Valley: Neuromusclar Diseases Flashcards
Are muscular dystrophy neuromuscular diseases hereditary?
Yes
Painless degeneration and atrophy of skeletal muscles (associated with mental retardation)
Muscular dystrophy
What are the 4 classifications of muscular dystrophy?
- Pseudohypertrophic muscular dystrophy
- Limb-girdle muscular dystrophy
- Facioscapulohumeral muscular dystrophy (heart not involved)
- Nemaline rod muscular dystrophy
Which classification has the characteristics of: CHF, recurrent pneumonia, kyphoscoliosis, hyperkalemia with sux, susceptible to MH
Pseudohypertrophic muscular dystrophy
Which classification has the characteristics of: micrognathia, bulbar palsy
Nemaline rod muscular dystrophy
Which muscular dystrophy is the most common and most severe?
Duchenne’s muscular dystrophy
Is duchenne’s muscular dystrophy x or y / dominant or recessive DNA?
X-linked recessive
Duchenne’s muscular dystrophy affects the lung volume in what 2 ways?
- Reduce total lung capacity
- Reduce residual volume
What type of heart block is common with Duchenne’s muscular dystrophy?
Bundle branch block
Duchenne’s muscular dystrophy has an increased incidence of ——, so avoid —.
Malignant hyperthermia , succinylcholine
Characterized by random and multiple sites of demyelination of corticospinal tract neurons in the brain and spinal cord, exclusive of the peripheral neurons.
Multiple sclerosis
S/s of which neuromuscular disease: visual disturbances, ataxia, limb paresthesia and weakness, spastic paresis of skeletal muscles, exacerbations and remission
Multiple sclerosis
What are the 5 common treatments (palliative) for multiple sclerosis?
- Corticosteroids
- Avoid stress
- Avoid marked temperature changes
- Dantrolene
- Carbamazepine
Multiple sclerosis management of anesthesia: — in response to succinylcholine
Hyperkalemia
Multiple sclerosis management of anesthesia: prevent — body temperature postoperatively
Increased
A chronic autoimmune disease involving the neuromuscular junction. It is characterized by weakness and rapid exhaustion of skeletal muscles with repetitive use; in some recovery with rest
Myasthenia Gravis
What are the 5 most common signs and symptoms with myasthenia gravis:
- Ptosis and diplopia
- Weakness of pharyngeal and laryngeal muscles (aspiration risk!)
- Asymmetric extremity skeletal muscle weakness (atrophy absent!)
- Cardiomyopathy
- Hypothyroidism
What are the 5 most common treatments for myasthenia gravis:
- Anticholinesterase drugs
- Corticosteroids
- Cyclosporine
- Plasmapheresis
- Thymectomy (elective operation)
Myasthenia Gravis preoperative preparation: — opioids and inform pt of possible —— postoperative
Avoid , mechanism ventilation
Myasthenia gravis induction: —— IV drugs , tracheal intubation — muscle relaxants
Short acting , without
Can you use muscle relaxants for maintenance with Myasthenia Gravis pts?
Yes, short or intermediate acting muscle relaxants