Degenerative Diseases Flashcards

1
Q

List 2 characteristics of the early disease stage.

A
  1. Minimal Impairments or functional limitations

2. No disabilities

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2
Q

List 4 rehabilitation priorities for the early stage of disease.

A
  1. Prevention (fitness and energy conservation)
  2. Delaying the onset of movement disorders
  3. Remediation: education/psychological support
  4. Compensatory: Movement strategies, equipment, home modifications
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3
Q

List 4 resources the PT can suggest to a patient in the early disease stage. Why is it important to recommend these resources?

A
  1. Referral to speciality clinic
  2. Register for clinical trial
  3. Encourage contact and membership in state/national societies
  4. Support groups

Why?: Empowers the patient to seek out information and support outside of PT.

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4
Q

List 2 characteristics of the middle disease stage.

A
  1. Increasing number and severity of impairments and functional limitations.
  2. Some disabilities
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5
Q

List 3 rehabilitation priorities for the middle stage of disease.

A
  1. Prevention (fitness, energy conservation, and neuroprotection)
  2. Remediation: Dystonia management and ROM
  3. Compensatory: Bracing, splinting, care giver training, and AD prescription
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6
Q

List 2 characteristics of the late disease stage.

A
  1. Severe impairments

2. Complete disability

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7
Q

List 3 rehabilitation priorities for the late stage of disease.

A
  1. Compensatory: care giver training
  2. Preventative: skin and pulmonary management, contracture prevention
  3. Restorative: Palliative care
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8
Q

What is the pathophysiology of multiple sclerosis? (2)

A
  1. Inflammatory process causing patchy plaques on the myelin sheaths in CNS.
  2. Reduces the speed and effectiveness of nerve transmission
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9
Q

List the 4 criteria that make up the clinical diagnosis for MS.

A
  1. Two or more central nervous system pathologies.
  2. Two distinct episodes of nervous system dysfunction.
  3. Diagnosed between 15-50 years of age with a majority diagnosed in their 30’s
  4. Confirmed by CT scan or MRI
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10
Q

List 4 factors that contribute to a FAVORABLE prognosis of MS.

A
  1. Female
  2. Onset of sxs before 35-40 years of age
  3. No disability for 5 years
  4. Initial signs and sxs: optic neuritis and sensory dysfunction
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11
Q

List 1 factor that contributes to a UNFAVORABLE prognosis of MS.

A
  1. Initial signs and sxs: Cerebellar and motor dysfunction
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12
Q

________ is the most common pattern of MS where ____ % of cases remain benign.

A

Relapsing and Remitting

20%

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13
Q

List 3 characteristics of relapsing and remitting MS.

A
  1. Sudden onset of symptoms
  2. Symptoms last days or weeks
  3. Complete or partial disappearance of symptoms
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14
Q

List 2 characteristics of primary progressive MS.

A
  1. Continuous and gradual worsening of symptoms

2. No delineated exacerbations or periods of remission

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15
Q

List 2 characteristics of secondary progressive MS.

A
  1. Starts as Exacerbating and Remitting

2. Becomes progressive

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16
Q

_____ is the most common symptom of MS, affecting _____ % of people.

A

Fatigue

70-95%

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17
Q

Fatigue, relative to MS, occurs as a result of inefficient ______.

A

Nerve conduction

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18
Q

List 4 PT management interventions used to manage fatigue in patients with MS.

A
  1. Energy conservation
  2. Schedule activity during higher energy times
  3. Aerobic Exercise
  4. Teach exertion perception concepts
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19
Q

Why do patients with MS have decreased heat tolerance?

A

Increased heat increases the inflammatory process of the disease which could exacerbate symptoms

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20
Q

List 2 PT management interventions used to manage decreased heat tolerance in patients with MS.

A
  1. Education regarding: hydration, clothing management and cooling vests
  2. Aquatic therapy
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21
Q

List 3 interventions used to treat weakness in patients with MS.

A
  1. Prevent disuse atrophy of un-effected muscles
  2. Overcome spastic antagonists
  3. Increase strength of afffected muscle groups
22
Q

Aerobic exercise is associated with higher levels of _______ integrity and _____ concentration in patients with MS.

A

Higher levels of white matter integrity

BDNF

23
Q

Huntington’s disease is characterized by neuronal loss in the _____ and ______.

A

Caudate nucleus

Putamen

24
Q

What is used to confirm a diagnosis of Huntington’s disease?

A

Genetic testing

25
Symptoms of Huntington’s disease appear at ages _____ with a median survival rate of _____ years after symptom onset.
30-50 years of age 15-25 years = median survival rate after onset of sxs
26
List 2 behavioral and 2 cognitive impairments associated with Huntington’s disease.
Behavioral impairments: Depression and irritability Cognitive impairments: Slow processing and decrease attention
27
List 7 movement disorders characteristic of Huntington’s disease.
1. Difficulty modulating gait and bed mobility 2. Difficulty turning 3. Chorea of the hands, limbs and trunk (increases then decreases) 4. Dystonia 5. Hypokinesia 6. Bradykinesia 7. Hemiballismus
28
List 4 treatment considerations used to treat Huntington’s disease.
1. Cognitive and sensory strategies as per PD 2. Balance retraining in early stages 3. ROM of spastic agonists 4. Strengthening of antagonists
29
True or False: There is no evidence related to exercise having an impact on Huntington’s disease progression.
TRUE
30
ALS is caused by the degeneration and death of both ______ in the ____ of the brain, the _____ and the _____.
Death of both motor neurons (upper and lower) In the motor cortex Brain stem Spinal cord
31
List 2 things that are used to confirm a diagnosis of ALS.
1. Clinical: UMN and LMN signs | 2. MRI
32
ALS has a ___ year survival rate with a median/mean survival rate of ____ years.
5-10 years | Mean: 2-4 years
33
List 3 characteristics of a FAVORABLE ALS prognosis.
1. Age at onset under 40 2. Limb onset better than bulbar 3. Absence of dyspnea at onset
34
List 3 characteristics to describe the course of ALS.
1. Initially manifests as weakness (sporadic and progressive) 2. Bulbar impairments (swallowing and speaking affected) 3. Cognitive sxs (fronto-temporal dementia)
35
List 3 respiratory impairments that affect patients with ALS.
1. Initial Impairments present as fatigue and compensated for by activity limitation 2. 50% FVC –orthopnea, dyspnea at rest and ineffective cough 3. 25% FVC acidosis, coma, death
36
List 3 treatment considerations used to treat patients with ALS.
1. Strength and Endurance Exercise in early stage 2. Supporting weak muscles - wrist and cervical spine extensors 3. Airway Clearance-Mechanical Insufflation-Exsufflation
37
______ and ______ are common pathologies among patients with ALS.
Shoulder Hand Syndrome | Adhesive Capsulitis
38
Aerobic exercise is associated with improved ____ measures in humans with ALS.
QOL
39
_____ in every ____ people over 65 have Alzheimer’s disease.
1 in 9 | 11,000 in every 100,000
40
How is a diagnosis of Alzheimer’s disease determined?
Cognitive decline and ruling out other causes
41
The presence of _____ and _____ in the brain are characteristic of Alzheimer’s disease.
Amyloid plaques | Neurofibrillary tangles
42
The amyloid core becomes surrounded by _____, _____, and other _______, representing ______ areas.
Fragmented axons Altered glial cells Cellular debris Represent nonfunctional areas
43
Neurofibrillary tangles develop in the ______ cells, leading to _____ and _____.
Pyramidal cells Atrophy Necrosis
44
The first structure to show pathological cognitive behavioral changes in ALS patients is the ______.
Cerebral cortex
45
List 2 early signs of cognitive behavioral changes in patients with ALS.
1. Loss of ability to learn new information (declarative memory) 2. Spatial disorientation
46
List 3 late signs of cognitive behavioral changes in patients with ALS.
1. Global memory loss 2. Loss of comprehension 3. Frontal lobe disinhibition
47
The cognitive behavioral impairments associated with ALS are similar to those seen with ______.
Chronic traumatic encephalopathy (CTE)
48
It is possible for even severely demented patients to acquire and retain ___________ memories.
Motor type procedural memories
49
List 3 movement disorders that may be seen in patients with MS.
1. Akinsea 2. Dystonia 3. Rigidity
50
The movement disorders seen in patients with ALS are similar to those seen in ______ and ______ Disease.
Parkinson’s | Huntington’s
51
Exercise interventions improve _____ and decrease ____ and ______ in patients with Alzheimer’s and dementia.
Improve ADL function | Decrease fall risk and disease progression