Neurological Flashcards

1
Q

What is apgar score?

A

-screening test used worldwide to Ax infant 1 + 5min post birth

1 min score= how well newborn tolerated birthing process

5 min score= how well newborn adapting to environment

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What are neural contributors to muscle tone?

A

Sensory= impose on body to raise arousal/attention
–Vestibular, tactile, prop, visual–> = can increase or decrease tone
Motor= reflex contraction caused by muscle stretch, maintenance of body position
–modulate tone according to motor task + position
Cognitive= level of arousal, cognition, higher level integrative processes that map perception
–sleepy, asleep, sedated/paralysed = decreased tone
–Frightened, cranky/angry, upset, joy = increased tone

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What are non-neural contributors of muscle tone?

A
  • Muscle properties
  • Soft tissue properties
  • Biomechanics
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Describe low tone

A
  • usually genetic condition
  • cerebellar syndrome
  • upper/lower MN syndrome eg Flaccid spinal paralysis
  • autoimmune, infections
Head= to side
Sh= relaxed, flopping back into floor
Arms= ER, abd, contact with support surface
Trunk= flat back> sinking into support
Legs= ER, taking up support
Feet= on ground, abd/PF toes
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Describe high tone

A
  • usually pyramidal conditions impacting due to damage to motor cortex/corticospinal tract
  • spastic type tone
  • eg cerebral palsy, TBI, stroke, tumour, spinal cord
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Testing resting tone

A
  • Resistance to passive movement LL
  • Resistance to passive movement UL
  • ROM (scarf sign, popliteal angle)
  • recoil
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Testing active tone

A
  • Head and neck (pull to stand)

- Body prone suspension (landau)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is spasticity?

A

velocity dependent increase in tonic stretch reflex influenced by test posture, initial length, sensory, or emotional stimulation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Spasticity pathological mechanisma

A
  1. Brain or spinal cord injury= loss of central inhibition, hyper-excitability of primary MNs
    - brain damaged= won’t generate inhibition signal
    - Spinal cord= won’t send inhibition sign down
  2. Segmental hyper-excitability= increase reflex sensitivity at segmental level of spinal cord
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Testing spasticity

A

-tardieu scale

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is dyskinesia

A

Motor disorder characterised by changes in muscle tone and posture w/ varying element of voluntary movement–> caused primarily by damage of basal ganglia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is dystonia

A

Involuntary sustained or intermittent muscle contraction cause twisting/repetitive mvmts, abnormal postures

  • Strong ext positions + get stuck in those positions
  • Can be triggered by voluntary mvmts and may overflow into other muscles

Cause: damage to basal ganglia, thalamus, brain stem and/or cerebellum during prenatal, perinatal or infant period

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is athetosis?

A

Slow, continuous, involuntary, writhing movement–> prevent stable posture
-seen in fingers, hands, toes, feet, some cases see arms, legs, neck, tongue

Cause: lesions to basal ganglia, specifically corpus striatum- controls mvmt in relation to motivation
- most commonly due to intranatal asphyxia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is chorea?

A

Quick involuntary movements of feet and hands
-ongoing random appearing sequence of 1+ discrete involuntary movements, constant fidgeting

Cause: excess dopamine–> prevents basal ganglia from functioning normally

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

How to differentiate between dystonia and spasticity?

A

-Hypertonia Ax tool

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Clinical observation of spasticity

A

Distribution

  • more evident proximally
  • reduced movements in affected areas
  • no involuntary movements in severely affected parts

Secondary effects

  • contracture towards mid position
  • balance reaction affected
  • Functional problems
  • Faster child wants to move, more resistance they get