What does ALS stand for
Amyotrophic lateral sclerosis
What is ALS
Breakdown the ALS name
Amyotrophic (muscles wasting away) lateral (happens symmetrically) sclerosis (leads to firmness of the tissues)
Is cognition affected in ALS
No - they are still there (think of steven hawking)
What is the most common complication of ALS
Respiratory (lose muscles to swallow and cough, etc)
Is there a genetic form of ALS
Yes, but most people don’t have the genetic form (autosomal dominant pattern of inheritance) (they might have a genetic predisposition though)
What are risk factors for developing ALS 9
Who is more at risk for ALS
Higher incidence in men, but after menopause, both men and women incidence is equal
What is an early symptom of ALS that people usually write off
What are other common early symptoms of ALS
What do we use to help monitor a pt’s ALS progression
The ALS Functional Rating Scale (the higher the number the better, a decrease in number indicates further decline)
How do we diagnosis ALS
When do we see the typical onset of ALS? What if we see it earlier?
Typically ALS is seen around 65. If earlier, it is most likely the genetic form.
Are there any tx options for ALS?
Not really - tx is limited. There is riluzole, which can be given to help slow progression.
Go over vent management
What are some nursing interventions for ALS
What is Guillain-Barre Syndrome (GBS)? What can it lead to?
What are most GBS patients on
Vents
What is happening in GBS
Immune response, usually from IgG immunoglobulins (antibodies formed from bacteria or virus), after a bacterial or viral infection
Is GBS permanent
No, re-myelination can occur, which can help your body regain functions
Symptoms of GBS
What is the main feature of GBS
Ascending, rapidly progressing, symmetrical weakness of the limbs
What is the most common cause of death for someone with GBS
Respiratory arrest
How do we diagnosis GBS