Pediatric Status Epilepticus Clinical Presentation
- Author: Grace M Young, MD; Chief Editor: Richard G Bachur, MD more...
History
In the initial presentation of status epilepticus, a directed history suffices. Obtain a more detailed history after stabilization, including the following details:
- The course of current seizure activity - Time and nature of onset of seizure activity; involvement of extremities or other body parts; nature of movements (eg, eye movements, flexion, extension, stiffening of extremities), including any focal movements and details of postictal neurologic deficit; incontinence; cyanosis (perioral or facial); duration of seizure activity prior to medical attention; mental status after cessation of seizure activity
- Fever or intercurrent illnesses
- Prior history of seizures - If present, specify medications, anticonvulsant use, and compliance.
- Head injury (recent and remote)
- Central nervous system (CNS) infection or disease (eg, meningitis, neurocutaneous syndrome)
- Intoxication or toxic exposure (see Causes for examples)
- Other CNS abnormality (eg, ventricular-peritoneal shunt, prior CNS trauma)
- Birth history and developmental delay (eg, anoxic encephalopathy, cerebral palsy)
- Other medical history (eg, acquired immunodeficiency syndrome, systemic lupus erythematosus, type 1 diabetes mellitus)
Physical
Perform a rapid, directed physical and neurologic examination during status epilepticus, followed by a detailed examination when the child is stabilized.
Signs of sepsis or meningitis include the following:
- Temperature more than 38.5°C; in patients younger than 2-3 months, more than 38.0°C
- Respiratory distress
- Cyanosis
- Poor peripheral perfusion
- Bulging fontanelles in infant
- Meningismus (in children >12-18 mo)
- Presence of petechiae or purpura, herpetic vesicles
Evidence of head or other CNS injury includes the following:
- Bradycardia, tachypnea, and hypertension (Cushing triad for signs of increased intracranial pressure)
- Poor pupillary response
- Asymmetry on neurologic examination
- Abnormal posturing
- Gross deformity or soft tissue injury to head
Hallmarks of neurocutaneous syndromes (eg, port wine stain) may be noted.
Causes
Neonates (first month of life)
- Birth injury (eg, anoxia, hemorrhage) and congenital abnormalities
- Metabolic disorders (eg, hypoglycemia, hypocalcemia, hyponatremia) and inborn errors of metabolism (eg, lipidoses, amino acidurias)
- Infection (eg, meningitis)
Early childhood (< 6 y)
- Birth injury
- Febrile convulsions (3 mo to 6 y)
- Infection
- Metabolic disorders
- Trauma
- Neurocutaneous syndromes
- Cerebral degenerative diseases
- Tumors
- Idiopathic
Children and adolescents (>6 y)
- Birth injury
- Trauma
- Infection
- Epilepsy with inadequate drug levels
- Cerebral degenerative disease
- Tumor
- Toxins
- Idiopathic
Toxins and medications
- Topical anesthetics (eg, lidocaine)
- Anticonvulsant overdose
- Camphor
- Hypoglycemic agents (eg, insulin, ethanol)
- Carbon monoxide
- Cyanide
- Heavy metals (eg, lead)
- Pesticides (eg, organophosphate)
- Cocaine
- Phencyclidine
- Belladonna alkaloids
- Nicotine
- Sympathomimetics (eg, amphetamines, phenylpropanolamine [recalled from US market])
- Tricyclic antidepressants
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