Evaluation of a patient with weakness Flashcards

1
Q

What are the levels of the nervous system that can produce true weakness?

A
  • Upper motor neurons (descending tracts of the central nervous system)
  • Lower motor neurons (the anterior horn cell and the axons traveling through the peripheral nerve to the muscle)
  • The neuromuscular junction
  • The muscle.
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2
Q

How is strength graded?

A

A 5 point scale:

  • 5 being normal
  • 4 being weak
  • 3 being only strong enough to move against gravity and no additional resistance
  • 2 being unable to move against gravity
  • 1 being a flicker of contraction of the muscle, but no actual limb movement of any kind.
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3
Q

How can strength be tested functionally?

A
  • The patient can attempt to hold the arms out in front, with weakness of the whole upper limb reflecting in pronator drift.
  • Grip can be tested by squeezing of two of the examiner’s fingers.
    • Making an “OK” sign with the thumb and index finger tests the thenar muscles.
  • Abduction and adduction of the ulnar 4 digits tests interosseous and hypothenar muscles.
  • Walking on the toes and heels, climbing a small step, hopping on one foot or rising from a chair tests lower extremity muscles.
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4
Q

Other than actual weakness, what other symptoms might the patient be describing when they use the term “weak”?

A
  • Rigidity

- Incoordination

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5
Q

What is suggested by proximal, symmetrical distribution of weakness (hip and shoulder girdle)?

A

This is the pattern most often seen in a myopathic process.

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6
Q

What is suggested by distal, symmetrical distribution of weakness (feet and/or hands)?

A

This is the pattern most often seen in a neuropathic process.

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7
Q

What does it mean if the atrophy is out of proportion to the degree of disuse?

A

This indicates lower motor neuron lesion.

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8
Q

What would be suggested by fatigability of muscles?

A

Neuromuscular diseases, such as myasthenia gravis, can produce fatigue of muscles.

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9
Q

What conditions can cause transient weakness?

A
  • Transient ischemic attacks
  • Neuromuscular diseases (like myasthenia)
  • Peripheral nerve entrapment problems
  • Periodic paralysis family of conditions
  • Migraine can cause transient weakness.
  • Patients can also be transiently weak after a seizure (Todd paralysis).
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10
Q

What is suggested by a story of severe, global weakness associated with heavy meals or periods of exercise?

A

This is a story suggestive of one of the periodic paralyses (an ion channelopathy).
- There may be a family history of similar problems.

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11
Q

What systemic conditions can produce weakness?

A
  • Thyroid or adrenal dysfunction
  • Certain rheumatologic/inflammatory conditions can lead to muscle damage (myopathy).
  • Diabetes mellitus, hypertension, dyslipidemas predispose to cerebrovascular disease
    • Can damage upper motor neurons.
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12
Q

How can pain affect the diagnosis of the patient with weakness?

A
  • Pain may be part of the condition (particularly those that damage nerves or muscle).
  • Pain may also produce an unwillingness or even inability to use the body part.
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13
Q

What conditions can present as bilateral weakness of the lower limbs?

A
  • Myelopathy (damage or disease of the spinal cord) usually produces bilateral symptoms below a certain level, often with some bladder urgency (this may require urgent MRI scanning of the cord).
  • Cauda equina compression (syndrome) is suggested by flaccid weakness of the legs, often with urinary retention or overflow incontinence.
  • Guillain - Barre => progressive weakness of both legs, evolving over hours to days
  • Myopathic processes tend to affect the hip girdle muscles early
  • Lambert-Eaton myasthenic syndrome usually begins with proximal hip girdle muscle weakness.
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14
Q

What is the likely cause of weakness of one side of the body that is associated with a lower facial weakness on the same side?

A

The problem is with upper motor neurons above the level of the brainstem
- Usually cerebral cortex or internal capsule.

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15
Q

What is the likely cause of weakness of one side of the body that is associated with weakness on the opposite side of the head (tongue, jaw, palate or eyes)?

A

The damage is localized to the brain stem (usually the medial aspect).

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16
Q

What procedure can be used to objectively demonstrate whether nerves to a muscle are damaged?

A

EMG can determine whether lower motor neurons to a muscle are intact.
- The pattern of denervated muscles is then used to try to distinguish whether a single nerve is involved or whether this is due to damage to a nerve root or the nerve plexus.

17
Q

What is the effect of upper motor neuron damage upon muscle bulk, tone, deep tendon reflexes and superficial reflexes?

A

Upper motor neuron damage generally produces increased deep tendon reflexes, along with diminished normal superficial reflexes and some pathological reflexes

  • Babinski
  • Muscle tone is usually increased in a pattern of spasticity (clasp-knife).
18
Q

What is the effect of lower motor neuron damage upon muscle bulk, tone, deep tendon reflexes and superficial reflexes?

A
  • Lower motor neuron damage generally produces decreased deep tendon reflexes in the effected area.
    • Superficial reflexes are usually not effected unless the weakness is very severe.
  • Muscle tone is usually decreased and there is often severe atrophy that develops over time.
    • If the motor neuron itself is damaged, fasciculations are usually prominent.
19
Q

What is the effect of muscle or neuromuscular disease on muscle bulk, tone, deep tendon reflexes and superficial reflexes?

A

Usually all of these are normal

- Very late in muscular disease there may be atrophy.

20
Q

What kinds of problems produce diffuse muscle damage (myopathy)?

A
  • Congenital/hereditary
    • Muscular dystrophy, congenital myopathy
  • Infection
    • Trichinosis
  • Connective tissue disease
    • Polymyositis, scleroderma, mixed connective tissue disorder
  • Endocrine
    • Hypo/hyperthyroid, hyperparathyroid, hypo/hyperadrenia
  • Neoplastic
  • Drug-induced (clofibrate, statins, corticosteroids).
21
Q

What kinds of conditions damage or block the neuromuscular junction?

A
  • Paraneoplastic (Lambert-Eaton Myasthenic syndrome)
  • Immunologic (Myasthenia gravis)
  • Toxins (botulism, snake venom, tick bite)
  • Drugs(antocholinesterase toxicity).
22
Q

What differences would be expected between myasthenia gravis and Lambert-Eaton myasthenic syndrome (LEMS)?

A

Myasthenia gravis

  • Progressive weakness during sustained or repeated contraction.
  • Affects eyes early (can affect speech and swallowing or be generalized).

LEMS

  • Get stronger with repetition
  • Affect hip girdle muscles
  • Tendon reflexes are usually diminished (and improve after exercise).
23
Q

What is the effect of lower motor neuron damage upon muscle bulk, tone, deep tendon reflexes and superficial reflexes?

A
  • Lower motor neuron damage generally produces decreased deep tendon reflexes in the effected area.
    • Superficial reflexes are usually not effected unless the weakness is very severe.
  • Muscle tone is usually decreased + severe atrophy that develops over time.
    • If the motor neuron itself is damaged, fasciculations are usually prominent.
24
Q

What disorders can damage peripheral nerves?

A
  • Trauma (including entrapment)
  • Toxins (lead, alcohol, several medicines)
  • Infections (diptheria, Lyme, HIV)
  • Inflammatory (CIDP, Guillain-Barre)
  • Metabolic (diabetes, porphyria)
  • Vascular (autoimmune arteritis)
  • Nutritional (vitamin B1 or B12 deficit or pyridoxine toxicity)
  • Heredity (Charcot-Marie-Tooth disease, etc)
  • Neoplasm
  • Abnormal proteins (amyloidosis).
25
Q

What kinds of conditions damage nerve roots?

A

Problems with nerve root(s) include:

  • Intervertebral disk herniation
  • Neoplasm
  • Foraminal encroachment
  • Radiation
  • Toxins
  • Chronic meningitis
26
Q

What kinds of conditions damage anterior horn cells?

A

Diseases directly damaging anterior horn cells include:

  • Infection (polio)
  • Spinal cord trauma
  • Tumors/paraneoplastic
  • Degenerative (ALS, progressive spinal muscular atrophy)
  • Disc (spondylotic myelopathy)
  • Radiation myelopathy
  • Vascular
27
Q

What kinds of problems are associated with upper motor neuron damage?

A
  • Vascular (stroke/TIA, AVM)
  • Tumor
  • Trauma
  • Infection (transverse myelitis, HIV)
  • Demyelination (MS)
  • Degeneration (ALS, primary lateral sclerosis)
  • Congenital (cerebral palsy)
  • Toxic/anoxic
  • Developmental (Chiari, spinal stenosis)