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EEG Basics & Interpretation A/Prof Ong Hian Tat Senior Consultant & Associate Professor Division of Paediatric Neurology & Developmental Paediatrics University Children’s Medical Institute National University Health System Singapore

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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