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Seizure (peds)
From WikEM
(Redirected from Pediatric seizure)
This page refers to pediatric patients; see seizure for adult patients.
Contents
Background
- Todd paralysis
- Temporary focal deficit up to 36 hr post-seizure
- Lateral tongue biting - 100% specificity
Seizure Types
Classification is based on the international classification from 1981[1]; More recent terms suggested by the ILAE (International League Against Epilepsy) task Force.[2]
Focal seizures
(Older term: partial seizures)
- Without impairment in consciousness– (AKA Simple partial seizures)
- With motor signs
- With sensory symptoms
- With autonomic symptoms or signs
- With psychic symptoms (including aura)
- With impairment in consciousness - (AKA Complex Partial Seizures--Older terms: temporal lobe or psychomotor seizures)
- Simple partial onset, followed by impairment of consciousness
- With impairment of consciousness at onset
- Focal seizures evolving to secondarily generalized seizures
- Simple partial seizures evolving to generalized seizures
- Complex partial seizures evolving to generalized seizures
- Simple partial seizures evolving to complex partial seizures evolving to generalized seizures
Generalized seizures
- Absence seizures (Older term: petit mal)
- Typical absence seizures
- Atypical absence seizures
- Myoclonic seizure
- Clonic seizures
- Tonic seizures
- Tonic–clonic seizures (Older term: grand mal)
- Atonic seizures
Clinical Features
- Abrupt onset, may be unprovoked
- Brief duration (typically <2min)
- AMS
- Jerking of limbs
- Postictal drowsiness/confusion
Differential Diagnosis
Pediatric seizure
- Seizure
- Febrile seizure
- First-Time afebrile seizure
- Neonatal seizure
- Epileptic seizures
- Seizure with VP shunt
- Impact seizure (trauma)
- Status epilepticus
- Meningitis
- Intracranial mass
- Epidural/subdural infection or hematoma
- Toxic ingestion
- Hydrocephalus
- Pyridoxine responsive seizure[3]
Evaluation
Seizure with a Fever
- See Febrile Seizure
First-Time Afebrile Seizure
- If patient returns to baseline no labs/imaging necessarily indicated
- Consider glucose, chemistry,
- LP only necessary if concern for meningitis (peds)
- EEG should be performed within 24-48hr
- Neuroimaging
- Preferred test is outpatient MRI
- Consider emergent imaging for focal deficit, no return to baseline
- 40% have 2nd seizure
Neonatal Seizure
- Often subtle, focal, poor prognosis
- Less often have generalized tonic-clonic seizures
- Findings include lip smacking, eye deviation, staring, ALTE
- Less often have generalized tonic-clonic seizures
- Work-up
- CBC, chemistry, UA, CSF (including HSV), utox (withdrawal)
- Consider neuroimaging if concern for abuse, [intracranial hemorrhage]], mass
- Consider lactate, ammonia if concern for inborn errors of metabolism
- Treatment
- Start IV antimicrobials (including acyclovir)
- Consider B6 and folic acid responsive etiologies unresponsive to benzos[4]
- Pyridoxal phosphate 10mg/kg/dose q2h x 2 doses
- If persistent, folinic acid 5mg q6h x 2 doses
- EEG monitoring during this period is helpful
Epileptic Seizures
- Epilepsy = 2 or more seizures with out acute provocation (fever, trauma)
- Often due to patient "outgrowing" their dosage
- Check levels of:
- Phenytoin, carbamazepine, valproic acid
- If low consider medication non-adherence, "outgrowing" dose, vomiting, med interaction
- Phenytoin, carbamazepine, valproic acid
- Patients with epilepsy may have lower seizure threshold with febrile illness
- Usually can limit ED work up to fever evaluation
Seizure with VP shunt
- Consider underlying epilepsy, shunt malfunction, CNS infection
- If patient has fever seizure more likely secondary to infection than malfunction
- Consult pediatric neurosurgeon to tap the shunt
- If patient has fever seizure more likely secondary to infection than malfunction
- Imaging
- Obtain shunt series and head CT or MRI to evaluate for increased ventricular size
Seizure with Pediatric Head Trauma
- "Impact seizures" (seizures that occurs within in minutes of head trauma)
- Not associated with severe head injuries
- Seizures that occur after this time more likely to represent intracranial injury
Status Epilepticus
- Seizure or recurrent seizure lasting >5min with out regaining consciousness
- If prolonged postictal state or longer than usual consider nonconvulsive status
- Obtain emergency EEG; if not available, trial of anticonvulsants appropriate
- If prolonged postictal state or longer than usual consider nonconvulsive status
- Management
- Glucose, chemistry, CBC, LFT, ?CSF, ?neuroimaging
- Intubate if evidence of apnea and persistent hypoxia
- If paralytic used, EEG monitoring should be arranged
Management
1st Line
Drug[5] | Route | Dose* | Maximum | Onset of Action | Duration of Action |
---|---|---|---|---|---|
Lorazepam | IV, IO, IN |
0.1mg/kg | 4mg | 1–5 min | 12–24 h |
IM | 0.1mg/kg | 4mg | 15–30 min | 12–24 h | |
Diazepam | IV, IO | 0.1–0.3mg/kg | 10mg | 1–5 min | 15–60 min |
PR | 0.5mg/kg | 20mg | 3–5 min | 15–60 min | |
Midazolam | IV, IO | 0.1–0.2mg/kg | 4mg | 1–5 min | 1–6 h |
IM | 0.2mg/kg | 10mg | 5–15 min | 1–6 h | |
IN | 0.2mg/kg | 10mg | 1–5 min | 1–6 h | |
Buccal |
0.5mg/kg | 10mg | 3–5 min | 1–6 h |
2nd Line
- If seizure persists for another 5 min after 2 doses of benzodiazepines switch to fosphenytoin or phenobarbital
- Fosphenytoin is usually preferred 2nd line agent
- Consider phenobarb over fosphenytoin if febrile illness, <2yr
Drug | Route | Loading Dose | Repeat Dose | Maximum | IV Infusion |
---|---|---|---|---|---|
Fosphenytoin | IV, IM | 15–20mg/kg PE | 5–10mg/kg PE | 30mg/kg PE | 3mg/kg/min PE |
Phenobarbital | IV | 15–20mg/kg | 5–10mg/kg | 40mg/kg | 1–30mg/min |
Valproic acid | IV | 20mg/kg | 15–20mg/kg | 40mg/kg | 5mg/kg/hr |
Levetiracetam | IV | 20–30mg/kg | — | 3 grams | — |
Pentobarbital | IV | 5–15mg/kg | 1–2mg/kg | 15mg/kg | 0.5–5.0mg/kg/hr |
Propofol | IV | 0.5–2.0mg/kg | 0.5–1.0mg/kg | 5mg/kg | 1.5–4.0mg/kg/hr |
Midazolam | IV | 0.1–0.2mg/kg | 0.1–0.2mg/kg | 10mg | 0.05–0.4mg/kg/hr |
3rd Line
- Consider valproic acid 20mg/kg over 1-5min; then infusion of 5mg/kg/hr
Hypoglycemia
- Defined as <50mg/dL
- All seizing patients with hypoglycemia should be treated with 2 mL/kg 25% dextrose
Hyponatremia
- Consider as cause of seizure, especially if Na <120 mEq/L
- Goal of therapy is to correct quickly to >120, slowly thereafter
- In actively seizing patient, treatment of choice is 3% NaCl
- 3% NaCl (513 mEq/1000 mL)
- Na deficit in total mEq = [(wt in kg)x(130 – serum Na level)x0.6] over 20min OR
- 3% NaCl: 4-6 mL/kg over 20min
- 3% NaCl (513 mEq/1000 mL)
- If no seizure activity but Na <120 start 4-6 mL/kg 3% NaCl or 20 mL/kg of NS over 1hr
- Check Na level after bolus to see if second bolus is necessary
- If 3% unavailable, start NS 20mL/kg
- In actively seizing patient, treatment of choice is 3% NaCl
Hypocalcemia
- Administer 10% calcium gluconate 0.3 mL/kg over 5-10min
Other
- Consider Pyridoxine (vitamin B6) 1g per g of INH ingested (in D5W IV over 30 min) [6]
- Consider Pyridoxine Responsive Seizure Disorder - 100mg/pyridoxine is generally effective [7]
Disposition
If negative workup
- EEG and MRI as outpatient
- Diastat (diazepam) Rectal Kit
- 2-5 yrs: 0.5mg/kg
- 6-11 yrs: 0.3mg/kg
- 12+ yrs: 0.2mg/kg
See Also
External Links
References
- ↑ Proposal for revised clinical and electroencephalographic classification of epileptic seizures. From the Commission on Classification and Terminology of the International League Against Epilepsy. Epilepsia 1981; 22:489.
- ↑ Epilepsia 2015; 56:1515-1523.
- ↑ Baxter P. et al. Pyridoxine‐dependent and pyridoxine‐responsive seizures. Developmental Medicine & Child Neurology 2001, 43: 416–42
- ↑ Robert Surtees and Nicole Wolf. Treatable neonatal epilepsy. Arch Dis Child. 2007 Aug; 92(8): 659–661.
- ↑ LaRoche SM, Helmers SL. The New Antiepileptic Drugs: Scientific Review. JAMA. 2004;291:605-614.
- ↑ Minns AB, Ghafouri N, Clark RF. Isoniazid-induced status epilepticus in a pediatric patient after inadequate pyridoxine therapy. Pediatr Emerg Care. 2010; 26(5):380-1.
- ↑ Pyridoxine dependent seizures a wider clinical spectrum. Archives of Disease in Childhood.1983 (58) 415-418. http://adc.bmj.com/content/58/6/415.full.pdf