Unit 2: Assessment & Interventions for MS & ALS Flashcards

1
Q

Patient History:
What do we want know about Sxs r/t MS

A

Sx Progression (timeline, severity, frequency)
Aggravating factors (fatigue, stress, overexertion, temp. changes)

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2
Q

Multiple Sclerosis (MS) or Amyotrophic Lateral Sclerosis (ALS)?
Intention Tremors

A

MS

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3
Q

Multiple Sclerosis (MS) or Amyotrophic Lateral Sclerosis (ALS)?
Muscle Atrophy

A

ALS

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4
Q

Multiple Sclerosis (MS) or Amyotrophic Lateral Sclerosis (ALS)?
Parasthesias

A

MS

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5
Q

Multiple Sclerosis (MS) or Amyotrophic Lateral Sclerosis (ALS)?
Muscle weakness, Dysarthria, + Dysphagia

A

BOTH!

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6
Q

Multiple Sclerosis (MS) or Amyotrophic Lateral Sclerosis (ALS)?
Visual disturbances (acuity + perception), Nystagmus, Diplopia (double vision)

A

MS
(ALS doesn’t affect vision!)

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7
Q

Multiple Sclerosis (MS) or Amyotrophic Lateral Sclerosis (ALS)?
Respiratory failure

A

ALS (Major cause of death!!)

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8
Q

Multiple Sclerosis (MS) or Amyotrophic Lateral Sclerosis (ALS)?
Bladder dysfunction

A

MS
(ALS doesn’t affect bladder function!)

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9
Q

Multiple Sclerosis (MS) or Amyotrophic Lateral Sclerosis (ALS)?
Highest risk for Depression

A

MS :(

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10
Q

What are the 3 main complications r/t MS?

A
  1. Infection (asp. pneumonia, UTI, urosepsis)
  2. Paralysis
  3. Mood changes (depression)
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11
Q

What are the 3 main complications r/t ALS?

A
  1. Paralysis
  2. Respiratory Failure
  3. Infection (asp. pneumonia)
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12
Q

What are the 4 Tx goals for MS?

A

(1) Prevent exacerbations
(2) Optimize function
(3) Sx Management
(4) Modify disease’s effects on immune system

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13
Q

What are the 3 Tx goals for ALS?

A

(1) Slow Progression
(2) Optimize Function
(3) Ensure Comfort

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14
Q

Why are pts with MS more susceptible to infection? (3)

A

Treated with immunomodulators
Bladder dysfunction (UTI, urosepsis)
Dysphagia (asp. pneumonia)

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14
Q

Why are pts with MS more susceptible to infection? (3)

A

Treated with immunomodulators
Bladder dysfunction (UTI, urosepsis)
Dysphagia (asp. pneumonia)

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15
Q

Why are pts with MS more susceptible to infection? (3)

A

Treated with immunomodulators
Bladder dysfunction (UTI, urosepsis)
Dysphagia (asp. pneumonia)

16
Q

Multiple Sclerosis (MS) or Amyotrophic Lateral Sclerosis (ALS)?
Implement Fall Precautions + Pressure Injury Prevention

A

BOTH!
Immobility an issue for boooooth

17
Q

Multiple Sclerosis (MS) or Amyotrophic Lateral Sclerosis (ALS)?
ROM exercises, Rest + Activity balance, Avoid rigorous activity

A

MS
Hyperthermia worsens mobility, fatigue, + vision

18
Q

Multiple Sclerosis (MS) or Amyotrophic Lateral Sclerosis (ALS)?
Swallow evaluation

A

BOTH!

19
Q

Multiple Sclerosis (MS) or Amyotrophic Lateral Sclerosis (ALS)?
Enteral nutrition

A

ALS

20
Q

Multiple Sclerosis (MS) or Amyotrophic Lateral Sclerosis (ALS)?
Self-catheterization, Bladder Pacemaker

A

MS

21
Q

Multiple Sclerosis (MS) or Amyotrophic Lateral Sclerosis (ALS)?
BIPAP, Trach, Vent, Diaphragmatic Pacemaker

A

ALS

22
Q

Multiple Sclerosis (MS) or Amyotrophic Lateral Sclerosis (ALS)?
Drug therapy aimed at Sx Mx + altering Immune system

A

MS

23
Q

Multiple Sclerosis (MS) or Amyotrophic Lateral Sclerosis (ALS)?
Drug therapy aimed at slowing progression

A

ALS

24
Q

Multiple Sclerosis (MS) or Amyotrophic Lateral Sclerosis (ALS)?
Eye-tracking board

A

ALS

25
Q

Multiple Sclerosis (MS) or Amyotrophic Lateral Sclerosis (ALS)?
Neurosurgery (Deep brain stimulation, Thalamotomy)

A

MS

26
Q

Multiple Sclerosis (MS) or Amyotrophic Lateral Sclerosis (ALS)?
Palliative/Hospice care Consult

A

ALS :(