Parkinson's tx Flashcards

1
Q

PD disease progression

A

-over 5-10 years w inc in motor sx
-cognitive sx after several years
-~15 year life expectancy after dx

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2
Q

PD clinical presentation

A

-tremor
-bradykinesia
-rigidit
-gait
-anxiety/depression
-constipation
-dementia
-insomnia
-hypotension
-psychosis/delirium
-sexual dysfunction

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3
Q

Goals of PD therapy

A
  1. minimize sx
  2. QOL
  3. ADLs
  4. minimize se
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4
Q

Non-pharmacologic tx of PD

A

-exercise/PT
-nutrition
-occupationaly therapy
-psych and speech therapy

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5
Q

PD tx

A
  1. rule out drug-induced
  2. Dopamine precursor
  3. DA agonist
  4. MAO-B inhibitor
  5. COMT inhibitor
  6. Amantadine
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6
Q

First line tx of PD

A

-rule out drug-induced
-dopamine precursor
-dopamine agonists
-MAO-B inhibitor

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7
Q

2nd line tx of PD

A

-COMT inhibitors
-Amantadine

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8
Q

Treatment initiation

A

-Levodopa for most
-can use dopamine agonist if <60 and higher risk for dyskinesia (risk of dyskinesia inc w time)
-IR > CR
-start low
-LDOPA > DA > MAOB for motor sx

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9
Q

AVOID DA agonists if

A

->70
-hx of ICD
-cognitive impairment
-xs daytime sleepiness
-hallucinationa

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10
Q

PD meds w better efficacy for motor sx

A

-LDOPA > DA > MAO-B

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11
Q

LDOPA

A

-gold standard
-N/V
-LD motor fluctuations/dyskinesia
-hallucinations

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12
Q

LDOPA clinical (or duodenal gel)

A

-inc absorption w empty stomach
-food dec nausea
-25/100mg PO BID-TID wf to start
-can inc freq as needed (5-6x day!)
-titrate to weigh risk v benefit

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13
Q

Patterns of motor fluctuations in PD

A

-duration of LDOPA concentration shortens w progression of disease
-doses go over threshold = dyskinesia

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14
Q

LD motor fluctuations

A

-wearing off: sx before next dose
-freezing (inability to move bc DA levels)
-delayed onset (benefits delayed)
-peak-dose dyskinesias (involuntary movements bc dose too high)

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15
Q

Dopamine agonist drugs

A

-Non-ergot
-Pramipexole (Mirapex®)
-Ropinirole (Requip®)
-Rotigotine (Neupro®)
-Apomorphine (Apokyn®
injection and SL film)

-Ergot (rarely use bc toxicity)
-Bromocriptine
(Parlodel®)
-Cabergoline (Dostinex®)

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16
Q

non-ergot Dopamine agonist clinical

A

-first line for initial tx
-minimize LD motor fluctuations
-long-acting formulations
-N/V
-suddeen onset sleep
-hallucinations
-impulse control disorder (ICD)
-Edema
-orthostatic hypotension

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17
Q

MAO-B inhibitors

A

-first line mild sx
-second line for adj
-motor and depression management

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18
Q

MAO-B inhibitors side effects

A

-N/V
-HA
-insomnia (selegiline)
-Hypo/Hyper tension
-avoid tyramine rich foods
-risk of serotonin syndrome (sertonergic antidepressants, dextromethorphan, serotonergic opioids)

19
Q

MAO-B clinical

A

-once/twice daily dosing
-avoid tyramine-rich foods

20
Q

COMT inhibitor side effects

A

-N/V
-brown/orange urine!! (entacapone)
-hepatotoxicity (toclcapone use limiting side effect)

21
Q

COMT clinical

A

-prob no benefit in early stage PD

22
Q

Anticholinergic drugs

A

-benztropine
-trihexyphenidyl

23
Q

anticholinergic side effects

A

-confusion
-blurry vision
-urinary retention
-dry mouth
-constipation

-AVOID if >65 yo

24
Q

Amatadine use

A

-manage LD motor fluctuations
-rarely monotherapy
-reserved for CD/LD peak dose dyskinesias

25
Q

Amatadine side effects

A

-insomnia
-confusion
-hallucination
-livedo reticularis
-use is limited bc SE

26
Q

Medications that can worsen PD:

A

Dopamine antagonists: antipsychotics, metoclopramide,
prochlorperazine, promethazine

27
Q

Pros of dopamine agonists

A

-once daily dosing
-better tolerated by young pt
-limited motor fluctuations

28
Q

Dopamine agonist cons

A

-$$
-less sx benefit than CD/LD
-many adverse effects

29
Q

Who is treated w dopamine agonists

A

-age < 60 and higher risk of dyskinesia
-avoid in >70, ICD hx, cognitive impairment, drowsiness, hallucinations

30
Q

MAO-B pros

A

-well tolerated
-delays onset of motor fluctuations

31
Q

MAO-B cons

A

-least effective 1st line agent against motor sx
-dietary restrictions = risk of serotonin syndrome

32
Q

MAO-B for who

A

-minor sx
-higher risk of motor fluctuations

33
Q

Wearing off tx

A

-inc CD/LC dose or frew
-add DA, MAO, COMT
-XR CD/LD

34
Q

freezing tx

A

-inc CD/LD dose/freq
-add DA agonist (apomorphine)
-add ODT CD/LD

35
Q

delayed onset tx

A

-take CD/LD on empty stomach
-ODT CD/LD
-avoid CR/XR CD/LD

36
Q

Peak-dose dyskinesia tx

A

-add amantadine
-dec dose of DA or CD/LD

37
Q

Deep brain stimulation

A

-surgical tx if motor fluctuations not managed
-risk infection
-neurotransmtter on clavivle

38
Q

Constipation in PD tx

A

-eval drug-induced
-inc fluids and activity
-laxatives

39
Q

Insomnia in PD tx

A

-melatonin
-AVOID benzos (-pams)

40
Q

Orthostatic hypotension in PD tx

A

-midodrine, droxidopa
-med equipment

41
Q

Anxiety/depression tx in PD

A

-CBT
-SSRI
-SNRI
-AVOID benzo
-caution tricyclic antidepressants

42
Q

Dementia in PD tx

A

-cholinesterase inhibitor
-AVOID: anticholinergics, benzos, antihistamines, sedatives

43
Q

Psychosis/delirium tx in PD

A

-reduce PD med dose
-pimavanserin (newish antipsychotic for psychosis
-atypical antipsychotics (clozapine, quetiapine)
-AVOID: haloperidol, olanzapine, paliperidone, risperidone