Neuromonitoring in the PICU
Indications for EEG monitoring
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Seizure detection
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Characterization of clinical events
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Encephalopathy evaluation
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Prognostication of outcome
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Medication titration (e.g. pentobarbital for ICP management)
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Evaluation of brain death
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Risks and Limitations
Risks
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Primary: scalp abrasions
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Secondary: potential adverse effects from medications administered due to EEG findings
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Limitations
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Cost and resources
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Frequently nonspecific –best used in conjunction with other modalities of neurological evaluation
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Orientation to EEG
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F- Frontal
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P- Parietal
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T- Temporal
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C-Central
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O-Occipital
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Odd numbers are left
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Even number are right
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Each column represents 1 sec
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Orientation to EEG Interpretation
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Frequency- number of times a repetitive wave recurs in 1 sec
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Delta (1-3 Hz), Theta (4-7 Hz), Alpha (8-13 HZ), Beta (>13 Hz)
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Amplitude- vertical distance of a wave in microvolts
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Waveform- shape of the wave
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Sharp (70-200ms)
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Spike (20-70 ms)
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Spike and wave complexes (spike followed by a slow wave)
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Continuity
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Nearly continuous : <10% attenuation < 10 uV
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Discontinuous: 10-50% with periods of attenuation < 10 uV
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Suppression-burst : discontinuous with interburst interval amplitude <10 uV > 50% of the time
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Suppression : all activity <10 uV
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Descriptors of periodicity and rhythmicity
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Periodic Discharges (PD)
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Rhythmic Delta Activity (RDA)
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Spike-Wave (SW; includes sharp-wave)
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Seizure definitions
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Electrographic Seizure - paroxysmal EEG change with or without associated clinical change
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Abnormal activity- sudden, repetitive, evolving, and stereotyped. amplitude at least 2µV p-p
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Minimum duration 10 secs and ≥10secs between
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Clinical Seizure - paroxysmal clinical change
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Electroclinical Seizure - seizure with both EEG and clinical manifestation
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Status Epilepticus (SE)
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Continuous seizure for ≥ 5 minutes or recurrent for > 5 minutes without return to baseline MS
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Neonates SE - recurrent seizures for ≥50% of 1hour EEG epoch
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Continuous EEG Monitoring
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High rate of electrographic only seizures (7-30% of patients in PICU, CICU and NICU)
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After seizure treatment 58% of neonates have only electrographic szs
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Several studies consistently report majority of seizures are noted in the 1st 24 hours of monitoring
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Consider monitoring for additional 24 hours after the last seizure
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Benefits of seizure identification
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Seizures are the symptom of a CNS insult
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Seizures can be associated with secondary injury (increased sz burden inversely associated with functional outcome)
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Early identification and treatment may improve outcome
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25% of infants thought to have seizures have no seizures on EEG
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44-70% of behaviors thought to be seizures have no EEG correlate
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Seizure mimics
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Clonus, jittery
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Benign neonatal sleep myoclonus
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Hyperekplexia (stiff when awake, startle)
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Dystonic posturing
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Electrographic Seizures
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Electrographic seizures (ES) are associated with
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worse outcome in PICU patients with no prior neurological dx
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unfavorable outcome in comatose PICU/NICU patients
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Greater decline of PCPC with higher seizure burden
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67% have decline if maximal seizure burden 15% per hour
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No decline if seizures 1.8% per hour
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Greatest decline if 20%/hour (12 min)
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Odds of decline increase 1.13 for every 1% increase in maximum hourly seizure burden
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Spike and wave complexes

Continuous

Discontinuous

Burst suppression

EKG Artifact
