Parkinson's Flashcards

1
Q

what are the pathological changes seen with Parkinson’s?

A

degeneration of dopamine neurones within the substantia nigra
accumulation of Lewy bodies (initially substantia nigra then widespread)

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2
Q

is Parkinson’s symmetrical or asymmetrical?

A

asymmetrical onset - initially affected side will always be worse
red flag -> absence of asymmetry

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3
Q

what are the main motor symptoms in Parkinson’s?

A

tremor
rigidity
bradykinesia

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4
Q

what are the main non motor symptoms in Parkinson’s?

A

REM sleep disorders
autonomic - constipation, urinary urgency, frequency
depression, dementia, personality changes

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5
Q

how is Parkinson’s diagnosed?

A

clinically

if there is any uncertainty SPECT scan can be done

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6
Q

what is the gold standard treatment for Parkinson’s?

A

levodopa and carbidopa
(dopamine precursor and peripheral antagonist to prevent breakdown)
- taken same time everyday

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7
Q

what are the side effects of levodopa?

A

nausea and vomiting
dyskinesia/dystonia (involuntary writhing movements)
‘off states’
psychosis, hallucinations, reduced impulse control

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8
Q

what are the names of some dopamine agonists?

A

roprinirole
pramipexole
apomorphine

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9
Q

what is the name of a COMT inhibitors?

A

entacapone

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10
Q

what are the names of some MOAB inhibitors?

A

selegeline

rasagiline

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11
Q

what is apomorphine used for in Parkinson’s?

A

rescue for sudden off states

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12
Q

what is one of the most common side effects of the medication for Parkinson’s? what is used to treat it?

A

nausea
-> domperidone
selective to peripheral dopamine so won’t affect activity of levodopa in brain

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13
Q

what is Parkinsonism? how is it different to PD?

A

associated symptoms but defined underlying cause

absence of asymmetry, fast progression, sensory disturbance and pyramidal signs

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14
Q

what is progressive supranuclear palsy?

A

vertical gaze palsy
lack of tremor
early insatiability and falls
speech and swallowing problems

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15
Q

what is seen on MRI in progressive supranuclear palsy?

A

Mickey Mouse sign

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16
Q

what is multi-system atrophy?

A

pyramidal signs
jerky, postural tremor
ataxia and cerebellar signs
early autonomic disturbance - postural hypotension, bladder dysfunction

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17
Q

what is seen on MRI of multi-system atrophy?

A

hot cross bun sign

cerebellar and pontine atrophy

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18
Q

how is vascular Parkinson’s differentiated from PD?

A

caused by multiple small infarcts
mainly gain disturbance
poor levodopa response

19
Q

how is dementia with lewy bodies differentiated from PD?

A

cognitive decline with visual hallucinations

- cognitive decline before Parkinson symptoms

20
Q

what drugs can cause drug induced Parkinson’s?

A

anti-psychotics
amiodarone
metaclopramide

21
Q

what is Wilson’s disease?

A

hepatic and renal failure
behavioural changes and cognitive decline
- keyser fisher rings in the eyes

22
Q

what is a resting tremor?

A

a tremor that occurs when muscles are relaxed

23
Q

what is a postural tremor?

A

tremor that is absent at rest and worse when maintaining a posture
doesn’t get worse with movement

24
Q

what can cause a postural tremor?

A

anxiety
alcohol withdrawal
benign essentail tremor

25
Q

what is the genetic aspect of a benign essential tremor?

A

autosomal dominant condition

26
Q

what are the features of a benign essential tremor?

A

worse if arms outstretched
bilateral, fast, low amplitude tremor
symptoms improve with alcohol and rest

27
Q

what is the treatment for a benign essential tremor?

A

propanolol

28
Q

what is an intention tremor?

A

task orientated and made worse throughout the range of movement

29
Q

what can cause an intention tremor?

A

cerebellar disease (MS, stroke, haemorrhage)

30
Q

what is dystonia?

A

involuntary, sustained muscle spasms that result in abnormal posturing and repetitive movements in the context of an associated tremor

31
Q

what can cause drug induced dystonia?

A

levodopa
anti-psychotics
metoclopramide

32
Q

how does acute dystonia present?

A

torticollis (cervical neck)
trismus (jaw clenching)
oculogyric crisis (eyes drawn up)

33
Q

how do you treat dystonia?

A

anti-spasmodics -> baclofen
botox (focal dystonia)
anti-cholinergic -> procyclidine (acute dystonia)

34
Q

what is chorea?

A

non-rhythmic irregular purposeless movements that move from one body part to another

35
Q

what genetic condition is chorea seen in?

A

Huntington’s disease

36
Q

what is the genetic mutation seen in Huntington’s disease?

A

autosomal dominant

CAG expansion on chromosome 4

37
Q

what does it mean if Huntington’s shows acceleration?

A

gets worse as it is passed down through the generations

38
Q

what are the early symptoms seen in huntington’s disease?

A

clumsiness, chorea

irritability, agitation, depression

39
Q

what are the advanced symptoms seen in hungtington’s disease?

A

chorea, myoclonus, rigidity, fits
cognitive decline and dementia
loss of ability to speak of swallow
saccadic eye movements

40
Q

what is the management for Huntington’s disease?

A

supportive treatment

15 year life span after diagnosis

41
Q

what is syndemans chorea?

A

self-limiting chorea usually seen in children

develops after strep throat

42
Q

what is myoclonus?

A

sudden, involuntary focal or generalised muscle jerks

43
Q

what condition is myoclonus seen in? what is the triad of symptoms it presents as?

A

Creutzfeldt–Jakob disease

dementia, ataxia, myoclonus