Paediatric Seizure Disorders Guide Febrile Seizures Absence JME Status Epilepticus Explained
Paediatrics

Paediatric Seizure Disorders Guide Febrile Seizures Absence JME Status Epilepticus Explained

Here is a complete, exam-oriented yet concise paediatrics reference covering seizure disorders, febrile seizures, absence epilepsy, JME, epilepsy syndromes, and status epilepticus.


🧠 SEIZURE DISORDERS (PAEDIATRICS)

Definition

A seizure = transient occurrence of signs/symptoms due to abnormal excessive synchronous neuronal activity in the brain.


Classification (ILAE-based simplified)

1. Focal seizures

  • Origin: one hemisphere
  • Types:

* Aware (no LOC)

* Impaired awareness

  • May evolve → bilateral tonic-clonic

2. Generalized seizures

  • Both hemispheres from onset:

* Tonic-clonic

* Absence

* Myoclonic

* Atonic

* Tonic

3. Unknown onset


Causes in Children

  • Idiopathic/genetic
  • Structural (malformations, tumors)
  • Metabolic (hypoglycemia, hypocalcemia)
  • Infection (meningitis, encephalitis)
  • Perinatal insult (HIE)
  • Trauma
  • Fever (febrile seizures)

Clinical Features

  • Motor: tonic, clonic, myoclonic
  • Non-motor: staring, behavioral arrest
  • Autonomic: cyanosis, tachycardia
  • Postictal phase: confusion, sleepiness (absent in absence seizures)

Investigations

  • Blood glucose, electrolytes, calcium
  • EEG (key diagnostic tool)
  • MRI brain (structural causes)
  • CSF (if infection suspected)

General Management

  • Ensure airway, breathing, circulation
  • Position: lateral
  • Treat underlying cause
  • Antiepileptic drugs (AEDs)

🌡️ FEBRILE SEIZURES

Definition

Seizures occurring in 6 months–5 years with fever, without CNS infection.


Types

Simple febrile seizure

  • Generalized
  • <15 minutes
  • Single episode in 24 hrs
  • Normal neuro exam

Complex febrile seizure

  • Focal / >15 min / recurrent

Pathophysiology

  • Immature brain + rapid temperature rise → neuronal hyperexcitability

Clinical Features

  • Generalized tonic-clonic seizure
  • Occurs early in fever
  • Rapid recovery

Investigations

  • Usually NOT required (simple type)
  • Do:

* Lumbar puncture → if meningitis suspected

* EEG → NOT routine


Management

Acute

  • Usually self-limiting
  • If >5 min → benzodiazepine

Long-term

  • No routine AED
  • Parental reassurance
  • Antipyretics (do not prevent seizures)

Drugs

Diazepam

  • Indication: prolonged seizure
  • Dose: 0.2–0.3 mg/kg IV / rectal
  • MOA: GABA-A agonist
  • Adverse: respiratory depression
  • Monitor: respiration

Prognosis

  • Excellent
  • Slight ↑ risk of epilepsy (esp. complex)

⚡ ABSENCE SEIZURES (Childhood Absence Epilepsy)

Definition

Brief episodes of impaired awareness (staring spells)


Pathophysiology

  • Thalamocortical circuit dysfunction

Clinical Features

  • Sudden staring
  • No postictal confusion
  • Automatisms (lip smacking)
  • Multiple times/day
  • Hyperventilation triggers

EEG

  • 3 Hz spike-and-wave pattern

Treatment

Ethosuximide (drug of choice)

  • MOA: T-type Ca²⁺ channel blocker
  • Dose: ~20 mg/kg/day
  • Side effects: GI upset, lethargy

Alternatives

  • Valproate
  • Lamotrigine

⚡ JUVENILE MYOCLONIC EPILEPSY (JME)

Definition

Common genetic epilepsy in adolescents


Clinical Triad

  • Myoclonic jerks (early morning)
  • Generalized tonic-clonic seizures
  • ± Absence seizures

Triggers

  • Sleep deprivation
  • Stress
  • Alcohol
  • Photosensitivity

EEG

  • 4–6 Hz polyspike-and-wave

Treatment

Valproate (drug of choice)

  • MOA: ↑ GABA, Na channel block
  • Dose: 10–60 mg/kg/day
  • Side effects: weight gain, hepatotoxicity, teratogenic

Alternatives

  • Levetiracetam
  • Lamotrigine

Prognosis

  • Lifelong tendency
  • Good control with medication

🧬 EPILEPSY SYNDROMES (IMPORTANT)

1. West Syndrome (Infantile Spasms)

  • Age: <1 year
  • Triad:

* Infantile spasms

* Developmental regression

* EEG: hypsarrhythmia

Treatment

  • ACTH
  • Vigabatrin

2. Lennox-Gastaut Syndrome

  • Age: 1–8 years
  • Multiple seizure types
  • Intellectual disability
  • EEG: slow spike-wave

Treatment

  • Valproate
  • Lamotrigine
  • Ketogenic diet

3. Benign Rolandic Epilepsy

  • Focal seizures during sleep
  • Good prognosis

4. Dravet Syndrome

  • Severe, prolonged febrile seizures
  • SCN1A mutation

🚨 STATUS EPILEPTICUS (PAEDIATRICS)

Definition

  • Seizure >5 minutes

OR

  • Recurrent seizures without recovery

Pathophysiology

  • Failure of inhibitory mechanisms (↓ GABA)
  • Excitotoxicity → neuronal injury

Clinical Features

  • Continuous convulsions
  • Altered consciousness
  • Autonomic instability

Emergency Management (STEPWISE)

Step 1 (0–5 min)

  • ABC stabilization
  • Oxygen, IV access
  • Check glucose → give dextrose if low

Step 2 (5–10 min)

Benzodiazepine (first-line)

  • Lorazepam: 0.1 mg/kg IV

OR

  • Diazepam: 0.2 mg/kg IV

Step 3 (10–20 min)

Second-line AED

  • Phenytoin: 20 mg/kg IV

OR

  • Levetiracetam: 20–60 mg/kg IV

Step 4 (Refractory)

  • Phenobarbital
  • Midazolam infusion
  • ICU care

Drugs Summary

Lorazepam

  • MOA: GABA enhancement
  • Longer CNS action
  • Less respiratory depression vs diazepam

Phenytoin

  • MOA: Na channel blocker
  • Side effects: arrhythmia, gingival hyperplasia
  • Monitor: ECG, BP

Levetiracetam

  • MOA: SV2A modulation
  • Fewer interactions
  • Well tolerated

Complications

  • Hypoxia
  • Brain injury
  • Metabolic acidosis

Prognosis

  • Depends on cause & duration
  • Early control → better outcome

🔑 HIGH-YIELD SUMMARY

  • Febrile seizure → benign, no long-term AED
  • Absence → 3 Hz spike-wave, treat with ethosuximide
  • JME → morning myoclonus, lifelong, valproate
  • West syndrome → ACTH
  • Status epilepticus → benzodiazepine first

If you want, I can convert this into:

  • MCQs (exam practice)
  • Flowcharts for quick revision
  • Comparison tables (very useful for viva)

Interactive MCQ Quiz

MCQ Exam Mode

20 Questions
Question 1 of 20

Frequently Asked Questions

A seizure disorder in children refers to recurrent episodes of abnormal electrical activity in the brain leading to motor, sensory, or behavioral changes. It may be due to genetic, structural, metabolic, or infectious causes.
Febrile seizures occur in children aged 6 months to 5 years associated with fever and are usually benign, whereas epilepsy is defined as recurrent unprovoked seizures without fever or acute triggers.
Simple febrile seizures are generalized, last less than 15 minutes, and occur once in 24 hours. Complex febrile seizures are focal, prolonged more than 15 minutes, or occur multiple times within 24 hours.
Ethosuximide is the first line treatment for absence seizures as it blocks T-type calcium channels and effectively controls typical absence episodes.
Juvenile myoclonic epilepsy presents with early morning myoclonic jerks, generalized tonic-clonic seizures, and sometimes absence seizures, often triggered by sleep deprivation.
Valproate is the drug of choice for juvenile myoclonic epilepsy due to its effectiveness against myoclonic and generalized seizures.
Status epilepticus is defined as a seizure lasting more than 5 minutes or recurrent seizures without regaining consciousness in between and requires emergency management.
Benzodiazepines such as lorazepam or diazepam are the first line drugs for the management of status epilepticus.
West syndrome is a severe epilepsy syndrome in infants characterized by infantile spasms, developmental regression, and hypsarrhythmia on EEG.
Lennox Gastaut syndrome is a childhood epilepsy syndrome with multiple seizure types, intellectual disability, and characteristic slow spike-wave EEG pattern.
Lumbar puncture is required when there are signs of meningitis such as neck stiffness, altered consciousness, or in infants where infection cannot be ruled out clinically.
Common triggers include fever, sleep deprivation, metabolic disturbances like hypoglycemia, infections, and missed antiepileptic medications.
Absence seizures show a characteristic generalized 3 Hz spike and wave pattern on EEG.
Carbamazepine can worsen generalized epilepsies such as absence seizures and juvenile myoclonic epilepsy by increasing seizure frequency.
Febrile seizures generally have an excellent prognosis with most children outgrowing them and only a small risk of developing epilepsy later.