Richard Caton, in his studies on rabbits and monkeys, was the first to identify electrical activity of the brain utilizing scalp electrodes. Hans Burger is credited with identifying similar electrical activity utilizing scalp electrodes in humans. In 1929 describing Caton's work he stated, "There were found distinct variations in currents which increased during sleep with the onset of death strengthened and after death became weaker and completely disappeared" [1]. This suggests that he saw the high-amplitude delta activity of slowwave sleep, with the "onset of death" an encephalopathic state and "after death became weaker," electrocerebral silence. As the electroencephalogram (EEG) evolved it was not only able to identify abnormal electrical activity of the brain including seizures, but also offered great diagnostic and prognostic utility. With neuroimaging and genetic advances, the diagnostics utility outside of the field of epilepsy has become somewhat limited. It is still an inexpensive, widely available, and benign procedure, which in many instances may drive diagnostic decision-making. It still has great utility in defining encephalopathic states and prognosticating recovery. In this chapter, an evidence-based approach for the necessity of its use or the lack thereof will be discussed. The use of the electroencephalogram in identifying a seizure, risk of epilepsy, and identifying epilepsy syndromes will be outlined.