parkinsons Flashcards

1
Q

causes of parkinsonism

A

idiopathic parkinsons, parkinsonian plus, degenerative, secondary- vascular, drugs, post encephalitic, genetic

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2
Q

what is it caused by

A

Lewy bodies and neuronal cell death in substantia nigra (loss of dopaminergic neurones)

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3
Q

key features

A

bradykinesia, tremor, rigidity UNILATERAL

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4
Q

other features

A

gait abnormalities, GOOD RESPONSE TO LEVODOPA, anosmia, postural hypotension, urinary urgency, constipation, micrographia

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5
Q

type of tremor

A

pill rolling. resting tremor.

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6
Q

what are the types of rigidity

A

lead pipe which is stiffness on passive movement and not velocity dependent. cogwheel rigidity is stiffness occuring with tremor

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7
Q

what diagnostic tool can be used

A

DaT scan- dopamine transporter imaging. assess extent of nigrostriatal loss can be used to distinguish PD from other causes of tremor but cant be used to distinguish between PD and other akinetic eg drug induced

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8
Q

treatment of PD

A

levodopa- combined with co beneldopa or carbidopa to reduce peripheral adverse effects. dopamine agonists- used in combination or monotherapy with younger patients with mild-mod

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9
Q

other drugs used in PD

A

sergiline, rasagiline- MAOB; amantadine; anticholinergics; apomorphine

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10
Q

what is entacapone

A

COMT- which can be added in

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11
Q

examples of dopamine agonists

A

cabergoline

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12
Q

what drugs can induce parkinsonism

A

typical and atypical antipsychotics, GI prokinetics eg metoclopramide

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13
Q

cognitive and psych changes in PD

A

cognitive impairment in late stage PD. may develop into dementia. visual hallucinations on treatment and psychosis. cholinesterase inhibitors may be helpful

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14
Q

symptoms of progressive supranuclear palsy (PSP)

A

Parkinsonism, postural instability with falls, vertical supranuclear gaze palsy, pseudobulbar palsy, dementia

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15
Q

what is seen deposited in PSP

A

tau protein

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16
Q

how can differentiate PSP from PD

A

not a good response to levodopa and symmetrical in onset

17
Q

what is different in Multiple system atrophy (MSA) from PD

A

autonomic symptoms eg bladder, bp; and ataxia in addition to Parkinsonism

18
Q

what is seen pathologically in MSA

A

alpha- synuclein positive glial cytoplasmic inclusions

19
Q

what is seen in corticobasilar degeneration

A

alien limb phenomenon (hand moves without person being aware or having any control over it), myoclonus, dementia

20
Q

what occurs with Parkinsonian plus syndromes

A

very progressive, only sometimes responds to levodopa, usually causes death within a decade

21
Q

red flag symptoms suggesting one of the Parkinsonian plus syndromes

A

symmetrical onset and absence of tremor; levodopa unresponsiveness, early falls (within the first year), additional neurological features

22
Q

what should be excluded in any patient

A

wilsons disease

23
Q

what is wilsons disease

A

copper deposition in the basal ganglia, cornea, liver, intellectual impairment, reversible neurological damage. check serum Cu and caeruloplasmin. treat with chelating agent penicillamine

24
Q

what are the symptoms of essential tremor

A

bilateral, fast, low amplitude, mainly in the upper limbs but can affect head and voice sometimes. usually starts early in life and is slowly progressive but rarely results in severe disability

25
Q

what is the tremor in ET

A

postural (eg when holding cutlery) or action, differentiating it from PD which is resting

26
Q

what treatments can be used in ET

A

often no treatment is necessary. B blocker (propranolol), primidone, gabapentin

27
Q

what treatment will make any tremor worse

A

sympathomimetics (salbutamol)