SN6
SHORT NOTE
5M
★ High-yield
Define status epilepticus. Describe its stepwise management.
Definition
Status epilepticus is a seizure lasting more than 5 minutes, or two or more seizures without full recovery of consciousness between them. It is a medical emergency with a mortality of 10 to 20%.
- The old definition of 30 minutes has been abandoned, because irreversible neuronal injury begins well before then and self-termination becomes unlikely after about 5 minutes — the change in definition was made to prompt earlier treatment
- Precipitants — antiepileptic withdrawal or non-adherence (the commonest), alcohol withdrawal, infection (meningitis, encephalitis, cerebral malaria, neurocysticercosis), stroke, head injury, metabolic disturbance (hypoglycaemia, hyponatraemia, hypocalcaemia), drugs, eclampsia
Stepwise Management
| Time | Action |
|---|---|
| 0–5 minutes | ABC — airway, oxygen, position; check glucose immediately (give glucose with thiamine if low or unknown in an alcoholic); intravenous access; blood for electrolytes, calcium, drug levels, toxicology |
| 5–20 minutes — first line | Benzodiazepine: intravenous lorazepam 4 mg (preferred — longer duration of anticonvulsant action and less redistribution than diazepam), or diazepam 10 mg, or intramuscular midazolam where there is no venous access. May be repeated once |
| 20–40 minutes — second line | Intravenous phenytoin 20 mg/kg (or fosphenytoin), valproate 40 mg/kg, or levetiracetam 60 mg/kg — all comparable in trials |
| 40–60 minutes — refractory | General anaesthesia with intubation and ventilation — midazolam infusion, propofol or thiopentone; continuous EEG monitoring |
| Throughout | Treat the cause — antibiotics for meningitis, antimalarials, correction of sodium or glucose, delivery in eclampsia (with magnesium sulphate) |
CLINICAL PEARL
Lorazepam is preferred to diazepam although diazepam enters the brain faster. Diazepam is highly lipid-soluble, so it acts within seconds but redistributes out of the brain within about 20 minutes and the seizure returns. Lorazepam is less lipid-soluble, enters slightly more slowly, and stays in the brain for hours. In status, duration of effect matters more than speed of onset.
Practical Points on Individual Drugs
- Phenytoin must be given slowly, no faster than 50 mg per minute, with cardiac monitoring — rapid infusion causes hypotension and arrhythmia, largely from the propylene glycol diluent
- Phenytoin must never be mixed with glucose solutions, in which it precipitates; normal saline is used
- Fosphenytoin is a water-soluble prodrug that can be given faster and is less irritant, and can be given intramuscularly
- Extravasation of phenytoin causes severe tissue necrosis — the "purple glove" syndrome
- Do not under-dose the benzodiazepine — giving too little for fear of respiratory depression is a common error and prolongs the seizure, which is itself far more dangerous
Applied Aspects
- Always check the blood glucose — hypoglycaemia is a readily reversible cause and is missed if the seizure dominates attention
- Consider eclampsia in any woman of childbearing age; magnesium sulphate, not a conventional antiepileptic, is the treatment, and delivery is definitive
- In India, consider cerebral malaria, neurocysticercosis, tuberculous meningitis and hyponatraemia — the causes differ from those in Western texts and change management substantially
- Non-adherence is the commonest precipitant in a known epileptic; ask about it, and address cost, supply and understanding rather than simply increasing the dose
- Prolonged seizures cause hyperthermia, rhabdomyolysis, acidosis and aspiration, all of which require specific attention alongside stopping the seizure
- Buccal or intranasal midazolam can be given by family members at home and prevents many hospital presentations; teaching the family is a practical, high-value intervention
- Non-convulsive status must be considered in any patient who fails to wake after a seizure; it requires an EEG and is easily missed
All questions in Central Nervous System Drugs
- Q1Classify general anaesthetics. Describe MAC and the factors governing induction, the stages of anaesthesia and the individual agents. ★
- Q2Classify local anaesthetics. Describe their mechanism of action, techniques of use and systemic toxicity. ★
- Q3Classify antiepileptic drugs by mechanism. Describe the choice of drug by seizure type and compare phenytoin, carbamazepine and valproate. ★
- Q4Classify opioid analgesics. Describe the pharmacological actions, uses and acute poisoning of morphine. ★
- Q5Classify antipsychotic drugs. Describe the dopamine pathways, extrapyramidal syndromes and adverse effects. ★
- SN1Classify sedative-hypnotics. Describe the mechanism, uses and adverse effects of benzodiazepines. ★
- SN2Classify antidepressants. Compare SSRIs with tricyclic antidepressants. ★
- SN3Describe the drugs used in Parkinson disease. Add a note on drug-induced parkinsonism. ★
- SN4Describe lithium with its adverse effects, interactions and monitoring. Add a note on other mood stabilisers. ★
- SN5Describe the acute and chronic effects of ethanol, alcohol withdrawal and methanol poisoning. ★
- SN6Define status epilepticus. Describe its stepwise management. ★
- SN7Define drug dependence, tolerance and addiction. Describe the opioid antagonists and the principles of managing dependence.