Week 6- Additional Neurological Disorders Flashcards
(88 cards)
PART 1: MYASTHENIA GRAVIS
PART 1: MYASTHENIA GRAVIS
What is Myasthenia Gravis?
-A neuromuscular junction disorder characterized by progressive muscular weakness and fatigability on exertion.
Myasthenia Gravis is a chronic progressive ____________ disease in which we have antibody-mediated attack on _____ receptors at NMJ.
- autoimmune
- ACh receptors at NMJ
Myasthenia Gravis will worsen with _______ and improve with _______.
-worsen with activity, improve with rest
What is the cause of Myasthenia Gravis?
Unknown
Myasthenia Gravis Risk Factors:
- Average age of onset = ___ years
- ________ > _______
- Prior _________ disorder
- 59 years
- Female > Male (2:1)
- Prior autoimmune disorder
What are the main S/Sx of Myasthenia Gravis?
- LMN Disorder
- WEAKNESS
- Diplopia and ptosis
- Larryngeal irritation
- Weakness with Myasthenia Gravis worsens with _________ and improves with ______.
- Which muscles are affected the most?
- Patients have generalized weakness throughout the body.
- worsens with contraction, improves with rest
- muscles of face and throat (intercostals will also be affected)
50% of patients with Myasthenia Gravis will have first symptoms be ______ in nature.
-ocular
What does laryngeal irritation cause? (3)
- voice impairments
- dysphonia
- increased risk for choking/aspiration
What are some exacerbating factors? (5)
- Fatgue
- Illness
- Stress
- Extreme Heat
- Some Medications (beta-blockers, calcium-channel blockers, some antibiotics)
What are the subtypes of Myasthenia Gravis? (4)
- Ocular Myasthenia
- Mild Generalized Myasthenia
- Severe Generalized Myasthenia
- Myasthenic Crisis
_______ Myasthenia only affects the muscles that move the eyes and eyelids. Can cause double vision, blurry vision, and ptosis.
-Ocular Myasthenia
Myasthenic Crisis:
- Myasthenic Crisis = S/Sx of MG + ______________
- ___-___% of myasthenic patients are affected by a myasthenic crisis at least once in their lives.
- __-__ months is the median time to first myasthenic crisis from onset of MG.
- What are some potential complications from a myasthenic crisis?
- What does treatment include?
- respiratory failure (upper airway muscles and respiratory muscles)
- 15-20%
- 8-12 months
- fever, infection, DVT, cardiac complications
- IVIg, Plasmaphoresis
Myasthenic Crisis Precipitating Factors.
- Physical Stressors
- Environmental Stressors
- Aspiration Pneumonia
- Infection
- Perimenstrual state
- Pregnancy
- Sleep deprivation
- Surgery
- Pain
- Temperature extremes
- Tapering of immune-modulating meds
What are some tests performed for diagnosis of Myasthenia Gravis? (5)
- Edrophonium Test
- Blood Analysis
- Ice Pack Test
- Electrodiagnostic Testing (Repetitive Nerve Stimulation)
- Pulmonary Function Tests
What is Edrophonium Test?
-Injection of edrophonium to look for sudden improvement in muscular strength temporarily.
What do they look for with a Blood Analysis?
-Abnormal antibodies
What is the Ice Pack Test?
-Cooling thought to improve neuromuscular transmission. Take ice pack and stick over eye and see if ptosis looks better (most common with ocular subtype).
What is Electrodiagnostic Testing?
-Repetitive Nerve Stimulation
What are the main ways Myasthenia Gravis is medically managed?
- IVIg, Plasmapheresis
- Cholinesterase Inhibitors
- Corticosteroids
- Immunosuppressants
What is IVIg and Plasmapheresis mainly used for?
-Myasthenia Crisis (but may be used even if someone isn’t in crisis)
What are the 2 ways Myasthenia Gravis is surgically managed?
- Videothoracoscope
- Tracheostomy
What is surgical management mainly used for?
-Secondary sequelae related to MG.