-
-
kids cranial bones
thin, not developed
-
kids brain are highly
vascular with small subarachnoid space
-
neonates have
immature mylineation
-
kids have excessive
spinal mobility
-
kids have what kind of vertebrae
wedge-shaped cartilaginous
plasticity
-
ICP means
total pressured exerted by brain, blood, CSF w/in cranial fault
-
ICP %
- brain: 80%
- CSF: 10%
- blood: 10%
-
which only two compartments in ICP can compensate
-
what causes increased CBF
changes in pCO2! MOST POTENTIAL MEDIATOR
increase pCO2 will cause vasodilation and increase ICP
-
what causes CBF
acidosis / hypoxemia = vasodilation and increased ICP
-
what causes CBF
seizures and fever=increased CBF and increased metabolic rate
-
causes of increased ICP
- traumatic brain injury:
- hematoma
- cerebral edema
- cerebral ischemia
- IVH
- intracerebral hemorrhage
-
causes of increased ICP
- hydrocephalus
- infections: inflammatory response, cerebral edema, hydrocephalus, cerebral hyperemia (IICP following ischemia)
- brain tumor: mass effect, peritumoral edea, hydrocephalus
- intracranial hemorrhage: mass effect, cerebral edema
- intraventricular hemorrhage: hydrocephalus
-
history clues to etiology
- family hx
- pregnancy hx: fetal distress, labor/delivery, apgar scores, maternal drug use, maternal diabetes
-
MITTEN
- M: metabolic (blood sugar abnormalities), electrolyte imbalances, inborn errors of metabolism
- I: infection, menigitis, congential viral infections
- T: toxins, CO, lead, NAS
- T: trauma; subdural hemotoma, shaken baby syndrome
- E: endocrine; blood sugar abnormalitites
- N: neur/neoplasm; malformations, intracranial hemorrhage, HIE
-
NEURO assessment
- "just doesn't act right"
- eyes: crossed, droopy eyelids, unequal pupils, blurred or double vision
- behavior: subtle initially, irritability, restlestness, lethargy
- motor function: movement? spontaneous?
- skin: dry vs diaphoretic?
-
Cushing's triad: Signs of Increased ICP
- systolic: increases
- diastolic: decreases
- pulse: decreases (brady)
- *wide pulse pressure
- maybe irregular breathing (Cheyvne-Stokes)
- elevated temp (hyperpyrexia)
-
neuro assessment in infant
- irritability
- restlessness
- full/bulging fontanels
- poor feeding
- poor sucking
- vomiting (even projectile)
- distention of superficial scalp veins
- sunset sign
- shrill/ high pitched cry
- nuchal rigidity and seizures (LATE SIGNS)
-
EARLY SIGNS NEURO
- sudden change in mood
- HA, poor feeding
- vomiting
- difficulty waking
- weakness on one side
- nuchal rigidty
- deterioation of cogn. ability
-
LATE SIGNS
- changes in vitals (Cushing's)
- seizures
- photophobia
- positive Kernig's and Brudzinski's sign (infection)
- opisthotonus (spasms causing backward arching of head, neck, spine)
-
decerbrate posture
- damange to upper brain stem
- arms abducted and extended, wrists pronated and fingers flexed
- legs are stiffly extended, plantar flexion of feet
-
decorticate posture* worse
- damage to one or both corticospinal tracts adducted and flexed, wrists and fingers on CHEST
- legs are stiffly extended and internally rotated with plantar flexion of feet
-
lab tests
- CBC: increase in WBC(infection) and decrease H&H (bleeding)
- metabolic panel: blood sugar-hypo or hyperglycemia (DKA), sodium, calcium
- toxiocology screen (urine drug screen)
- UA
- blood gas: O2 and acid-base status
- blood culture
- CSF analysis and culture
- infants: ammonia, metabolic screen
-
lumbar puncture
- cell count: over 40 WBCs
- grain stain: presence of organism
-
KEY TO LUMBAR PUNCTURE
POSITION!
-
EEG Testing
- may withhold sleep
- no caffeine several hours prior
- adminster sedatives as ordered
- help attach electrodes to head
- monitor
-
neurodiagnostic testing
CT scan: study of choice in child with acute neuro impairment or deteroiation
MRI: assessment of brain tissue; precautions: metal, implants, o2 cycliners
-
neuro monitoring
- GCS <8!
- signs of increased ICP
- post resusciation of acute traumatic IC hematoma or other procedure
- others who have high chance of IICP
- gold standard is intraventricular monitoring
-
Increased ICP
- A: rapid sequence intubation may be neccessary
- B: ventilation (normoventilation) or hyper for some
- C: avoid hypotension
- positioning: midline to facilitate JVdrainage (elevate for 15-30 degrees)
- osmotic therapy: mannitol bolus every 4-6 hours, hypertonic saline infusion
-
Increased ICP
- maintain normal temp
- prevent shivering, fever
- sedation, anagelisc
- seizure prevention, prophylaxis in kids <1 or those with TBI
- no steriods
- surgical intervetion: only for lesions producing mass effects
- euvolemic, normoglycemic, avoid dextrose for 48 hours
-
Seizures
paradoxical electrical discharge of neurons in the brain that result in a change in function or behavior
- 30k diagnoses / year
- 10% of pop. will have 1 in lifetime
- epilepsy: recurrence of seizures
-
risk factors for seizures
- genetic predisposition
- acute febrile state
- head trauma
- cerebral edeam
- abrupt cessation of AED meds
- infections
- metabolic disorders
- exposure to toxins (leads)
- hypoxia
- acute drug and ETOH withdrawal
-
triggering factors for seizures
- increased physical activity
- excess stress
- overwhelming fatigue
- acute EOTH ingestion
- exposure of flashing lights
- caffeine, coacine, aersols, glue products..
-
subtle seizures in neonate/infant
- more common in preterm
- eye deviation
- repetitive blinking, fluttering of eyelids, fixed stare (preemie)
- repetitive mouth and tongue movements (drooling, sucking, tongue - thrusting, yawning)
- apnea: 'if aint breathin, they a seiz'ing"
-
tonic clonic in neonate/infant
- single limb jerking
- extension of arms/legs
- decorticate like movements
- myclonic jerks
- abnormal movements: pedaling, swimming, rowing
-
tonic clonic
- eyes roll upward
- LOC
- tonic contractions
- salivation
- apnea->cyanosis
- violent jerk
- incontinence
- gradual slowing til cessation
-
post-ical phase
- difficulty arousing
- confused for several hours
- impaired fine motor function
- lack of coordination
- possible vomit, HA
- sleepy
- no recollection of event
-
absence seizures
- 4-12 years common
- brief periods of altered consciouness with sublte motor activity
- appears to be day dreaming
- lasts about 10 sec
- no hisotry of motor involvemtn or resp. compromise
-
myclonic
- sudden, jerking or stiffening of extremities
- may occur 100x a day
- each episode lasts 1-2 sec
-
atonic:
- sudden loss of muscle tone and consciousness
- lasts a few seconds wihtout resp. signs
- HIGH FALL RISK
-
infantile spams
- first 8 months of life
- sudden, brief, symmetric contraction
- head flexed with arms and legs extended
- possible eye deviation
- possible cry, giggle
- possible flushing, pallor, cyanosis
-
simple partial
- aversive seizure
- rolandic: tonic-clonic movements of face, most common during sleep
- tinglining, numbness may spread
-
complex partial
- altered behavior
- unable to respond to environment
- impaired consciousness
- confusion, amneisa
- aura*****
- last 2-3 min to up to 10 min
-
jitterness
- responsive
- resolves with touch-passive flexion of extrememity
- NO autonomic changes
- gaze normal
- predominant motion: tremors
-
seizure
- not responsive to stimuli
- abnormal gaze
- autonomic changes occur
- predominant motion: clonic jerking
-
tests for seizures
- EEG
- ct
- mri
- lumbar punct
- metabolic panel
- tox screen
- consider metabolic screenin for inborn errors of metabolism
-
EEG interventions
- adminster sedatives as ordered
- assist w. position
- no caffeine for several hours prior
- wash hair before/after
- may need to take deep breaths
- withhold sleep if instructed
- not painful!!
-
Seizure treatment
- AEDs: phenobarbital, valium, phenytonin, carbamazepine, depakote, cerbyx, levitracin
- monitor levels
- be aware of food/med interaction
-
vagal nerve stimulator
implanted device used to abort or shorten seizures
-
ketogenic diet
- high-fat foods
- limited CHO
- useless in kids whose seizures cant be controlled by meds, start diet in hospital and supervise by a doctor
-
brain surgery
- kids with persistent seizures unresponsive to meds
- remove part of brain responsible for seizures (corpus callosotomy, focal resection)
-
cannabidiol
major nonphyschoactive ingredient in weed
- used for unrelenting seizures
- mechanism is unkwonw
- studies underway
-
status epilepticus
greater than 10 min long or cluster of seizures where child does not awake between seizures
- EMERGENCY: CALL AMBULANCE
- if prescribed: give Diazepam gel (DIASTAT) into rectum
-
documenting seizure
- time begins and ends
- precipating event
- body parts involved
- description of motor involvement
- description of eye movement
- resp. status, color, desaturation
- behavioral state (LOC)
- postical state
- all nursing interventions and childs response
-
SEIZURE NUSING DX
- RISK FOR INJURY!
- know warning signs
- use padded side rails and keep up
- move child away from furniture
- bed in lowest position
- safety helmet for repetitive seizures
- use TM themometer
- remove glasses
- do not restrain!
- reorient, obtain v/s after
- adminster meds as ordered
-
seizure nursing dx
- ineffective airway clearance
- avoid gum, small candy
- supine with head turned to side
- loosen restrictive clothes
- no padded tongue blades
- sunction prn
- provide O2 ,,PPV if indicated
- emergency equipment ready
-
after seizure
- maintain sidelying
- check vitals
- assess injuries
- perform neuro check
- allow rest
- orient
- encourage child to describe before/after and if aura?
- no foods/liquids until fully awake and can swalow
- try to determien trigger
- complete documentation
-
low self-esteem nursing dx for seizure
- explore feelings about self and disorder
- ecournage expression
- use play therapy
- treat child as nomrla and not vulnerable
- refer to suppor group
- routine eval for sucidie risk
-
knowledge deficient for seizure
- discss triggers
- promote good dental care
- what to do
-
seizure education
- avoid biking, skating, skateboarding on streets with heavy traffic
- avoid activities at height
- supervise around water
- tell teachers
- ID bracelet
- driving restrictions by state
- counsel on effects of seziures and AEDS on sex
- avoid recreational drugs and EOTH
-
neural tube defect
- most common birth defect in CNS
- results: neural tube failure to close during embyronic development in 1st 3-5 weeks of gestation
- latin term: "spilt" or "open" spine
- elevated alpha-feto-protein in mother may indicate fetus with NTD
- most common in girls
-
risks for spina bifida
- insufficent folic acid intake during pregnancy
- maternal malnutrition
- medications
- exposure to radiation/chemicals
- prepregnancy conditions; diabets, obseity, hyperthermia, low b12
- genetic predisposiiton
-
incidence of spina bifda
- 0.7 per 1000 in Us
- 4.45 per 1000 in TN
*significant decrease since folic acid supplement was made mandatory
-
spina bifida occulta
- veretebral body fails to close
- spinal cord is intact
- no meninges are exposed
- no neuro deficient seen
-
menigocele
- protustion involves sac-like cysts that contains CSF in the midline of the back
- spinal cord not involved
- neuro deficient usually not present
-
myelomeningocele
- protrustion involves meninges, CSF, nerve roots, and spinal cord
- neuro deficients evident*
-
s/s of spina bifida
- visible spinal defect-inspect to see if intact
- flaccid paralysis of legs
- hip/joint deformtities
- altered bowel and bladder function
-
preop care of spina bifida
- prepare parents for surgery within 24-48 hours
- position prone with hips flexed and legs abducted
- cover defect with a moist, nonadhearing dressing using NS, change q 2 hours
- maintain infant in open warmer
- inspect sac closely for leaking, irritation
-
postop care of spina bifida
- monitor vitals
- assess for infection
- provide pain relief
- incisional care as prescribed
- assess for CSF leak
- maintain PRONE until okayed by neurosurgeon
- begin ROM to lower extremities
- monitor HC daily
-
d/c care of spina bifida
- teach ROM, incisional care
- allergies
- teach signs of ICP
- asses bowel/bladder function
-
nuring dx for spina bifida
- risk for infection:
- monitor temp
- ATB
- change dressing
- prevent soiling of wound from urine and feces
- meticulous aspetic technique
- monitor for UTIs
-
at risk for injury SB*
- avoid rectal temp
- keep pressure off site
- coordinate OT/PT
- monitor HC in infants
- evaluate nutritional status
- keep pressure of bony prominences
- reposition q 1-2 hours
- observe skin under splints and braces
- ROM to legs
- position in proper alignment
-
bowel/urniary incontinence nrusing dx for spina bif
- intermittent self-cath
- note color and blah blah crap
- monitor for UTIs
- no rectal temps
- adminster laxative or enmeas as needed
- antispasmodics as prescribed
-
at risk for latex allergy -sb nursing dx
- nonlatex gloves, caths, equipment
- provide parents iwth list of household items
- s/s of latex allergy
- provide info on epi-pen
-
mobility: impaired physical d/tneuro muscular impairment ---nursing dx for sb
- assess mobilit skills
- assist devices
- passive ROM TID
-
surgical recovery:delayed --nursing dx for sb
- measure Hc and abd girht
- signs of IICP
- DO NOT POSITION ON SIDE OF SHUNT
- Monitor for skin breakdown
- reposition
- monitor for bleeding
-
school aged children with sp
- IEP
- legal
- created by parents
-
teens with spina bif -independnece
- foster it
- encourage act. with friends
- talk to professionals about sexuality
- contraception, folic acid intake
- safety important
-
hydrocephalaus
a syndrome, sign, resluting from distrubances in the dynamics of CSF which may be caused by several diseases
-
hydrocephalus incidence
- 3-4 q 1000 births
- congenital or acquired
- congential: due to maldevelopment of intraurterine infection
- acquired: due to infection, neoplasms (rare), or hemorrhage (common)
-
patho of hydrocephalus
- CSF is formed by 2 mechanisms:
- secretion by choroid plexus
- lymphatic-like drainage by the ECF in brain
CSF circulates thru ventricular system and is absorbed within subarachnoid spaces by unknown mechanisms
-
mechanisms of fluid imbalance
- hydrocelphalus results from:
- impaired absorption of CSF within the subarachnoid space (communicating hydrocephalus) or
- obstruction to the flow of CSF: through the ventricular system (noncommunicating)
- both lead to increase accumulation of CSF in ventricles
- ventricles become dilated and compress brain---> cranial sutures are closed, skull enlarges
-
non communication (obstructive) hydrocephalus
result from development malformations
other: neoplasms, intrauterine infections, trauma
-
Arnold Chiari Malformation
type 2 malformation of brain seen most exclusively with myelomeningocele, is charactered by herniation of a small cerebellum, medualla, pons, and 4th ventricle into cervical spinal canal through enlarged foramen magnum
-
manifesations of hydrocephlaus
depends on acutiy of onsent and presence of preexisitng structural lesions
-
signs of hydrocephalus
- head grows at alarming rate!
- 1st signs: bulging of fontanels without head enlargement
- tense, bulging, non-pulsatile ant. fontanel
- thin skull bones with separated sutures (cracked pot head sounds on percussion)
- increasing HC: more than 0.5 cm/day
- setting sun eyes, may signify brain damage
- vomiting, lethary, irritability
-
best way to detect hydrocephalus in neonate
- ultrasound
- easy, quick, not painful
-
preterm infants 30 weeks or less (some say 32 weeks)
should have ultrasound at 7 days or age (sooner if suspect significant IVH)
see dilated ventricles on ultrasound
-
goals of hydrocephalus
- releive it
- treat complications
- manage problem resutling from effects of disorder on psychomotor development
- usually surgical!
-
lumbar puncture- hydrocephalus
- for infants with hydro from IVH: lp done to relieve pressure
- espeically if infant to small for surgery
- Allow CSF to drain freely (amount depends on MD)
-
lumbar puncture-hydro
- key is successful positioning!
- sitting up or lying on side
-
care during lumbar puncture
- monitor CP status
- hold infant still in proper position
- chin to chest
- bend in C shape
- send CSf to lab for cell count, glucose, protein, culture, gram stain
-
surgical treatment for hydro
- therapy of choice!
- direct removal of source of obstruciton (neoplasm, cyst, and hematoma)
- most require shunt procedure to drain CSF from ventricles to extracranial area; usually peritoneum (VP shunt), or right atrium (VA shunt) for absorption
-
VP shunt
- neonates and young infants
- greater allowance for excess tubing: which minimizes number of revisions needed as child grows
-
VA shunt
- older children who have attained most of smoatic growth or children with abnromal patho
- contraindicated in children with cardiopulmnoary diseaes or with elevated CSF protein
-
major complications of shunt
- infection!****
- greatest risk period: 1-2 months following placement
- staph and strep most common organisms
-
complications of shunt
- mechanical difficulities; kinking, plugging, migration of tubing
- malfunction is most often by mechanical obstructin!
- look for signs of increased ICP, fever, lethargy, vomiting
-
post op care for shunt
- place on un-operated side to prevent pressure on shunt valve
- keep HOB flat: rapid decrease in IC fluid cause subdrual hemotoma due to small vien rupture in cerebral cortex
- DO NOT PUMP SHUNT WITHOUTH SPECIFIC DIRECTION FROM DOCTOR! too many different devices..
-
VP shunt requires
incision on the head, behind ear, and on the abd
-
post op care for shunt
- OBSERVE FOR SIGNS OF INCREASE ICP!
- may indicate obstruction of shunt
- assess pupil size; as pressure on oculomotr nerve may cause dilation on same side as pressure
- blood pressure may be variable due to hypoxia to brainstem
- abd distention: due to CSf peritonitis or post-op ileus due to cath placement
-
postop for shunt
- monitor for I/O: may be on fluid restriction or NPO for 24 hours to prevent fluid overload
- monitor VS : increased temp may indicate infection
- give good skin care to prevent tissue damage
-
family support
- fear
- support: provide info
- prepare for discharge: teach signs of ICP and when to call the doctor
- teach positioning, wound care
- have PT/OT teach parents
-
hypoxic-ischemic encephalopathy
dx based on clicnal and lab evidence of brain injury due to lack of O2 and reduced blood flow to brain
-
hypoxia
partial or complete lack of O2 in the brain or blood stream
-
asphyia
state in which the placental or pulmonary gas exchange is compromised or cases
-
birth asphyxia
occurs during 1st and 2nd stages of labor when fetus is otherwise nml
-
perinatal asphyxia
occurs anytime during the perinatal period from conception through 1st month of life
-
HIE
abnormal neuro behavior in neonates from hypoxic-ischemic event
-
HIE incidence
- 2-8 gases per 1k live births
- 23% of all neonatal deaths worldwide
- severe cases: mortality rate: 25-50%
-
causes of HIE
- antepartum risk factors
- labor/delivery
- postnatal events
-
definition of HIE
profound metabolic or mixed acidosis (ph less than 7)
perisistance of an Apgar score of 3 or less for longer than 5 min
neontal neuro sequalae, such as seizures or hypotonia
multiple organ involvement
-
neonatal brain
- immature: lower metabolic rate
- immature balance of neurotransmitters
- plasticity of immature CNS
- glucose: only substrate used for energy metabolism
-
cooling the brain and or total body
- reduces cerebra metabolism, decreases rate of energy ultiziation
- decreases neurotrans release
- supresses free radical activity
- reduces vascular permeability and edema
- reduces secondary neurnoal death
- decreases degree of global brain damage
-
indications for cooling
- infants born at 36 weeks or greater
- within 6 hours of insult
- evidence of acute injury around the time of birth
- specific criteria for cooling events
-
prognosis of HIE
good signs: 7 days old, EEg with normal background activity, absence of seizures, adequate head growth, able to take oral feedings
poor signs: lack of spontaneous resp. effort 30 min after birth, seizures, persistent feeding difficulty, poor head growth
-
states on HIE
- 10%: generally healhty
- 10%: minor disabilites
- 30-50 may develop mod-severe disability
- 30 may have disabling CP
- 16% epilepsy
- 14-70 blindness
- 6 hearing impair
- others: ADD, ADHD, intellect challenges
-
neonatal abstinence syndrome
- infant born to a drug affected mother-withdrawal
- withdrawal:set of symptoms as the body attempts to remove an addictive substance
- accurately assessed*
- therapetuic measures and often medication
-
common symptoms of NAS baby
- depends on drug
- how each individual baby metabolizes the drug
- baby's own tolerance
*no two babies will react the same. responsibility of caregiver to monitor and read the infant and signs
-
hypersensitivty to stimuli-NAS baby
- common trait
- little tolerance
- swallowing, closenes, sound, can escalate baby into frantic state
babies need protection from overstimulation but should NOT be stimulus-deprieved
-
NAS baby muscle tone
- muscle tone is degress of stiffness
- unusually limp of stiff
- particularly in limbs and neck
- stiffness may come and go
- tremors, jerking, other signs of distress-sign of baby tryin to control uncomfortable sensations
-
GI problem-NAS baby
- drugs attack gastric system-at 12 mon
- watery stool, explosive diarrhea, excoiatred butttocks, gas, constipation
- need proper handling to prevent serious health concerns
- distress and high stimulation can increase
- diarrhea can irritate fragile lining of the intestines and also lead to dehydration
-
other r/t complications of NAS baby
- chronic ear infection
- unexplained fecer(opioates and opioids)
- sleep/week irregualr
- extreme appetitie (barbitures, cocaine)
- hyperrefleia, moro
-
critical for management of NAS baby
- comforting techniques !
- basica principeles of handling apply to all
-
8 principels of NAS baby
- swaddling: contains extremties
- C position: allows infant to relax
- vertical rock
- clapping: stop if infant does not respond
- feeding: get infant relaxes, minimize stimulation
- controlling environment: next
-
prinicple 7 - control environment
- limit number of caregivers
- offer calm surroujndings
- minimize loud noise--low volume
- keep lights low
- caregiver should have calm presence
- rountine beneficial *
-
Neonatal abstience scoring
- determines level of therapetuic intervetion necessary
- helps to determine effectivness of intervnetions being used
- assess sjmptoms
- oringiallydevelped by Loretta Finnegan
-
NAS scoring tool
- set of observed signs and sympotms in the infant
- obsereved at regular intervals=every 3 hours
- should refelct all symptoms obsereved sing the last scoring
- high scores are nOT lowered by therapuetic handling should assessed for medical intervention
-
medication for NAS baby
- begun depneding on Finnegan scores
- once stable, medicated is tapered, based on Fs
- med of choice: morphine sulfate
- 2nd line: clonidine
- 3rd line: phenobarbital (use contravseral )
-
SB1391
- ENacted 4/29/14
- expires 7/1/16
- prosecuted for illegal use of narcotic if infant is harmed
- aggravated assault (up to 15 years)
- homicide if infant dies!
-
YOUR BABY LIFE SHOUL DNT BEGIN WITH DETOX
- BORN DRUG FREE TN
- new to redue NAs babies
- inform, resoureces, newroom, hint for families and firneds
- explore website
-
menigititis
- viral: wide variety of viral agents or enterovirus
- bacterial: haemophilus influenzae (type B), streptococcus pneumonia, neisseria minigities (meningococcal)
-
priority nursing dx for menigities
- risk for ineffective breathing pattern
- pain
- risk for injury
- risk for ineffective thermoregulation
-
bacterial medication therapy for menigititis
Iv ATB senstive to culture oragnism for 7-14 days (droplet precautions for 24 hours)
- viral: tylenol for symptomoatic treatment
- preventive carE: HiB vaccine to prevent from hemo in B infection
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