts as to the NEBA technology’s value in the overall diagnosis and management of ADHD. Currently the evaluation of ADHD is a complex process utilizing observation, behavior analysis, and psychological testing. Whether the NEBA adds significant help in this process is uncertain. One concern is how much does the use of this technology add to the overall cost of an evaluation.

 
Of course, time will reveal the usefulness of this new technology. Stay tuned. We will keep you informed as additional research data comes in.

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