Common Neurological Conditions in infants Flashcards

1
Q

cerebral palsy definition

A

a group of permanent disorders of the development of
movement and posture, causing activity limitation, that are
attributed to non-progressive disturbances that occurred in
the developing fetal or infant brain”

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2
Q

name the rate of incidence of cerebral palsy in children

A

100-150 children born with CP in Ireland each year
17 million worldwide yearly

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3
Q

how can cerebral palsy be classified

A

using the classification tree for sub-types
Gross motor function classification system
topographical classification system
functional classification e.g. Manual ability classification system (MACS), communication function classification system (CFCS), Eating and drinking ability classification system (EDACS)

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4
Q

How does the classification tree put cerebral palsy into sub categories

A

increased(spastic) /decreased (hypotonia) muscle tone
if increased muscle tone is bilateral or unilateral
if the tone is varying (dyskinetic) or consistent
if there is hypotonia is paired with signs of ataxia
https://www.intechopen.com/chapters/63463

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5
Q

how does topographical classify cerebral palsy

A

unilateral - monoplegia or hemiplegia
bilateral - diplegia, triplegia or quadriplegia

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6
Q

what is the level I of the Gross motor function classification system

A

can walk and climb stairs independently unaided but will have difficulty running or jumping

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7
Q

describe level II of Gross Motor Function Classification system

A

can walk independently unaided short distances on level surface but may need upper limb support from a hand rail when climbing stairs. cannot run or jump

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8
Q

describe level III of Gross Motor Function Classification System

A

can walk independently with a hand held mobility device on level surface but will need assistance from adults climbing stairs, or will need help travelling long distances, outdoors or uneven surfaces

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9
Q

describe level IV of Gross Motor Function Classification System

A

at best can walk independently with a mobility device and adult supervision but can have difficulty maintaining balance on uneven surfaces.
can use self powered wheelchair

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10
Q

describe level V of Gross Motor Function Classification System

A

Requires the assistance and mobility device to mobilise regardless of ambulatory distance or surface level

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11
Q

symptoms of cerebral palsy

A

altered muscle tone e.g. spasticity can cause impaired lengthening of muscle fibres, impaired voluntary muscle control, difficulty isolating movements, impaired recipricol inhibition => altered resting posture of limbs, difficulty balancing agonist/antagonist
muscle weakness, delayed milestones
persistence of primitive reflexes

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12
Q

describe how spasticity may present itself across CP

A

worse in LL in B/L CP
worse in UL in U/L CP

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13
Q

What causes spasticity

A

UMN lesion

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14
Q

define spasticity

A

A velocity dependent increase in stretch
reflex

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15
Q

describe the F words ICF framework

A

body structure = fitness
activity = functioning
participation = friends
environment = family
personal = fun
https://canchild.ca/system/tenon/assets/attachments/000/004/249/original/ICFFramework_and_Fwords_ENG-ACCESS.pdf

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16
Q

motor types

A

spastic
ataxic
dyskinetic

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17
Q

dyskinesia

A

involuntary movement from basal ganglia damage

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18
Q

ataxia

A

shaky movements - affects balance and sense of positioning
cerebellum damage

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19
Q

what is the importance of regulating muscle tone

A

maintain posture
for purposeful co-ordinated movement

20
Q

children with CP are at risk of developing

A

hip joint condition
joint or muscle contracture
emergent dystonia
increase body mass and possible underlying muscle weakness

21
Q

describe the integrated pathway of cerebral palsy

A

established integrated pathway in australia, UK
Pelvic X ray at age 2, 6 and 16
more frequent x rays increased if possible risk of hip dislocation is detected
a clinical exam is conducted every 6 months between the ages 2-6
clinical exam completed annually from 6-16

22
Q

spina bifida definition

A

congenital malformation in which the spinal column is split (bifid) as a result of failed closure of the embryonic neural tube, during the fourth week post-fertilization
https://www.cdc.gov/ncbddd/spinabifida/facts.html

23
Q

list three types of spina bifida

A

occulta - mildest form with a gap in the spine but not sac and the spinal cord and nerves are normal and intact
meningocele - a gap in spine but a formation in a sac of fluid but no nerve damage
myelomeningocele - most severe sac formation comprised of nerves and spinal, involves nerve damage

24
Q

how can neural tube defect be detected during pregnancy

A

scan conducted at 20 wks
ultrasound
AFP - alpha fetoprotein the foetus produces and is sent to mother’s bloodstream. higher AFP levels can indicate spina bifida

25
Q

purpose of MRI for spina bifida

A

determines level of lesion in antenatal period

26
Q

if the child has a spina bifida lesion at thoracic level T1 T2 will they able to walk, will they require a shunt, will the bowels be affected

A

all children will be wheelchair users
9/10 require shunt
bowels affected

27
Q

if the child has a spina bifida lesion at lumbar level L1 L2 will they able to walk, will they require a shunt, will the bowels be affected

A

all children will be wheelchair users
10/10 require shunt
bowels affected

28
Q

if the child has a spina bifida lesion at lumbar level L3 will they able to walk, will they require a shunt, will the bowels be affected

A

8/10 children will be wheelchair users
9/10 require shunt
bowels affected

29
Q

if the child has a spina bifida lesion at lumbar level L4 will they able to walk, will they require a shunt, will the bowels be affected

A

5/10 can walk
7/10 require shunt
all children bowels affected

30
Q

if the child has a spina bifida lesion at lumbar level L5 will they able to walk, will they require a shunt, will the bowels be affected

A

3/4 children walk
7/10 require a shunt
all children bowels affected

31
Q

if the child has a spina bifida lesion at sacral level will they able to walk, will they require a shunt, will the bowels be affected

A

9/10 children walk
6/10 require shunt
all children bowels affected

32
Q

describe motor function of child with meningomyelocele spina bifida at thoracic level and L1-3

A

cannot stand unsupported
wheelchair bounds
may face spinal curves, hip dislocation, knee contracture, talipes
needs assistance with ADLs

33
Q

describe motor function of child with meningomyelocele spina bifida at L4-5

A

assistive device needed for walking, may need wheelchair for longer distances
orthotics - AFO, KAFO
may face hip dislocation, knee contractures, talipes
need help w/ ADL

34
Q

describe motor function of child with meningomyelocele spina bifida at sacral level

A

stands unsupported
may need AFO/orthotics
may have orthopaedic needs

35
Q

surgical intervention of spinal bifida

A

not all children with spina bifida get surgery
children with hydrocephalus get surgical stunt

36
Q

signs of spina bifida

A

Full or bulging fontanelle (soft spot), Seizures, Enlarged
head size, Headache, Swelling or redness along the shunt tract,
Fever, Irritability, Vomiting, Drowsiness, Loss of previous abilities,
Change in appetite, Prominent veins on scalp

37
Q

what other complications can children with spina bifida face

A

syringomyelia - collection of CSF in spinal cord
tethered spinal cord - loss of free movement. of spinal cord may require surgery
bladder issues - may require clean intermittent catheterisation
may require bowel management through diet, regular routine and medical support

38
Q

list rate of incidence in obstetric brachial plexus

A

1 in 200 births

39
Q

method of injury in obstetric brachial plexus injury

A

baby’s shoulder stuck in mother’s pelvis - shoulder’s dystocia

40
Q

symptoms of upper obstetrics brachial plexus injury

A

cannot flex elbow

41
Q

symptoms of lower obstetrics brachial plexus injury

A

loss of wrist/hand function
flexed claw like position of fingers
scapular control issues

42
Q

what possible stretch nerve injury could occur in obstetrics in birth

A

neuropraxia
rupture - can be partial and may require surgery
avulsion injury - nerve pulled from cord mat require surgery or nerve transplant

43
Q

what is developmental co-ordination disorder / dyspraxia

A

child has difficulty co-ordinating movement

44
Q

diagnosis of DCD

A

Childhood onset - longstanding problems w/ motor function
no alternative explanation
at least 5 years old
subjective axam - DCD-Q-R
objective 5th centile for age on M-ABC2 = unequivocal

45
Q

what is the physio intervention for children with DCD

A

flexibility
strength
endurance

46
Q

transverse myelitis

A

inflammation of spinal cord

47
Q

hereditary spastic paraplegia

A

inherited disorder including weakness, spasticity, and stiffness or paralysis of legs