Parkinson's Flashcards

1
Q

Pathophysiology of Parkinson’s Disease

A
  • dopamine deficiency in brain
  • imbalance between inhibitory dopamine and excitatory acetylcholine
  • loss of dopaminergic cells
  • formation of Lewy Bodies
  • required 30-80% of nigral cell death before disease manifests clinically
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2
Q

Diagnostic Criteria for Parkinson’s

A

Bradykinesia (slowness and difficulty initiating voluntary movement)

+ at least one of the following
- limb muscle rigidity
- resting tremor
- postural instability

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3
Q

Levodopa

A

MOA: precursor to dopamine, crosses BBB

Dosing: 200-300 mg/day -> inc by 100mg/wk -> 800-1000mg/day

CI: Breast feeding, closed angle glaucoma, melanoma

DDI: dopamine antagonists (metoclopramide and APS), MAOIs, high protein intake, pyridoxine

ADE: dyskinesia, On-off, decreased effectiveness over time, psych disturbances, vivid dreams, nausea, ortho hypo, saliva/sweat/urine discoloration, NMS w/ abrupt dc

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4
Q

Carbidopa

A

MOA: inhibit breakdown of levodopa in the periphery (increases both absorption and T1/2)

Dosing: 70-100mg/day

CI: pregnancy / lactation

ADE

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5
Q

Carbidopa

A

MOA: inhibit breakdown of levodopa in the periphery (increases both absorption and T1/2)

Dosing: 70-100mg/day

CI: pregnancy / lactation

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6
Q

Sinemet CR

A

Carbidopa / Levodopa
25/ 100 mg
50 / 200 mg

less bioavailable than IR (consider giving 25% more per day)

pats complain of slowed onset

when switching from IR to CR start with 50% reduction in frequency

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7
Q

Inbrija

A

Levodopa powder for inhalation
for intermittent treatment of OFF episodes

ADE: somnolence, hallucinations, dyskinesia, COUGH, nausea, URTI, discolored sputum

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8
Q

Tolcapone (Tasmar)

A

MOA: reversible selective inhibitor of COMT -> prevents breakdown of L-dopa

Dosing: 100mg TID

CI: hepatic disease

DDI: nonselective MAOI, other drugs metabolized by COMT (apomorphine, bitolterol, dobutamine, dopamine, epinephrine, isoetharine, isoproterenol, methyldopa, norepinephrine)

ADE: hepatocellular injury, similar ADE to levodopa

Generally Entacapone is preferred over Tolcapone

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9
Q

Entacapone (Comtan)

A

MOA: reversible selective inhibitor of COMT -> prevents breakdown of L-dopa

Dosing: 200mg with each dose of levodopa/carbidopa

DDI: nonselective MAOI, other drugs metabolized by COMT (apomorphine, bitolterol, dobutamine, dopamine, epinephrine, isoetharine, isoproterenol, methyldopa, norepinephrine)

ADE: similar to levodopa + brown/orange urine

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10
Q

Stalevo

A

Carbidopa / Levodopa / Entacapone
12.5 / 50 / 200
25 / 100 / 200
50 / 150 / 200

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11
Q

Selegiline (Eldepryl, Zelapar [transbuccal])

A

MOA: noncompetitive, selective MAO-Bi -> decrease breakdown of dopamine
- increase L-dopa peak, can dec L- dopa dose up to 50%

Dosing:
-Eldepryl (PO): 5mg QD-BID
-Zelapar (dissolving tablet): 1.25 mg QD - 2.5 mg QD after 6 weeks. no food or drink 5 minutes before/after

DDI: nonspecific MAOI, TCA, SSRI, SNRI, DXM, tyramine containing foods at doses > 10 mg, sympathomimetics

ADE: CNS, GI, hypertensive crisis, serotonin syndrome, insomnia, jitteriness HA

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12
Q

Rasagiline (Azilect)

A

MOA: noncompetitive, selective MAO-Bi -> decrease breakdown of dopamine
- decrease in free radicals -> may be disease modifying

Dosing: 0.5 mg QD w/ levodopa
- 1 mg as monotherapy

DDI: nonspecific MAOI (2 week washout), TCA, fluoxetine (5 week washout), sympathomimetics

ADE:
-monotherapy: HA, arthralgia, GI upset, falls
- w/ levodopa: dyskinesia, GI upset, HA, weight loss, arthralgia, orthostasis (during first 2 months)

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13
Q

Safinamide (Xadago)

A

MOA: selective MAOBi
- Na and K channel blocker, dec glutamate release
- adjunct to L-dopa for wearing off symptoms

Dosing: 50mg PO QD -> 2 weeks -> inc to 100mg QD if needed

CI: Child-Pugh class C, do not exceed dose of 50mg in hepatic impairment

ADE: dyskinesia, hallucinations/psychosis, impulse control, behavior change, nausea, daytime somnolence, NMS in withdrawal, retinal pathology

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14
Q

Amantadine (Symmetrel, Gocovri, Osmolex ER)

A

MOA: not understood, decreases rigidity, tremor, bradykinesia, L-dopa induced dyskinesia

Dose:
-Symmetrel IR: 300 mg/day PO div
-Gocovri ER: 137 mg PO QD 1w -> 274 mg PO QD
- Osmolex ER: 129 mg PO QD 1w -> 322 mg PO QD

CI: CHF, orthostatic hypotension, peripheral edema

DDI: Flumist, Quinine/Quiidine, HCTZ, triamterene

ADE: orthostatic hypotension, hallucinations, sedation, anticholinergic AEs, livedo reticularis - mottling of skin with LE edema (resolves with dc), NMS with abrupt disruption

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15
Q

Pramipexole (Mirapex)

A

MOA: Dopamine agonist

Dosing:
-IR 0.125mg TID -> MDD 1.5mg TID
-ER 0.375 mg QD -> MD 4.5 mg QD

PK: smoking may decrease levels (induces CYP1A2)

CI: abrupt discontinuation, hepatic disease

ADE: edema, impulsivity, psychosis, N/V, orthostasis, sedation, vivid dreams, pedal edema, plum fibrosis (Ergots), cardiac valvopathy

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16
Q

Ropinirole (Requip)

A

MOA: Dopamine agonist

PK: smoking may decrease levels (CYP1A2)

Dosing:
IR 0.25 mg TID -> MDD 24mg
ER 2mg QD -> MDD 24mg

CI: abrupt discontinuation, hepatic disease

ADE: edema, impulsivity, psychosis, N/V, orthostasis, sedation, vivid dreams, pedal edema, plum fibrosis (Ergots), cardiac valvopathy

17
Q

Bromocriptine (Parlodel)

A

MOA: dopamine agonist

CI: breast feeding, eclampsia, ergot alkaloid hypersensitivity, uncontrolled HTN

DDI: antihypertensive agents, erythromycin

ADE: CNS, GI, pulmonary fibrosis (chest radiograph at BL, once yearly)

18
Q

Rotigotine (Neupro)

A

MOA: dopamine agonist, transdermal patch

Dosing: 2mg/24h -> inc weekly by 2mg/24h up to 6mg
-4mg minimum effective dose

DDI: dopamine antagonists (APS and metoclopramide)

ADE: application site reaction, CNS, GI, peripheral edema

19
Q

Apomorphine (Apokyn)

A

MOA: stimulates postsynaptic D2 type receptors
- used as needed or for off episodes

Dosing: 2mg SC test dose under medical supervision
-monitor BP pre-dose, 20 min, 40min, 60min
-may increase dose by 1mg every few days as needed up to 6mg
-pretreat with antiemetic (3 days before, continue for 2 months and reassess) -NOT 5HT3 antagonists or antidopaminergic

ADE: N/V dizziness, somnolence, chest pain/pressure, dyskinesia, falls, yawning, rhinorrhea

20
Q

Non-pharm treatments for Parkinson’s

A

surgery (deep brain stimulation)
physical therapy and exercise
nutrition
- fluids
- fiber
- omega 3 fatty acids
- occupational therapy and fall precautions

21
Q

Management of wearing off syndrome

A

increase frq
switch to CR (decreased frq may require IR morning dose)
adjunctive DA (MAOI/COMT/Amantadine)

22
Q

Management of OFF NO ON

A

delayed stomach emptying / decreased absorption?
- inc dose
- inc frq
- take on empty stomach
- use ODT

advanced disease > APO SQ

23
Q

Management of delayed onset

A

empty stomach
water
avoid protein
if CR: consider switching off CR or adding IR

24
Q

Management of peak effect dyskinesia

A

dec dose
inc frq
add amantadine
use CR Sinemet
add DA agonist

25
Q

Management of dystonia

A

add early morning dose
CR at HS
DA agonist
Baclofen
Botox

26
Q

Management of freezing

A

inc dose
DA agonist
gait modification
physical therapy

27
Q

Management of depression in parkinson’s

A

pramipexole
SSRIs
venlafaxine

28
Q

Management of dementia in parkinson’s

A

rivastigmine

29
Q

Management of insomnia in parkinson’s

A

eszopiclone
melatonin

30
Q

Management of excessive daytime sleepiness

A

modafanil

31
Q

Management of orthostatic hypotension

A

fludrocortisone
midodrine
droxidopa

32
Q

Management of sexual dysfunction

A

sildenafil

33
Q

Management of constipation

A

PEG
probiotics
lubiprostone

34
Q

Management of urinary frequency

A

solifenacin

35
Q

Management of drooling

A

glycopyrrolate
botox

36
Q

Management of psychosis

A

evaluate for other causes (pathological, drug)
simplify regimen
consider atypical antipsychotics
- Quetiapine
- Clozapine
- Pimavanserin tartrate (Nuplazid)