Dr. Louie: Neuropathy and EMG Flashcards

1
Q

What are the clinical features of neuropathy?

A

stocking/glove numbness
exclusively or initially in legs
loss of sensation: feet feel like walking on logs
tingling: pain and needles
pain: burning, shooting, allodynia
unsteadiness/imbalance particularly when vision taken away
weakness (greater distally)

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2
Q

What are some characteristics of the weakness associated w neuropathy?

A

greater distally than proximally
unable to grip, open jar, execute fine movements
foot drop / tripping over feet
dropping objects from hands

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3
Q

What are some bulbar/cranial nerve symptoms associated w neuropathy?

A

diplopia
ptosis
dysarthria

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4
Q

What are some sensory features associated w neuropathy?

A

loss of pinprick sensation in distal extremities
loss of temperature
hypersensitivity/allodynia
proprioception testing (Romberg test)

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5
Q

What are some motor features associated w neuropathy?

A

mostly distal atrophy with or without fasciculations
weakness evident in distal groups
tremor
diminished to absent deep tendon reflexes
pes cavus deformity of foot
steppage gait with foot drop

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6
Q

What are some bulbar features that are notable during a physical exam?

A
diplopia
ptosis
facial asymmetry
tongue weakness/atrophy
pupillary abnormalities
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7
Q

What is one caveat when performing EMGs?

A

slowing latencies or conduction velocities can be due to cold limb skin temperature

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8
Q

What could decreased sensory or motor amplitudes suggest?

A

axonal damage

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9
Q

What may delayed distal latencies or slowed conduction velocities suggest?

A

demyelination

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10
Q

What may abnormal temporal dispersion or conduction block be suggestive of?

A

demyelination disease or focal nerve impingement

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11
Q

What may delayed or absent F-responses or H-reflexes be suggestive of?

A

demyelination disease
radiculopathy
focal nerve compression

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12
Q

In a needle electrode exam, what can increased insertional activity suggest?

A

muscle irritability, which can be seen in neuropathy or myopathy

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13
Q

motor units are high-amplitude, polyphasic with decreased recruitment

A

denervation

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14
Q

motor units are low-amplitude, polyphasic with increased recruitment

A

myopathic muscle

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15
Q

What is EMG good for?

A

diagnosis of classification of peripheral neuropathy
diagnosis of major compressive mononeuropathies
diagnosis of myopathy
diagnosis of severe radiculopathy

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16
Q

Decreased or absent sensory and motor amplitudes on NCS
Increased insertional activity with fibs and p-waves and possibly CRDs as abnormal spontaneous activity
High-amplitude, polyphasic motor unit potentials with decreased recruitment on motor unit analysis

A

axonal neuropathy

17
Q

NCS showing markedly delayed distal latencies and slowed conduction velocities
Abnormal temporal dispersion or conduction block
Markedly delayed F-wave latencies or absent F-waves
Needle EMG: Increased insertional activity with p-waves, fibs as abnormal spontaneous activity
High-amplitude, polyphasic motor unit potentials with decreased recruitment

A

deymyelinating neuropathy

18
Q

Decreased sensory amplitudes or absent sensory responses
Decreased or absent motor responses
EMG showing fibs, p-waves, fasciculations exclusively in muscles supplied by suspect nerve. Motor unit potentials of those muscles are large, polyphasic with decreased recruitment

A

compressive neuropathy

19
Q

Normal sensory nerve conductions
Normal or decreased motor amplitudes
Delayed or absent F-responses
EMG: fibs, p-waves, CRDs in appropriate myotome. In those muscles, motor unit potentials are large and polyphasic with decreased recruitment. Paraspinous muscles are most sensitive for these changes.
EMG/NCS can be normal in patients with a significant radiculopathy. Need to correlate with imaging.

A

Radiculopathy

20
Q

Diabetic Neuropathy
Other metabolic neuropathies
Vasculitic neuropathy
Hereditary neuropathy

A

types of axonal neuropathy

21
Q

Guillain-Barre syndrome
MGUS-related neuropathies
Selected toxic neuropathies—Toluene
Hereditary demyelinating neuropathies—Charcot-Marie-Tooth Disease

A

demyelinating neuropathy

22
Q

What should you do if a neuropathy is not treatable?

A

supportive care