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Guillain Barre Synd
| Question | Answer |
|---|---|
| Patho | Acute autoimmune disorder attacking peripheral nerve myelin sheaths (demyelinating polyneuropathy). Often post-infection. |
| GBS Trigger | Most commonly preceded by bacterial (Campylobacter jejuni) or viral (H. influenzae, CMV) infection 1-4 weeks prior. |
| Key Symptoms | Ascending, symmetric paralysis or weakness. Starts in lower extremities, progresses upward to trunk, arms, cranial nerves. |
| Respiratory | Paralysis can ascend to diaphragm. Monitor for respiratory failure. Priority sign: Drooling (cannot swallow secretions). |
| Autonomic Involvement | Can cause instability: tachycardia/bradycardia, hypertension/hypotension, diaphoresis. |
| Prognosis | Most patients experience significant recovery over months to years with rehabilitation (PT/OT). High mortality if respiratory failure occurs. |
| ANS Signs | Labile BP & HR, cardiac arrhythmias, paralytic ileus, urinary retention, diaphoresis. Requires cardiac monitoring. |
| Lumbar Puncture | Albuminocytologic dissociation: Elevated CSF protein with normal cell count. May be normal in first week. |
| Peak Illness | Weakness typically progresses for up to 4 weeks, then plateaus (plateau phase) before recovery begins. |
| Plasmapheresis | Removes circulating antibodies. Most effective if started within 2 weeks of symptom onset. 5 exchanges over 8-10 days. |
| IV Immunoglobulin (IVIG) | Equal efficacy to plasmapheresis. 2 g/kg over 2-5 days. Can cause aseptic meningitis, flu-like symptoms. |
| Pain Management | Neuropathic pain is common. Use gabapentin, pregabalin, or tricyclic antidepressants. Opioids often less effective. |