Pediatrics Neuro

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Last updated 9:01 PM on 3/27/26
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55 Terms

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children are top heavy, HUGE proportion to body, poor neck musckles

Anatomic differences between children's and adults' nervous

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24 months (2 years)

how long does sutures stay unfused

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posterior within first 2 months and then anterior is close between 12 and 18 months

when to the anterior and posterior fontanel close

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LOC, cognitive function, cranial nerves, skull, pupils, vital signs, posture and movement, neck stiffness, pain

what is in a nero assessment

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intracranial pressure (ICP)

with an altered LOC you want to look for signs of increased

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sequential pattern (initial changes may be subtle, restless, or fussy, failure to soothe)

Decline in LOC often follows a

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-confusion

-delirium

-lethargy

-stupor

-coma

altered LOC categories

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lethargy

profound slumber in which speech and movement are limited. Arousable with moderate stimulation, but falls asleep easily once stimulation is removed

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headache, visual disturbances, diplopia, N/V, dizziness, a slight change in vitals, pupils not reactive or equal, a slight change in LOC

early signs of ICP

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bulging frontale, wide sutures, increased head circumference, dilated scalp veins, irritabile, high pitched, catlike cry

early signs of increase ICP specifically in infants

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sunsetting eyes, a significant decrease in LOC, seizure, fixed/dilated pupils, Cushing triad

late signs of increased ICP

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increased systolic BP (widened pulse pressure), bradycardia, and irregular respirations

cushing triad

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seizure

A sudden surge of electrical activity in the brain that cause involuntary movement, and behavior and sensory alterations

• Symptoms depend on type of seizure and duration

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partial seizures

caused by abnormal electrical brain function in one hemisphere or a specific area of the cerebral cortex.

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simple and complex

types of partial seizures

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Simple Partial (Focal) Seizure

a type of partial seizure

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no LOC

lasts <30 sec

no post ictal phase confusion

no aura

limited to an isolated muscle group (fingers, arms, or legs)

Simple Partial (Focal) Seizure description:

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complex partial seizure

2nd type of partial seizures

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Altered behavior

• Unable to respond to environment

• Impaired LOC (regains in <5 min)

• Automatisms: unusual body movement without purpose -lip smacking or chewing

• Aura frequently occurs

• Postictal period: confusion and inability to recall event

complex partial seizure description

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Generalized Seizures


Involve both sides of the brain at the sametime

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Tonic-Clonic Seizure

most common generalized

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tonic, clonic, postictal

three phases of tonic clonic seizure

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last 10-20 seconds:

Stiffening of body and limbs, back arched

• Eyes roll upward

• LOC

• Mouth snaps shut (may bite tongue)

• Possible piercing cry

• Pallor

• Increased salivation

• Apnea leading to cyanosis

tonic phase of seizure:

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last 30-50 seconds:

Clonic jerks of limbs, body, and head

• Foaming of the mouth

• Incontinence

• Gradual slowing of movements until stop

clonic phase of tonic clonic

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30 min or longer:

Limbs and body limp

• Remains semiconscious - aroused with difficulty

• Confused for several hours

• Impairment of fine motor movements

• Lack of coordination

• May have headache, vomiting, visual, or speech difficulties

• Sleep for several hours

• Feels tired

• May complain of muscle soreness

• Do not recall seizure

postical state of tonic clonic

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Brief altered state of consciousness

• LOC lasts 5 to 10 seconds

• Motionless

• Blank stare

• Do not recall episodes

• Immediately resumes previous activity

• May be mistaken for a learning problem or behavioral problem

• Onset between ages 4 to 12 years

• End by teenage years

Absence Seizures:

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Also called "drop attacks"

• Onset is between 2 to 5 years of age

• Muscle tone lost few seconds = risk for fall

• Period of confusion follows

• May need to wear helmet

atonic seizures

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Variety of seizure episodes

• Symmetric or asymmetric involvement

• Brief contractions of muscles/group of muscles• May not lose consciousness

• No postictal state

Myoclonic Seizures

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Infantile spasms and Febrile seizures

Types of unclassified seizures

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Infantile Spasms(AKA West Syndrome)

rare disorder of unknown origin and peaks around 3-7 months of age

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Sudden, brief symmetric muscle contractions

• May cry before or after

• May occur in a cluster, up to 150 seizures

• Even with proper therapy, they can have long-term complications

infantile spasms:

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Febrile Seizures

Associated with sudden spike in temperature

• Duration of 15 to 20 seconds

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Status Epilepticus

Prolonged seizure activity lasting 30 minutes or longer or continuous seizure activity where child does not enter postictal phase

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Phenobarbital, Dilantin, Tegretol, Depakote, Zarontin, Keppra

Seizure Medications

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gum hyperplasia, sleepiness, decreased attention and memory, difficulty with speech, ataxia and diplopia (must monitor therapeutic levels)

side effects of these drugs:

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2 years without medications. In most cases if seizures recur, they will happen within the first year of AED withdrawal.

A trial of medication withdrawal is often attempted for children who have been seizure free for 2 years or longer. Medications are tapered slowly, over a few months. Approximately 70% of children remain seizure free for

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Stay with child - ensure SAFETY

• Maintain airway

• Supplemental oxygen

• Monitor vital signs

• Medication

• Provide emotional support and education

what to do with a seizure

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Meningitis

Bacterial: prognosis depends on how quickly care is initiated

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newborns and infants

greatest risk for meningitis

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Streptococcus pneumoniae and Neisseria meningitides cause the majority of cases in the U.S

causative agents of meningitis

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infections, injuries, and crowded living conditions

risk factors for meningitis

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  • fever (cold hands + feet)

  • refuses to eat

  • PETECHIAE like rash below the CHEST

  • bulging fontanelle

  • seizure

  • unusual cry

  • increased resp

S/S of meningitis in (think of ICP symptoms and what happens with meningitis when inflamed)

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blood work (causative agent), Lumbar puncture, and CT or MRI (to see increased IOP/abscess)

Meningitis: Diagnostic Procedures

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cloudy color, elevated WBCs, elevated protein (bacteria excretes) , decreased glucose level (bacteria eats it) , positive gram stain

Bacterial findings in CSF for a LP

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isolate ASAP droplet precautions

what kind of precaution for meningitis pt

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ampicillin, gentamicin, cefotaxime, penicillin G, vanc

Antibiotics that cross blood-brain barrier

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ASAP

when to start antibiotics for bacterial meningitis

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dexamethasone

most effective med for reducing neuro complicationswith Hib infection

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Reye Syndrome

Acute encephalopathy

• Primarily affects the liver and brain

cause not understood

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using aspirin products for fevers caused by viral infections

risk for reye

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Lethargy, irritability

• Combativeness, confusion, delirium

• Profuse vomiting

• Seizures, Loss of consciousness

findings with reye synrdrome

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Hydrocephalus

Imbalance between production and absorption of cerebrospinal fluid (CSF)

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Rapidly increasing head circumference

• Full or bulging anterior fontanel

• Split skull sutures

•Bossing (protrusion) of frontal area; face disproportionate to skull size

• Difficulty holding head up

• Prominent or distended scalp veins

• Increased tone or hyperreflexia

• Irritability or crying

• Decreased appetite or poor feeding

• Fever

• Decline in LOC

early signs of hydrocephalus (think ICP)

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Sunsetting eyes

• Apnea episodes

• Shrill, high pitched cry

late s/s of hydrocephalus

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A catheter or shunt is placed in the ventricle and passes the CSF to the peritoneal cavity; CSF is regulated by a one-way valv

Hydrocephalus: Therapeutic Procedure

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