parkinson's Flashcards

(45 cards)

1
Q

what is parkinson’s

A

progressive idiodegeneration of the dopaminergic pathways in the substantia nigra

loss of dopaminergic neurones in the substantia nigra that leads to inadequate dopamine transmission.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

characteristic neuropathological finding

A

lewy body formation in affected neurones

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

gold standard for diagnosis for parkinsons

A

brain bank criteria

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

brain bank criteria for the diagnosis of Parkinson’s disease

A

step 1:
clinical syndrome involving bradykinesia (+rigidity important

plus at least one of

  • tremor - 4-6 Hz - corase, pill-rolling, disappears during voluntary movement, asymmetrical
  • rigidity
  • postural instability

step 2: exclude other potential conditions

step 3
PLUS 3 OR MORE

  • Unilateral onset
  • stooped posture
  • loss of arm seing
    • Rest tremor present
    • Progressive disorder
    • Persistent asymmetry affecting side of onset most
    • Excellent response (70-100%) to levodopa
    • Severe levodopa-induced chorea
    • Levodopa response for 5 years or more
    • Clinical course of ten years or more
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Other parkisonian features apart from the triad

A
  • Depression, anxiety, and fatigue.
  • Reduced sense of smell.
  • Cognitive impairment.
  • Sleep disturbance.
  • Constipation.
  • lack of facial expression
  • lsck of spontanrous movements
  • greasy skin - autonomic dysfunction
  • decreased blinking
    tibulation - nodding head involuntarily
  • dribbling of saliva
  • festinating gait
  • stooped posture
  • increased tone
  • impotence
  • sweating
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

what is lead pipe rigidity

A

constant resistance felt when a limb is passively flexed in the presence of increased tone without tremor,

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what is cogwheel rigidity

A

regular intermittent relaxation of tension felt when a limb is passively flexed in the presence of tremor and increased tone.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

what may be seen when examining a parkinson patient

A

reduced facial expression
slow
shuffling, festinating gait

pill rolling
‘pull test’ - tendency to fall back when pulled by examiner

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

other causes of parkinsonism

A

drug-induced parkinsonism

antipsychotics
antiemetics
- prochlorperazine
- metocloperamide

amiodarone
antidepressants - SSRIs

wilson’s
repeated head injury
cerbrovascular disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

other causes of tremor

A

1) essential tremor
- bilateral stress, caffeine, sleep deprivation

exaggerated psychological tremor

dystonic tremor

hyperthyroidism

drugs - B2 agonists

2) intention - cerbellar

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

name of scales used to assess progression of parkinson

A

Hoehn and Yahr

Unified Parkinson’s Disease Rating Scale

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

classification of Unified Parkinson’s Disease Rating Scale

A

Part 1: non-motor experiences of daily living
Part 2: motor experiences of daily living
Part 3: motor examination
Part 4: motor complications

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

drugs available for parkinson

SEs

A

levodopa - pass thru BBB - converts levodopa into dopamine

neuroepileptic malignant syndrome

monomine oxidase B inhibitors - dizzy, insomnia, orthostatic hypotension, joint pain

and COMT - coloured urine, diarrhoea, liver damage, impulsive and compulsive behaviours

stop breakdown of dopamine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

4 phases of parkinson

A
  1. Early stage - Soon after diagnosis, symptoms are mild and normal life possible
  2. Maintenance stage - Good response to treatment and no major disability
  3. Advanced stage - Poor response to drugs with motor side effects
  4. Palliative stage - Unable to live independently and in need of multidisciplinary support
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

clinical features of vascular pseudoparkinsonism

A
  • bilateral symmetrical rigidity;
  • bradykinesia, predominantly involving - lower limbs
  • postural instability; shuffling gait
  • falls;
  • dementia
  • corticospinal findings.
    resting tremor maybe absent
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

clinical features of benign essential tremor

A

Begin gradually, usually more prominently on one side of the body

Worsen with movement
Usually occur in the hands first, affecting one hand or both hands

Can include a “yes-yes” or “no-no” motion of the head

May be aggravated by emotional stress, fatigue, caffeine or temperature extremes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

dementia with lewy bodies

A

cognitive symptoms develop within the year whereas IPD is after a year

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

features of progressive supranuclear palsy

A

postural instability and falls
— patients tend to have a stiff, broad-based gait

impairment of vertical gaze (down gaze worse than up gaze - patients may complain of difficultly reading or descending stairs)

parkinsonism
— bradykinesia is prominent

cognitive impairment
— primarily frontal lobe dysfunction

pseudobulbar palsy

supranuclear opthalmoplegia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

progressive supranuclear palsy ?

A

brain cells in certain parts of the brain are damaged as a result of a build-up of a protein called tau

20
Q

features of multiple system atrophy

A

alpha synuclein build up

parkinsonism + autonomic disturbance

  • erectile dysfunction: often an early feature
  • postural hypotension
  • atonic bladder

POOR RESPONSE TO LEVODOPA

  • rapid progression
  • pronounced autonomic failure

cerebellar signs

autonomic NS affected

bladder problems
low BP

Problems with co-ordination, balance and speech
slow moving and feeling stiff

21
Q

types of multiple system atrophy

A

1) MSA-P - Predominant Parkinsonian features

2) MSA-C - Predominant Cerebellar features

22
Q

first line treatment for parkinson

A

if the motor symptoms are affecting the patient’s quality of life: levodopa

if the motor symptoms are not affecting the patient’s quality of life: dopamine agonist (non-ergot derived), levodopa or monoamine oxidase B (MAO‑B) inhibitor

23
Q

impulse control disorders more significant

features

A
  • dopamine agonist therapy
  • a history of previous impulsive behaviours
  • a history of alcohol consumption and/or smoking
24
Q

SEs of levodopa

A

dyskinesia (involuntary writhing movements), ‘on-off’ effect, dry mouth, anorexia, palpitations, postural hypotension, psychosis, drowsiness

25
what happens if you stop levodopa acutely
acute dystonia
26
examples of dopamine receptor agonists
bromocriptine, ropinirole, cabergoline, apomorphine
27
SEs fo dopamine receptor agonists
(bromocriptine, cabergoline) have been associated with pulmonary, retroperitoneal and cardiac fibrosis. impulse control disorders excessive daytime somnolence more likely to cause hallucinations comapred to levodopa nasal congestion postural hypotension
28
examples of monoamine oxidase B inhibitors
e.g. selegiline | inhibits the breakdown of dopamine secreted by the dopaminergic neurons
29
SEs of amantadine
ataxia, slurred speech, confusion, dizziness and livedo reticularis
30
COMT eg
entacapone, tolcapone | COMT is an enzyme involved in the breakdown of dopamine, and hence may be used as an adjunct to levodopa therapy
31
antimuscarinics?
block cholinergic receptors now used more to treat drug-induced parkinsonism rather than idiopathic Parkinson's disease help tremor and rigidity e.g. procyclidine, benzotropine, trihexyphenidyl (benzhexol)
32
DDx fro parkinson
vascular pseudoparkinsonism benign essential tremor parkinsonism + syndromes drugs antipsychotics toxins - CO, MPTP depression
33
What is meant by on/off fluctuations in patients who are taking levodopa preparations and why do they occur?
Unpredictable fluctuations in motor function due to “wearing off”.
34
causes of parkinsonism
``` Parkinson's disease drug-induced e.g. antipsychotics, metoclopramide* progressive supranuclear palsy multiple system atrophy Wilson's disease post-encephalitis dementia pugilistica (secondary to chronic head trauma e.g. boxing) toxins: carbon monoxide, MPTP ```
35
excessive daytime sleepness remedy
modafinil reviewed every 12 months cant drive infrom DVLA
36
orthostatic hypotension remedy
midodrine hydrochloride then fludrocortisone acetate
37
drooling of saliva
glycopyrronium bromide 2nd line botulinum toxin A
38
Managing motor Sx of parkinsons
offer levodopa w carbedopa or benserazide in early stages of parkinson's disease whose motor Sx impact their quality of life QOL not affected OFFER levodopa, non-ergot-derived dopamine-receptor agonists (pramipexole, ropinirole or rotigotine) or monoamine-oxidase-B inhibitors (rasagiline or selegiline hydrochloride). ADJUVANT THERAPY Patients who develop dyskinesia or motor fluctuations despite optimal levodopa therapy should be offered a choice of - non-ergotic dopamine-receptor agonists (pramipexole, ropinirole, rotigotine) - MAOI (rasagiline or selegiline hydrochloride) - COMT inhibitors (entacapone or tolcapone) as an adjunct to levodopa. ergot-derived dopamine-receptor agonist (bromocriptine, cabergoline or pergolide) should only be considered as an adjunct to levodopa if symptoms are not adequately controlled with a non-ergot-derived dopamine-receptor agonist. If dyskinesia is not adequately managed by modifying existing therapy, amantadine hydrochloride should be considered.
39
What info should be given when starting Mx for motor Sx
impulse control disorders esp w dopamine agonists excessive sleepiness sudden onset of sleep w dopamine agonists Psychotic Sx THESE 3 Sx more likely to be seen with dopamine receptor agonists Levodopa treatment is associated with motor complications, including response fluctuations and dyskinesias. Response fluctuations are characterised by large variations in motor performance, with normal function during the ‘on’ period, and weakness and restricted mobility during the ‘off’ period.
40
Long term problems of parkinsons
50-90% of people who have received L-dopa for 5-10 years may experience the following - motor fluctuations-> when the dose is wearing off, "on" may experience involuntary movements DYSKINESIAS - Axial problems are balance, speech and gait disturbance which do not respond to Parkinson's disease medication -> Due to degeneration outside the substantia nigra where dopamine is not the NT -> Mx- SALT and physio, OT Parkinson's dementia -> occurs more than one year after diagnosis of Parkinson's - Presence of Parkinsonism in the limbs. - Frequent visual hallucinations. - Frequent fluctuations in lucidity.
41
Mx of nocturnal akinesia
levodopa or oral dopamine-receptor agonists should be considered 2nd line -> rotigotine
42
Mx of psychotic Sx
No CI -> quetiapine to treat hallucinations and delusions. above ineffective -> clozapine offered
43
Mx of rapid eye movement sleep behaviour disorder
clonazepam | melatonin
44
Mx of advanced parkinson's disease
apomorphine hydrochloride w domperidone if they ahve N/V chech ECG due to cardiac effects deep brain stimulation - IF DRUG DO NOT WORK
45
what is impulse control disorders
compulsive gambling, hypersexuality, binge eating, or obsessive shopping on dopaminergic therpay modify Mx