Upper neuro exam Flashcards

1
Q

What is chorea?

A

brief irregular movements that are not repetitive or rhythmic

often in patients with Huntington’s disease

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2
Q

What is opthalmoplegia?

A

wide range of neurological disorders

e.g. MS and myasthenia gravis

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3
Q

What is pronator drift?

What does the outcome mean?

A

assesses mild upper limb weakness and spasticity

  1. hold arms out in front with palms upwards
    look for signs of pronation
  2. no pronation, ask patients to close their eyes and observe again
Interpretation=
pronation with(out) downward movement= pronator drift= contralateral pyramidal tract lesion
(UMN lesion= supinator muscles in forearm are weak)
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4
Q

How do you test for tone in muscle groups?

A

support arm

relax patient and fully control their movement (elbow= flexion and extension, shoulder and wrist= circumduction)

feel for:
-spasticity, rigidity, cogwheeling, hypotonia

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5
Q

Spasticity vs rigidity?

A

spasticity= pyramidal tract lesions (stroke)
(faster move limb= worse + linked weakness)

rigidity= extrapyramidal tract lesions (parkinson’s disease)
(same feeling if move limb rapidly or slowly- velocity independent)

**both increased tone

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6
Q

What type of rigidity is linked to parkinson’s disease?

A

cogwheel

tremor superimposed on hypertonia, resulting in intermittent increases in tone during movement of limb

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7
Q

What is lead pipe rigidity? What is it associated with?

A

increased tone throughout the movement of the muscle

linked to: neuroleptic malignant syndrome

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8
Q

Shoulder abduction test

A

C5

flex elbow and abduct shoulders to 90˚
apply downward resistance on lateral side of upper arm

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9
Q

Shoulder adduction test

A

C6/7

adduct shoulder to 45˚ bringing elbows closer to body
apply upward resistance on medial side of upper arm

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10
Q

Elbow flexion test

A

C5/6

flex elbow
apply resistance by pulling the forearm whilst stabilising shoulder joint

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11
Q

Elbow extension test

A

C7

elbow flexed
apply resistance by pushing the forearm towards patient + stabilise shoulder joint

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12
Q

Wrist extension test

A

C6

hold arm out in front of them with their palms facing downwards
make a fist and extend their wrist joints, keep their wrists in this position whilst apply resistance

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13
Q

Wrist flexion test

A

C6/7

patient still holding arms out in front of them
flex their wrist joints and keep position whilst you apply resistance

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14
Q

Finger extension test

A

C7

hold fingers out straight whilst you apply downwards resistance

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15
Q

Finger abduction test

A

T1

abduct fingers against resistance

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16
Q

Thumb abduction test

A

T1

patient to turn their hand over so their palm is facing upwards and to position their thumb over midline of palm
apply downward resistance with own thumb

17
Q

patterns of muscle weakness

UMN vs LMN

A

UMN:
pyramidal pattern of weakness disproportionately affects upper limb extensors and lower limb flexors

LMN:
focal pattern of weakness, only muscles directly innervated damaged neurone affected

18
Q

MRC muscle power assessment scale:

A

0- no contraction
1- flicker or trace of contraction
2- active movement, with gravity eliminated
3- active movement against gravity
4- active movement against gravity and resistance
5- normal power

19
Q
  1. biceps reflex C5/6
  2. supinator reflex C5/6
  3. triceps reflex C7
A
  1. thumb of non-dominant hand over tendon and then tap thumb with tendon hammer
  2. locate brachioradialis reflex (4 inches proximal to base thumb) tap with tendon hammer
  3. relax triceps tendon, 90˚ flexion on their lap/support patient’s forearm
    (triceps tendon= superior to olecranon process of ulna, tap with hammer)
20
Q

hyperreflexia vs hyporeflexia

A

hyperreflexia:
UMN lesions

hyporeflexia:
LMN lesions

pendular (less brisk and slower in their rise and fall):
cerebellar disease

21
Q

How to examine sensation?

A
  1. check one modality from dorsal columns and spinothalamic tracts
  2. eyes closed for assessment
  3. normal sensation on patient’s sternum
  4. upper limb dermatomes compare L and R
22
Q

Arm dermatomes?

C5-T1

A

C5: lateral aspect of lower edge of deltoid muscle
C6: palmar side of the thumb
C7: palmar side of middle finger
C8: palmar side of little finger
T1: medial aspect antecubital fossa (proximal to medial epicondyle of humerus)

23
Q

Types of sensation tests

A

light touch sensation
(DCML and spinothalamic tracts)

pin-prick sensation
(spinothalamic tracts)

vibration sensation
(DCML)
-use tuning fork

24
Q

What do you examine after sensation?

A

proprioception

at interphalangeal joint of thumb

25
Q

How to these present:

  • mononeuropathies
  • peripheral neuropathy
  • radiculopathy
  • spinal cord damage
  • thalamic lesions
  • myopathies
A
  • localised sensory disturbance in area
  • symmetrical sensory deficits glove and stocking distribution in peripheral limbs
  • nerve root damage= sensory disturbances associated dermatomes
  • sensory loss at and below
  • contralateral sensory loss
  • symmetrical proximal muscle weakness
26
Q

What does finger to nose test tell us?

A

cerebellar pathology:

  1. dysmetria: lack of coordination of movement. Clinically this results in the patient missing the target by over/undershooting
  2. intention tremor: a broad, coarse, low-frequency tremor that develops as a limb reaches the endpoint of a deliberate movement. =tremor that becomes apparent as the patient’s finger approaches yours. Be careful not to mistake an action tremor (which occurs throughout the movement) for an intention tremor

(both present= ipsilateral cerebellar pathology)

27
Q

What is dysdiadochokinesia?

A

inability to perform rapid, alternating movements

feature of ipsilateral cerebellar pathology

(cerebellar ataxia if movements appear slow and irregular)