parkinsons Flashcards

1
Q

what is parkinson’s disease

A

a progressive neurodegenerative disease which leads to the death of dopaminergic cells in substantia nigra part of the brain

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2
Q

describe the motor symptoms of parkinson’s disease

A
  • hypokinesia (decreased muscle movement)
  • bradykinesia (slow movement)
  • rigidity
  • rest tremor
  • postural instability
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3
Q

describe the non-motor symptoms of parkinson’s disease

A
  • dementia
  • depression
  • sleep disturbances
  • bladder and bowel dysfunction
  • speech and language changes
  • swallowing problems and weight loss
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4
Q

TRUE OR FALSE

patients with parkinson’s disease should inform the DVLA and car insurer when they are diagnosed

A

TRUE

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5
Q

what is the aim of parkinson’s disease treatment

A

to control symptoms and improve quality of life (it is incurable)

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6
Q

what non-drug treatment can be offered to patients with parkinson’s disease

A
  • physiotherapy if balance or motor function problems are present
  • speech and language therapy if they develop communication
  • swallowing or saliva problems, occupational therapy if they experience difficulties with their daily activities.
  • Dietitian referral should be considered.
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7
Q

what is the first line treatment for the motor symptoms of parkinson’s disease

A
  • if motor symptoms decrease quality of life: levodopa combined with carbidopa (co-careldopa) or benserazide (co-beneldopa)
  • if motor symptoms DO NOT affect quality of life: choice of levodopa, non-ergot-derived dopamine-receptor agonists (pramipexole, ropinirole or rotigotine) or monoamine-oxidase-B inhibitors (rasagiline or selegiline hydrochloride)
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8
Q

name some of the adverse reactions from antiparkinsonian drugs

A
  • psychotic symptoms
  • excessive sleepiness and sudden onset of sleep with dopamine-receptor agonists
  • impulse control disorders with all dopaminergic therapy (especially dopamine-receptor agonists)
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9
Q

why may the use of the levodopa in parkinson’s disease be associated with motor complications

A

motor complications= fluctuations and dyskinesias (involuntary muscle movements)

  • the patient may have a large variation in their motor performance due to “on” and “off” periods whilst taking levodopa. “on” period= normal motor function, “off” period= weakness + restricted mobility.
  • the patient’s motor skills may also deteriorate near the end of their dose known as “end-of-dose” deterioration. modified release preparations help to reduce this and nocturnal immobility
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10
Q

compare the advantages + disadvantages of levodopa vs non-ergot dopamine-receptor agonists (pramipexole, ropinirole or rotigotine)

A

advantages levodopa:
- provides more noticeable improvement in motor skills

disadvantage of levodopa:
- causes motor complication (fluctuations in motor ability during “on” and “off” period)

advantages of non-ergot dopamine-receptor agonists (pramipexole, ropinirole or rotigotine):
- motor complications are less likely to occur when used alone long-term

disadvantages of non-ergot dopamine-receptor agonists (pramipexole, ropinirole or rotigotine):
- excessive sleepiness, hallucinations, and impulse control disorders are more likely to occur with dopamine-receptor agonists than with levodopa

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11
Q

what do you do if a patient with Parkinson’s disease develops dyskinesia or motor fluctuations, despite being on optimal treatment with levodopa

A

add on another drug. choice of:

  • non-ergotic dopamine-receptor agonists (pramipexole, ropinirole, rotigotine)
  • monoamine oxidase B inhibitors (rasagiline or selegiline hydrochloride)
  • COMT inhibitors (entacapone or tolcapone)
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12
Q

what is the only time you would use ergot dopamine-receptor agonists

name some examples of them

A

ergot-derived dopamine-receptor agonist should only be considered as an adjunct to levodopa if symptoms are not adequately controlled with a non-ergot-derived dopamine-receptor agonist.

examples of ergot-derived dopamine-receptor agonist:
bromocriptine, cabergoline or pergolide

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13
Q

how do you manage Daytime sleepiness and sudden onset of sleep in parkinson’s disease

A
  • adjust parkinson’s drug under specialist treatment. If reversible pharmacological and physical causes have been excluded, modafinil should be considered
  • note review this every 12 months*
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14
Q

how do you manage Nocturnal akinesia in parkinson’s disease

A

nocturnal akinesia = difficulty turning in bed + getting up to pass urine

  • levodopa or oral dopamine-receptor agonists should be considered as first-line options
  • rotigotine as second-line (if both levodopa or oral dopamine-receptor agonists are ineffective).
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15
Q

how do you manage Postural hypotension in parkinson’s disease

A
  • review drug treatment to check if there’s a pharmacological cause. if you need drug therapy:
  • midodrine hydrochloride should be considered as the first option
  • fludrocortisone acetate [unlicensed indication] as an alternative
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16
Q

how do you manage psychotic symptoms of parkinson’s

A

if hallucinations + delusions are well tolerated, do not treat. otherwise:

  • reduce dose of drug that may be causing hallucinations + delusions (specialist advice)
  • patients with no cognitive impairment, quetiapine [unlicensed indication] can be considered to treat hallucinations and delusions. clozapine as an alternative if not tolerated
17
Q

which symptoms of parkinson’s disease can some antipsychotics worsen

A
  • can worsen motor symptoms

antipsychotic medicines (such as phenothiazines and butyrophenones)

18
Q

how to manage Rapid eye movement sleep behaviour disorder in parkinson’s disease

A

first address any pharmacological causes then

  • Clonazepam [unlicensed indication] or melatonin [unlicensed indication]
19
Q

how do you manage Drooling of saliva in parkinson’s disease

A
  • first try speech and language therapy. if ineffective or not available, then:
  • Glycopyrronium bromide [unlicensed indication] should be considered as first-line treatment and botulinum toxin type A as second-line
20
Q

how do you manage Parkinson’s disease dementia

A

in mild/moderate/severe dementia:

  • offer a acetylcholinesterase inhibitor (donepezil, rivastigmine and galantamine)
21
Q

how do you treat advanced parkinson’s disease

what is the MHRA recommendation for this

A
  • Apomorphine hydrochloride as intermittent injections or continuous subcutaneous infusions. Add Domperidone whilst taking this to reduce nausea + vomiting associated with taking Apomorphine

MHRA recommendation:

  • assessment of cardiac risk factors and ECG monitoring because risk of serious arrhythmia due to QT prolongation when taking domperidone + apomorphine hydrochloride
  • do not use Domperidone in those weighing less than 35 kg

note advanced parkinson’s disease is when symptoms become more complex + antiparkinsonian drugs become less effective

22
Q

how do you manage Impulse control disorders in patients with parkinson’s disease

name some examples of Impulse control disorders

A
  • inform patients about the different types of impulse control disorders so they know what to look out for
  • dopamine-receptor agonist therapy may be reduced or stopped if problematic impulse control disorders develop. This would be done gradually

examples of Impulse control disorders:

  • compulsive gambling
  • hypersexuality
  • binge eating
  • obsessive shopping
23
Q

how do COMT inhibitors help to manage parkinson’s disease

name a few examples

A

They are a new class of antiparkinsons medication.

work by inhibiting the enzyme catechol-o-methyl-transferase (COMT), they prevent peripheral degradation of levodopa, allowing a higher concentration to cross the blood-brain barrier

examples:
Comtan® (entacapone)
Tasmar® (tolcapone)
Ongentys® (opicapone)