Parkinson’s Disease (2) Flashcards

1
Q

What is it the most common type of?
→ What is this characterised by?

What is its pathophysiology?

A

➊ Parkinsonian Syndrome
→ Bradykinesia + 1 of rigidity, tremor or postural instability

➋ Loss of dopaminergic neurons in substantia nigra

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2
Q

What are the motor symptoms it presents with?

What are the features of a Parkinsonian gait?

What are the non-motor symptoms most present with?
→ What does very prominent autonomic dysfunction point towards?

A

Parkinsonian Triad:
Bradykinesia - Actions slow and decrease in amplitude with repetition, e.g. parkinsonian gait, blink rate, micrographia, hypomimia
Resting tremor - often ‘pill-rolling’ of thumb over fingers
Rigidity

➋ Shuffling, forward tilt, stooped posture with reduced arm swing and asymmetric tremor – There is also, festination (tendency to pick up speed)

➌ • Autonomic dysfunction – constipation, postural hypotension, sweating, impotence, nausea, sexual dysfunction
REMS disorder
Loss of smell
• Cognitive impairment – affects most in the end
• Psychiatric features – depression, anxiety, hallucinations
MSA

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3
Q

How does a Parkinson’s tremor differ from a Benign Essential tremor?

A

Parkinson’s tremor:
Asymmetrical
Present at rest
• Goes with intention
• Other PD features
• No change with alcohol

Benign Essential Tremor:
Symmetrical
Not present at rest
Postural - Worse with intention
• No other PD features
• Improves with alcohol

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4
Q

How is it investigated?

A

DAT scan

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5
Q

Management:
What will these pts have with medication?
→ Why is this important to take into account?

What is the best drug for it?
→ What is the main SE? When does it occur?

What are other drug options?

What will occur as the disease progresses?

A

➊ On and off periods, which become more common as the drug decreases in efficacy over time
→ So you know when to start pharmacological management – May be better to start late (e.g. when 70+) or when PD seriously interferes with life

Levodopa - Best drug for symptoms but becomes less effective over time, therefore is often kept for when other options are no longer effective
Dyskinesia, which occurs when the dose is too high – Dystonia, Chorea, Athetosis (writhing movements)

➌ DA, COMT-I, MAOB-I, NMDA R Antagonists

➍ • End-of-dose effects – Motor activity declines as the previous dose wears off
On-off phenomena – Random fluctuations in drug effect

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6
Q

Parkinson-plus Syndromes:
What are the different types? How does each present?

A

• Progressive Supranuclear Palsy (PSP) – Parkinsonism and Vertical gaze palsy, rigidity of trunk >limbs; symmetrical onset, bulbar symptoms, little tremor
• Multiple System Atrophy – Degeneration of neurones of multiple systems in brain, affecting basal ganglia – Parkinsonism and early autonomic dysfunction (postural hypotension, constipation, sexual dysfunction)
• Lewy Body Dementia – Cognitive impairment and visual hallucinations before Parkinsonism
• Corticobasal Degeneration – Parkinsonism and spontaneous activity or akinetic rigidity of a limb

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