Publication: Editorial Perspective: How should child psychologists and psychiatrists interpret FDA device approval? Caveat emptor
Editorial Perspective: How should child psychologists and psychiatrists interpret FDA device approval? Caveat emptor
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Arns, M., Loo, S. K., Sterman, M. B., Heinrich, H., Kuntsi, J., Asherson, P., Banaschewski, T., & Brandeis, D. (2016). Editorial Perspective: How should child psychologists and psychiatrists interpret FDA device approval? Caveat emptor. Journal of Child Psychology and Psychiatry, 57(5), 656–658. https://doi.org/10.1111/jcpp.12524
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Recently several new tests have received US Federal Drug Administration (FDA) marketing approval as aids in the diagnostic process for attention deficit hyperactivity disorder (ADHD), including the Neuropsychiatric electroencephalogram (EEG)-Based ADHD Assessment Aid (NEBA) Health test. The NEBA test relies upon an EEG-based measure, called the theta to beta ratio (TBR). Although this measure has yielded large differences between ADHD and non-ADHD groups in studies prior to 2009, recent studies and a meta-analysis could not replicate
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- Arns, Martijn
- Loo, Sandra K
- Sterman, M Barry
- Heinrich, Hartmut
- Kuntsi, Jonna
- Asherson, Philip
- Banaschewski, Tobias
- Brandeis, Daniel
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Arns, M., Loo, S. K., Sterman, M. B., Heinrich, H., Kuntsi, J., Asherson, P., Banaschewski, T., & Brandeis, D. (2016). Editorial Perspective: How should child psychologists and psychiatrists interpret FDA device approval? Caveat emptor. Journal of Child Psychology and Psychiatry, 57(5), 656–658. https://doi.org/10.1111/jcpp.12524
