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Folio edition · Set in Instrument Serif & Archivo

Paeds Vivasfetal-neonatal-and-perinatal

Paeds Vivas · fetal-neonatal-and-perinatal

Neonatal seizures and encephalopathy — branching viva

Branching viva from the recognition of a neonatal seizure through the seizure-versus-jitteriness distinction, the cooling decision in the encephalopathic term infant, and the refractory-seizure search for a metabolic cause.

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Target exams

RACP General PaediatricsRACP DCEMRCPCH ClinicalRCPSC Pediatrics

Target exams

RACP General PaediatricsRACP DCEMRCPCH ClinicalRCPSC Pediatrics
Prompt
You are the neonatal registrar on the postnatal ward. The midwife asks you to review three newborns with abnormal movements of differing cause and severity. The examiner releases information in stages about an encephalopathic term infant, a well-looking term infant with tremulous movements, and a preterm infant with apnoea and desaturation.

Station opening

Examiner: "Define a neonatal seizure and explain why the great majority are described as provoked rather than epilepsy." [5]

Strong candidate (must-hit)

  • Defines a neonatal seizure as the clinical or electrographic expression of abnormal, excessive neuronal discharge in the immature brain, almost always provoked by a treatable brain insult (HIE commonest, then stroke, haemorrhage, infection, metabolic derangement, malformation); explains that provoked (acute symptomatic) seizures reflect an acute insult, whereas epilepsy is a chronic tendency to unprovoked seizures. [5]

Weak candidate

  • "A seizure is when the baby shakes." [5]

Branch A — The encephalopathic term infant

Examiner: "A term infant born after placental abruption with cord pH 6.85 has focal clonic seizures and lethargy at 2 hours. What is your diagnosis, your first-line drug, and the neuroprotective decision?" [1]

Strong

  • Diagnoses moderate hypoxic-ischaemic encephalopathy (Sarnat stage 2) with provoked seizures; checks blood glucose first, gives phenobarbital 20 mg/kg IV as first-line antiseizure medication, starts continuous EEG; activates therapeutic hypothermia to 33.5 to 34.5 °C for 72 hours within the 6-hour window, citing the TOBY (Azzopardi 2009) and NICHD (Shankaran 2005) trials and the Jacobs 2013 Cochrane meta-analysis for the mortality and disability benefit. [1] [5]

Weak

  • "Give phenytoin and observe; consider cooling if it gets worse." [1]

Branch B — The tremulous well-looking infant (the jitteriness trap)

Examiner: "A well-looking term infant has fast, rhythmic trembling that started when the incubator was opened and stopped when the nurse held the limb. The baby is alert. A colleague wants to start phenobarbital. What do you say?" [5]

Strong

  • States this is jitteriness (a tremor), not a seizure: fast, stimulus-sensitive, abolished by holding the limb flexed, preserved consciousness, no ocular or autonomic features. Jitteriness is the commonest mimic of neonatal seizures and must not be treated with antiseizure drugs; the response is reassurance and correction of any underlying cause (hypoglycaemia, drug withdrawal). [5]

Weak

  • "Yes, give phenobarbital to be safe — any abnormal movement in a neonate could be a seizure." [5]

Branch C — The preterm infant with apnoea

Examiner: "A 28-week infant on the NICU has recurrent apnoea, bradycardia and desaturation with no visible motor activity. The team thinks it is apnoea of prematurity. What is your concern and your next step?" [8]

Strong

  • Recognises that apnoea, bradycardia and desaturation can be the only sign of a seizure in a preterm infant (an autonomic/subtle seizure); triggers continuous EEG to confirm or exclude an electrographic seizure, because clinical observation alone misses most NICU seizures; treats to an electrographic endpoint if confirmed, and searches for the cause (IVH, metabolic, sepsis). [5] [8]

Weak

  • "It is apnoea of prematurity — increase the caffeine dose." [8]

Branch D — The refractory seizure and the missed cause

Examiner: "Seizures persist despite phenobarbital 20 mg/kg and levetiracetam 50 mg/kg. The initial glucose and electrolytes were normal. What is your principle, and which two causes must you not miss?" [5]

Strong

  • States the principle: a refractory neonatal seizure is often a missed cause, not a drug-ladder failure. Re-screens for a metabolic cause (ammonia, lactate, amino acids, organic acids) and performs a lumbar puncture and cranial MRI. Two must-not-miss causes: HSV encephalitis (start aciclovir 20 mg/kg IV every 8 hours empirically while awaiting CSF PCR) and a pyridoxine- or pyridoxal-phosphate-dependent seizure (trial the cofactor). [5]

Weak

  • "Add a third antiseizure drug and continue." [5]

Close

Examiner: "Summarise your approach to a neonatal seizure in one sentence." [5]

Strong

  • "A neonatal seizure is a provoked event — so I stabilise, check the glucose, confirm with continuous EEG, treat reversible causes, give phenobarbital 20 mg/kg IV first line and escalate to an EEG endpoint, and cool moderate-to-severe HIE within 6 hours at 33.5 to 34.5 °C for 72 hours; I stop the antiseizure drug before discharge if the infant is neurologically normal, because the cause drives the prognosis." [1] [5]

References

  1. [1]Azzopardi DV; Strohm B; Edwards AD; et al Moderate hypothermia to treat perinatal asphyxial encephalopathy. N Engl J Med, 2009.PMID 19797281
  2. [4]Painter MJ; Scher MS; Stein AD; et al Phenobarbital compared with phenytoin for the treatment of neonatal seizures. N Engl J Med, 1999.PMID 10441604
  3. [5]Pressler RM; Abend NS; Auvin S; et al Treatment of seizures in the neonate: Guidelines and consensus-based recommendations-Special report from the ILAE Task Force on Neonatal Seizures. Epilepsia, 2023.PMID 37655702
  4. [7]Sharpe C; Reiner GE; Davis SL; et al Levetiracetam Versus Phenobarbital for Neonatal Seizures: A Randomized Controlled Trial. Pediatrics, 2020.PMID 32385134
  5. [8]Shellhaas RA; Chang T; Tsuchida T; et al The American Clinical Neurophysiology Society's Guideline on Continuous Electroencephalography Monitoring in Neonates. J Clin Neurophysiol, 2011.PMID 22146359
  6. [9]Nyman J; Mikkonen K; Metsäranta M; et al Poor aEEG background recovery after perinatal hypoxic ischemic encephalopathy predicts postneonatal epilepsy by age 4 years. Clin Neurophysiol, 2022.PMID 36183624