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NEUROLOGY · NEONATAL CONDITIONS

Neonatal Seizures

A practical guide for SCN clinical staff  ·  Often subtle, usually symptomatic - check the glucose, find the cause, treat early

GLUCOSE FIRST -
THEN FIND
THE CAUSE
SEIZURES AT A GLANCE
Definition
An electrographic event: abnormal, sudden, repetitive and evolving electrical activity in the brain, with or without visible signs.
Incidence
About 1-3 per 1000 term births; much higher in preterm babies. Most start in the first 2 days.
Causes
Usually acute and provoked: HIE (about half), stroke, intracranial haemorrhage, infection, metabolic. Epilepsy syndromes are less common.
The trap
Only about a third of EEG seizures have visible signs, and many movements that look like seizures are not.
Diagnosis
Confirmed by EEG (gold standard) or aEEG. On the SCN it starts as a clinical suspicion - capture it on video.
First moves
Bedside glucose, blood gas with electrolytes, call the consultant, treat, and look for the cause.
WHY NEWBORNS SEIZE · GO DEEPER
1

An excitable brain

The newborn brain favours excitation: glutamate receptors mature early, and inhibitory circuits mature late.

2

GABA can excite

Immature neurons have high intracellular chloride (high NKCC1, low KCC2), so GABA can depolarise rather than inhibit. One reason phenobarbitone and benzodiazepines often only partly work.

3

Focal, not generalised

Poorly myelinated connections limit spread, so seizures are focal or multifocal. Generalised tonic-clonic seizures do not occur in newborns.

4

Electroclinical uncoupling

Many seizures are electrographic only. After phenobarbitone the visible signs often stop while EEG seizures continue.

5

Seizures add injury

A high seizure burden is linked to worse outcome independent of the cause. Treating early to reduce burden is the aim.

6

Timing points to cause

First 24-48h: HIE, haemorrhage, infection, hypoglycaemia. Days 2-3 in a well term baby: think stroke. After day 3: metabolic disorders, genetic epilepsy, late hypocalcaemia.

INVESTIGATIONS

  • Now: bedside glucose; blood gas with Na, K, ionised Ca, lactate
  • Bloods: FBC, CRP, blood culture, UEC, Ca, Mg, phosphate, LFTs, ammonia
  • Lumbar puncture when stable (include HSV PCR)
  • Imaging: cranial ultrasound early; MRI is the key test for stroke and injury
  • EEG/aEEG via NICU; metabolic and genetic tests guided by NICU and neurology

RED FLAGS

  • Encephalopathy after a difficult birth: assess for cooling now (6-hour window)
  • Unwell, febrile or abnormal CSF: treat as meningitis or HSV until proven otherwise
  • Seizures after feeds start, with poor feeding or vomiting: think inborn error (check ammonia)
  • Recurrent or prolonged seizures despite a first drug
  • Apnoea or loss of airway after loading doses

JITTERINESS

  • Triggered by handling or noise; stops when the limb is held
  • Fine, even tremor with no fast and slow phase
  • No eye or autonomic signs; baby otherwise alert
  • Common and usually benign - still check glucose and calcium

BENIGN SLEEP MYOCLONUS

  • Jerks only during sleep; stop when the baby is woken
  • Often repetitive clusters in a well, normal baby
  • Normal examination and EEG
  • Resolves in the first months; no treatment

MANAGEMENT

Stabilise, check the glucose, treat with phenobarbitone, and look for the cause. Most babies with seizures need NICU care and EEG, so involve the consultant and NETS early.

First 15 minutes

  • Airway, breathing, circulation; oxygen and monitoring
  • Bedside glucose - treat hypoglycaemia (10% glucose 2 mL/kg IV)
  • Gas with electrolytes; correct low calcium or magnesium per local protocol
  • Video the event if parents consent; call the consultant

Antiseizure treatment

  • First line: phenobarbitone 20 mg/kg IV over 20 minutes
  • If seizures continue: further 10 mg/kg, to a total of 40 mg/kg
  • Second line on NICU/NETS advice: levetiracetam, phenytoin or midazolam
  • Watch for apnoea and hypotension; be ready to support the airway

Find the cause & refer

  • Start antibiotics and aciclovir if infection is possible
  • Assess for cooling if HIE is possible
  • Call NETS: most babies with seizures need NICU, EEG and MRI
  • Stop antiseizure drugs before discharge once provoked seizures settle (ILAE)
Nursing considerations
  • Note the time, duration and exact movements; video if parents consent.
  • Check a bedside glucose straight away and tell the doctor.
  • Gently hold the limb: jitteriness stops, a seizure does not.
  • After phenobarbitone, watch breathing, saturations and BP closely.
  • Parents are often the first to notice - take their concern seriously and keep them informed.
DISCUSSION QUESTIONS
1

How do you tell jitteriness from a seizure at the cot side?

2

Which causes of seizures can you treat in the first 15 minutes?

3

Why can a baby still be seizing after the visible movements stop with phenobarbitone?

4

A well term baby has focal clonic seizures on day 2. What is the likely cause and the key test?

RESOURCES
❝

Take-home message: Neonatal seizures are usually a sign of an acute problem - most often HIE, stroke, haemorrhage, infection or a metabolic upset. They are often subtle and easy to over- or under-call. Check the glucose, correct what you can, give phenobarbitone, look for the cause, and involve the consultant and NETS early.

For educational purposes only. Doses are a guide only - check your local formulary. Always align management to your local SCN/NICU or NETS protocols.

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