Assignment: Myasthenia Gravis: Read the following article:
- Moore, A.S. & Shepard, L.H. (2014). Nursing Made Incredibly Easy! 12 (4). 21-30.
Initial Discussion Post:
Select one (1) of the following Nursing Diagnoses:
Impaired Spontaneous Ventilation
Impaired Swallowing
Care Giver Role StrainAddress the following:
Is the nursing diagnoses that you selected appropriate for the patient with a diagnosis of myasthenia gravis, Guillain-Barre syndrome or both? Explain your answer.
Provide an outcome for the nursing diagnosis that you selected making sure that is specific to the needs of the patient with myasthenia gravis or Guillain-Barre syndrome.
Identify two (2) interventions that will help your patient with myasthenia gravis or Guillain-Barre syndrome reach the outcome for the nursing diagnosis.
350 words minimum APA format in text citation
Myasthenia Gravis
Definition
Myasthenia gravis (MG) is an autoimmune neuromuscular disorder that is characterized by fatigue and exhaustion of muscles. The most commonly affected muscles are those of the eyes, face, and swallowing. It can affect people of any age, typically starting in women under 40 and men over 60. It can result in double vision, drooping eyelids, trouble talking, and trouble walking. Onset can be sudden. Those affected often have a large thymus gland or develop a thymoma.
It occurs when communication between nerve cells and muscles becomes impaired. This impairment prevents crucial muscle contractions from occurring, resulting in muscle weakness. It is generally treated with medications known as acetylcholinesterase inhibitors such as neostigmine and pyridostigmine. Immunosuppressants, such as prednisone or azathioprine, may also be used.
Myasthenia gravis affects 50 to 200 per million people. It is newly diagnosed in three to 30 per million people each year. Diagnosis is becoming more common due to increased awareness.
Causes, Sign and Symptoms of Myasthenia Gravis
Myasthenia gravis is a neuromuscular disorder that’s usually caused by an autoimmune problem. It is caused by a problem with the signals sent between the nerves and the muscles. It’s an autoimmune condition, which means it’s the result of the immune system, which is the body’s natural defence against illness and infection mistakenly attacking a healthy part of the body.
In myasthenia gravis, the immune system damages the communication system between the nerves and muscles, making the muscles weak and easily tired. It’s not clear why this happens, but it has been linked to issues with the thymus gland (a gland in the chest that’s part of the immune system).
In many people with myasthenia gravis, the thymus gland is larger than normal, and in around 1 in 10 people there is abnormal growth of the thymus called a thymoma.
The main symptom of Myasthenia gravis is weakness in the voluntary skeletal muscles, which are muscles under patient’s control. The failure of muscles to contract normally occurs because they can’t respond to nerve impulses. Without proper transmission of the impulse, a blocked communication occurs between nerve and muscle and weakness results.
Common symptoms of myasthenia gravis include:
- droopy eyelids
- double vision
- difficulty making facial expressions
- problems with chewing and difficulty swallowing
- slurred speech
- weak arms, legs or neck
- shortness of breath and occasionally serious breathing difficulties
In a myasthenic crisis, a paralysis of the respiratory muscles occurs, necessitating assisted ventilation to sustain life. Crises may be triggered by various biological stressors such as infection, fever, an adverse reaction to medication, or emotional stress.
Not everyone will have every symptom, and the degree of muscle weakness can change from day to day. The severity of the symptoms typically increases over time if left untreated.
Diagnosis and Treatment of Myasthenia Gravis
Myasthenia Gravis can be difficult to diagnose, as the symptoms can be subtle and hard to distinguish from both normal variants and other neurological disorders.
Three types of myasthenic symptoms in children can be distinguished:
- Transient neonatal myasthenia occurs in 10 to 15% of babies born to mothers afflicted with the disorder, and disappears after a few weeks.
- Congenitalmyasthenia, the rarest form, occurs when genes are present from both parents.
- Juvenile myasthenia gravis is most common in females.
Congenital myasthenias cause muscle weakness and fatigability similar to those of MG. The signs of congenital myasthenia usually are present in the first years of childhood, although they may not be recognized until adulthood.
There is no cure for myasthenia gravis. The goal of treatment is to manage symptoms and control the activity of your immune system.
Medication: Corticosteroids and immunosuppressants can be used to suppress the immune system. These medications help minimize the abnormal immune response that occurs in MG.
Thymus Gland Removal: Removal of the thymus gland, which is part of the immune system, may be appropriate for many patients with MG. Once the thymus is removed, patients typically show less muscle weakness.
Plasma Exchange: Plasmapheresis is also known as a plasma exchange. This process removes harmful antibodies from the blood, which may result in an improvement in muscle strength.
Intravenous Immune Globulin: Intravenous immune globulin (IVIG) is blood product that comes from donors. It’s used to treat autoimmune MG. Although it’s not entirely known how IVIG works, it affects the creation and function of antibodies.
Lifestyle Changes: There are some things people can do at home to help alleviate symptoms of MG:
- Get plenty of rest to help minimize muscle weakness.
- If they are bothered by double vision, talk to doctor about whether they should wear an eye patch.
- Avoid stress and heat exposure, as both can worsen symptoms.
These treatments cannot cure MG. However, patient will typically see improvements in their symptoms. Some individuals may go into remission, during which treatment is not necessary.
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