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Guillain Barre Syndrome A Simple Guide To The Condition, Treatment And Related Conditions

Kenneth Kee
pubblicato da Kenneth Kee

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Guillain-Barre syndrome (GBS) is a disorder in which the body's immune system attacks part of the peripheral nervous system
Guillain-Barre Syndrome is a rare autoimmune progressive disease with relatively symmetrical weakness of 2 or more limbs due to neuropathy, areflexia and mild sensory symptoms of not more than 4 weeks duration.
Causes are:

  1. A nonspecific respiratory or gastrointestinal viral illness
  2. Vaccination (rarely)
  3. Extreme exposure to cold
    The result of the antibodies attack on the peripheral nerves is inflammation of myelin and blockage of nerve conduction resulting in muscle paralysis with sensory or autonomic deficits.
    The first symptoms of this disorder are varying degrees of weakness or tingling sensations in the legs.
    In many cases the symmetrical weakness and abnormal sensations spread to the arms and upper body.
    These symptoms can increase in intensity until certain muscles cannot be used at all and when severe the person is almost totally paralyzed.
    Such an individual is often put on a ventilator to assist with breathing and is watched closely for problems such as an abnormal heart beat, infections, blood clots, and high or low blood pressure.
    Absence of fever is one of the sign of Guillain Barre Syndrome.
    Recovery usually begins 2-4 weeks after progression of disease stops
    The diagnosis of Guillain-Barre Syndrome involve
  4. History of a rapid onset and progression of ascending motor weakness, areflexia and the absence of fever.
  5. Physical and neurological examinations for peripheral neurological deficit.
  6. Cerebrospinal fluid examination-
    a. An elevated protein level (100 - 1000 mg/dL)
    b. Absent pleocytosis (increased cell count)
  7. Electromyography studies and nerve conduction studies may show prolonged distal latencies, conduction slowing, nerve conduction blockage suggestive of demyelization.
  8. Computed tomography or MRI may show actual demyelization of the nerve.
    There is no known cure for Guillain-Barre syndrome.
    The most critical part of the treatment for this syndrome consists of keeping the patient's body functioning during recovery of the nervous system.
    This can sometimes require placing the patient on mechanical ventilatory assistance, a heart monitor, or other machines that assist body function.
  9. Hospitalization and early intubation with a respirator on standby in case of difficulty in respiration
  10. Treatment of the underlying cause is started as soon as possible:
    Currently, plasma exchange (also called plasmapheresis) and high-dose immunoglobulin therapy are used.
    Both of them are equally effective but immunoglobulin is easier to administer.
    a. High dose intravenous immune globulin, which temporarily modifies the immune system and provides the body with normal antibodies from donated blood
    In high-dose immunoglobulin therapy, doctors give intravenous injections of the proteins that, in small quantities, the immune system uses naturally to attack invading organisms.
    Giving high doses of these immunoglobulins, derived from a pool of thousands of normal donors, to Guillain-Barre patients can lessen the immune attack on the nervous system.
    b. Plasmapheresis in which abnormal antibodies are removed from the blood.
    Plasmapheresis seems to reduce the severity and duration of the Guillain-Barre episode
  11. Rehabilitation is started after the patient is stable and will focus on improving activities of daily living functions such as brushing teeth, washing and getting dressed.
  12. Physiotherapy to strengthen muscles
  13. Speech therapy for speech and swallowing
    Patients sometimes need psychological counseling to help them adapt.
    The recovery period may be as little as a few weeks or as long as a few years.
    TABLE OF CONTENT
    Introduction
    Chapter 1 Guilla

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Generi Salute Benessere Self Help » Self Help » Malattia , Scienza e Tecnica » Medicina

Editore Kenneth Kee

Formato Ebook (senza DRM)

Pubblicato 16/12/2016

Lingua Inglese

EAN-13 9781370755639

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