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Increased ICP
manifestations (infants):
tense bulging fontanel
separated cranial sutures
high-pitched cry
increased FOC
distended scalp veins
sun-setting sign
manifestations (children):
HA
N/V
blurred vision
seizures
decline/diminished performance
lethargy
LATE MANIFESTATIONS:
bradycardia
decreased response to verbal and sensory
pupil size and reactivity altered
decerebrate or decorticate posturing
cheyne-stokes respirations
pailledema
decreased LOC / coma
Hydrocephalus
causes: congenital (chiari malform., idiopathic intracranial HTN, dandy-walker syndrome); acquired (meningitis, trauma, brain tumor, hemorrhage), obstructive vs nonobstructive
assessment: INCREASED ICP
diagnosis: serial FOC, progressive neuro signs, CT/MRI
nursing care: TREAT CAUSE
congenital = surgical intervention
choroid plexus cauterization
shunts
chiari decompression
pre-op
daily FOC
freq neuro checks
monitor signs ICP
family surgical prep
post-op
pain control
freq neuro checks
surgical site assess
VS monitoring
through GI assessment → peritoneal shunt
Neural Tube Defects - Spina Bifida
Occulta: may go undiagnosed if asymptomatic, skin depression or port-wine stain, bowel and bladder sphincter
Cystica: US and elevated alpha fetoprotein, dependent on level of defect → motor and sensor defects (meningocele or myelomeningocele)
nursing care:
pre-op
radiant warmer
sterile moist non-adherent dressing
prevent infection
site assess
neuro check
post-op
pain control
prone position
feeding
surgical site assess
neuro checks
no latex
Neural Tube Defects
Anencephaly: defect in neural tube formation
Chiari Malformation: cerebrum extends below opening and into upper spinal canal
Myelomeningocele: sac w CSF, meninges, and spinal cord
Seizures
Acute
Focal
Generalized
Unknown Onset
Febrile → fever lowers the threshold for seizures (self resolving)
Epilepsy
Chronic: 2 or more unprovoked seizures more than 24 hours apart
Seizure: Diagnostics
medical and family history
seizure observation
EEG
Labs: CBC, BMP, glucose, urine, lumbar puncture, toxicology, anticonvulsant levels*
epilepsy monitoring unit
Seizure: Treatment and Nursing Care
Treatment:
medication manage → action plan
clonazepam, levetiracetam,
diet → keto
surgical intervention → vagal nerve stimulator / epilepsy surgery
Nursing Care:
maintain airway → suction and O2
turn child onto side
O2 monitor
nothing in mouth
timing
rescue meds
Meningitis
manifestations: Kerning, Brudzinski, nuchal rigidity, photophobia, irritability, HA, vomiting
diagnosis: lumbar puncture → positioning, comfort measure, monitor site
nursing care: droplet precautions, ANTIMICROBIAL THERAPY, manage shock
TBI - Concussions (accidental trauma)
assessment: HA/dizziness, N/V, diplopia, increased emotional behavior, foggy thinking, difficult sleeping or staying awake
EMERGENCY findings: unequal pupils, difficult to arouse, worsening HA, LOC, repeated vomiting, inability to recognize, numbness
nursing care: rest and recovery time, progress as tolerated, low stimulation, prevention
TBI - Nonaccidental Traumas
assessment: hematomas, retinal hemorrhages, skull fractures
nursing care: shaken baby → extensive interview, CARE team consult, full skeltal survery, CPS report
Cerebral Palsy
assessment: varying degrees in disturbances in movement, muscle tone, coordination
types: spastic, dyskinetic, ataxic, mixed
nursing care: baclofen, PT/OT, orthotics, surgery