Parkinson's disease / parkinsonism Flashcards

1
Q

What is parkinson’s disease

A

Chronic disorder of the brain/substansia nigra with parkinsonism features

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2
Q

How common is it and who gets it

A

0.6% at 60-64yrs and 3.5% at 85-89years

typical onset = 65yrs

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3
Q

What is the cause

A
  • Mitochondrial DNA dysfunction
    –> Degeneration of dopaminergic neurons in substantia nigra pars compacta (ass w. Lewy bodies)
  • Reduced levels of dopamine
    = slower/abnormal nerve messages
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4
Q

What is the clinical presentation of parkinson’s

A
  • Bradykinesia/hypokinesia – slow voluntary + autonomic reduced arm swing
  • Tremor – 4-6Hz resting tremor, induced by concentration + absent during activity.
  • Postural instability +/- muscular rigidity - resistance to passive movement
  • Gait – small shuffling steps w/ unsteadiness on turning + difficulty stopping (festination)
  • NON-MOTOR FEAT = sense smell, constipation, visual hallucination, frequency/urgency, dribbling of saliva, depression/dementia
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5
Q

What are the features of parkinsonism

A

TREMOR
- worse at rest, ‘pill-rolling’ of thumb over fingers, 4-6 cycles/sec

RIGIDITY/^ TONE
– rigidity + tremor = Cogwheel rigidity felt by examiner during rapid pronation/supination (jerky)

BRADYKINESIA/HYPOKNESIA
• slow to initiate movement
• slow, low-amplitude excursions in repetitive actions e.g. blink rate, monotonous
• hypophonic speech, micrographia

GAIT: arm swinging, festinance (shuffling steps w/ flexed trunk), freezing at obstacles/doors, expressionless face (hypomimesis)

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6
Q

What are the differential diagnoses

A
  • Benign essential tremor - worse on movement
  • Drug/toxin induced tremor
  • HUNTINGTON’S - can Px w. rigidity 1st + not chorea
  • LEWY BODY DEMENTIA - parkinsonian feat
  • Creutzfeldt-Jakob Disease - dementia apparent w. myoclonic jerking + ataxia
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7
Q

What investigations do you perform

A
  • refer to specialist
  • Diagnoses = clinical –> investigations exclude other causes
  • CT/MRI if pt fails to respond to L-DOPA
  • PET scan can show dopamine deficiency
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8
Q

How do you treat parkinson’s

A
  • Specialist review every 6-12 months
    LEVODOPA
  • most effective
  • given w. peripheral dopa-decarboxylase inhibitor - prevents peripheral conversion

DOPAMINE AGONISTS - ropinirole, pramipexole
- Delay starting L-DOPA
- SE: drowsiness, nausea, hallucinations, compulsive behaviour
AMANTADINE (weak DA) - used for drug-induced dyskinesia in late PD

ANTICHOLINGERICS - Benzhexol, orphenadrine

  • Help tremor but cause confusion in elderly
  • SE: dry mouth, confusion, anxiety, dizziness, urinary retention, decrease vision + memory, hallucinations

MAOB INHIBITORS - rasagiline, selegiline

  • Alt to DA-agonist given in early PD
  • SE: postural hypotension + AF

COMP INHIBITORS - entacapone + tolcapone
- Lessen ‘off’ time in those w. end-of-dose wearing off

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9
Q

What is on and off time

A
Off = bradykinesia + tremor +/- rigidity 
On = (more) normal movements
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