parkinsons Flashcards

(67 cards)

1
Q

what is parkinsons

A

parkinsons is a neurodegenerative disease that affects the dopamine production in the brain

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2
Q

what part of the brain is affected by parkinsons disease

A

substania nigra

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3
Q

what build up leads to a decreased production of dopamine

A

lewy bodies

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4
Q

what is the acronym given to the motor symptoms of parkinson

A

TRAP

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5
Q

what does trap relate to and stand for

A

trap relates to the motor symptoms in parkinsons

t = tremor
r = rigidity
a = akinesia
p = postural instability

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6
Q

what are the four different types of non motor symptoms a patient with parkinsons may experience

A

psychiatric
sleep disturbance
pain
autonomic disturbance

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7
Q

what are some psychiatric symptoms a patient with parkins may present with

A

depressed
anxious
angry

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8
Q

what are the different autonomic disturbances that a patient with parkinsons may experience

A

constipation
urinary dysfunction
sexual dysfunction

weightloss
polyphagia

sweating
salivation

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9
Q

what are the different treatment options for a patient with parkinson

A

physiotherapy / exercise

occupational therapy

speech and language therapy

nutritional advice

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10
Q

What is the main aim of pharmacological treatment

A

increase the levels of dopamine inside the substantia nigra

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11
Q

what are the different medications that are used in the management of parkinsons

A

dopadecarboxylase inhibitors
comt inhibitors
Maob inhibitors

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12
Q

what is the first line treatment in parkinsons

A

levodopa

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13
Q

if a patient has motor symptoms affecting quality of life what do we give instead of levodopa

A

levodopa and carbidopa /benseramide

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14
Q

what is dyskinesia

A

Dyskinesias are involuntary, erratic, writhing movements of the face, arms, legs or trunk. They are often fluid and dance-like.

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15
Q

when it comes to learning this subject what is the main bulk of the content

A

drugs

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16
Q

what is levodopa a precursor to

A

dopamine

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17
Q

what is levodopa converted to dopamine by

A

decarboxylation

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18
Q

why is levodopa given with dopa-decarboxylaze inhibitors

A

levodopa when given on its own is broken down before it can cross the blood brain barrier

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19
Q

what are two examples of dopa-decarboxylaze inhibitors

A

carbidopa
benserazide

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20
Q

what is sinemet made up of

A

levodopa and carbidopa

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21
Q

what is madopar made up of

A

levodopa and benserazide

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22
Q

when treating parkinsons with levodopa what period of treatment is most effective and why

A

first few years but as time goes on the effect of levodopa drops

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23
Q

why is levodopa taken before food

A

levodopa is taken one to two hours before food as it can inhibit its absorption

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24
Q

what are the main side effects experienced with levodopa

A

GI
Discolouration of urine
Drowsy
Postural hypotension

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25
What is the "on off effect"
Patients experience significant improvement in their motor control but when off there is significant akinesia
26
what are the main interactions with levodopa
MOAB inhibitors = ^ chance of hypertensive crisis Antihypertensives = ^ chance of postural hypotension pyroxidine = ^ peripheral breakdown of levodopa
27
If a patient is taking levodopa and carbidopa and is switching to another how long do they need to wait
12 hours
28
if a patient is currently taking immediate release co-careldopa and is swapping to prolonged release how much do we need to increase the dosing interval
50%
29
what is duodopa
intestinal gel
30
when is duodopa used
extreme parkinsons but that is still responsive to levodopa
31
if a patient is taking madopar modified release and is swapping to the dispersible how long do we redduce the dose by
30%
32
when should we avoid madopar
liver impairment
33
Give two examples of non ergotic dopamine agonists
ropinrole pramipexole
34
what is noteable about pramipexole in over 65
longer half life 8 -> 12
35
whaat does ropinrole and pramipexole have an affinity for
d2 + d3 receptors
36
what are three ergotic dopamine agonists
bromocriptine cabergoline pergolide
37
what is bromocriptines selectivity
partil d1 agonist partial d2 agonist
38
what do we need to moniotor for bromocriptine
pituitary enlargement visiot
39
what dopamine agonist needs to be avoided in pregnatn and postpartem women with hypertensive disorders
bromocriptine
40
what are the common side effects associated with dopamine agonists
gi drowsy diskensia neuropsychiatric symptoms hypotension
41
When is apomorphine used
as a last line and is given sc
42
what is the most common side effect of apomorphine
nausea and vommiting
43
name 3 anti-emetics
domperidone metocloprimide cyclizine
44
what is the most common anti-emetic that is given with apomorphine
domperidone
45
does apomorphine have a long or short duration of acction
short
46
what are some other side effects of apomorphine
hallucination dyskinesia abnormal behaviour
47
what is the mechanism of action of MAO-B inhibitors
MAO-b breaks down dopaamine and the inhibitors prevent this
48
what are the two mao-b inhibitors to be aware of
rasagiline selegine
49
what is the dosing requirements for maob inhibitors
once daily in the morning
50
when are mao-b inhibitors most effective
early pd as there is less build up of lewy bodies
51
what are the cautions for mao-b inhibitors
psychosis hypertension arrythmias
52
what should we avoid mao-b inhibitors
gastric ulcers postural hypertension anti-depressants linezolid
53
what sort of foods do we need to avoid in rasagaline
aged foods e.g. wine and cheese there is an increased risk of hypotensive crisis
54
why do we avoid linezolid and mao-b inhibitors
serotonin syndrome
55
why do we avoid opioids with mao-b inhibitors
serotonin syndrome
56
what are comt inhibitors used in conjunction with
levodopa
57
name two comt inhibitors
tolcapone entacapone
58
how do comt inhibitors work
prevent the peripheral breakdown of levodopa before it crosses the blood brain barrier
59
if initiated how long do we need to wait to see if we should continue with a comt inhibitor
if improvement after 3 weeks
60
what special requirements to do with dosing marks comt inhibitors as different compared to other medications used to treat parkinsons
can be taken WITH or WITHOUT FOOD
61
what do comt inhibitors bind to
plasma proteins
62
what are comt inhibitors metabolised byq
liver
63
what is a common side effect of comt inhibitors
brown / disccoloured urine
64
what are the common side effects of the comt inhibitors
gi sleep disorders drowsy hallucinations
65
with tolcapone what monitoring is required
LFTs every 2 weeks for first year > 4 weeks for 6 months > 8 weeks thereafter
66
what important risk do we need to identify with tolcapone
HIGH CHANCE OF HEPATOTOXICITY
67