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Myasthenia gravis

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MYASTHENIA GRAVIS MANALI H SOLANKI F.Y.M.SC.NURSING J G COLLEGE OF NURSING
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Page 1: Myasthenia gravis

MYASTHENIA GRAVIS

MANALI H SOLANKI

F.Y.M.SC.NURSING

J G COLLEGE OF NURSING

Page 2: Myasthenia gravis

ANATOMY AND PHYSIOLOGY

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DEFINITION:

• Myasthenia gravis is an autoimmune disorder affecting the myoneural junction, is characterized by varying degrees of weakness of the voluntary muscles.

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CAUSES:• In MG, the receptors at the muscle

surface are destroyed or deformed by antibodies that prevent a normal muscular reaction from occurring.

• The causative factor is unknown, but the disorder may have a genetic link.

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RISK FACTORS:

Risk factors for myasthenia gravis include:

• Female gender and age under 40 years• Male gender and age over 60 years• Other autoimmune disorders

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Factors that can worsen myasthenia gravis

• Fatigue• Illness• Stress• Extreme heat• Some medications — such as beta

blockers, calcium channel blockers, quinine and some antibiotics

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PATHO PHYSIOLOGY:

POSTER

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SIGN AND SYMPTOMS:

• Diplopia and ptosis

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• Weakness of the muscles of the face and the throat, and generalized weakness. Weakness of the facial muscles results in bland facial expression.

• Laryngeal irritation causes voice impairment and dysphonias and increases the patient’s risk for choking and aspiration.

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• Generalized weakness of all the extremities and the intercoastal muscles resulting in decreased respiratory capacity and vital capacity.

• Myasthenia gravis is purely a motor disorder with no effect on the sensation and coordination.

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DIAGNOSTIC TEST:

• Edrophonium test:

Injection of the chemical edrophonium (Tensilon) may result in a sudden, although temporary, improvement in muscle strength - an indication that patient may have myasthenia gravis.

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Blood analysis

• A blood test may reveal the presence of abnormal antibodies that disrupt the receptor sites where nerve impulses signal muscles to move.

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Ice Pack Test

• Cooling may improve neuromuscular transmission. In a patient with myasthenia gravis who has ptosis, placing ice over an eyelid will lead to cooling of the lid, which leads to improvement of the ptosis.

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• Repetitive nerve stimulation

• Pulmonary function tests

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MEDICAL MANAGEMENT:

• Cholinesterase inhibitors. • Corticosteroids• Immunosuppressant

Plasmapheresis

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SURGICAL MANAGEMENT

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DIETARY MANAGEMENT

• Reduce protein intake to 10 percent of total calories; replace animal protein as much as possible with plant protein

• Eliminate milk and milk products (substitute other calcium sources).

• Eat more fruits and vegetables (make sure that they are organically grown).

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• Eliminate polyunsaturated vegetable oils, margarine, vegetable shortening, all partially hydrogenated oils, and all foods (such as deep-fried foods) that might contain trans-fatty acids. Use extra-virgin olive oil as your main fat.

• Take ginger.

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NURSING MANAGEMENT

• Ineffective breathing pattern related to intercoastal muscle weakness

• Impaired verbal communication related to weakness of the larynx ,lips, mouth, paharynx and jaw

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• Impaired physical mobility related to voluntary muscle weakness

• Risk for aspiration related to weakness of the bulbar muscles

• Disturbed sensory perception related to ptosis,and decreased eye movements.

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ASSIGNMENT

Write down Nursing Care plan of patient with Myasthenia Gravis.

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BIBLIOGRAPHY

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