Med Surg-Quiz 13 Flashcards

1
Q

inflammatory condition of the joints of the axial skeleton.

A

Ankylosing Spondylitis

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2
Q

occurs when neck is forcefully whipped opposite direction while the shoulder is depressed on the same side. (Ex: Left sh depression, right neck SB). Causes trauma to the nerves and blood vessels of the brachial plexus.
Common in MVA, sports injuries, falls.

A

Brachial Plexus Injury

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3
Q

are felt after mild injury and usually resolve independently. (Brachial Plexus Injury)

A

“Stingers” or “burners”

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4
Q

(formerly RSD; reflex sympathetic dystrophy)- develops after trauma. Insidious c/o pain. Edema. Erythemia. Movement disorders.
Sympathetic nervous system is out of whack! Exaggerated pain response. Constant state of arousal. No relief.
Treatment: variety of tactile cues, light PRE, gentle stretching, modalities, education

A

Complex Regional Pain Syndrome- CRPS

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5
Q

progressive, insidious etiology, destruction of motor neurons in the lateral aspect of the spinal cord, brain stem and cerebral cortex via scarring. Results in peripheral nerve damage and muscle atrophy. Very debilitating. Terminal diagnosis. Will eventually paralyze respiratory muscles.
Incidence: 5,000 per year in US (approx 2/100,000) inherited autosomal trait

A

Amyotrophic Lateral Sclerosis- ALS

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6
Q

progressive, hereditary disease. Involves involuntary abnormal motor patterns and dementia. Brain atrophy is evident on MRI

A

Huntington’s Disease

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7
Q

Idiopathic facial paralysis. Unilateral effects.

A

Bell’s Palsy

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8
Q

auto-immune demyelination of PNS.

A

Guillain-Barre Syndrome

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9
Q

multiple sclerotic plaques throughout the myelin sheaths of the CNS. Inhibits nerve transmission including motor and sensory input. (demyelinating) Chronic and progressive condition.

A

Multiple Sclerosis

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10
Q

an idiopathic, chronic, progressive condition that affects the basal ganglia’s motor control of the CNS.

A

Parkinson’s Disease

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11
Q

slow initiation of movement

A

Bradykinesia

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12
Q

lack of emotional expression in face

A

Flat affect

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13
Q

controls smooth movement; medication is given to patients to control symptoms of PD. Important to time therapy around “on” times.

A

Dopamine

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14
Q

disruption of the nerve root originating from the spinal cord.

A

Radiculopathy- (radiculoneuropathy)

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15
Q

Chromosomal error. Feet will present with unusually high arches and claw toes. hereditary neuropathy that affects the joints. Initially affects LE, then progresses to UE.

A

Charcot Marie Tooth Disease

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16
Q

entrapment of the nerves of the foot, usually between 3rd and 4th toes.
Presents as: pain with weight bearing. Typical onset in female aged 45-60.
Treatment: orthoses, anti-inflammatory meds, modalities, stretching, ther ex; surgery only if debilitating to patient

A

Morton’s Neuroma

17
Q

viral infection that presented as flu-like symptoms, but developed quickly into paralytic symptoms. Attacked the motor nerves. Most affected persons were able to recover, but may have variable residual paralysis. Vaccine developed in 1950.

A

Poliomyelitis

18
Q

symptoms occur years after initial onset. Patients >50 y/o. The regenerated motor nerves are no longer capable of compensating and thus weakness reappears.

A

Post-polio syndrome

19
Q

TOS, CTS, TTS

A

Nerve compression injuries