Electroencephalogram

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This diagnostic image displays a 12-channel electroencephalogram (EEG) recording showing significant pathological brain activity. The recording utilizes a longitudinal bipolar montage with labels including Fp1-T3, T3-O1, Fp2-T4, T4-O2, Fp1-C3, C3-O1, Fp2-C4, C4-O2, T3-C3, C3-Cz, Cz-C4, and C4-T4. The waveforms are organized in alternating red and blue traces against a vertical grid representing time intervals. The visual findings are characterized by high-amplitude, generalized discharges including frequent spikes, sharp waves, and irregular slow-wave complexes. There is a notable lack of normal background synchronicity, with chaotic and paroxysmal activity present across all frontal, temporal, and central derivations. These features are clinically indicative of generalized seizure activity (ictal state). The tracing demonstrates high-voltage electrical instability and rhythmic discharges consistent with a drug-induced or spontaneous epileptiform event. The image serves as an educational tool for identifying disorganized EEG patterns, spike-and-wave morphology, and the electrographic manifestation of generalized seizures in a neurodiagnostic context.

This diagnostic image displays a 12-channel electroencephalogram (EEG) recording showing significant pathological brain activity. The recording utilizes a longitudinal bipolar montage with labels including Fp1-T3, T3-O1, Fp2-T4, T4-O2, Fp1-C3, C3-O1, Fp2-C4, C4-O2, T3-C3, C3-Cz, Cz-C4, and C4-T4. The waveforms are organized in alternating red and blue traces against a vertical grid representing time intervals. The visual findings are characterized by high-amplitude, generalized discharges including frequent spikes, sharp waves, and irregular slow-wave complexes. There is a notable lack of normal background synchronicity, with chaotic and paroxysmal activity present across all frontal, temporal, and central derivations. These features are clinically indicative of generalized seizure activity (ictal state). The tracing demonstrates high-voltage electrical instability and rhythmic discharges consistent with a drug-induced or spontaneous epileptiform event. The image serves as an educational tool for identifying disorganized EEG patterns, spike-and-wave morphology, and the electrographic manifestation of generalized seizures in a neurodiagnostic context.

This diagnostic figure displays representative electroencephalogram (EEG) recordings demonstrating various epileptiform discharges in a model of post-traumatic epilepsy (PTE). Panel A shows a baseline normal EEG tracing characterized by regular oscillations with an amplitude of 80μV. Panels B through F illustrate diverse pathological waveforms associated with PTE: (B) multiple sharp-wave polyspikes with a 400μV amplitude; (C) two- and three-phase sharp waves on a 0.5-second timescale; (D) a 10-second window of continuous abnormal discharges with an inset providing an enlarged view of individual high-amplitude spikes (400μV); (E) a 20-minute recording showing explosive, sustained abnormal activity with occasional high-amplitude spikes exceeding the background; and (F) a singular, sudden high-amplitude spike against a quieter baseline. These recordings highlight the progression from normal brain activity to distinct ictal and interictal patterns, including increased amplitude (up to 1,000μV) and altered frequency characteristic of epileptic seizures. The imagery serves as a comparison chart for identifying specific neurological markers in epilepsy research and clinical neurophysiology.

This diagnostic figure displays representative electroencephalogram (EEG) recordings demonstrating various epileptiform discharges in a model of post-traumatic epilepsy (PTE). Panel A shows a baseline normal EEG tracing characterized by regular oscillations with an amplitude of 80μV. Panels B through F illustrate diverse pathological waveforms associated with PTE: (B) multiple sharp-wave polyspikes with a 400μV amplitude; (C) two- and three-phase sharp waves on a 0.5-second timescale; (D) a 10-second window of continuous abnormal discharges with an inset providing an enlarged view of individual high-amplitude spikes (400μV); (E) a 20-minute recording showing explosive, sustained abnormal activity with occasional high-amplitude spikes exceeding the background; and (F) a singular, sudden high-amplitude spike against a quieter baseline. These recordings highlight the progression from normal brain activity to distinct ictal and interictal patterns, including increased amplitude (up to 1,000μV) and altered frequency characteristic of epileptic seizures. The imagery serves as a comparison chart for identifying specific neurological markers in epilepsy research and clinical neurophysiology.

This diagnostic image shows a standard scalp electroencephalogram (EEG) recording from a human subject. The tracing is organized into multiple horizontal channels, with electrode derivations labeled on the left side of the display (e.g., Fp1-F3, F3-C3, C3-P3, P3-O1), representing the 10-20 system in a longitudinal bipolar montage. The recording displays continuous electrical activity of the brain, characterized primarily by high-frequency waves of 8 Hz and higher, consistent with alpha and beta rhythms. The wave morphology is relatively symmetric and regular across the hemispheres, without evident epileptiform discharges, focal slowing, or lateralized periodic discharges. Vertical green grid lines provide a temporal scale for frequency analysis, while vertical deflections in frontal channels (Fp1, Fp2) likely represent physiological artifacts such as eye blinks. This tracing is identified as a normal EEG in the context of a patient presenting with metabolic-induced seizures, serving as an educational example of how systemic conditions like hypoglycemia from an insulinoma can mimic primary epilepsy despite a normal interictal EEG.

This diagnostic image shows a standard scalp electroencephalogram (EEG) recording from a human subject. The tracing is organized into multiple horizontal channels, with electrode derivations labeled on the left side of the display (e.g., Fp1-F3, F3-C3, C3-P3, P3-O1), representing the 10-20 system in a longitudinal bipolar montage. The recording displays continuous electrical activity of the brain, characterized primarily by high-frequency waves of 8 Hz and higher, consistent with alpha and beta rhythms. The wave morphology is relatively symmetric and regular across the hemispheres, without evident epileptiform discharges, focal slowing, or lateralized periodic discharges. Vertical green grid lines provide a temporal scale for frequency analysis, while vertical deflections in frontal channels (Fp1, Fp2) likely represent physiological artifacts such as eye blinks. This tracing is identified as a normal EEG in the context of a patient presenting with metabolic-induced seizures, serving as an educational example of how systemic conditions like hypoglycemia from an insulinoma can mimic primary epilepsy despite a normal interictal EEG.

This diagnostic image shows a multi-channel electroencephalogram (EEG) recording, utilized in clinical neurology for assessing brain electrical activity. The tracing demonstrates a bipolar montage across frontal, temporal, parietal, and occipital derivations. A prominent finding is a generalized, rhythmic theta-frequency background of approximately 6 Hz, particularly visible in the posterior channels. This slowing of the normal alpha rhythm represents moderate diffuse encephalopathy, a common finding in metabolic, toxic, or infectious central nervous system disorders. The waveforms are generally sinusoidal but show some irregularity in amplitude and frequency, indicating synchronization across different cortical regions. Critically, there is an absence of epileptiform activity such as spikes, sharp waves, or pleomorphic discharges. A bottom channel labeled as EKG is included for artifact identification, showing relatively flat activity with minimal cardiac signal interference. This EEG is characteristic of an encephalopathic state where basic brain function is altered without focal neurological deficits or active seizure activity.

This diagnostic image shows a multi-channel electroencephalogram (EEG) recording, utilized in clinical neurology for assessing brain electrical activity. The tracing demonstrates a bipolar montage across frontal, temporal, parietal, and occipital derivations. A prominent finding is a generalized, rhythmic theta-frequency background of approximately 6 Hz, particularly visible in the posterior channels. This slowing of the normal alpha rhythm represents moderate diffuse encephalopathy, a common finding in metabolic, toxic, or infectious central nervous system disorders. The waveforms are generally sinusoidal but show some irregularity in amplitude and frequency, indicating synchronization across different cortical regions. Critically, there is an absence of epileptiform activity such as spikes, sharp waves, or pleomorphic discharges. A bottom channel labeled as EKG is included for artifact identification, showing relatively flat activity with minimal cardiac signal interference. This EEG is characteristic of an encephalopathic state where basic brain function is altered without focal neurological deficits or active seizure activity.

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Electroencephalogram (EEG)

Definition and Historical Background

An electroencephalogram (EEG) is a recording of the spontaneous electrical activity generated in the cerebral cortex, obtained via electrodes placed on the scalp. It was developed by Hans Berger in 1929 and remains one of the fundamental investigations in clinical neurology.
The activity recorded reflects the summated excitatory and inhibitory postsynaptic potentials of cortical neurons - not individual action potentials (which are too small to be detected by scalp electrodes). This spontaneous cortical activity is highly influenced and synchronized by subcortical structures, particularly the thalamus and brainstem reticular formation, which entrain cortical neurons into characteristic rhythmic patterns such as the alpha rhythm and sleep spindles.
  • Adams and Victor's Principles of Neurology, 12th Ed.

Technical Setup

Electrodes: Silver or silver-silver chloride discs (~0.5 cm diameter) placed on the scalp using a conductive medium.
Amplifiers: 8 to 32 or more amplifying units, recording simultaneously from multiple scalp areas. Frequency range: 0.5 to 30 Hz, displayed at 3 cm/s. Recordings are now stored digitally.
Montage - International 10-20 System: The standard electrode placement system uses 10 or 20% inter-electrode intervals of the hemi-circumference of the skull, ensuring reproducibility across patients of different head sizes. Electrode labels include Fp1/Fp2 (frontopolar), F3/F4/Fz (frontal), C3/C4/Cz (central), T3/T4 (temporal), P3/P4/Pz (parietal), O1/O2 (occipital).
10-20 EEG electrode placement system and sample tracings
Figure: The International 10-20 electrode placement system (A) and sample EEG tracings showing normal alpha rhythm posteriorly, blink artifact, and eye-opening suppression of alpha (B), plus photic driving response (C). - Adams and Victor's Principles of Neurology
Each channel represents the voltage difference between two electrodes over time - a voltage-versus-time graph. Positive deflections go downward; negative deflections go upward by convention.
  • Adams and Victor's Principles of Neurology, 12th Ed., p. 40-41

EEG Frequency Bands

BandFrequencyCharacteristics
Delta< 4 HzDeep sleep; pathological if in waking adult
Theta4-7 HzDrowsiness, light sleep; abnormal if dominant in awake adult
Alpha8-13 HzNormal awake, eyes closed; posterior dominant; attenuates with eye opening
Beta> 13 HzNormal awake, eyes open; frontal regions; increased by benzodiazepines
  • Goldman-Cecil Medicine, p. 3806; Costanzo Physiology 7th Ed.

Normal EEG Patterns

Awake, eyes closed: Dominant alpha rhythm (8-12 Hz, ~50 mV sinusoidal waves) over occipital and posterior parietal regions. These wax and wane spontaneously and are suppressed by eye opening or mental activity (alpha blocking). Frontal regions show beta waves (>12 Hz, 10-20 mV).
Awake, eyes open: Beta rhythm (13-30 Hz) dominates - low-voltage, high-frequency, desynchronous.
Sleep staging:
  • Stage 1 (N1): Alpha waves interspersed with theta waves
  • Stage 2 (N2): Low-frequency waves + sleep spindles (bursts of high-frequency activity) + K complexes (large slow potentials)
  • Stage 3-4 (N3): Delta waves predominate (slow-wave sleep)
  • REM sleep: Desynchronized, low-voltage, high-frequency - resembles the awake EEG ("paradoxical sleep"). Characterized by rapid eye movements, loss of muscle tone, and dreaming.
  • Costanzo Physiology 7th Ed., p. 3517-3523

Activating Procedures

Performed during EEG to provoke abnormalities:
  1. Hyperventilation - breathing 20x/min for 3 minutes; may activate characteristic seizure patterns
  2. Photic stimulation - strobe light at 1-20 flashes/second; normal subjects show photic driving (occipital response to each flash); epileptic patients may show a photoparoxysmal response (spike-and-wave activity)
  3. Sleep deprivation and sleep recording - drowsiness and sleep transitions can reveal hidden abnormalities
  4. Long-term/ambulatory monitoring - continuous EEG over hours to days, often combined with video (video-EEG) for seizure characterization

Clinical Indications

Primary UseDetails
Epilepsy diagnosisMost important use; classifies seizure types; EEG positive in ~50% of patients on a single recording, up to 90% with repeated studies and provocative maneuvers
Status epilepticusIncluding non-convulsive status epilepticus in comatose patients
EncephalopathyMetabolic (hepatic, renal, toxic); earliest change is diffuse theta slowing
Brain deathElectrocerebral silence (isoelectric tracing)
Coma evaluationICU monitoring; prognosis after cardiac arrest
Creutzfeldt-Jakob diseaseCharacteristic pseudo-periodic sharp wave complexes (~1/second)
Sleep disordersPolysomnography
Intraoperative monitoringCerebral activity monitoring under anesthesia
Herpes simplex encephalitisPeriodic lateralized epileptiform discharges (PLEDs) - temporal predominance
  • Adams and Victor's Principles of Neurology; Bradley and Daroff's Neurology in Clinical Practice; Goldman-Cecil Medicine
Note: EEG has been largely supplanted by CT/MRI for localization of structural lesions, but remains irreplaceable for seizure evaluation.

EEG Abnormalities

Background rhythm abnormalities:
  • Generalized slowing - most metabolic encephalopathies
  • Triphasic waves - hepatic, renal, and other metabolic encephalopathies (frontal predominance)
  • Focal slowing - large mass lesions (tumor, large stroke); delta waves over the affected area
  • Electrocerebral inactivity - neocortical death, hypothermia, drug overdose
Paroxysmal abnormalities:
  • 3-Hz spike-and-wave (augmented by hyperventilation) - childhood absence epilepsy
  • 3-4 Hz spike-and-wave in light sleep/photic stimulation - juvenile myoclonic epilepsy
  • Centrotemporal spikes - benign epilepsy with centrotemporal spikes (BECTS)
  • Anterior temporal spikes/sharp waves - mesial temporal lobe epilepsy
  • Periodic lateralized epileptiform discharges (PLEDs) - stroke, herpes simplex encephalitis
  • Generalized periodic sharp waves - Creutzfeldt-Jakob disease
  • Burst suppression - severe anoxic brain injury, barbiturate coma
  • Goldman-Cecil Medicine, Table 366-5

Sensitivity and Specificity

  • A single EEG is positive in only ~50% of patients with seizures
  • Repeated EEGs with provocative maneuvers raise sensitivity to ~90%
  • About 1% of normal adults and 3.5% of normal children have pseudo-epileptiform activity without ever having a seizure (specificity limitation)
  • EEG is neither highly sensitive nor fully specific (range cited: 78-98%)
  • Goldman-Cecil Medicine, p. 3806

Preparations for EEG

  • Patient should not be sedated (sedatives alter the recording)
  • Should not be hypoglycemic (relative hypoglycemia modifies normal patterns)
  • Avoid caffeine if a sleep study is planned
  • For epilepsy patients, anti-epileptic medications are generally continued during routine EEG; they may be weaned during inpatient monitoring to increase seizure yield

Sample EEG Images

Generalized seizure activity:
Generalized epileptiform EEG showing spikes and slow-wave complexes
Normal scalp EEG (alpha/beta rhythm, 10-20 system):
Normal EEG with alpha and beta rhythms in bipolar montage
Diffuse encephalopathy (theta slowing):
EEG showing generalized theta slowing consistent with encephalopathy

Quick Reference Video


Key sources: Adams and Victor's Principles of Neurology (12th Ed.) | Costanzo Physiology (7th Ed.) | Goldman-Cecil Medicine | Bradley and Daroff's Neurology in Clinical Practice
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