Movement Disorder and Neurosurgery Flashcards

1
Q

What is a movement disorder?

A

A category of neurological conditions that cause problems with movement. This could be:
▪️ Increased
▪️ Decreased
▪️ Voluntary
▪️ Involuntary

Including PD, HD (chorea), dystonia, parkinsonism, TS etc

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2
Q

How do you subclassify disorders of movement?

A

▪️ Hyperkinetic movement (e.g., chorea, tremor, tics, myoclonus, dystonia, ataxia, spasticity)
▪️ Hypokinetic movement (e.g., bradykinesia, rigidity, balance problems, parkinsonism)

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3
Q

What does the basal ganglia do?

A

▪️ Motor control
▪️ Motor learning
▪️ Executive functions and behaviours
▪️ Emotions

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4
Q

How are the basal ganglia organised?

A

Group of subcortical nuclei:
1. Input nuclei (e.g., caudate nucleus, putamen, nucleus accumbens)
2. Output nuclei (e.g., GPi and substantia nigra pars reticulata)
3. Intrinsic nuclei (e.g., GPe, subthalamic nucleus, substantia nigra pars compacta)

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5
Q

What is the effect of dopamine on the basal ganglia?

A

Dopamine can enhance the activity of neurons in the basal ganglia, involved in movement, motivation, and reward-processing

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6
Q

Why do so many basal ganglia disorders affect cognition and emotion?

A

Because the basal ganglia are interconnected with many parts of the brain responsible for cognitive and emotional processing

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7
Q

What is the difference between Parkinson’s disease and Parkinsonism?

A

Parkinsonism = umbrella term describing symptoms of tremors, muscle rigidity, and slowness of movement

Parkinson’s disease = most common type of parkinsonism caused by degeneration of dopaminergic neurons

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8
Q

How may imaging differentiate pre and post-synaptic Parkinsonism?

A

▪️ PET/SPECT to measure level of dopamine transporter in the brain, responsible for reuptake of dopamine
▪️ In presynaptic parkinsonism, there is a loss of dopamine transporters (e.g., PD)
▪️ In postsynaptic parkinsonism, there is a loss of dopamine receptors (e.g., atypical parkinsonian disorder)

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9
Q

What is an ‘atypical Parkinsonian disorder’ and how might you know?

A

▪️ Progressive disease with similar symptom presentation to PD as well as changes in BP, breathing, and eye movements
▪️ BUT loss of dopamine receptors so don’t respond as well to levodopa

E.g., MSA, PSP, CBD

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10
Q

Why are there so many non-motor symptoms in Parkinson’s disease?

A

▪️ Dopamine also plays a role in mood, cognition, and sleep
▪️ Disruption of other brain areas due to spread of pathology (Lewy bodies)

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11
Q

What is DBS?

A

A reversible means of altering physiological circuits in the brain through electrodes implanted into deep structures

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12
Q

Who is the ideal PD candidate for DBS according to the NICE guidelines?

A

▪️ Medically refractory disease
▪️ Presence of dystonia

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13
Q

What movement disorders can DBS be used for?

A

▪️ Parkinson’s disease
▪️ Dystonia (involuntary spasms)
▪️ Essential tremor

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14
Q

What are the advantages of DBS?

A

▪️ Non-destructive (compared to traditional method of thalamotomies)
▪️ Reversible
▪️ Adjustable - can increase voltage is symptoms get words

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15
Q

What are the disadvantages of DBS?

A

▪️ Usually surgical risks and complications (e.g., infection, mortality)
▪️ Expensive
▪️ High maintenance

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16
Q

What types of pain can be helped with DBS?

A

▪️ Neuropathic
▪️ Nociceptive

17
Q

How are patients selected for DBS surgery?

A

Through a multidisciplinary team

18
Q

Where are the electrodes typically placed for DBS in PD?

A

Motor area of the subthalamic nucleus

19
Q

What is the role of the neurologist during DBS surgery?

A

To monitor movement

20
Q

What are the main components of the DBS system?

A

▪️ Battery pacemaker generates electricity (external to begin with then placed in chest)
▪️ Two electrodes
▪️ Two cables

21
Q

What complications are associated with DBS surgery?

A

▪️ 1% risk of mortality/severe morbidity
▪️ 2-10% risk of infection
▪️ 10% risk of lead breakage or hardware failure
▪️ Target specific complications (usually reversible)
▪️ Cognitive and mood disturbance

22
Q

What psychiatric conditions may DBS be experimentally tried in?

A

▪️ Tourette’s syndrome
▪️ Depression
▪️ OCD
▪️ Epilepsy?

(Newer trials in AD, AN, and addiction not yet clear)

23
Q

How might DBS be used in TS?

A

▪️ Electrodes in centromedian nucleus/intralaminar thalamic nucleus
▪️ >60% reduction in tic scores in intractable cases

24
Q

How might DBS be used in depression?

A

Target subgenual cingulate which shows overactivity in treatment resistant depression and decreased activity after clinically effective therapy

25
Q

What target might you consider for DBS in OCD?

A

Subthalamic nucleus

26
Q

What is ataxia?

A

Impairment in muscle control, causing clumsy voluntary movements, usually related to the cerebellum

Can affect coordination, balance, and speech

27
Q

What is apraxia?

A

Loss of ability to carry out skilled movements and gestures, despite maintaining physical ability and desire to perform them

28
Q

What symptoms might occur from basal ganglia dysfunction?

A

Trouble starting, stopping, or sustaining movement

29
Q

What is the difference between tics, myoclonus, and chorea?

A

▪️ Tics = sudden, brief repetitive movements usually preceded by an urge
▪️ Myoclonus = sudden, brief involuntary muscle twitch/jerk, either spontaneous or in response to stimulus
▪️ Chorea = irregular, rapid, jerky, involuntary movements that are not repetitive, ‘dancing’