Parkinsons Disease Flashcards

1
Q

Why is levodopa used instead of dopamine to treat Parkinson’s disease?

A

Dopamine cannot cross the blood-brain barrier (BBB), so it cannot reach the brain to replenish dopamine levels.

Levodopa is a precursor to dopamine that can cross the BBB and be converted into dopamine in the brain.

To reduce peripheral side effects (e.g., nausea, vomiting), levodopa is combined with carbidopa, a DOPA decarboxylase inhibitor that prevents peripheral conversion of levodopa to dopamine.

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2
Q

How is Parkinson’s disease classified?

A

A neurodegenerative disorder caused by the progressive loss of dopaminergic neurons in the substantia nigra pars compacta, leading to motor and non-motor symptoms.

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3
Q

What are the core motor symptoms of Parkinson’s disease?

A

Bradykinesia – slowness of movement
Rigidity – resistance to passive limb movement
Resting tremor – occurs when limbs are at rest
Postural instability – impaired balance, leading to falls

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4
Q

What are some non-motor symptoms of Parkinson’s disease?

A

Depression, cognitive impairment, sleep disturbances, autonomic dysfunction (e.g., constipation, orthostatic hypotension).

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5
Q

How is Parkinson’s disease diagnosed?

A

Clinical diagnosis based on motor symptoms, with supportive criteria such as response to levodopa. No definitive lab test.

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6
Q

What imaging tests may help in uncertain cases?

A

DaTscan (dopamine transporter scan) – Shows reduced dopamine activity in the substantia nigra.
MRI/CT scan – Used to rule out other conditions (e.g., stroke, tumors).

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7
Q

What is the first-line treatment for Parkinson’s disease?

A

If motor symptoms affect quality of life → Levodopa + carbidopa (co-careldopa) or benserazide (co-beneldopa)

If motor symptoms do not affect quality of life → Choice of:
Levodopa
Non-ergot dopamine agonists (pramipexole, ropinirole, rotigotine)
MAO-B inhibitors (rasagiline, selegiline)Levodopa + Carbidopa (e.g., Sinemet) or Levodopa + Benserazide (e.g., Madopar)
Most effective for improving bradykinesia and rigidity, but long-term use can lead to motor complications.

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8
Q

non-drug treatments are available for Parkinson’s disease?

A

Physiotherapy for balance/motor issues
Speech therapy for communication/swallowing problems
Occupational therapy for daily activities
Dietitian referral if needed

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9
Q

What are treatment options for advanced Parkinson’s disease?

A

Apomorphine (subcutaneous injection or continuous infusion)
Domperidone (for nausea, ECG monitoring required)

Deep Brain Stimulation (if symptoms are uncontrolled on medication)

Intestinal levodopa gel or subcutaneous foslevodopa/foscarbidopa infusion (if apomorphine & DBS fail)

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10
Q

hat impulse control disorders can occur in Parkinson’s?

A

Compulsive behaviors: Gambling, hypersexuality, binge eating, shopping
More common with: Dopamine agonists

Management:
Reduce or stop dopamine agonists gradually
Monitor for withdrawal symptoms
Consider cognitive behavioral therapy (CBT)

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11
Q

second-line treatment options for Parkinson’s disease?

A

Dopamine agonists (e.g., pramipexole, ropinirole, bromocriptine) – Used in younger patients to delay levodopa use.
MAO-B inhibitors (e.g., selegiline, rasagiline) – Reduce dopamine breakdown.
COMT inhibitors (e.g., entacapone, tolcapone) – Extend the effect of levodopa.
Amantadine – Helps with dyskinesias (levodopa-induced involuntary movements).

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12
Q

adverse effects of levodopa?

A

Nausea, vomiting (due to peripheral dopamine activation)
Dyskinesias (involuntary movements, common with long-term use)
“On-Off” phenomenon (fluctuations in symptom control)
Postural hypotension

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