Neuro Misc. Flashcards

1
Q

Describe protective vs diminished monofilament testing

A

5.07 and 10 g of force for protective

The 5.07 Semmes-Weinstein monofilament is calibrated so that it takes 10 grams. of force to bend it when touched on the skin of the foot. Inability to detect this. degree of force indicates that the client has a loss of protective sensation.

5.07 OR UNDER FOR PROTECTIVE SENSATION

ANYTHING ABOVE MEANS LOSS OFF EITHER, POSITIVE TEST

4.18 OR UNDER for light touch…polyneuropathy

4.18 and 1 g of force for diminished b/c seeing if its there
A positive test for the 1g monofilament (4.17) occurs when the patient cannot feel the monofilament when applied to specific areas of the skin.

This indicates diminished light touch sensation and suggests early sensory loss or mild neuropathy.

Testing DCML b/c light touch.

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2
Q

What tract does crude touch fall under

A

Spinothalamic

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3
Q

Describe keyy diff in ACA vs MCA vs PCA lesion

A

ACA - Impacts LE more
MCA -Impacts UE and face more
PCA - Vision, cerebellar

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4
Q

What is prosopagnosia

A

Inability to recognize names, faces due to occipital lesion (PCA)

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5
Q

Main traits of frontal lobe

A

Motor, brocas area (non fluent aphasia), executive, judgement

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6
Q

Main traits for the parietal lobe

A

Interpretation, sensory + perception, memory

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7
Q

Temporal lobe

A

Memory, Wernickis area (fluent aphasia), auditory, all comprehension (related to Wernickes)

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8
Q

Occipital

A

Vision

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9
Q

Hippocampus

A

Memory

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10
Q

Basal Ganglia

A

Voluntary movement, muscle tone, posture, control

Parkinsons, Huntingtons, Tourettes, OCD, ADD, Dyskinetic CP

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11
Q

Amygdala

A

Emotion

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12
Q

Thalamus

A

Relay or processing center
(thalamic pain syndrome) spontaneous pain cont side

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13
Q

hypothalamus

A

Receives from autonomic ns, regulates hormones

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14
Q

Epithalamus

A

Pineal gland, melatonin, circadian rhythm

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15
Q

Cerebellum

A

Controls muscle tone, coordination, balance

CAUSES IPSILATERAL IMPAIRMENT

ataxia, nytsagmus, tremor, hypermetria, poor balance, dysmetria (under/over shoot)

Dysdiadochokinesia (rapid alternating movements)

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16
Q

Pons

A

Respiratory rate norm is 12-20 CN 5-8 come out of pons
30-60 for 0 to 1 yo
20-40 for 2 to 5 yo
20-30 for 3 to 11

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17
Q

Medulla oblongata

A

Regulation of respiration and HR, reflex centers e.g vomiting, cough, sneeze

Relay somatic sensory info

Causes contralateral effects. All tracts cross in the medulla accept ALS (spinothalamic tracts)

CN 8-12 come from here

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18
Q

ACA

A

Cont LE involvement…bowel and bladder, frontal lobe so personality changes, aphasia

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19
Q

MCA

A

Most common. Cont UE and face, Wernickes aphasa, If dominant side, then all aphasias

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20
Q

Global aphasia

A

is issue both understanding and producing speech

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21
Q

PCA

A

Thalamic pain syndrome* and cortical blindness
Cont pain and temp loss
Ataxia
Homonymous hemianopsia e.g Left 50 percent of both eyes is out
Prosopagnosia - difficulty recognizing faces
Visual agnosia - issues processing visual input

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22
Q

Vertebral basilar artery

A

Brainstem and cerebellum involvement
Locked in syndrome, vegetative state, vertigo, nystagmus, loss of consciousness

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23
Q

Signs of meningitis

A

Fever, headache, neck stiffness

Light sensitivity

Brudzinkis sign - neck flexion causes hip and knee flex
Kernigs sign - pain with hip flex and knee ext

Lumbar puncture, refer out

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24
Q

DCML

A

vibration, proprioception, two-point discrimination
graphesthesia - the ability to identify letter numbers etc.

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25
Q

spinothalamic

A

Ant - crude touch and pressure
Lat- pain and temp (ALS) - crosses at spinal cord

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26
Q

Corticospinal tract related to

A

Positive babinski (toes spread and extend with swipe under foot), absent superficial abdominal and cremasteric, loss of voluntary movement

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27
Q

Rubrospinal tract

A

Muscle tone control

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28
Q

Reticulospinal tract

A

Voluntary and reflex activity

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29
Q

Tectospinal tract

A

Cont postural tone related to auditory and visual stimuli

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30
Q

A fibers

A

fasted and myelinated for motor and sensory

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31
Q

Superficial abdominal reflex

A

L8-T1
stroke quadrant near umbilicus and should move in that direction

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32
Q

Corneal blink superficial reflex

A

involved trigeminal (sensory) to facial (motor) closes eye
stroke eye

33
Q

Cremasteric superficial reflex

A

L1-L2 scratch medial thigh, scrotum should elevate on that side

34
Q

Gag reflex

A

CN IX and X touch back of throat and gag should occur

35
Q

Plantar reflex

A

L5-S1 Stroke lat aspect of sole of foot
Normal response is flexio of toes
Babinski would be ext and spreading toes (abd)

36
Q

Superficial reflex test grading and indications

A

Absent or present
Consider peripheral neuropathy if pathology

37
Q

Deep tendon reflex

A

0 (nothing), 1+, 2+ (normal), 3+ (brisk), 4+ (very brisk)

Biceps is more C5
Brachioradialis more C6
Could overlap though

Consider peripheral neuropathy if pathology

38
Q

Dominant hemisphere is

A

opposite of the dominant hand. If im R hand dominant its because I’m L brain dominant.

39
Q

L hemispehere (assuming dominant)

A

Brocas, Wernicke, global aphasia, positive thoughts, logical, judgment

40
Q

R hemisphere (assuming nondominant)

A

Creativity
Negative thoughts
Spatial
Kinesthesia

41
Q

Why is preservation of pinprick relevant post stroke

A

proximity corticospinal tracts and spinothalamic tract so if its preserved then better prognosis for moto recovery

42
Q

Asia A

A

Complete. No sensory or motor below the leesion

43
Q

Asia B

A

Sensory below the lesion (at least in sacral segments)

44
Q

Asia C

A

Motor preserved in less than half of levels below lesion have more than 3/5

45
Q

Asia D

A

Motor preserved in more than half of levels below lesion have more than 3/5

46
Q

Asia E

A

Normal both sensory and motor

47
Q

Spinal shock

A

Sympathetic loss, everything decreased (reflex, sensation, power, bowl and bladder flacid)

Edema buildup 3-6 days

48
Q

Autonomic dysreflexia vs orthostatic hypotension

A

AD: if face is red, raise the head. Sit up to get blood flow to body

OH: If face is pale, raise the tail (Trendelnberg) to get blood flow to head

49
Q

Autonomic dysreflexia

A

Lesion is at or above T6

Raise in BP flushed face

Sit pt up, check for stimulus, activate EMS in that order

50
Q

Conus Medullaris

A

L1 typically, termination of spinal cord

Injury above will act as UMN (spastic, hyperreflexxixc bladder and bowel)
- suprapubic tapping for intervention to cause reflex
- Digital stimulation

Injury below will act as LMN
(flaccid, areflexic)
- catheter or valsalva to force out
- Manual evacuation

Catherization for both initially

51
Q

How may breathing chnage visually with SCI

A

Normal is elevation and expansion at chest wall and epigastric region without abdominal rising

Paradoxical: Upper ribcage moves inwards and abdominals move out
*IN cervical or upper thoracic due to loss of external intercostals

Decreased functional cough due to internal intercostals

52
Q

Pressure relief every 15 min

A

Lean forwards more than 45 degrees

Tilt in space more than 65

53
Q

Intrinsic plus position for tenodesis grip

A

Wrist 20 ext
MCP 90 ( so that they stay tight so there is no give when stretched during active wrist extension)
IP sligjt flexion

54
Q

Hamstrings and QL

A

Dont overstretch

HS 100 to 110 stretch in supine

55
Q

Upright positioning

A

Gradually increase angle
May use abdominal binder or compressions

If symptoms of OH
Bring down to supine or trendelenberg (COMPLETELY GO DOWN) and let symptoms subside before proceeding

56
Q

Connus medullaris

A

L1

Above is UMN spastic
Below is LMN Areflexic flacid

57
Q

Internal capsule lesion causes

A

Contralateral hemiparesis in body and contralateral facial weakness (ON BOTTOM HALF OF FACE CONT)

58
Q

Most common UE spasticity early stroke

A

Adductors, pronation, wrist, finger flexion

59
Q

Dyspraxia

A

Impairment of skilled learned movement

60
Q

vertebrobasilar insufficiency

A

Signs are visual field cuts, visual dysfunction, drop attacks, unsteadiness/incoordination

61
Q

Location of cranial nerves in relation to infarct locations

A

CN 1, 2 anterior brain (vision, smell)
CN 3, 4 midbrain (eye movment)

CN 5,6,7,8 Pons
CN 9, 10, 11, 12 Medulla

62
Q

Cerebrum

A

Cont sx in body and face

63
Q

Brain stem

A

Face and body opposite side sx

64
Q

Anosognosia

A

Denial, neglect, lack of awareness of paralaysis

65
Q

Somatoagnosia

A

Perceptual disorder relayed to body scheme (aware of body and relationship of parts of body)

66
Q

Prosopagnosia

A

Perceptual disorder inability to recognize faces

67
Q

Visual agnosia

A

Inability to recognize objects in general

68
Q

Monofilament

A

5.07 monofilament or less is normal sensation

Anything above , means loss of protective sensation

69
Q

ALS

A

ALS
pain
crude touch
temperature

70
Q

DCML

A

fine touch
proprioception
Two point discrimination

71
Q

Key for bowel/bladder spasticity or flaccid quesitons

A

If the specific organ system (bowel/bladder/sexual dysfunction) is referenced → Use S2-S4 Reflex Arc…S2 is cutoff
If the question is more general motor control or spasticity/flaccidity → Use UMN vs. LMN ….L1 is cutoff

72
Q

Cauda equina

A

Areflexic bowel dysfunciton

73
Q

Myelomeningocele

A

Flaccid bowel

74
Q

Parietal info

A

Impairments such as neglect, somatosensory loss, and impaired spatial relationship are common with resections in the parietal lobe

75
Q

Basal ganglia info

A

Individuals who have basal ganglia dysfunction have difficulty initiating movements, and this can be addressed through the augmentation of sensory cues

76
Q

Tongue towards

A

affected side

77
Q

Crude touch vs fine touch

A

DCML is fine touch

78
Q

Wallenberg syndrome is also called lateral medullary and posterior inferior cerebellar artery syndrome.

A

Signs (horners syndrome = decreased pupil size, drooping eyelid, decreased sweating) due to sympathetic loss

double vision,
slurred speech
dizziness

79
Q

Medial medullary syndrome distinguishing factor

A

Ipsilateral tongue atrophy and deviation

BUT

LE and UE is affected on contralateral side