Neuromuscular Dysfunction Flashcards

1
Q

what is the most common permanent physical disability in childhood?

A

cerebral palsy

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2
Q

what is cerebral palsy?

A

group of disorders affecting movement and posture

non progressive disturbances to the developing brain

abnormal muscle tone and coordination

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3
Q

what does CP affect?

A

sensation

perception

cognition

communication

behaviour

MSK problems

epilepsy

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4
Q

what are the causes of CP?

A

prenatal brain abnormalities
- chorioamnionitis
- preterm infants
- perinatal ischemic stroke
- meningitis
- periventricular leukomalacia
- shaken baby syndrome

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5
Q

what are the 3 types of CP movement disorders?

A
  1. spastic
  2. dyskinetic
  3. ataxic
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6
Q

what is spastic CP?

A

increased stretch reflexes

hypertonic

poor posture/balance/coordination

impaired motor skills

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7
Q

what is dyskinetic CP?

A

non spastic

athetoid

dystonic

drooling

dysarthria

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8
Q

what is athetoid?

A

chorea
- involuntary jerking

slow, worm-like movements

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9
Q

what is dystonic?

A

slow twisting movements

abnormal posture

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10
Q

what is ataxic CP?

A

wide gait

rapid, repetitive movements

inability to hold objects

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11
Q

what are some possible signs of CP?

A

persistent primitive reflexes (4+ months)

poor head control > 3 months

stiff/rigid limbs

arching back

floppy tone

unable to sit without support > 8 months

clenched fists > 3 months

no smiling > 3 months

feeding difficulties

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12
Q

persistence of what reflexes are a sign of CP?

A

tonic neck

moro

crossed extensor

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13
Q

what are some signs of CP related feeding difficulties?

A

tongue thrusting

gagging

choking

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14
Q

what are some other problems that might be a sign of CP?

A

poor bladder control

urinary retention

RT infection

aspiration pneumonia

GER

poor nutrition

late toilet training

ADHD

vision abnormalities

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15
Q

what are the therapeutic interventions for CP?

A

ankle-foot braces

wheelchairs

orthopaedic surgery

antispastics

baclofen pump

antiepileptic drugs

dental hygiene

physiotherapy

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16
Q

what are the anti spastics for GENERAL spasms?

A

dantrolene sodium

baclofen

diazepam

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17
Q

what is the antispastic for LOCAL spasms?

A

botox (botulinum toxin A)

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18
Q

how does the implanted baclofen pump work?

A

infuses baclofen directly into intrathecal space around spine

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19
Q

what are the anti epileptic drugs?

A

carbamazepine

divalproex

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20
Q

why is dental hygiene important for CP?

A

to prevent gum hyperplasia

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21
Q

what is spina bifida?

A

failure of osseous spine to close

22
Q

what are the 2 types of spina bifida?

A
  1. occulta
  2. cystica
23
Q

what is occulta SB?

A

not visible

lumbosacral area

24
Q

what is cystica SB?

A

visible saclike protrusion

25
what are the 2 types of cystica SB?
1. meningocele: encases meninges + spinal fluid 2. myelomeningocele: encases meninges + spinal fluid + nerves
26
what are the clinical manifestations of spinal bifida?
hydrocephalus partial paralysis of lower extremities incontinence lack of bowel control kyphosis scoliosis hip dislocation
27
how is spina bifida diagnosed?
based on clinical manifestations anatomical ultrasound (second trimester)
28
what is muscular dystrophy?
degeneration of muscle fibres muscle weakness and wasting
29
what is the most common and severe form of muscular dystrophy?
Duchenne muscular dystrophy
30
what is Duchenne muscular dystrophy?
psuedohypertrophic muscular dystrophy
31
what causes Duchenne muscular dystrophy?
x-linked recessive trait male children inherit from carrier mothers
32
__________ are more affected by Duchenne muscular dystrophy
males
33
what is the age of onset for Duchenne muscular dystrophy?
2-7 years
34
what are some clinical manifestations of Duchenne muscular dystrophy?
waddling (weak glute muscles) lordosis (weak pelvic muscles) frequent falls Gower sign enlarged muscles (eventually atrophy) cognitive impairment
35
with Duchenne muscular dystrophy, ambulation is impossible by _________________
12 years
36
what are some complications associated with Duchenne muscular dystrophy?
osteoporosis fractures constipation obesity respiratory and cardiac failure
37
how is Duchenne muscular dystrophy diagnosed? which is the most reliable?
creatinine kinase EMG muscle biopsy* DNA test
38
when do CK levels rise in Duchenne muscular dystrophy?
first 2 years (before symptoms present)
39
what does an EMG measure?
electrical pattern of muscle contraction
40
what are the mechanisms of spinal cord injuries?
indirect trauma MVAs sports injuries birth trauma surgery
41
how do sports injuries cause spinal cord injuries?
vertebral compression
42
what birth position is more likely to result in spinal cord injury?
breech
43
with spinal cord injuries, the _____________ the damage, the more _______________ the injury
high damage = more extensive
44
what are the 3 types of spinal damage?
1. paraplegia 2. tetraplegia 3. high cervical cord injury
45
what is paraplegia?
complete or partial paralysis of lower extremities
46
what is tetraplegia?
lack of function in all 4 extremities
47
what does a high cervical cord injury affect?
phrenic nerve
48
what does a high cervical cord injury cause?
paralyzed diaphragm ventilator dependent
49
what are some clinical manifestations of spinal cord injuries?
flaccid paralysis loss of sensation loss of motor function autonomic dysfunction
50
what is flaccid paralysis?
below level of damage spinal shock syndrome
51
what are some manifestations of autonomic dysfunction?
hypotension poor thermoregulation loss of bladder and bowel control dysreflexia