5. PD, Huntington's, and Dystonia Flashcards

1
Q

PD signs and symptoms Main 4

A

Resting tremor
Bradykinesia
Rigidity
Postural Instability

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2
Q

Resting tremor rate pathological vs non

A

4-6 pathological

8-12 non

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3
Q

Resting tremor

A

Tremor when body weight supported this is more common in early Parkinson’s

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4
Q

Intention tremor

A

Intention tremor (part of cerebellar disease not PD) is when the tremor is small in amplitude to begin with and increases as approach closer to target

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5
Q

Rigidity

A

Cogwheel

Leadpipe

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6
Q

Parkinsons symptoms

A

Difficulty with swallowing and chewing
Speech impairments: Speak too softly, monotone, hesitant, slurred, repeating words
“Masked” face (flat affect)
Fatigue
Sleep problems
Decreased strength in muscles of respiration
Dementia or other cognitive problems

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7
Q

PD- Posture

A

Kyphotic, forward flexed trunk
Forward head
Crouched legs

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8
Q

PD- Gait Deficiency

A
difficulty initiating
freezing gait
festinating gait
Decrease trunk rotation
Decrease arm swing
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9
Q

PD progression

A

In the later stages of the disease, PD-related complications can lead to death, such as choking, pneumonia, and falls
Progression of symptoms may take 20 years or more (In some, PD progresses more quickly)

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10
Q

Hoehn & Yahr- Stage 1

A

Unilateral, one side of the body
Symptoms mild, inconvenient but not disabling
Usually presents with tremor of one limb
Friends noticing change in posture, gait, facial expression

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11
Q

Hoehn & Yahr- Stage 2

A

Bilateral, both sides of the body
Minimal disability
Posture and gait affected

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12
Q

Hoehn & Yahr- Stage 3

A

Significant slowing of movement
Early impairment of equilibrium on gait or standing
Generalized dysfunction that is moderately severe
By the time people reach Stage 3, quality of life is usually significantly affected

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13
Q

Hoehn & Yahr- Stage 4

A
Severe symptoms
Can still walk to a limited extent
Rigidity and bradykinesia
No longer able to live alone
Tremor may be less than earlier stages
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14
Q

Hoehn & Yahr- Stage 5

A

Cachectic stage: loss of weight and muscle wasting secondary to serious disease or disorder:
Invalidism complete
Cannot stand or walk
Requires constant nursing care

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15
Q

PD diagnoses

A

Must have two or more classical signs
Positive response to dopamine-like medications
CT or MRI in PD usually appear normal, but may be needed to rule out other diseases

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16
Q

PD meds- Ldopa

A

Levodopa (L-dopa)
A dopamine precursor that crosses the blood-brain barrier and then converts to dopamine
aim is BG

17
Q

Ldopa Side effects

A

Nausea, Hypertension, Dyskinesias
“Tolerance” develops with continued usage
Period of effectiveness after each dose begins to shorten
Larger doses may be needed to be effective

18
Q

PD meds- carbidopa

A

Carbidopa: inhibits Dopa decarboxylase, prevents premature conversion in the bloodstream
Often 4:1 ratio of carbidopa to levodopa (sometimes 10:1 ratio)
Carbidopa does not cross the BBB which is good since do not want levadopa to not convert to dopamine once it is in the brain

19
Q

Carbidopa effects

A

Therapeutic Effect: decreases symptoms of Parkinson’s less muscle rigidity, less bradykinesia

20
Q

carbidopa side effects

A

GI irritation: severe nausea and vomiting with initial administration
Postural hypotension/orthostatic hypotension
Cardiac arrhythmias
Large incidence of dyskinesias (chorea-athetoid movements)
Psychosis(limbic system), depression, anxiety

21
Q

PD Ablation (stereotaxic surgery)

A

Selectively destroying specific cells that contribute to the symptoms
Pallidotomy (reduce tremor, rigidity, and bradykinesia)
Thalamotomy (reduce tremor)

22
Q

PD DBS

A

Deep brain stimulation (DBS)
Electrodes implanted in thalamus, subthalamic nucleus, and globus pallidus
Electrodes connected to a pulse generator
The pulse generator and electrodes painlessly stimulate the brain
Blocks electrical signals from targeted areas
Reduces the need for medications

23
Q

PD: hypokinetic

A

SUBSTANTIA NIGRA PARS COMPACTA IMPAIRED TO RELEASE DOPAMINE  UNDERFACILITAED CORTEX  HYPOKINETIC

24
Q

Huntingtons

A

Dominant genetic disease
Degeneration of SNr & LGP
Hyperkinetic

25
Huntingtons onset and progression
Onset: 30 YOA Death: 15-20 years later
26
Non huntingtons chorea like movements
children who have had anoxia or cerebral palsy | Medicated PD patients
27
Huntingtons symptoms
``` Chorea Akinesia and bradykinesi HYPOTONIA staggering gait speech lacks rhythm swallowing difficulty poor saccadic control ```
28
Huntingtons cognitive symptoms
``` Dementia Poor judgment Loss of long term memory Depression IQ decreases Irritability ```
29
Huntingtons early stage
MOTOR SYMPTOM BEGIN DISTAL Cognitive difficulty thinking through complex tasks Behavioral: irritability and disinhibition
30
Huntingtons midstage
Losing independence: may be unable to perform chores work or drive Motor: eating becomes a challenge Cognitive: cannot organize info Behavioral: losing interest
31
Huntingtons late stage
Totally dependent for all care, combined to bed, SNF Unable to speak Tube feeding, choking concerns Motor: severe rigidity, chorea stopped, cannot initiate Behavioral: some have psychosis
32
Huntingtons Medications
``` Cholinergic or GABA-containing agonists Perphenazine Haloperidol (Haldol) Reserpine Riluzole ```
33
Dystonia
``` Idiopathic early onset has a defected gene OFTEN SECONDARY TO OTHER DISORDERS Lesions at caudate, putamen or globus Hyperkinetic ```
34
Dystonic movements
abnormal muscle tone with simultaneous contraction of agonist and antagonist Co-contraction of muscles around a joint causes the joint to be rigid
35
Dystonia: Focal: pharyngeal
intercostals and diaphragm often affected Distorted speech Treated with botox
36
Dystonia progression onset: generalized
8 YOA | Begins in legs
37
Dystonia progression onset: focal
30-50 YOA | Progresses for 5 years and then plateaus