1 / 13

Guillain-Barre’

Guillain-Barre’. Guillain-Barre’ Syndrome. Post-infectious polyneuropathy; ascending polyneuropathic paralysis An acute, rapidly progressing and potentially fatal form of polyneuritis. Guillain-Barre’ Syndrome. Affects the peripheral nervous system. Guillain-Barre’.

taylor
Download Presentation

Guillain-Barre’

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Guillain-Barre’ Neurology Chapter of IAP

  2. Guillain-Barre’ Syndrome • Post-infectious polyneuropathy; ascending polyneuropathic paralysis • An acute, rapidly progressing and potentially fatal form of polyneuritis Neurology Chapter of IAP

  3. Guillain-Barre’ Syndrome • Affects the peripheral nervous system Neurology Chapter of IAP

  4. Neurology Chapter of IAP

  5. Guillain-Barre’ • T-cell sensitization occurs which causes loss of myelin which disrupts nerve impulses • Loss of myelin, edema and inflammation of the affected nerves, causes a loss of neurotransmission to the periphery. • 85% of patients recover with supportive care. Neurology Chapter of IAP

  6. Pathophysiology • Etiology unknown • May be cell-mediated immunological reaction directed at the peripheral nerves • Frequently preceded by viral infection, trauma, surgery or other immune system stimulation. Neurology Chapter of IAP

  7. Myelin Sheath Neurology Chapter of IAP

  8. Clinical Manifestations • Usually develop 1 to 3 weeks after URI or GI infection • Weakness of lower extremities (symmetrically) • Parathesia (numbness and tingling), followed by paralysis • Hypotonia and areflexia (absence of reflexes) • Pain in the form of muscles cramps or hyperesthesias (worse at night). Neurology Chapter of IAP

  9. Clinical manifestations • Autonomic nervous system dysfunction results from alterations in sympathetic and parasympathetic nervous systems. • Results in respiratory muscle paralysis, hypotension, hypertension, bradycardia, heart block, asystole. • Involvement of lower brainstem leads to facial and eye weakness Neurology Chapter of IAP

  10. Complications • Most serious is respiratory failure. • How do we manage? Neurology Chapter of IAP

  11. Diagnostic studies • Based on history and physical • EMG and nerve conduction studies will be abnormal Neurology Chapter of IAP

  12. Therapeutic management • Ventilator support! • Plasmapheresis used within the first 2 weeks of onset. If treated within the first 2 weeks, LOS of morbidity is reduced. After three weeks, plasmapharesis no benefit. • IV immunoglobin • Nutritional support (TF, TPN, Diet) Neurology Chapter of IAP

  13. Nursing management • See handout! • Read Nursing Implementation: Lewis, 1607-1608. Neurology Chapter of IAP

More Related