Neuro Book Flashcards

(27 cards)

1
Q

**understand the different types of seizures
what nursing interventions should be done

A

partial/focal: one hem, aura, unprovoked, sudden
generalized: both hem, tonic clonic, postictal
febrile: generalized
- simple: one less than 15 min and no reoccurrences
- complex more than 15 min and reoccur
status epi: +30 min slides/15 min book, or intermittent with no recovery

left side lying
maintain air way
jaw thrust
O2
nothing in mouth
clear space
remove restrictive clothing

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2
Q

**what are febrile seizures and why do they occur

A

seizure with fever over 101/38.3
due to immature neuro system
6mo-5 years

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3
Q

**understand viral and bacterial meningitis, what is the treatment for each what are symptoms (pay attention to age)

A

bacterial: more dangerous, abx and dexmethosone, decrease CSF gluc
- infants: hypothermia, change in feeding, bulging or flat fontanelle, V/D
- older: fever, muscle pain, photophobia, nuchal rigidity

viral: supportive, norm CSF gluc
- abrupt onset of fever, menegial signs, malaise, V/D, upper resp s/s

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4
Q

**understand how to conduct kerning and brudzinski assessment

A

kerning is brining knee up
brud is brining the neck down and knees bend up

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5
Q

**what is hydrocehlapus and how is it treated

A

imbalance between CSF produced and absorbed
TX: shunt
s/s infant
- increase head circ
s/s older
- increase ICP

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6
Q

** what is a VP shunt, how do we know if the shunt is working vs malfunctioning

A

passes CSF to perinetional area, r atria, pleural space, or subgaleal space
infant s/s
- nonspecific, irritability, vomiting, decrease appetite, change in sleep
older s/s
- N/V, HA, decrease loc

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7
Q

**s/s of increase ICP

A

early:
diplopia
sunset eyes
N/V
pupils not reactive
change in LOC
restless

late
Cushing
seizures
fixed and dilated

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8
Q

** spina bifida
meningocele
myelomeningocele

A

spina bifida: defect in 1 or more vertebrae that allows spinal cord contents to protrude

meningocele: protrusion of meningeal sac filled with CSF through a vertebral defect

myelomeningocele: malformation of spinal cord and canal

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9
Q

**understand how a child with CP might present, what are goals of treatment

A

motor, hearing, vision, communication, perceptions, cognitive, or behavioral prob

provide adequate nutrition, maintain skin integrity and promote physical mobility/saftey/growth and dev

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10
Q

when does the neural tube develop

A

4th week

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11
Q

suture lines between skull interlock by

A

6 mo

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12
Q

when are suture lines ossified

A

12 year old

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13
Q

a full term infant has what nervous system

A

immature

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14
Q

myelination progresses and that leads to

A

newborn reflexes disappear
- cephalocaudal direction

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15
Q

lumbar puncture should be postponed for any signs of

A

herniation/ increase ICP

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16
Q

with viral why do we want to use nonasprin

A

reye syndrome

17
Q

neonatal seizures apperence

A

subtule with roving eye movement, receptive blinking, sucking, lip smacking, tongue thrusting, swimming movement with arms

18
Q

bacterial men is comfy in what position

19
Q

why should pts with a shunt be careful of MRI

A

could lead to pressure issues of the shunt

20
Q

when is new shunt replaced after shunt infection

A

when CSF culture is sterile

21
Q

when can fetal surgery be performed for neural tube issues

22
Q

CP spastic

A

majority of cases
increase muscle tone, contractures, increase DTR, clonus, persistent newborn reflexes

23
Q

CP dyskinetic ~ Athetosis

A

abnormal musc tone, difficulty with fine motor, tremors

24
Q

CP dyskinetic ~ dystonia

A

muscle contraction, posturing, twitching, rigid when awake and normal to decrease when asleep

25
CP ataxic
abnormal volume, wide gait, Dif maintaining posture, increase or decrease in tone, difficulty controlling hand and arm during reaching
26
CP diet
increase cal and soft foods due to aspiration, increase fluids, and fiber
27