Parkinson's disease Flashcards

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1
Q

5 pharm therapies for patients with dyskinesias or motor fluctuations despite optimal levodopa therapy

A
  1. COMT Inhibitors (prolong LDopa) ex. entacapone
  2. MAO-B inhibitors (motor sx) ex. rasagiline, selegiline
  3. Dopamine agonists (motor sx) ex. rotigotine patch, ropinirole, pramipexole
  4. Controlled release levodopa
  5. Intrajejunal levodopa-carbidopa enteric gel through perc gastrostomy
  6. Amantadine (dyskinesias, anticholinergic)
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2
Q

REM SBD can be a precursor to what 4 ND conditions? Less commonly seen in other 3 conditions?

A
  1. Idiopathic Parkinson’s disease
  2. Levy body dementia
  3. Multisystem atrophy (MSA)
  4. MCI non-amnestic
    Less Common
  5. PSP
  6. FTD
  7. ALS
  8. Huntington disease
  9. Alzheimer’s disease
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3
Q

Management of REM SBD

A
  1. Decrease/discontinue SSRI/antidepressant
  2. Melatonin 3-12 mg
  3. Clonazepam 0.25-2 mg
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4
Q

Medications that can cause hallucinations in PD patient

A
  1. Sinemet (DA)
  2. Tolterodine (anticholinergic)
  3. Amantadine (DA, anticholinergic)
  4. Pramipexole (DA)
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5
Q

Management for hallucinations in Parkinson’s disease

A
  1. Discontinue/decrease offending drug (anticholinergics, anxiolytics/sedatives, amantadine, DA, MAO-B, COMTi, levodopa)
  2. Start antipsychotic - in Parkinsonism can only safely use quetiapine, alternative is clozapine but requires monitoring
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6
Q

Management of constipation in PD

A
  1. Increase fluid and fibre intake
  2. Mobilize as able
  3. Discontinue anticholinergics
  4. Bulk forming laxative - Metamucil, psyllium
  5. PEG (osmotic)
  6. Senna (stimulant)
  7. Add domperidone
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7
Q

PD Palliative care recommendations

A
  1. Offer discussion of prognosis
  2. Provide information on progression, med sfx, end of life, advanced care planning, options for future tx, support services
  3. Recognize family and patient may need different information
  4. Consider palliative care team referral at any stage of PD
  5. Palliative care requirements (including the option of medical assistance in dying) should be considered throughout all phases of the disease
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8
Q

MDS Criteria - 2 features of a dramatic and significant response to levodopa therapy

A
  1. Marked improvement with dose increases or marked worsening with dose decreases
    a. Objectively >30% UPDRS III
    b. Subjectively - documented hx from reliable source
  2. Unequivocal and marked on/off fluctuations which must have at some point included predictable end of dose wearing off
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9
Q

PD Diagnostic Criteria (clinically established)

A
  1. Need bradykinesia PLUS tremor OR rigidity
    Then:
  2. Absence of absolute exclusion criteria
  3. At least 2 supportive criteria
  4. No red flags
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10
Q

Supportive criteria for PD

A
  1. Clear and dramatic response to dopaminergic therapy
  2. Presence of levodopa induced dyskinesia
  3. Rest tremor of limb
  4. Olfactory loss OR cardiac sympathetic denervation on MIBG scintigraphy
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11
Q

PD absolute exclusion criteria (9)

A
  1. Unequivocal cerebellar abnormalities (gait, limb ataxia, oculomotor)
  2. Downward vertical supra nuclear gaze palsy
  3. Dx of probable bvFTD or PPA within first 5 yrs of disease
  4. Parkinsonian features only in lower limbs for >3 years
  5. Tx with dopamine blocker or depleting agent (drug induced)
  6. No observable response to high dose LD despite at least moderate severity of disease
  7. Unequivocal cortical sensory loss (grapesthesia, stereognosis), limb ideomotor apraxia or progressive aphasia
  8. Normal functional neuroimaging of presynaptic dopaminergic system
  9. Documented alternate condition known to produce Parkinsonism
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12
Q

PD red flags (10)

A
  1. Rapid progression of gait, regular wheelchair within 5 yrs
  2. Complete absence of progression of motor sx over 5+ years (unless due to tx)
  3. Early bulbar dysfunction (sev dysphonia or dysarthria, sev dysphagia) within 5 yrs
  4. Severe autonomic failure in first 5 years (orthostasis, urinary retention or incontinence)
  5. Inspiratory respiratory dysfunction
  6. > 1 fall per year due to impaired balance within 3 years
  7. Disproportionate anterocollis or contractures of hand or feet in 10 yrs
  8. Absence common non motor symptoms in 5 yrs
  9. Pyramidal tract signs (weakness or hyperreflexia)
  10. Bilateral symmetric Parkinsonism
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13
Q

Non-oral treatment for patient on Sinemet, entacapone, selegiline and DA with wearing off and dyskinesias

A

Rotigotine patch (if stopping other DA) OR
Intrajejunal levodopa carbidopa gel via perc gastrostomy

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14
Q

Fluctuating non-motor symptoms in advanced PD (6)

A
  1. Neuropsychiatric (Hallucinations, cognition, depression, anxiety)
  2. Constipation
  3. Orthostasis HOTN
  4. Excessive drooling
  5. Urinary incontinence
  6. Sleep disturbance
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15
Q

Criteria for absence of response to levodopa

A

Item is: absence of observable response to high dose levodopa despite at least moderate severity of disease
1. Must have received 600+mg/day
2. Absence clearly reported by patient/witness or confirmed objectively (improvement <=3 pts on UPDRS)
3. Patient must have at least moderate severity Parkinsonism (UPDRS >2 of rigidity or bradykinesia)

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16
Q

Ddx for REM SBD

A
  1. Adverse effect of SSRI
  2. Overlap parasomnia disorder
  3. Sleep related movement disorder like RLS
  4. Sleep disordered breathing like OSA
17
Q

6 differences between essential tremor and Parkinson’s tremor

A
  1. Bilateral vs. unilateral (initially)
  2. Low amp high freq vs. high amp low freq
  3. Better with alcohol/BB vs. better with levodopa
  4. Action/postural vs. resting
  5. Familial vs. not often familial
  6. Not associated with other TRAP features vs. associated
  7. Progresses over decades vs. years
18
Q

Prodromal symptoms of PD

A
  1. REM SBD
  2. Hyposmia/Anosmia
  3. Constipation
  4. Mood disorders
19
Q

4 main causes of sleep disturbance in PD and tx

A
  1. Insomnia from pain, tremor, med sfx, depression, nocturia (tx sleep hygiene, melatonin, night time levodopa, doxepin, trazodone)
  2. Excessive daytime somnolence (tx modafanil)
  3. REM SBD (melatonin, clonazepam)
  4. Restless leg (check if IDA, optimize dopaminergic therapy, pregabalin)
20
Q

5 non-pharm strategies for gait freezing

A

2022 review
1. Gait training on treadmill
2. Obstacle training
3. General exercises
4. Action observation training
5. Conventional PT
Other
1. Dual task training
2. Robotic assisted walkng
3. Real time biofeedback
4. External cueing
5. Psychoeducation
6. Mind body - tai chi, dance, yoga

21
Q

Serotonin syndrome vs. NMS

A

Onset: hrs vs. days
Etiology: SSRI/SNRI/MAOI/TCA/opioids vs. antipsychotics/sudden cessation dopaminergic
Vitals: inc HR/BP/sweaty vs. inc HR/labile BP/sweaty
Temp: maybe febrile vs. febrile for sure
Pupils: dilated vs. normal
Reflexes: hyperreflexia and myoclonus vs. hyporeflexia and no clonus, lead pipe
GI: diarrhea/inc BS vs. normal
CK: can be raised vs. raised for sure

22
Q

Vascular Parkinsonism vs. IPD 6 features

A
  1. Symmetrical
  2. Lower body predominant
  3. Absence of tremor
  4. Absent/poor response to dopamine
  5. Gait unsteadiness
  6. Pyramidal signs/CS tract signs: spasticity, brisk reflexes, positive Babinski, diminished power
23
Q

8 changes in gait with PD

A
  1. Stooped posture
  2. Shuffling
  3. En bloc turning
  4. Reduced arm swing
  5. Festination
  6. Freezing
  7. Slow gait speed
  8. Reduced step height
  9. Shorter step/stride length
  10. Increased truncal rigidity
24
Q

Define ideomotor apraxia and ideational apraxia

A

Ideomotor apraxia: unable to perform skilled gesture with a limb by command and/or imitation ex. toothbrush, wave goodbye
Ideational apraxia: unable to plan movements related to interaction with objects b/c don’t understand purpose of object and can’t do series in sequence ex. using fork to brush hair, put on shoes before socks

25
Q

5 adverse effects from dopaminergic agonists

A
  1. Excessive daytime somnolence: drowsiness, or sudden onset of sleep
  2. Ankle edema
  3. Impulse control disorders
  4. Skin reaction (rotigotine)
  5. Hallucinations
  6. Nausea
26
Q

5 ocular findings in PD

A
  1. Decreased blink rate
  2. Eyelid opening apraxia
  3. Impaired upward gaze and convergence
  4. Hypometric saccades (undershoot)
  5. Impaired vestibulo-ocular reflex