Seizures in Children ==================== þ Neonatal Seizures: - Pyridoxine, 100 mg intravenously, should be considered for neonates with intractable seizures of unclear etiology [Kwon KT, Tsai VW. Metabolic emergencies. Emergency medicine clinics of North America 2007;25:1041-60, vi.] þ Febrile Seizures: þ American Academy of Neurology Clinical Practice Guidelines: (for common ED seizures) - < 6 months: admit, consult neuro - > 6 months: + check glucose + tox screen, electrolyes: only if clinical suspicion + EKG: ? not in practice guidelines, but often done; most with cardiac syncope don't have prolonged tonic-clonic true seizure, do only if question of cardiac syncope + EEG: have PCP schedule as outpatient + CT? 5-10% will have some abnormality, 33% if get MRI, but few influence management. - CT if: Todd's paralysis focal seizure < 3 years persistent MS changes predisposing factors: sickle, bleeding problems CNS disease, malignancy HIV, hemihypertropy hydrocephalus, travel to cysticercosis closed head injury þ New afebrile seizure: + In most cases, don't need to start anticonvulsant right away; + don't need to get CT scan if patient looks OK. + 50% of normal looking kids will not have a second seizure; + it's hard to take kids off an anticonvulsant. + If second seizure, go ahead and start anticonvulsant. þ Seizure 3 days later: just admit. þ IM Versed - For kids with seizures, IM Versed worked better than IV Valium - Midazolam 0.2 mg/kg (max 7 mg) IM þ History: Was it really a seizure? What kind of seizure was it? þ Presentations: - Febrile Seizure - Afebrile Seizure (recent or remote) - Status Epilepticus - Breakthrough Seizure in Patient with Known Seizures. þ Classsify seizure: - Partial; Generalized; Unclassifies; Status Epilepticus. - Partial: + Simple (consciousness preserved) + Complex (consciousness impaired) + (either may generalize) + (Complex may have staring, amnesia, automatisms, - Generalized: + Absence ("Petit Mal") 10-20 sec. + Tonic-Clonic ("Grand Mal") + Myoclonic ("Minor Motor") brief shock-like motor twitches, usually bilaterally; more often than normal myoclonic jerks - Non-Epileptic seizures: + Anoxia (faints, febrile syncope, breath-holding) + Apnea or Bradycardia in infants + Paroxysmal Vertigo - ?migraine equivalent; - run to and hug parents tightly; - may see nystagmus; - resolves in minutes; - toddlers to 7-8 years age group? - +FH of migraine helpful in diagnosis) - Psychiatric + hyperventilation; + pseudoseizures: + avoid eye contact, hold eyes shut; + very atypical movements; + usually have severe psychiatric illness - Migraine or similar Periodic Syndromes + Tics and other abnormal movements (most disappear during sleep) - Paroxysmal Nocturnal Events: + night terrors, + somnambulism, + abnormal movements during sleep; + narcoplepsy; + cataplexy; + sleep paralysis; + hypnagogic/hypnopompic hallucinations þ Precipitant Drugs for Pediatric Seizures: - adrenergics, - sedative withdrawal, - phenothiazines, - tricyclics þ Drugs: - Current Fad: MONOTHERAPY push levels of a single drug for monotherapy - phenobarb: + 20mg/kg IV; or + PO twice maintenance for 3 days. + Maint 5mg/kg/day - Dilantin (phenytoin): + 20mg/kg IV; or, + 20 mg/kg divided into 2-5 hourly doses 1 mg/kg/min infusion - lorazepam (Ativan): + onset 2-20 minutes, duration 2-4 hours; + 0.05-.01 mg/kg IV (Max 4-8mg); or, + 0.05-0.15 mg/kg SL; or, + 0.05 mg/kg rectal - Valium: + .5-1.0 mg/kg IV solution rectal; + useful for home for preventing febrile seizures - Paraledehyde: + good IV 200mg/kg loading via 4% solution IV 200 mg/kg/hr; + good level is 300 mg - valproate (valproic acid/depakene): + may load with 60/mgkg/day rectal with depakene syrup in cocoa butter; + may cause hepatic toxicity in children; + causes N/V/anorexia, easy bruising; + may get breakthrough from hepatic toxicity - Tegretol (carbemazapine): + thrombocytopenia and neutropenia significant side effects; + get baseline in ED if starting in ED. - Pyridoxine: + 25 - 50 mg of should be administered intravenously in neonatal seizures as some neonates will have seizures secondary to a syndrome of pyridoxine dependence (a metabolic disorder requiring lifelong pyridoxine therapy). + Tintinalli 3rd ed. p 480-1, Schwartz 3rd ed. p 364. þ Choice of Anticonvulsant for Pediatric Seizures: - Abscence: + Valproate (depakene)/ + ethosuximide (Tegretol known for worsening of abscence episodes.) - Tonic-clonic: + Dilantin/ + Phenobarb - Partial: + Dilantin/ + Tegretol (carbamezapine) - Myotonic/Atonic: + benzodiazepines - Neonatal: + lorazepam (Ativan) is preferred over diazepam (Valium) when using a benzodiazepine to control neonatal seizures in a jaundiced baby; Diazepam uncouples the bilirubin-albumin complex and may worsen hyperbilirubinemia. Ref: Tintinalli 3rd ed. p 481 + pyridoxine; see above - Febrile: see þ Status Epilepticus (may also be ascence or partial status epilepticus) After 60 minutes (or a bit more in children), permanent damage. 0-5 minutes: ABC's, look for trauma, infection, good IV access 6-9 minutes: give glucose and B vitamins 10-30 minutes: Dilantin, benzodiazepine, or phenobarb. Dilantin preferred in kids: fast response, goes through BBB, doesn't cause CNS depression; if that doesn't work, try .1mg/kg bolus of lorazepam x2; then phenobarb; then general anaesthesia. þ Breakthrough Seizure: + check levels, + look for trauma, + do tox screen, + check routine labs including Mg, PO4, Ca, lytes/BUN/Cr/Glucose