Parkinson's Disease Flashcards

(31 cards)

1
Q

This is the immediate precursor to dopamine. It is the gold standard for treatment of Parkinson’s. Crosses the BBB

A

Levodopa

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2
Q

This drug inhibits aromatic L-amino acid decarboxylase in the periphery

A

Carbidopa

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3
Q

What are 3 strategies to address wearing off of Levodopa/Carbidopa

A
  • increase dose or dose number
  • add a dopamine agonist
  • use a COMT inhibitor
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4
Q

ADRS are N/V/anorexia, tachycardia, arrhythmias, visual and auditory hallucinations, depression, mania, anxiety, dyskinesia

A

Levodopa/Carbidopa

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5
Q

Drug interactions with vitamin B6 (pyridoxine), MAO inhibitors, antipsychotics

A

Levodopa/Carbidopa

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6
Q

This class of drugs have reduced risks of motor complications and dyskinesias compared to Levodopa/Carbidopa

A

Dopamine agonists

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7
Q

These two dopamine agonists are FDA indicated as monotherapy

A

Pramipexole

Ropinirol

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8
Q

This class of drugs can be neuroprotective. It decreases autooxidation and free radical formation in the brain. Reduces levodopa requirements

A

Dopamine agonists

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9
Q

ADRs include N/V, orthostasis, psychosis, narcolepsy

A

Dopamine agonist

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10
Q

Can cause increased risk of compulsive gambling due to stimulation of dopamine release in the mesolimbic pathway

A

Dopamine agonists

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11
Q

This dopamine agonist has a 3 hour half life, high first pass metabolism and is highly protein bound

A

Bromocriptine

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12
Q

This dopamine agonist has an 8-12 hour half life and is renally excreted

A

Pramipexole

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13
Q

Adverse effects include sedation, hypotension, delusions or psychosis, dyskinesias, N/V, and leg edema

A

Dopamine agonists

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14
Q

This dopamine agonist is transdermal, has a high affinity for DA receptor subtypes, and can be used as monotherapy or adjunct therapy

A

Rotigotine

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15
Q

AEs of this dopamine agonist include application site rxns, nausea, somnolence, sudden onset of sleep, and brief LOC while driving

A

Rotigotine

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16
Q

This MAOB inhibitor can extend the time before l-dopa is needed by 9 months and can extend its action for up to an hour

17
Q

ADRs include insomnia, jitteriness, HTN, worsen preexisting hallucinations and delusions. Can cause a rare serotonin syndrome with concomitant SSRI treatment

18
Q

This is transdermal Selegiline

19
Q

This is a selective, irreversible MAO-B inhibitor that is 5x more potent than Selegiline

20
Q

2 Parkinsons drugs metabolized by CYP 1A2

A

Ropinirole, Rasagiline

21
Q

This drug is used as an adjunct to L-dopa, is more efficacious than anticholinergic agents, and relieves symptoms of bradykinesia, rigidity, and tremor

22
Q

This drug has fewer side effects than L dopa or anticholinergic agents. Can cause hallucinations. confusion, and nightmares when administered with an anticholinergic

23
Q

ADRs include insomnia, dizziness, and slurred speech. CAUTION in patients with renal disease

24
Q

Indicated for tx in pts with PD experiencing end of dose wearing off with l-dopa

A

COMT inhibitors

25
These agents have NO ROLE AS MONOTHERAPY
COMT inhibitors
26
This COMT I is highly protein bound and readily absorbed. You need to do strict LFT monitoring, DC if signs of liver failure (there is even an informed consent on package insert)
Tolcapone
27
Can cause delayed onset diarrhea and brownish orange fluid discoloration, and orthostasis
Tolcapone
28
This COMT I causes diarrhea and orthostasis, brownish-orange urine discoloration, but NO evidence of hepatotoxicity
Entacapone
29
This drug is a combo of carbidopa, levodopa, and entacapone
Stalevo
30
These 2 anticholinergic drugs arent as effective as l-dopa but CAN be effective against tremor and dystonic features. Ineffective against bradykinesia
Trihexphenidyl | Benzotropine
31
ADRS: dry mouth, blurred vision, constipation, urinary retention, sedation memory impairment, confusion, dysphoria, hallucinations
Anticholinergics