neurologic emergencies.ppt
TRANSCRIPT
pediatric neurologic pediatric neurologic emergenciesemergencies
may 2002 core rounds
contentscontents
seizures– approaches to
febrile seizure new onset non-febrile seizure established seizure disorder with recurrence neonatal seizures status epilepticus
– investigation, treatment, disposition headache
– discussion (as little evidence to support) migraine treatment imaging indications
case 1case 1
2 year old parents “shaking episode” lasting “10 mins” EMS called - child no longer shaking V/S - BP 105/60 HR 100 RR 18 Sat N T39
approach?
– well looking child first event multiple events
– sick looking child
case 2case 2
8 year old parents describe good history for tonic-clonic activity
lasting 2 mins 1st event post event confusion - improving in ED - V/S N, N sensorium, N neuro exam otherwise healthy, no meds, no allergies
approach?
case 3case 3
16 year oldknown seizure disorder, on phenytointypical seizure presenting complaintV/S N, neuro N, otherwise looks well
approach?
case 4case 4
2 week old parents - “doesn’t look right”, “mouth opening and
closing” one episode lasting 1 minute child not interested in feeding, sleepy V/S - BP 90/50 HR 130 RR 38 sat N T 37.8 otherwise normal exam
approach?
definitionsdefinitions
febrile seizure – NIH defn - event of infancy/childhood, typically between age 3mo and 5yrs, with no evidence intracranial infection or defined cause
epilepsy - two or more seizures not provoked by a specific event such as fever, trauma, infection, or chemical change
definitionsdefinitions
neonatal seizure – in first 28 days of life (typically first few days)
status epilepticus– seizure lasting >30 mins
NB rosen 5-10 mins
– sequential seizures without regain LOC >30min
classificationclassification
generalized – LOC– tonic, clonic, tonic-clonic, myoclonic, atonic, absence
partial – focal onset– simple partial – no LOC– complex partial – LOC– partial secondarily generalized
unclassified
etiologyetiology
infectiousmetabolictraumatictoxicneoplasticepilepticother
differential diagnosisdifferential diagnosis
syncopebreath holdingsleep disorders (eg. narcolepsy)paroxysmal movement disorder
– tics,tremors
migrainespsychogenic seizures
approach to febrile seizuresapproach to febrile seizuresthe numbersthe numbersepidemiology
– age 3mo – 5yrs– peak age 9-20 mo– 2-5% children will have before age 5– 25-40% will have family history– 80 – 97% simple– 3 - 20% complex
simple febrile seizuresimple febrile seizure
< 15 minsno focal featuresno greater than 1 episode in 24hneurologically and developmentally normal
complex febrile seizurecomplex febrile seizure
>15 min– febrile epilepticus >30min or recurrent without
regaining consciousness > 30min
focal recurrence within 24h
what do parents want to what do parents want to know?know? recurrence
– risk recurrence 25-50%– risk recurrence after 2nd – 50%– most recurrences within 6-12 mo
(20% within same febrile illness)
risk of epilepsy– 2-3% (baseline 1%)– increased in
family history of epilepsy abnormal developmental status complex febrile seizure
neonatal seizureneonatal seizure
brief and subtle– eye blinking– mouth/tongue movements– “bicycling” motion to limbs
typically sz’s can’t be provoked/consoledautonomic changesEEG less predictable
neonatal seizureneonatal seizure
etiology– hypoxic-ischemic encephalopathy
Presents within first day
– congenital CNS anomalies– intracranial hemorrhage– electrolyte abnormalities – hypoglycemia and
hypocalcemia– infections– drug withdrawal– pyrodoxine deficiency
status epilepticusstatus epilepticus
definition– deizure lasting >30 mins
NB Rosen 5-10 mins
– sequential seizures without regain LOC >30min
mortality in pediatric status epilepticus 4%morbidity may be as high as 30%
SE treatment considerationsSE treatment considerations
ABC’sbrief directed Hx and Px
glucose antibiotics/antivirals
– if meningitis/encephalitis considered
SE treatmentSE treatment
1st line anticonvulsants– IV
lorazepam 0.1mg/kg diazepam 0.2 mg/kg midazolam 0.2 mg/kg
– rectal diazepam 2-5 yrs – 0.5 mg/kg 6-11 yrs – 0.3 mg/kg >12 yrs – 0.2 mg/kg
– IM, intranasal, buccal midazolam
SE treatmentSE treatment
2nd line agents– phenytoin 20 mg/kg @ 1mg/kg/min (upto 50 mg/min)– fosphenytoin 15-20 PE/kg @ 3 mg/kg/min (upto 150
mg/min)
3rd line agents– phenobarbital 20mg/kg @ 100mg/min– repeat prn 5-10mg/kg– maximum 40 mg/kg or 1 gram
refractory SE treatmentrefractory SE treatment
consider midazolam– 0.2 mg/kg bolus– then 1-10 mcg/kg/min infusion
induce barbiturate coma– pentobarbital 5-15 mg/kg @ 25 mg/min– then 1-5 mg/kg/hour
others– valproic acid– paraldehyde, chloral hydrate– propofol, inhalational anesthesia, paralysis– lidocaine
approach – stable post szapproach – stable post sz
history– pre-seizure
what was child doing when attack occurred precipitants – fever, trauma, poisoning, drug/med use aura
– deizure what movements – incl. eyes how long LOC? consequences – resp distress, incontinence, injury
– post seizure Post-ictal
approach to stable patientapproach to stable patient
physical directed towards– systemic disease– infection– toxic exposure– focal neuro signs
laboratorylaboratory
blood glucose? electrolytes? magnesium, calcium?
anything at all? what about first time seizures? recurrent?
laboratorylaboratory
yes if…– neonatal– abnormal mental status persistent– diabetics, renal disease– diuretic use– dehydration– malnourishment
laboratorylaboratory
septic work-up (CBC, BC, urine C+S, CXR, LP)– as indicated
sick child < 12 - 18 mo
therapeutic drug levels
other– ABG– toxicologic screen– TORCH, ammonia, amino acids in neonate– CPK, lactate, prolactin – ?confirm seizure?
lumbar puncturelumbar puncture
patients at greatest risk for meningitis– under 18 months of age– seizure in the ED– focal or prolonged seizure– seen a physician within the past 48 hours
other indications– concern about follow-up– prior treatment with antibiotics
The American Academy of Pediatrics “strongly consider” in infants under 12 months of age with a first
febrile seizure
neuroimagingneuroimaging
WHO? which patients?
WHAT? CT vs. MRI– ultrasound in neonates
WHEN? emergent vs. elective
ACEP guidelines - >6 yoACEP guidelines - >6 yo
consensus indication for non-contrast CT first time seizure patients
– if suspect structural lesion – partial onset seizure– age > 40– no other identified cause
recurrent seizure patients– change in pattern– prolonged post-ictal period– worsening mental status
neuroimagingneuroimaging predictors of abnormal findings of computed tomography of the head in
pediatric patients presenting with seizures
Warden CR - Ann Emerg Med - 01-Apr-1997; 29(4): 518-23 – retrospective case series– predicts CT scan results normal if
no underlying high-risk condition – malignancy, NCT, recent CHI, or recent CSF shunt revision
older than 6 months sustained a seizure of 15 minutes or less no new-onset focal neurologic deficit
– not prospectively validated
emergent EEG?emergent EEG?
not generally available on emergent basisbut consider in..
– persistent altered mental status (?non convulsive status epilepticus)
– paralyzed patients– pharmacologic coma
dispositiondisposition
can be discharged home if– single seizure– stable, returning to baseline neuro status– no underlying condition/cause requiring
treatment in hospital– arranged follow-up
EEG – 1EEG – 1stst non-febrile seizure non-febrile seizure
follow-up EEG– within 24h
Lancet 1998;352:1007-11 improved pick-up 51% vs 34% ? how soon do we get ours ?
– inter-ictal EEG’s often normal neuro may do sleep deprivation study (provocation)
– absence epilepsy and infantile spasms are invariably associated with an abnormal EEG
– spike and wave 3HZ
idiopathic seizureidiopathic seizure
recurrence risk stratification – normal EEG – 25%– abN EEG – 60%– 2nd seizure – 75%
neuroimagingneuroimaging
MRI superior
not emergently available
?defer imaging until follow-up MRI available in low risk patients?
treatmenttreatment
correct underlying pathology, if any antipyretics ineffective in febrile seizure anti-epileptic choice often trial and error
no anti-epileptic 100% effective febrile seizure – diazepam, phenobarbital, valproic acid
– Currently AAP does not recommend neonatal - phenobarbital generalized TC – phenytoin, phenobarbital, carbamazepine, valproic
acid, primidone absence – ethosuximide, valproic acid new anti-epileptics – felbamate, gabapentin, lamotrigine, topiramate,
tiagabine, vigabatrine
in consultation with neurologist
pediatric headachepediatric headache
case 5case 5
14 year old mother’s chief complaint - “having headaches all the
time, getting worse, this is not normal!!” etc. etc…….. V/S N looks in discomfort but otherwise well
approach?– treatment– imaging?
classificationclassification
classify based on temporal pattern
acute headaches– any febrile illness, sinus/dental infection, intracranial
infection/bleed (AVM,SAH,trauma) acute recurrent chronic progressive chronic non-progressive
– tension, psychogenic, post-traumatic, ocular refractive error
acute recurrent headacheacute recurrent headache
migraine
other– cluster headache – typically >10 yo– sinusitis– vascular malformation
migraine - terminologymigraine - terminology
classic migraine– biphasic
neuro aura headache, N/V, anorexia, photophobia
– either unilateral (older) / bilateral(younger) or both
common migraine– malaise, dizziness, N/V, feels and looks sick– unilateral/bilateral
migraine equivalent/”complicated migraine”– transient neuro deficits– +/- headache
migraine variants– Cyclic N/V, abdo pain– BPV
migraine treatmentmigraine treatment
very little supporting evidence for pharmacologic treatment in children compared to adults
classes of medication– acetaminophen– NSAIDS– phenothiazines (dopamine antagonists)– dihydroergotamine– triptans
the simple stuffthe simple stuff
acetaminophen 15 mg/kg PO 30mg/kg PR ibuprofen 10 mg/kg PO
Hamalainen ML Ibuprofen or acetaminophen for the acute treatment of migraine in children: A double-blind, randomized, placebo-controlled, crossover studyNeurology 48:103-107, 1997 – N = 88 age 4-16– relief at 2 hours
acetaminophen 54% ibuprofen 68%
other NSAIDSother NSAIDS
naproxen 5-7 mg/kg PO– no pediatric evidence
ketorolac IV 0.5 mg/kg (max 30mg dose)– not studied in pediatric migraine– not approved <16 yo– Houck CS – Safety of intravenous ketorolac in children and cost savings with a unit
dosing system. J Pediatr - 01-Aug-1996; 129(2): 292-6 1747 children 0.2% hypersensitivity 0.1% renal complications (in patients with renal disease) 0.05% gi bleed
dihydroergotaminedihydroergotamine
not approved?dose – 0.1 – 0.5 mg IVnot studied in emergency population
Linder SL – Treatment of childhood migraine with dihydroergotamine mesylate Headache - 1994 Nov-Dec; 34(10): 578-80 – N = 30– inpatient protocol– IV DHE and PO metoclopramide – average 5 doses!– 80% response
phenothiazinesphenothiazines
again no studies
metoclopramide 1-2 mg/kg IV (max 10mg)prochloperazine 0.1 – 0.15 mg/kg
IV/IM/PO/PR (max 10mg)
children may be more susceptible to EPS– ? pre-treat with benadryl
triptanstriptans
mostly studied in adolescent groups sumitriptan subcutaneous 0.06mg/kg
– Linder S: Subcutaneous sumatriptan in the clinical setting: The first 50 consecutive patients with acute migraine in a pediatric neurology office practice. Headache 36:419–422, 1996
– N = 50 age 6-18– 78% effective at 2 hours– 6% recurrence
sumitriptan intranasal– long term treatment studies done– no emergent studies
triptans PO– studies plagued by high placebo response
chronic progressive headachechronic progressive headache
least common presentation
most worrisome for increased ICP– pseudotumor cerebri– space occupying lesion
imaging indications? discussimaging indications? discuss
lack of evidence to help– small studies lack power to guide decision
making
MRI preferred in non-urgent indication
imaging indications? discussimaging indications? discuss
classically based on historical and physical– sudden severe headache– rapid increase over days - weeks– chronic progressive– suggestive of increased ICP
severe nocturnal headache (wakes or upon waking), changes in pain with position, coughing
– following head trauma– persistent neuro findings
? include migraine equivalents ?
– growth abnormality– age (? <3 ?)