Parkinson's Disease Flashcards

1
Q

What is the aetiology of PD?

A

Unknown

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2
Q

Outline the pathophysiology of PD

A

Chronic, progressive movement disorder

Triad of bradykinesia, tremor and rigidity

Degeneration of substantia nigra = deficiency of dopamine

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3
Q

What are the symptoms and signs of PD?

A

Tremor = resting

Bradykinesia - shuffling gait, falls

Hypertonia = rigidity (lead-pipe, sometimes cog-wheel)

Hypophonia

Reduced facial expression

Micrographia (small cramped handwriting)

Dementia (can see lewy-body before PD)

Depression

Falls

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4
Q

How should PD be investigated?

A

Hx - timeline, lifestyle, previous head injury, DH (antiepileptics, antipsychotics)

Neurological exam - tone, power, gait, handwriting

Bloods = Hb, TFT (hypo), U+Es, LFTs, B12/folate

MSU = rule out infection

Imaging = CT, MRI, PET

DAT scan = used to diff PD from central tremor

Carbidopa-levodopa test - do symptoms improve

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5
Q

How is PD managed?

A

LIFESTYLE = aerobic exercise

CARBIDOPA-LEVODOPA

  • SE = nausea, orthostatic hypo (no B-blockers)
  • Short half life = take every few hours
  • Don’t suddenly stop = neuroleptic malignant syndrome (fever, marked rigidity, altered consciousness, leucocytosis, high CK)
  • End up stop working (converted in dopaminergic neurons, eventual loss of pre-synaptic - give dopamine agonist ropinirole (SE impulsivity))

MAO B inhibitors = prevent breakdown of dopamine by inhib monoamine oxidase B - rasagiline

COMT inhibitors (have to use with levodopa) = entacapone, tolcapone

DBS = electrodes in STN, generator in chest (need to be responding to levodopa but having severe SE)

SLEEP = melatonin

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6
Q

What are the possible complications of PD?

A

Dementia

Depression

Swallowing difficulties

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7
Q

How is PD clinically diagnosed?

A

Clinical diagnosis

Bradykinesia + at least ONE of the following

  • Muscular rigidity = typically lead pipe (can be cog wheel - when tremor present)
  • 4 – 6 Hz rest tremor = pill rolling
  • Postural instability not caused by primary visual, vestibular, cerebellar, or proprioceptive ◦ dysfunction
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8
Q

What are the features of supportive criteria for a PD Dx?

A

Unilateral

Rest tremor present

Progressive

Persistent asymmetry

Excellent response (70 – 100%) to LD

Severe LD-induced chorea

LD response for ≥5 years

Clinical course of ≥10 years

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9
Q

What are the non-motor symptoms of PD?

A
Neuropsychiatric dysfunction
◦ Mood Disorders
◦ Apathy + anhedonia
◦ Frontal executive dysfunction
◦ Dementia + Psychosis
Sleep Disorders
◦ Sleep fragmentation + insomnia 
◦ RBD 
◦ PLMS / RLS
◦ Excessive daytime somnolence

Autonomic dysfunction
◦ Orthostatic hypotension
◦ Urogenital dysfunction
◦ Constipation

Sensory symptoms + pain
◦ Olfactory dysfunction
◦ Abnormal sensations
◦ Pain

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10
Q

What is a DAT scan?

A

Focus on the activity of the dopamine transporter

Loflupane I123 injection

Used with single-photon emission computed tomography (SPECT)

Detecting dopamine transporters (DaT) in suspected parkinsonian syndromes

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11
Q

What is deep brain stimulation?

A

Deep brain stimulation involves the implantation of a wire, with 4 electrodes at its tip, into one of 3 target sites in the brain:

  • the thalamus (this procedure is known as thalamic stimulation)
  • the globus pallidus (this procedure is pallidal stimulation)
  • the subthalamic nucleus (this procedure is subthalamic stimulation)
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12
Q

Outline Hoehn and Yahr scale

A
  • STAGE 1 = Unilateral disease
  • STAGE 2 = Bilateral disease, without impairment of balance
  • STAGE 3 = Mild to moderate bilateral disease; some postural instability; physically independent
  • STAGE 4 = Severe disability; still able to walk or stand unassisted
  • STAGE 5 = Wheelchair bound or bedridden unless aided
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13
Q

Outline UPDRS

A

Unified Parkinsons Disease Rating Scale

42 question assessment
• 1 = mentation, behaviour, mood
• 2 = ADL
• 3 = motor sections
• 4 = modified Hoehn and Yahr scale
• 5 = Schwab and england ADL scale
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14
Q

What is an essential tremor?

A

Progressive tremor of the upper extremities and head, present in posture and action, without other neurological signs or symptoms

Mainly symmetrical, rhythmic, involuntary oscillation movement disorder of the hands and forearms (69% of patients) that is usually absent at rest and present during posture and intentional movements

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