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Definition
Varying and changing, operationally defined as:
≥5 minutes of continuous seizure activity, or ≥1 seizure without recovery in between
Seizure ≥30 minutes may cause permanent brain damage
Epidemiology
5% of the world population will have at least 1 episode of seizure
Annual incidence is higher in developing country
Lower mortality rate in children (30% vs 3%)
Equal prevalence in males and females
Binomial age distribution (extremes of ages)
Causes
New cases: Idiopathic (62%), stroke (9%), head trauma (9%), alcohol (6%)
Old cases: Incompliance
After episode, go A&E if it is the first epilepsy episode; or else not necessary (check medical history!)
Assessment
First investigations Anticonvulsant blood levels
Toxicology screening
Comprehensive metabolic profile: Electrolyte imbalances, other reversal causes
Complete blood count: Check WBC for infection; PLT for haemorrhage
Electrocardiogram: Arrhythmia or cardiac ischemia may occur
Blood glucose: Hypo-/Hyperglycaemia
Others to consider EEG, ABG, CT head, lumbar puncture, MRI head, blood cultures
Management
Treat underlying causes
Causes Treatment
Bacterial infection Anti-bacterial
Metronidazole
Viral infection Anti-viral
Abscess Surgery
Increased intracranial pressure Neurosurgical decompression
Eclampsia Magnesium and BP management, early delivery
Isoniazid overdose Pyridoxine
Sodium channel blocker overdose Sodium bicarbonate, intralipid
Pharmacologic management (thiopental, methohexitol, no ketamine)
Time phase Management
0-5 min - Airway ± mechanical ventilation;
Stabilization Preferred: IV propofol or midazolam – Anti-convulsant properties
Not preferred: IV etomidate or neuromuscular blocking agents
(If required, prefer suxamethonium chloride or rocuronium – Short acting)
Neuromuscular blocking may block motor manifestations
EEG monitoring should be used to monitor disease progress
- Thiamine 100mg + glucose
Hypoglycemia is an uncommon cause of Status Epilepticus
**Thiamine should always be given BEFORE glucose infusion to avoid
Wernicke’s Encephalopathy: Activation of glycolysis consume thiamine**
- Pyridoxine should be given for children until metabolic causes been ruled out
- IV access
- Rectal paracetamol for hyperthermia or vasopressors for hypotension
5-20 min - Benzodiazepines (First-line agent)
Initial Therapy IV Diazepam: High lipophilicity
Fastest onset (10-20s);
Shortest duration (<20 mins), IV access required
IV Lorazepam
Longer duration of action (4-12 hours), fast onset (2 mins)
IV access required
IM Midazolam (or buccal)
IV access NOT required
Short half-life in CNS
- Can be re-dosed after 5 minutes if ineffective
- Side effects: hypoventilation, cardiac rhythm disturbances
20-40 min - Likely to be equally effective and have similar rates of adverse effects
Secondary Therapy - IV Fosphenytoin (20mg/kg IM or IV)
Better tolerability and faster infusion than phenytoin
(i.e., local site irritation, less hypotension from propylene glycol)
Life threatening rash in Asians with HLA-B*1502
IM should not be used due to unpredictable level and slow onset
- IV Valproate acid
May be more efficacious/tolerable than fosphenytoin
Risk of hepatoxicity and coagulopathy
- IV levetiracetam (not preferred on HA formulary)
Least drug interactions and hepatotoxicity, need renal dose adjustments
Least risk on major birth defects or effect on oral contraceptive efficacy
40-60 min - Repeat previous treatments
Refractory phase - Induce coma by pentobarbital, midazolam and propofol
(10-20% of cases) - Midazolam
Tachyphylaxis rapidly develops within 24-48 hours
Dose may need to be increase after 1-2 days
- Propofol (Continuous infusion: Half-life is very short 3-10 minutes)
Less seizure recurrence than midazolam
Contraindicated in patients with hypotension, always check BP!
- Pentobarbital/phenobarbitone
More hypotension but maybe better efficacy
- Send to ICU as soon as possible for EEG monitoring and further management