Degenerative Diseases Flashcards

1
Q

What are the diseases?

A
PD
MS
ALS
HD
Alzheimers
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2
Q

What happens in early stages of disease?

Priorities of rehab?

A

minimal impairments/limitations
usually just starting to struggle.

Priority:
neuro protection* and plan energy conserve but workout.
delays regression*
educate and home modifications

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3
Q

Some things to do for early stage?

A

consider referral
register for Clinical Trial
Membership in societies
support groups.

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4
Q

Middle stages of diseases?

A

impaiments/disabilities pile up
use same type of prevention

WORK ON:
range*
dystonia
bracing
AD* plan for disease progression
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5
Q

late stage diseases?

A

Severe impairments/ completely disabled.

Rehab:
Caregiver training*
prevent contractures/skin.
palliative care.

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6
Q

What is MS?

A

inflammation causing plaque in myelin sheaths.

reduces speed and effectiveness of nerve transmission

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7
Q

Dx and Px of MS?

A
PT can Dx.
2 CNS pathologies*
2 episodes of nerve dysfx.*
lots of sensory issues
CT/MRI.

Favorable Px?
female/35 y/o/ no disability for 5 yrs/
first symptoms are optic neuritis/sensory dysfx

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8
Q

What are MS patterns?

A

relapse/remitting: sudden onset->disappearance of symptoms

Primary progressive: continuous worsening. no remission

2ndary progression:
starts with remitting but then becomes progressive.

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9
Q

Sxs and symptoms of fatigue?

A

FATIGUE: work around this (time/save energy)

Dec heat tolerance: hydrate/cooling vest/hydrotherapy

Weak: prevent disuse/overcome spasticity/strengthen

increased BDNF after exercise. so u want to do that to keep white matter.

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10
Q

What is huntington’s disease?

Dx/Prognosis

A

neuronal loss in caudate and putamen

Dx: genetic testing

Px: survive 15-25 yrs after onset usually 30y/o

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11
Q

Sx and symptoms of HD?

A

Depression/irritable
Slow processing/Dec attention

move slow/dystonia/cant modulate gait/chorea
difficulty turning.

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12
Q

Tx for HD?

A

Cognitive/sensory strategy
Balance retraining
ROM of spastic and strengthen antagonist

neuroprotections.. rn exercise isn’t that great for this like it is for PD

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13
Q

Patho of ALS?

A

Degenerations of motor neurons in Brain/BS/SC.

Dx: UMN/LMN signs
Px: 5-10 yr survival.

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14
Q

Signs and symptoms of ALS?

A

at first weak/sporadic/fatigue
Bulbar impairments
Cognitive symptoms (usually later unlike HD)
Respiratory impairments(dec activity to match impairment)*

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15
Q

50% FVC?

25?

A

orthopnea/ineffective cough

acidosis/coma/death

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16
Q

Tx for ALS?

A

exercise in early stage (strength/endurance)
Support weak muscles
Airway clearance
*progresses rapidly

aerobic exercise ^ QOL

17
Q

Alzheimers notes?

A

cognitive decline and rule out other stuff.

have neurofibrillary tangles inside. and amyloid plaques outside

18
Q

1st structure to show patho change in alzheimers is

A

cerebral cortex: no ne memory/lose declarative memory

Late:global memory loss/loss comprehension/ Frontal lobe disinhibition.

19
Q

What is important for demented patients to acquire and retain?

A

motor-type procedural memories

20
Q

Movement disorders of alzheimers?

A

akinesia/dystonia
rigidity

similar to parkinson’s.

21
Q

effects of Interventions for Alzheimers

A

aerobic + strengthen improve ADLs.

decrease fall risk

deterioration slows

decrease caregiver burden

slow development of dementia