Movement Disorders Review Sheet Flashcards

1
Q

average age of onset for Parkinson’s

A

58-60 years old

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2
Q

PD is more often seen in which sex?

A

slightly more in men

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3
Q

What is the cellular mechanism behind PD?

A

clumping of proteins (Lewy bodies) appear in neurons of the substania nigra, brainstem and other areas of the brain

degenerationa nd death of dopamine-producing neurons in the substania nigra

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4
Q

What primary symptoms make up Step 1 of PD diganosis process

A

Tremor- resting
Rigidity
Akinesia or bradykinesia
Postural instability

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5
Q

What exclusion criteria make up Step 2 of PD diagnosis process?

A

poor response to large doses of levodopa
symptomatic parkinsonism syndrome where symptoms appear to be related to some other cause such as exposure to toxins, head trauma, vascular, etc.
other neurodegenerative conditions in addition to PD type signs

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6
Q

What are the features which support diagnosis of Step III?

A

unilateral onset
rest tremor (but one does not have to have this for diagnosis of PD)
excellent early response to levodopa
levodopa induced dyskinesias
progressive signs and symptoms, asymmetry of signs; at least initially
clinical onset > 10 years

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7
Q

Bradykinesia

A

major sign of PD
slow movement
can’t realease thalamus enough to generate bugger bursts to create bigger movements

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8
Q

Akinesia

A

major sign of PD
too much inhibition of the thalamus; can’t release it
masked facies (lack of expression) and reptilian stare (infrequent blinking)
arm swing decreased
difficulty stopping movement once started (festination)
difficulty stopping backwards movement (retropulsion)
“freezing” episodes

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9
Q

What makes akinesia or bradykinesia worse?

A

dual tasking

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10
Q

Rigidity

A

major sign of PD
increased resistance throughout the range
due to outputs to the pedunculopontine nuclei
-with a loss of dopamine, the pedunculopontine nucleus is inhibited so that it can no longer inhibit the reticulospinal and vestibulospinal tracts
-this leads to excitation of postural muscles
muscles are active even when the person is at rest
does NOT cause akinesia or bradykinesia

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11
Q

Resting tremor

A

major sign of PD
rhythmic, alternating bursts of antagonistic muscles
due to different output pattern from BG
goes away with purposeful movement
“pill rolling” is the most common form
over 90% of those with a PD tremor have some degree of an action tremor

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12
Q

Postural Instability

A

co-activation resulting in a rigid body and inability to recover stability

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13
Q

What ANS problems occur with PD?

A

postural hypotension
excessive salivation and sweating
constipation and urinary disturbance

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14
Q

What cranial nerve nucleus is involved with ANS problems

A

dorsal motor nucleus of X

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15
Q

Mood and cognitive deficits of PD

A
  • mild to moderate cognitive impairment
    • dysexecutive syndrome
  • depression
  • impulse control behavior disorder
  • psychosis
  • sleep disorders
  • nutritional deficits
  • speech
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16
Q

What are the symptoms of dysexecutive syndrome?

A

impaired attention
verbal fluency reduced but language is preserved
visuospatial deficits
difficulty initiating planning and sequencing
impaired free recall
personality change

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17
Q

What are the speech deficits of PD due to?

A

bradykinesia, akinesia and decreased chest excursion causes a decreased volume and slurred speech as the disease progresses

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18
Q

what is forward festination?

A

inability to stop forward movement once it has started

bradykinesia issue; difficulty releasing thalamus to generate bigger bursts

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19
Q

what is backward festination?

A

also called retropulsion
inability to stop backward movement
bradykinesia issue; difficulty releasing thalamus to generate bigger bursts

20
Q

Elements PT addresses in Parkinson’s

A
Gait
mobility deficits
Balance and falls
Loss of ROM/contracture/fixed, stooped posture
muscle atrophy and weakness
fatigue
cardiopulm deconditioning
osteoporosis
ulcers
21
Q

Gait of someone with PD

A

slow, shuffling and flat-footed
decreased arm swing
forward and backward festination
difficulty changing direction, going through doorways or over things which can trigger a freezing response

22
Q

main medication used for PD

A

Levodopa

23
Q

What are the major problems with this treatment?

A
  • doesn’t help with tremors
  • difficulty in delivery
  • dual therapy with carbidopa has extreme side effects
  • dyskinesias after prolonged use
  • diminished response over time
24
Q

Advantages of dopamine agonists

A

effective as an early monotherapy
avoids levodopa side effects
has neuroprotective effects

25
Q

Disadvantages of dopamine agonists

A
less potent
long titration
requires levodopa addition eventually
cognitive side effects
confusion and hallucinations
\$\$$ expensive
26
Q

population for dopamine agonists

A

first line treatment for early PD in young, cognitively preserved patients

27
Q

population for carbidopa/levodpa

A

patients with more advanced PD that are older and more cognitively impaired

28
Q

Describe Chorea

A
Abrupt
Brief
Irregular
Purposeless
Unpredictable
Non-stereotypical
Involuntary movement
29
Q

when do the first symptoms of Huntingtons occur

A

onset at 35 and 42

30
Q

what NT are lost with huntingtons?

A

loss of Ach and GABA because there is too much dopamine and too much release of thalamus

31
Q

general development of huntingtons

A

first symptoms are mood/mental disorder with depression being the most common
then neurobehavioral changes
chorea

32
Q

what is a common sign of chorea?

A

milkmaids sign

increase and decrease in grip strength involuntarily

33
Q

what is hemiballismus

A

rotary nature/choreatic movements on one side of the body

caused by lesion of the subthalamic nucleus

34
Q

What causes tardive dyskinesia?

A

drug induced disorder secondary to use of antipsychotic drugs

35
Q

signs and symptoms of tardive dyskinesia

A

involuntary fragmented movements of the tongue, mouth and jaw
smacking, sucking noises
choreoathetoid movements
dystonia of neck and trunk

36
Q

characteristics of dystonia

A

PROLONGED muscle contractions of limbs/axial that are either repetitive or sustained

37
Q

what triggers dystonia

A

VOLUNTARY movement

38
Q

what worsens dystonia

A

fatigue and anxiety

39
Q

what is the most common type of dystonia

A

focal which includes task specific (writer’s cramp, musicicians) and spasmodic toricollis

40
Q

what is spasmodic torticollis

A

turning fo the neck that causes spasm

41
Q

how can spasmodic toritcollis be suppressed

A

only be self-touch sensory trick “gest”

42
Q

define a tic

A

major distinguishing characteristic is that if asked it can be suppressed
involves quick, involuntary movements that are repetitive at irregular intervals

43
Q

tourette’s syndrome

A

a simple or complex motor tic that may involve vocal tics(swearing)

44
Q

define myoclonus

A

quick muscle jerks, irregular or rhythmic that cannot be suppressed and result from cortical, cerebellar, brainstem or spinal cord disorders

45
Q

types of tremors

A

resting: rhythmic, alternating bursts of antagonistic muscles that goes away with purposeful movement
postural: type of action tremor that is not seen at rest

Intentional: type of action tremor where the closer you get to the target the wilder the movement; successive overshoots an undershoots about a goal that leads to oscillations