Parkinsons disease and ALS Flashcards

1
Q

main neurotransmitter that is affected in parkinsons

A

dopamine

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2
Q

extrapyramidal tracts

A

part of the brain controls semiautomatic functions and coordinated movmt

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3
Q

level of dopamine in parkinsons

A

down to 80%

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4
Q

resting tremors

A

tremors disappear with movement and sleeping

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5
Q

rigidity

A

resistance to passive limb movement

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6
Q

passive movement of the extremity

A

causes limb to move in jerky in increments called cogwheel rigidity

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7
Q

shuffling gait (postural instability)

A

pt tries to walk faster trying to move feet forward under center of gravity - steps are shorter in stride and drag their feet and reduce arm movement

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8
Q

freezing gait (postural instability)

A

difficultly in initiating walking – feet are glued to the floor

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9
Q

psychiatric changes in parkinsons patients

A

depression, anxiety, dementia, delirium, hallucination

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10
Q

hypokinesia

A

decresed range of bodily mvmt/slow

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11
Q

dysphonia

A

voice impairment– voice is hoarse/nasal

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12
Q

levodopa “on-off syndrome”

A

sudden periods of immobility (seems like drug is not working/then working again)

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13
Q

dyskinesia

A

involuntary repetitive of facial and oral muscles

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14
Q

Anticholingeric drug info

A

-Trihexyphenidyl hydrochloride- control tremors
-Benztropine mesylate- counteract the action of the acetylcholine
SE: constipation, urinary retention, blurred vision; CI: patient with narrow angle glaucoma

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15
Q

amantidine hydrochloride

antiviral

A

reduces rigidity and tremor, bradykinesia in early parkinsons
se: hallucination; depression

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16
Q
Bromocriptine mesylate
(dopamine agonist)
A

secondary drug used after levodopa losses its effectiveness

SE hypotension, lightheadedness

17
Q

Ropinirole hydrochloride

Nonergot derivative

A

SE: dizziness, drowsiness

18
Q

what to do if patient has SE like insomnia, hallucination etc. ?

A

stop drug see if it subsides, if it doesn’t then it’s the disease not the drug

19
Q

pudding-thick

A

spoon-thick, holds own shape, requires a spoon (advanced parkinsons - those who can not swallow)

20
Q

risk factors for amyoptripic later sclerosis/ Lou Gehrig disease

A

smoking; viral infections; autoimmune disease; environmental exposure to toxins

21
Q

when/how does Lou Gehrig disease occur

A

Commonly occurs between 40-60 years of age; affects all social and racial background; men affected slightly more than women;
About 5-10% of cases are familial from an autosomal dominant trait

22
Q

diagnosis for Lou Gehrig disease

A

based ONLY on s/s - no labs specific

23
Q

Riluzole (Rilutek)- glutamate antagonist

A

– can prolong the survival ; Neuroprotective effect especially in early stage