Module 4.3.2 (Management of Parkinsons) Flashcards

1
Q

What are the principles of treatment?

ps: You must have bradykinesia plus either tremor or rigidity for a Parkinson’s diagnosis to be considered.

A
  • Maintain function as long as possible with minimum medication
  • Individualise therapy according to disease stage and main symptoms
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2
Q

What examples DDI and COMT inhibitors that are used with levodopa for therapy of PD?

A

DDI: carbidopa and benserazide

COMT-I: entecapone

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3
Q

Examples of ergot and non-ergot dopamine agonists?

A

Ergot: bromocriptine, cabergoline

Non-ergot: pramipexole, rotigotine (patch), apomorphine (inje)

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4
Q

Examples of MAO-B inhibitors?

A
  • Selegiline, rasagiline, safinamide
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5
Q

What is preferred 1st line therapy for parkinsons? What is it given with?

A

Levodopa

  • Always with DDI (>75 mg benserazide or carbidopa daily)
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6
Q

Why is levodopa/DDI 1st line therapy? What is the AE?

A

Greatest benefit with the least adverse effects

  • especially in elderly and cognitive decline

> improves bradykinesia (slowness of movement) and rigidity, reduces mortality; less effective for tremor

> ADRs: orthostatic hypotension, neuropsychiatric effects, hallucinations and confusion, impulse control disorders, dopamine dysregulation syndrome (compulsive overuse)

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7
Q

Long term levodopa syndrome develops within 5 years of starting LD, what are the two major complications of this? Who is more likely to occur in?

A

1. Motor fluctuations

> Wearing OFF, delayed ON and ON-OFF swings

2. Drug-induced chorea/dyskinesias

> involuntary erratic, writhing motions usually affecting face, arms, legs or trunk

Especially in patients with earlier onset PD, more severe disease, higher LD dose, longer duration of disease

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8
Q

What happens with increased duration with levodopa therapy?

A

TI window narrows

  • Spend more time ‘off’ and experiencing dyskinesias than their ‘on’ state
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9
Q

Describe the “Wearing OFF” stage of LD. How to manage?

A
  • End of dose failure = earliest and most common motor complication
  • Re-emergence of sx before next LD dose is due

> related to the progressive loss of neuronal storage capacity and short half life of LD

  • first sign = early morning tremor and immobillity = improves afterr 1st morning dose

Management

  • Smaller, more frequent doses (upto 5-6) doses per day
  • Add a dopamine agonist (or switch)
  • Use CR product –> bedtime dose at first, then during the day
  • Take on an empty stomach, reduce protein intake
  • Add a COMT inhibitor
  • Add rasgiline or selegiline
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10
Q

When does ON-OFF swings occur when using LD? How to amnage?

A
  • Occur in advanced PD, after extended therapy with LD
  • Rapid and sudden motor fluctuations unrelated to timing of last LD dose

> exact emchanism unclear; therapeutic challenge

Management

  • DBS (deep brain stimulation)

Continuous dopaminergic therapy –> continous infusion + boluses

> SC apomorphine

> Duodenal levopdopa continuous infusions

  • LD/CD gel given via percutaneous endoscopic gastronomy (PEG) tube into duodenum or jejunum
  • Reduces the fluctuations in concentrations due to erratic or delayed gastric emptying
  • Used only for uncontrolled advance disease with severe motor fluctuations, very expensive :(
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11
Q

What is meant by ‘freezing’ in PD? How to manage?

… issa motor complication

A
  • Sudden freezing of gait
  • Feet are stuck, difficulty initiating steps or turning
  • Exacerabted by stress or when obstacles are encountered
  • Symptom of disease or drug-related event

Management

  • Increase dopaminergic needs
  • Physiotherapy
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12
Q

What are dyskinesias/peak dose dyskinesias? How to manage?

…issa motor complication

A

Inability to control muscles giving rise to uncoordinated flailing of the arms or legs, or chorea, rapid repetitive movment of the limbs, face, tongue, mouth and neck

> not painful but very distressing

Management

  • Decrease LD dose (even though may worsen PD)
  • Smaller and more frequent LD doses
  • Add amantadine
  • Add dopamine agonists or increase dose
  • Switch dopamine agonists
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13
Q

How to treat advanced PD?

A

Combination therapy often required

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14
Q

What are examples of dopamine agonists used to treat advanced PD? Are they used on its own?

A

Rarely use as 1st line monotherapy (rotigotine (patch) for NBM patient, pramipexole for once-daily dosing); otherwise add on.

  • Pramipexole (preferred oral agent)
  • Rotigotine (transdermal patch)
  • Apomorphine SC injection prn or continuous infusion

> rescue medication for severe fluctuations refractory to conventional therapy

> effective within 5-10 minutes

> requires admission to specialised clinic or hosptial for intiation of therapy

> VERY emotgenic –> domeperidone required

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15
Q

AE of dopamine agonists? Which patients to avoid in? What to warn patients about?

> AE of dopamine agonists are 15% worse than levodopa

A

hallucinations and confusion common, impulse control disorder (ICD), sudden sleep onset, dopamine dysregulation syndrome

  • ICD: problem gambling, hypersexuality, overspending, binge eating, inappropriate internet use, punding

> avoid in patients with history of ICDs or similar, warn patients and carers, monitor behaviour

> If ICD develop, stop DA, taper gradually to avoid withdrawal syndrome

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16
Q

What COMT inhibitor is used to treat advanced PD? What is it given with? AE?

A

Entacapone with each LD dose

Take with each LD dose to prolong clinical response

  • reduce LD dose by 10-30%

AE

  • Worsens dopaminergic ADRs; also bright yellow/organge urine, increased LFTs

> taper slowly due to NMS-like withdrawal syndrome

NMS: high fever, irregular pulse, accelerated heartbeat (tachycardia), increased rate of respiration (tachypnea), muscle rigidity, altered mental status

17
Q

What MAO-B inhibitors are used to treat advanced PD? Advantage of using them? What are they used with? AE?

A

Adjunct to LD –> increase efficacy by 20% –> reduce “off” time

> may increase dopaminergic ADRs/dyskinesias

  • Rasagiline
  • Selegiline
  • Safinamide

AE​

  • Insomnia, neuro-psychiatric ADRs common
  • Associated with serotonin toxicity; C/I with serotonergic agents
  • Tyramine reaction rare; follow dietary restrictions if taken with moclobemide
18
Q

What is amantadine used with to treat advanced PD? When does it effectiveness reduce? What CNS side effects?

A

Adjunct therapy; useful for controlling LD-induced dyskinesias

> effectiveness drops off after 3 to 6 months

CNS side effects

  • nervousness, depression, nightmares, hallucinations, insomnia, dizziness; also livedo reticularis

> mottled discolouration of the skin

19
Q

Why may anticholinergics be used to treat advanced PD? What are examples of this? Why poorly tolerated?

A

Effective against tremor, may reduce sialorrhoea (hypersalivation)

  • Benzatropine
  • Biperiden
  • Trihexyphenidyl (benzhexol)

> poorly tolerated: blurred vision, cognitive impairment, constipation, dry mouth, urinary retention

  • avoid in eldely, cognitive impairemtn
20
Q

What drugs may worsen PD?

A
  • Antipsychotics (esp typical antipsychotics)
  • Dopamine antagnoist antiemetics (droperidol, metoclopramide, prochlorperazine)
  • Methyldopa
21
Q

What drugs not to use with MAO-B (+DDI) for PD?

A
  • Non selective MAOIs (phenelzine, tranylcypromine)
  • Moclobemide
  • Serotonergic drugs
22
Q

What are some non-pharmacological therapies in PD?

A

CAMs

  • No evidence, vitamin E/vitamin C, CoQ10 that signficantly delay PD progression

Multidisciplinary approach

  • Physiotherapy, speech therapy, occupational therapty, dietetics
  • Physical therapies (active music therapy, treadmill training, balance training) can improve function

Surgery (deep brain stimulation)

  • high frequency DBS with an inserted electrode
  • Must succeful in patients with motor fluctuations and dyskinesias
  • does not alloviated cognitive deficits, NMS (non-motor symptoms) and some motor effects

> C/I in major psychatric/medical illness, cognitive impairment, PPM, levodopa-resistant parkinsonism, +/- advanced age

23
Q

How to manage the following non-motor smyptoms (NMS) in PD (lifestlye advice and also medications used):

A) orthostatic hypotension (20 mmHg fall in SBP, 10mmg Hg in DBP; risk of falls, injuries)

B) constipation

C) sleep problems

D) psychosis

E) depression and anxiety

F) dementia

A

A)

  • review medications (antiparkinsond drug, antiHTN drugs)
  • avoid heat, alcohol, large meals, straining, standing up rapdily
  • increase sodium and water intake
  • smaller, more frequent meals
  • exercise in horizontal position (swimming)
  • compression sotckings
  • sleep with head of the bed raised

drug treatment:

> fludrocortisone 0.1 mg daily, increasing to 0.2 mg daily if needed

> alternatives: pyridostigimine, midodrine, ephedrine, octreotide

B)

  • Increse fluids, dietary fibre
  • remove anticholinergics
  • osmotic laxatives –> PEG, macrogol

C)

  • insomnia, RLS, hypersomnia
  • Parasomnia (REM sleep behaviour disorders) –> clonazepam 0.25mg nocte (monitor for decline in cognition and symptom control)
  • sleep hygiene

D)

  • common in PD, eldely have cognitive disturbance and anticholinergic drugs wihich worsen cogntive function
  • often drug induced –> reduce LD dose, simplify regimen

> withdrawl anticholinergics and DAs

Antipsychotic therapy (low dose second gen antipsychotics)

  • clozapine most effective but difficult to use, needs regular blood monitoring
  • quetiapine useful and often used empirically
  • avoid other second gen and first gen antispychotics

E)

  • Treat with standard pharmacotherapy
  • Common and often undertreated

F)

  • 2-6x increased risk with PD –> increases with time
  • cholinesterase inhibitors have mild-mod benefit

> donepezil, rivastigmine –> fewer ADRs –> can exacerbate motor symptoms in PD e.g. tremor

> Trial for 2-3 months; taper slowly if no benefit

check if patient on anticholinergic as it worsens cognitive function