Movement Disorders Flashcards

(80 cards)

1
Q

Pyramidal is

A

direct and monosynaptic

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2
Q

Extrapyramidal is

A

indirect and polysnaptic

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3
Q

What are four targets of the extrapyramidal system?

A
  • Control of motor tone
  • Control of movement amount and velocity
  • Suppression of undesirable motor activity
  • Reflexes
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4
Q

Where does things usually go wrong in the Extrapyramidal system?

A
Basal nuclei (collection of nuclei)
Striatum
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5
Q

Large collections of nuclei that modify movement constantly?

A

Basal nuclei and cerebellum

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6
Q

Cerebellum output?

A

excitatory

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7
Q

Basal nuclei output

A

Inhibitory

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8
Q

What is disturbance?

A

movement disorders

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9
Q

Hypokinetic

A

it will be slow

Parkinson disease

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10
Q

Hyperkinetic

A

(Huntington)

  • Dystonia
  • Chorea
  • Tic disorders
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11
Q

What 3 drugs causes drug induced movement disorders?

A

SSRIs, Stimulants, Anti-psychotics

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12
Q

What is the most common cause of postural or action tremor?

A

Essential tremor

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13
Q

What causes essential tremor?

A
Familial tremor (autosomal dominant w/ reduced penetrance)
environmental influence
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14
Q

What causes essential tremor?

A

UNEXPLAINED.. need more studies

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15
Q

What is usually not involved in essential tremor?

A

legs

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16
Q

What body parts are usually involved in essential tremor?

A
  • one or both hands (usually bilateral)

- Head (laryngeal muscles)

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17
Q

What disease usually improves with alcohol consumption?

A

essential tremors

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18
Q

What is seen on a physical exam for pts with a essential tremor?

A

difficulty handwriting, manual skills, speaking

Worsened w/ anxiety, excitement

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19
Q

When is treatment not necessary in a essential tremor?

A

symptoms are mild

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20
Q

What is the treatment for mild, situational exacerbations?

A

Propranolol (Inderal), Alprazolam (Xanax), small amount of
alcohol,
Primidone (Mysoline)

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21
Q

What is the treatment for persistent disability due to essential tremor?

A

Propranolol (Inderal), Primidone (Mysoline), OR combination

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22
Q

Treatment for continuous symptoms of essential tremor despite treatment?

A

Topiramate (Topamax), Gabapentin (Neurontin)
Botulinum toxin A- associated w/ muscle dependent
weakness at the injection site

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23
Q

Treatment for disabling tremor not responsive to meds?

A

High frequency thalamic stimulation

Subdural motor cortex stimulation

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24
Q

Where should all essential tremor patients be referred to?

A

Neurologist

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25
Bradykinesia + what 3 things meets for Parkinsonism?
- Resting tremor - Rigidity - Postural instability
26
What is the most common cause of Parkinson Disease?
Idiopathic
27
What 2 structures make up the Substantia Nigra?
- Pars Reticulata | - Pars Compacta
28
What two things are found in Parkinson Disease?
- Presence of Lewy Bodies | - Neuronal degeneration
29
What are lewy bodies?
Abnormal aggregates of protein within neuron cytoplasm in the substantia nigra or cortex
30
What is the patho of Parkinson Dx?
degeneration of dopaminergic nigrostriatal system
31
What causes the tremor in Parkinson?
lack of dopamine and cerebellar influence
32
What two pathways are affected in Parkinson?
direct and indirect
33
What are the 5 risk factors for Parkinson Disease?
- Age (45-65yrs) - Family Hx - Male - Herbicide/Pesticide exposure - PMH of head trauma
34
What is the biggest cardinal symptom seen in 70% of pts w/ Parkinson?
Resting tremor
35
How do symptoms usually spread in Parkinson?
Starts in one limb and spreads to the other limb on that same side
36
What are 5 facial symptoms of Parkinson?
- Immobile-masked facies - Widened palpebral fissures - Infrequent blinking - Scalp/face seborrhea - Soft voice
37
What is Myerson sign?
tapping pts face and they constantly blink
38
How do you diagnosis Parkinson dx?
Clinical dx: a minimum of bradykinesia + tremor or rigidity
39
When is the challenge test used?
if dx is in doubt
40
What are 2 components of the "challenge test"?
- Carbidopa levodopa | - Apomorphine (Apokyn)
41
What is the gold standard diagnosis for Parkinson?
neuropathologic examination
42
When is Parkinson dx , txt started?
when dx negatively impacts living
43
What is the DOC for Parkinson?
Levodopa (L-dopa) (converts to dopamine)
44
What is the txt for Parkinson?
- Dopamine agonists - Levodopa - Carbidopa - Sinemet - MAOIs - Amantadine (Symmetrel)
45
What does Carbidopa do?
limits extra-cerebral breakdown of levodopa
46
Two dopamine agonist for txt Parkinson?
Pramipexole (Mirapex) | Ropinirole (Requip)
47
What drugs are effective in early or advanced Parkinson?
Dopamine agonist
48
What drug improves all clinical features, but does not stop progression?
Levodopa (L-dopa)
49
Carbidopa/Levodopa?
Sinemet`
50
Used prior to starting levodopa or with Sinemet?
Dopamine agonist
51
2 MAOIs for txt of Parkinson?
Rasagiline (Azilect) | Selegiline (Eldepryl)
52
MAO of amantadine?
increase dopamine | release or block dopamine reuptake
53
Who gets deep brain stimulation in Parkinson dx?
Patients w/o cognitive impairment or psychiatric disorder w/ good response to levadopa, but having response fluctuations
54
What type of deep brain stimulation is used for Parkinson?
High frequency stimulation of subthalamic | region
55
Parkinson progress more quickly in ppl who:
- are older when symptoms begin | - Do not have tremor
56
T/F Parkinson is fatal?
False, but can reduce longevity
57
What causes Huntington dx?
Trinucleotide repeat on chromosome 4 (autosomal dominant inheritance)
58
What is the age of onset for Huntington?
30-50 yrs
59
T/F Huntington is fatal?
True, 15-20yrs
60
What is the patho for Huntington dx?
Degeneration of the striatal cortex, basal ganglia, GABA neurons (inhibitory) in the striatum
61
What are the 2 symptoms of Huntington?
Dementia and Chorea
62
What imaging is used for Huntington's?
CT scan or MRI | PET
63
DIAGNOSIS of choice for Huntington's?
GENETIC TESTING!!!
64
Txt for Huntington's chorea?
purely symptomatic: there is no cure, nor ability to slow progression
65
What 4 dx are used for Huntington's chorea?
- Tetrabenazine (Xenazine) - Haloperidol or phenothiazines - Quetiapine (Seroquel)
66
What should be done w/ all pts diagnosied w/ huntington?
offer GENETIC testing for . all family members
67
What is Tourette Syndrome?
complex interaction between social and environmental factors and multiple genetic abnormalities
68
What and where is Bilineal transmission seen in?
Tourette Syndrome: inheritance from both parents is clearly evident in most cases
69
What area does Tourette effect?
Disturbance in the striatal-thalamic-cortical | (mesolimbic) spinal system
70
What causes the motor and vocal tics in Tourette?
disinhibition of the motor and limbic system?
71
Whats the biggest intital presentation for tourette?
Motor tics (80%)
72
What age does Tourette present?
prior to age 21 (2-15yrs)
73
Why is actual diagnosis of Tourette delayed?
due to mis diagnosis
74
How is Tourette diagnosed?
Clinical diagnosis
75
How could Tourette be misdiagnosed?
- No abnormalities on physical exam | - Normal neuro exam
76
What is the DSM-5 Criteria for Tourette?
- Multiple motor + >1 vocal tics present at some time - Tics present >1 yr - ONSET BEFORE 18yrs - Not due to direct physiologic effects of substance or meds
77
Txt for mild disabling tics?
education and counseling WITHOUT tic suppression therapy meds
78
Txt for bothersome tics?
Tetrabenazine (Xenazine)
79
Txt for focal motor or vocal tics?
Botulism toxin injections into the affected muscles
80
Txt for bothersome tics who want non-med txt or who have failed meds?
Behavioral therapy w/ habit reversal training