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EEGBasics&Interpretation
A/Prof Ong Hian Tat
SeniorConsultant&AssociateProfessorDivisionofPaediatricNeurology&DevelopmentalPaediatrics
UniversityChildrensMedicalInstituteNationalUniversityHealthSystem
Singapore
Outline 1. EEG and its uses and limitations
2. EEG electrode placement, 10-20 international system
3. EEG Rhythms
4. Normal awake and sleep EEGs in adults and children
5. Activation procedures for EEG
6. Common benign variants in the EEG
7. EEG artifacts
8. Non-epileptiform abnormalities in the EEG
9. Epileptiform discharges
What is the EEG?
EEG (electroencephalogram) displays the electrical activity of the brain created by neurons generating the electrical signals
The brains electrical activity is picked up by electrodes attached on the patients scalp and amplified on the EEG machine to be viewed as brain waves
Hans Berger (1873-1941), a German psychiatrist, discovered the electroencephalography (EEG) in 1929
Analog EEG
Digital EEG
Allows more accurate interpretation of the EEG record by applying different montages/references, gain/sensitivity, filters and time constant
Use of the EEG Helps to confirm Epilepsy Syndrome (diagnosis)
Confirm seizures, classify seizures and epileptic syndrome Quantify seizures or epileptic burstsLocalising epileptic focus especially for pre-surgical evaluation
Help to indicate abnormalities that may suggest the following possibilities though definitive diagnosis is by other investigations/tests:Acute encephalitis/cerebral abscessBrain tumourIntracranial stroke haemorrhage/ischemic infarctionAny other non-specific encephalopathy e.g. Metabolic encephalopathy Brain death
Limitations of the EEG(sensitivity)
1. Some abnormal activity may not be detected when:The area is too small on the brains surface
- need 4 cm2 surface area of cortex to be involved
Foci located too deep in the brain
- mesial aspect and inferior aspect of the cortex (FLE or TLE)
Limited time sampling
2. Poor technical quality
3. Interpretation of the significance of the EEG abnormalities appropriate to the clinical setting
Limitations of the EEG(specificity)
1. Some non-specific EEG abnormalities in normal people- up to 10%
2. Paroxysmal epileptiform activity in the absence of any clinical seizures
- ~ 1% of normal people- much higher in patients with non-epileptic neurological disorders
e.g. migraine, cerebrovascular disorders
3. Benign focal epileptiform discharges in children without seizures
- 2 to 4 %
Electrode Placement
International 10-20 System
Fp2 = right frontal pole
F4 = right frontal
F8 = right fronto-temporal
C4 = right central
T4 = right temporal
P4 = right parietal
T6 = right postero-temporal
O2 = right occipital
A2 = reference to right ear
Fp1 = left frontal pole
F3 = left frontal
F7 = left fronto-temporal
C3 = left central
T3 = left temporal
P3 = left parietal
T5 = left postero-temporal
O1 = left occipital
A1 = reference to left year
G = ground
Fz = mid frontal
Cz = midline
Pz = mid posterior
EEG montages based on the 10-20 system
IPSI AP Bipolar
Coronal
The Routine EEG To include recordings (each at least 15min) of
- awake (eye open/close)- drowsiness, sleep (following partial sleep deprivation)- awakening
Activation procedures- intermittent photic stimulation- hyperventilation (with breath counting)- other forms of appropriate activation of reflex seizures e.g. reading, hot water, somatosensory stimuli, auditory stimuli
The Routine EEG
Simultaneous video-EEG recordings should be made routine - confirms seizure(s) and diagnosis of epilepsy
- excludes epileptic seizures and arrive at diagnosis of non-epileptic paroxysmal events, which are also very common in infants & children
- clinical signs during the seizure may be subtle, and not able to be picked up or recognised immediately by the EEG technologist e.g. absences during HV, myoclonic jerks, focal seizures
EEG Rhythms
Rhythm Hertz Description
Alpha 8-13 Hz Posterior dominant rhythm
Beta >13 Hz Normal in sleep especially in infants and young children
Theta 4-7 Hz Drowsiness and sleep
Delta
Alpha activity
Beta activity
Theta activity
Delta activity
Digital EEG
Interpretation of EEG can be enhanced by applying changes to the following: Sensitivity High frequency filter Time constant
Normal Awake EEG in Adults & Children
Normal adult awake EEG
2-3 Hz posterior rhythm seen in a 3 month old baby
5 Hz posterior rhythm seen in a 6 month old baby
6 Hz posterior rhythm seen in a 1 year old child
7.5 Hz posterior rhythm seen in a 2 year old child
9 Hz posterior rhythm seen in a 6 years old child
10 Hz posterior rhythm seen in children >8 years old
Normal Sleep EEG in Adults & Children
Asynchronous sleep spindles seen in a 2 month old infant
Hypnogogic burst
EEG during Activation Procedures
Photic driving
Rhythmic activity elicited by frequencies of 5-30 Hz that are time-locked to represent a harmonic of the stimulus frequency
Usually maximal over the posterior regions
Adults tend to drive best at frequencies near their alpha rhythm whereas children may drive at slower frequencies
An impressive driving response at very low flash frequencies of 0.5-3 Hz usually indicative of CNS dysfunction
Asymmetric or absence of photic driving may be seen in normal individuals
Photic Driving
Photomyoclonic Response
Consists of muscle spikes over the anterior regions in response to IPS
Spikes increase in amplitude as stimulation increases appearing maximal at flash frequencies of 12-18 Hz and disappearing abruptly with the end of stimulation
Photoconvulsive response is associated with anxiety, alcohol, or drug withdrawal states and parkinsonism
Considered a normal response
Photomyoclonic Response
slighthandjerk
Photoconvulsive Response
Characterized by generalized or posteriorly dominant spike/polyspike-wave complexes produced by photic stimulation
Lapses of consciousness or myoclonic jerks may accompany the spike discharges
Generalized discharges represent an abnormal response that suggests a predisposition to an epileptic disorder, particularly if sustained beyond the stimulus
Photoparoxysmal response is most frequently elicited at flash rates of 15-20 Hz and is elicited most often in people with primary generalized epilepsy
However, can also be seen in patients with toxic/metabolic or drug withdrawal states and is observed in 2% of normal persons
Photoconvulsive Response
Comparison of Photomyoclonic and Photoconvulsive responses
Photomyoclonic response Photoconvulsive response
Effective stimulus frequency 8-20 flashes/sec 3-20 flashes/sec
Eyelids, position for maximal effect Closed Closed (and open)
Clinical accompaniments Fluttering of eyelids Eyes turning, speech arrest
Consciousness Maintained Often disturbed
Distribution of electric changes Face, frontal regions Diffuse over scalp
EEG response, type Myoclonic spikes (polyspike) Spike-wave ot atypical spike-wave
Recruitment Marked Less frequent
After-discharge None Frequent
Age group Adult All ages
Variability of threshold Large Slight
Muscle tension Increases No effect
Nervous tension Increases No effect
Occurrence Normals frequent Normals rare
Photoparoxymsal Response
Prolonged (self-sustained) which continues for a short period after the stimulus has been withdrawn
High incidence of epilepsy
Patients with photoparoxysmal response often had other epileptiform abnormalities in their resting EEG
Photoparoxysmal Response
Slow waves activated by hyperventilation
Common Benign Variants in the EEG
Mu rhythm, which disappears when patient is told to make a clenched fist
Central rhythm of 7-12 Hz with arciform morphology
Observed in ~20% of normal young adults and less common in children and the elderly
Slightly more common in females than males
Mu rhythm does not attenuate with eye opening but does diminish with movement or tactile stimulation of the contralateral extremities, fatigue, arithmetic or problem solving
Mu Waves
Lambda Waves
Sharp transients characterized as biphasic or triphasic waveforms having initial small positive phase followed by a prominent negative component
Appears over occipital regions bilaterally
Elicited by looking at a patterned design in a well-lit room
Most commonly seen in children 2-15 years of age
May be asymmetric and misinterpreted as occipital spikes
Eye closure, reducing illumination of the room or having the patient stare at a blank card will eliminate lambda waves
Lambda Waves
Posterior Slow Waves of Youth (PSWY) superimposed on Posterior Rhythm
Also called sail waves and polyphasic waves
Moderate voltage, fused waves intermixed with the alpha rhythm that attenuate with eye opening and diminish with drowsiness
May not appear symmetric or synchronous, but asymmetries should not exceed 50%
Observed in children and young adults, maximal incidence between 8-14 years
Posterior Slow Waves of Youth
Positive Occipital Sharp Transients (POSTS)
Also referred to as occipital V-waves of sleep, lambdoids of sleep and rho waves
Surface positive sharp waves in stage I and II sleep most commonly in young adults (15-35 years)
Waves consist of sharp, surface-positive peak followed in some instances by low voltage surface-negative peak
Initial deflection has a slower duration than the ascending phase resulting in a checkmark morphology
Typically occur in runs of bilaterally synchronous 4-5 Hz waves that may be asymmetrical
Positive Occipital Sharp Transients (POSTs)
14- and 6-Hz Positive Spikes
Bursts consists of rhythmic arciform waveform of 0.5-1.0 second duration during drowsiness and light sleep
Maximal in amplitude over the posterior temporal regions
Usually unilateral or independent over both sides, but may be bilaterally synchronous
Appear most often in adolescents between 13-14 years but have been seen in children as young as 3-4 years
14- and 6- Hz Positive Spikes
Phantom spike-waves
Characterized by brief burst of 5-7 Hz generalized spike-wave discharges seen primarily in young adults in relaxed wakefulness or drowsiness
Hughes subdivided this pattern in 2 subgroups: FOLD & WHAM
FOLD occurs primarily in Females, maximal in the Occipital regions, Low in amplitude and present in Drowsiness
WHAM occurs in Waking state, is Higher in amplitude, more Anterior and observed primarily in Males
Observed in 2-3% of normal persons >50 years
Phantom Spike-Wave
Wicket spikes
Consists of monophasic arciform mu-like 6-11 Hz transients occurring singly or in trains in the temporal regions during wakefulness or sleep
Typically bilateral and independent, usually having a unilateral predominance
Seen in adults >30 years in ~1-3% of normal population
Wicket spikes are not associated with an aftercoming slow wave or background slowing
Wicket Spikes
Small Sharp Spikes (SSS)
Also referred to as benign epileptiform transients of sleep (BETS) and benign sporadic sleep spikes (BSSS)
Benign transients of low amplitude (
Breech Rhythm (Skull Defect)
Breech Rhythm (Skull Defect)
Associated with skull defects are focal mu-like rhythms in Rolandic or temporal region with sporadic slow waves and spiky or sharp transients
Rhythms are unrelated to epilepsy and do not indicate recurrence of a tumor
Rhythmic Mid-Temporal Theta of Drowsiness
Rhythmic Mid-Temporal Theta of Drowsiness
Also known as rhythmic midtemporal discharges (RMTDs)
Characterized by burst or trains of rhythmic 4-7 Hz theta waves in the temporal region
Often have flat-topped or notched appearance due to the superimposition of faster harmonic frequencies
Burst may be unilateral or bilateral, but often appear independently with shifting emphasis in the relaxed or drowsy state
Pattern evolves in amplitude, increasing at the beginning and gradually decreasing at the end
Found in 0.5 to 2% of normal adults
Description: The prominent feature here is the rhythmic 6 Hz activity at the vertex (arrow). This discharge spreads to the paracentral regions. The background frequencies are in the theta range with superimposed beta.
Significance: Normal, state transition
Central Theta
Description: This shows a mitten discharge during stage 2 sleep (arrows). The sharp component precedes the slow wave, with resulting appearance similar a sharp and slow wave complex. These may appear spontaneously or with auditory stimulation, and are best demonstrated with an ear reference
Significance: Normal, may be mistaken for pathological bifrontal sharp and slow wave complex
Mitten
EEG Artifacts
EEG Artifacts
Physiological Eye movements Lateral rectus spikes (muscle action potential) Eyelid flutter Sweat Glossokinetic ECG
Non-physiological Electrode pop Movement 60 Hz artifacts
Fp1 Fp2
F8F7
Asymmetrical slow eye movements of drowsiness (F7, F8), not to be mistaken for focal delta activity
Eye movements
Lateral Rectus Spikes (muscle action potentials)
Eyelid flutter
Sweat artifact
Prominent glossokinetic potentials resembling frontal intermittent rhythmic delta activity
Chewing
ECG artifact
Electrode Pop
Head movement
60 Hz Artifact
60 Hz Artifact (after using filter)
Non Epileptiform Abnormalities
Non Epileptiform Abnormalities
Intermittent slowing Generalized Focal
Intermittent rhythmic slowing Generalized Focal
Continuous slowing Focal (regional)
Non Epileptiform Abnormalities
Intermittent slowing generalized focal
Intermittent rhythmic slowing generalized focal
Generalized intermittent slowing
Focal intermittent slowing
Non Epileptiform Abnormalities
Intermittent slowing generalized focal
Intermittent rhythmic slowing generalized focal
Occipital Intermittent Rhythmic Delta Activity (OIRDA)
Frontal Intermittent Rhythmic Delta Activity (FIRDA)
Focal intermittent rhythmic slowingLeft temporal region (F7-T3)
Non Epileptiform Abnormalities
Intermittent slowing Generalized Focal
Intermittent rhythmic slowing Generalized Focal
Continuous slowing Focal (regional)
background asymmetry, continuous slowing right hemisphere
Epileptiform Discharges
Definition of Epileptiform Discharges Should be unarguably discrete events, not just accentuation of part
of an ongoing sequence of waves
Should be clearly separable from ongoing background activity, not only by their higher amplitude but also by their morphology and duration
Have bi- or triphasic waveform and have more complex morphology than even high-voltage background rhythms
Not sinusoidal but rather show asymmetric, rising and falling phases
Most spikes and sharp waves followed by slow wave
Should have a physiological potential field involving more than one electrode that helps distinguish them from electrode-related artifacts or muscle potentials
Rightcentrotemporalspikes(BFEDC)Bipolarmontageshowingphasereversal
BFEDC
staring
Characteristics of Ictal pattern
Repetitive EEG discharges with relatively abrupt onset and termination
Pattern of evolution lasting at least several seconds
Generally rhythmic, frequency displays increasing amplitude, decreasing frequency and spatial spread during the seizure
Grading of EEG Abnormalities in Diffuse Encephalopathy
Grade I (almost normal) Dominant activity is alpha rhythm with minimal theta activity
Grade II (mildly abnormal) Dominant theta background with some alpha and delta activities
Grade III (moderately abnormal) Continuous delta activity predominates, little activity of faster frequencies
Grade IV (severely abnormal) Low-amplitude delta activity or burst-suppressionpattern
Grade V (extremely abnormal) Nearly flat tracing or electrocerebral inactivity
Continuous Slow Waves
Triphasic Waves
Periodic Lateralized Epileptiform Discharges (PLEDS)
BiPLEDs
Bilateral Independent Periodic Lateralized Epileptiform Discharges (BiPLEDS)
Generalized Suppression(low amplitude delta)
Burst Suppression Pattern
Burst Suppression Pattern Differential Diagnosis1. Severe diffuse encephalopathy e.g. hypoxia, metabolic disorders
2. Iatrogenic e.g. general anesthesia e.g. thiopentone treatment for
GCSE
3. Normal pattern in prematurity
4. Early infantile epileptic encephalopathy:
- Othahara syndrome
- Early myoclonic encephalopathy
- West syndrome (EEG in sleep)
Summary 1. EEG and its uses and limitations
2. EEG electrode placement, 10-20 international system
3. EEG Rhythms
4. Normal awake and sleep EEGs in adults and children
5. Activation procedures for EEG
6. Common benign variants in the EEG
7. EEG artifacts
8. Non-epileptiform abnormalities in the EEG
9. Epileptiform discharges
Take Home Message 1. Not all sharply contoured transients or rhythmic activity
are epileptiform, but may represent normal findings or benign variants with no clinical significance.
2. Use various montages and references for analysis of the field potential (maximum negativity) instead of relying on visual pattern recognition.
3. Do not miss the wood for the trees, being over-interested in each individual spike but missing the big picture, especially in the presence of encephalopathy.
4. Conservative reading and interpretation should be the rule, as more damage is done by over-reading or over-interpretation of an EEG record.
References
Comprehensive Clinical Neurophysiology Cleveland Clinic Foundation
Atlas of ElectroencephalographyEd: MR Sperling & R Clancy
EEG Activation & Artifacts American Society of Electroneurodiagnostic Technologists
Pediatric EEG American Society of Electroneurodiagnostic Technologists
Thank You
University Childrens Medical Institute