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
Q

what are the 2 types of cystica SB?

A
  1. meningocele: encases meninges + spinal fluid
  2. myelomeningocele: encases meninges + spinal fluid + nerves
26
Q

what are the clinical manifestations of spinal bifida?

A

hydrocephalus
partial paralysis of lower extremities
incontinence
lack of bowel control
kyphosis
scoliosis
hip dislocation

27
Q

how is spina bifida diagnosed?

A

based on clinical manifestations

anatomical ultrasound (second trimester)

28
Q

what is muscular dystrophy?

A

degeneration of muscle fibres

muscle weakness and wasting

29
Q

what is the most common and severe form of muscular dystrophy?

A

Duchenne muscular dystrophy

30
Q

what is Duchenne muscular dystrophy?

A

psuedohypertrophic muscular dystrophy

31
Q

what causes Duchenne muscular dystrophy?

A

x-linked recessive trait

male children inherit from carrier mothers

32
Q

__________ are more affected by Duchenne muscular dystrophy

33
Q

what is the age of onset for Duchenne muscular dystrophy?

34
Q

what are some clinical manifestations of Duchenne muscular dystrophy?

A

waddling (weak glute muscles)

lordosis (weak pelvic muscles)

frequent falls

Gower sign

enlarged muscles (eventually atrophy)

cognitive impairment

35
Q

with Duchenne muscular dystrophy, ambulation is impossible by _________________

36
Q

what are some complications associated with Duchenne muscular dystrophy?

A

osteoporosis

fractures

constipation

obesity

respiratory and cardiac failure

37
Q

how is Duchenne muscular dystrophy diagnosed?

which is the most reliable?

A

creatinine kinase

EMG

muscle biopsy*

DNA test

38
Q

when do CK levels rise in Duchenne muscular dystrophy?

A

first 2 years
(before symptoms present)

39
Q

what does an EMG measure?

A

electrical pattern of muscle contraction

40
Q

what are the mechanisms of spinal cord injuries?

A

indirect trauma

MVAs

sports injuries

birth trauma

surgery

41
Q

how do sports injuries cause spinal cord injuries?

A

vertebral compression

42
Q

what birth position is more likely to result in spinal cord injury?

43
Q

with spinal cord injuries, the _____________ the damage, the more _______________ the injury

A

high damage = more extensive

44
Q

what are the 3 types of spinal damage?

A
  1. paraplegia
  2. tetraplegia
  3. high cervical cord injury
45
Q

what is paraplegia?

A

complete or partial paralysis of lower extremities

46
Q

what is tetraplegia?

A

lack of function in all 4 extremities

47
Q

what does a high cervical cord injury affect?

A

phrenic nerve

48
Q

what does a high cervical cord injury cause?

A

paralyzed diaphragm

ventilator dependent

49
Q

what are some clinical manifestations of spinal cord injuries?

A

flaccid paralysis

loss of sensation

loss of motor function

autonomic dysfunction

50
Q

what is flaccid paralysis?

A

below level of damage

spinal shock syndrome

51
Q

what are some manifestations of autonomic dysfunction?

A

hypotension

poor thermoregulation

loss of bladder and bowel control

dysreflexia