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ALS is also known as
Lou Gehrig’s disease
Number of canadians living with ALS
3000
Amyotrophic lateral sclerosis (ALS) (2)
Rare, progressive, neurological disorder characterized by loss of motor neurons in spinal cord and brain stem,
and by weakness and atrophy of the muscles of the hands, the forearms, and legs, spreading to most of the body and face
ALS cause (2)
Causative agent unknown
Combination of genetic component and environmental factors
Average survival after diagnosis
2 - 6 years (textbook)
3 - 5 years (ashley)
Signs and symptoms (13)
Tripping
Dropping things
Slurred speech
Difficulty swallowing
Weight loss
Decreased muscle tone
Shortness of breath
Increased or decreased reflexes
Uncontrollable periods of laughing or crying
Weakness
Fatigue
Muscle cramping or twitching
Muscle stiffness or rigidity
Usually the first S+S of ALS (2)
Tripping and dropping things
ALS diagnosis (5)
Clinical symptoms
MRI and Electromyography
Muscle and nerve function tests
to check conduction
No labs definite
Rule out other conditions
Management (12)
Emotional support
Supportive measures that address symptoms
Prevent aspiration
Prevent skin breakdown
Nutrition
Exercise to prevent spasticity
Facilitating communication
End of life decisions
Assistive devices (wheel chairs, mechanical lifts, etc.)
Pain management
Mechanical Ventilation
Medication
Supportive measures that address symptoms
End of life decisions
“If you can’t breathe do you want mechanical breathing?”
Prevent aspiration (2)
Raise HOB
Thick fluids
Prevent skin breakdown (2)
Prevlon boots, frequent repositioning
Nutrition
Want to maintain weight
Medication (2)
Riluzole (Rilutek)
slows the progression of ALS. This medication works to decrease the amount of glutamate (an excitatory neurotransmitter) in the brain.
Nursing interventions (6)
Facilitating communication
Reducing risk for aspiration
Early identification of respiratory insufficiency
Decreasing pain
Decreasing risk for fall-related injury
Providing diversional activities
Facilitating communication (4)
Tools like:
Eye gaze tracked by technology
Finger on mousepad
Printed pictures
Be creative
Reducing risk for aspiration (2)
Can aspirate on own secretions
Suction at bedside
Early identification of respiratory insufficiency
Always monitoring respiratory status
Providing diversional activities (4)
audio books, music, radio, TV