Myasthenia Gravis Flashcards
Define MG
A chronic disease of the myoneural (neuromuscular) junction which interferes with chemical transmission (acetylcholine) of impulses across the motor endplate is inhibited.
Characteristics of MG
Fatigue (improves with rest) Muscular weakness (improves with rest) Only affects myoneural junction, not sensory function
Anatomical alterations
Atelectasis
Alveolar consolidation
Excessive bronchial secretions
Airway obstruction
Noncardiopulmonary Manifestations
Drooping of upper eyelids (ptosis) Double vision (diplopia) Speech impairment Dysphagia Weakness skeletal muscles of arms and legs Weakness of striated muscles Ventilatory muscles weakness
Clinical manifestations provoked by
Emotional upset Physical stress Exposure to extreme temperature Febrile illness Pregnancy
Etiology
Circulating antibodies of the autoimmune system
Anti-Ach receptor antibodies
Thymus gland abnormal
Anti-Ach receptor antibodies
Block acetylcholine from the receptor sites
of the muscular cell
Accelerate the breakdown of acetylcholine
Destroy the receptor sites at the neuromuscular junction
Diagnosis of MG
Clinical history
Response to an injection of edrophonium chloride (Tensilon) parasympathomimetic
Short-acting cholinesterase inhibitor
Electrophysiology test of neuromuscular transmission
Assay of circulating antibodies
Ice pack test (ptosis improves confirms MG)
Treatment of MG
Drug therapy
Parasympathomimetic drugs
Cholinesterase inhibitors
Corticosteroid therapy
Adrenocorticotropic hormone therapy
Thymectomy
Removal of the thymus gland with a source
of the anti-Ach receptor antibodies
Respiratory Care Treatment (O2 therapy, Bronchopulmonary hygiene, Hyperinflation therapy, Mechanical ventilation)
Drug therapy
Drugs that enhance the action of acetylcholine – inhibit the function of cholinesterase • Tensilon • Neostigmine • Pyridostigmine
Nasty side effect
– increased secretion production
Effective in mild cases of myasthenia gravis
but not severe corticosteroid therapy
• prednisone
Long-term side effects include diabetes
Neurologic examination.
Evaluation of reflexes, muscle strength, muscle tone, senses of tough and sight, gait, posture, coordination, balance, and mental abilities
Electromyography
Performed to confirm the diagnosis of MG
Identify specific muscles involved
Determine degree of fatiguability
Entails the repetitive stimulation of a nerve with the simultaneous recording of the muscle response
Blood Analysis
Reveal presence of acetylcholine receptor antibodies.
75% of patients have elevated levels
Edrophonium (Telison)
Diagnosis confirmed with the injection of edrophonium
Short-acting drug, blocks cholinesterase from breaking down ACh after it has been released from the terminal axon.
Causes dramatic transitory improvement in muscle function (lasting 10 minutes)
Magnetic resonance imaging:
Identifies an abnormal thymus gland or the presence of thymoma