EEG For Dummies
EEG For Dummies
EEG For Dummies
Funfacts:
-EEG (electroencephalogram) uses electrodes placed on the scalp to measure brain electrical activity, BY COMPARING
ONE ELECTRODE TO ANOTHER.
-Average Reference: Compares all electrodes individually to the same, single fixed point of reference. Abnormal
electrode is the “biggest” deflection, with deflections in other electrodes getting bigger the closer you are to the
abnormal electrode.
-Transverse: Best to compare side to side. Field points TOWARD the abnormal electrode.
Theta: 4-7 Hz
Delta: 1-3 Hz
-3 years =8 Hz
2. Blinking: Big symmetric downward deflection in frontal/eye leads, b/c eyes roll up in head when you close your lids.
3. Eye movement: Look at F7 and F8. Eyes up=downward deflection, eyes down= upward deflection, eyes left or right =
“open vs. closed window” rule.
4. Muscle artifact: Dark super-fast squiggly lines, or big deflections in one lead without a field change or effect on other
leads
5. Breach rhythm: missing part of your skull, so over that region get high amplitude sharp fast discharges.
6. Positive occipital sleep transients(POSTs): sail-shaped, in posterior leads. Occur at end of stage 2 sleep.
7. Lambda: Basically awake POSTs, demonstrate patient is scanning with their eyes/watching TV. Putting blank piece of
paper in front of their eyes should end it.
9) EKG artifact
Sleep: **NOTE: Normal but scary-looking stuff happens during sleep/wake transitions, be careful what you call
abnormal here**
-Stage 1 (drowsiness): Central vertex waves, slow lateral eye movements, alpha waves <50% of epoch, intermittent slow
waves. Ends with POSTS (Positive occipital sharp transients of sleep, ie upside-down posterior sharps)
-Stage 2 (real sleep): K complexes (central-maximum big diphasic slow wave followed by spindles) and spindles (central
runs of Beta waves, < 2 seconds), markedly low amplitude background.
-REM: Rapid eye movements, muscles paralyzed, occasional runs of alpha. Central sawtooth waves.
2. Have you ruled out artifact (blinking, sleep/wake transition, EKG artifact, etc)?
5. Is it a seizure (does it evolve in frequency, location/spread; less importantly, does it have change in
morphology(sharp) or amplitude while being rhythmic/repetitive, does it have a beginning and end, does it last
>10 seconds)?
1) “Epileptiform activity”= pattern demonstrating increased risk of having seizure, usually from
the region you see the activity. Epileptiform patterns include spike and wave, sharps, PLEDs,
GPEDs, TIRDA, BIPLEDS. A seizure also counts as epileptiform activity. Slowing by itself is NOT
necessarily epileptiform.
2) Spikes= less than 70 ms long. Sharps= greater than 70ms long. Difference is arbitrary.
3. Focal slowing: Intermittent (non-specific neuronal dysfunction in that region) vs. constant (structural lesion)
4. Encephalopathy: Mild (mild slowing 7-8Hz PDR, normal sleep and reactivity), moderate (moderate slowing 4-6Hz,
lose sleep architecture but see background activity and variability), severe (<4 Hz, no variability, no sleep architecture),
profound (nearly flat).
5. PLEDS (periodic lateralized epileptiform discharges): 0.5-2Hz, big, stereotyped, repetitive. Seen most commonly after
infarction/acute injury, or seizure. Usually go away after a few weeks.
7. Burst suppression: long periods of suppression, punctuated by bursts of sharp/slow. Seen in hypoxia, hypothermia,
anesthesia, trauma.
8. BiPLEDS: bilateral INDEPENDENT PLEDs; 70% of people with this have seizures.
9. Triphasic waves: 0.5-2 second interval negative-positive-negative wave. Suggest metabolic or infectious process.
10. FIRDA: Frontally dominant intermittent rhythmic delta activity; big waves; suggests encephalopathy (most
commonly metabolic).
11. OIRDA: occipital “ “ “ “ (big, bilateral, synchronous). Associated with absence epilepsy.
12. TIRDA: Temporal “ “ “. Epileptiform from that region; associated with structural lesions (get imaging if you see it).
BASICALLY MEANS YOU HAVE EPILEPSY.
13) Status epilepticus: One single lasting longer than 30 minutes, or 30 minutes of seizures not returning to baseline.
3. ABNORMALITIES:
A) Any epileptiform activity? CAN IT BE A NAMED NORMAL VARIANT? Describe them (spikes/sharps/waves/sharply-
contoured, frequency, diffuse vs. focal, location, symmetry, continuous/intermittent/episodic/paroxysmal, quantity)
C) Any seizures (evolving (frequency, spread; less important change in amplitude or clear onset/ending), rhythmic,
different from background, etc)? Where do they start/spread to/how long they last/what is their frequency and
morphology/what happens clinically?
D) Any clinical events (describe them, and if they have EEG correlate; as a general rule, more than 3 seconds of
continuous epileptiform activity should impact behavior)
4. Stages of sleep
5. Photic driving? (ie, does PDR synchronize with at least one of the photic frequencies? Is it symmetrical? Does it bring
out abnormalities?)
7. EKG?
8. Read the patient’s story, prior imaging, prior EEGs, current meds that could be influencing EEG. Based on that, does
that change your read or make you want to look for something specific?
Mu rhythm
PLEDS: