SESSION TITLE: Wednesday Medical Student/Resident Case Report Posters SESSION TYPE: Med Student/Res Case Rep Postr PRESENTED ON: 10/23/2019 09:45 AM - 10:45 AM INTRODUCTION: Neuromuscular disorders should be considered for patients presenting with rapid onset bulbar weakness and shortness of breath. CASE PRESENTATION: A 30 y.o. man with no history of neurologic illness returned from a 4 day Caribbean trip with a 1 day history of dysphagia, voice change and dyspnea. He denied diplopia. He has history of Thyroid cancer post thyroidectomy and radiation, Hep B on Tenofovir. He had tachypnea, ptosis, dysphonia, dysphagia. Initial ABG revealed mild hypoxia with pO2 76 and hypercapnia with pCO2 52. He had proximal muscle weakness, intact reflexes and Negative Inspiratory Force (NIF) of -12cmH2O(normal:>-60cmH2O). He was intubated with differentials: Guillain Barre Syndrome(GBS), acute flaccid paralysis and Myasthenia Gravis(MG). He was given high dose steroids and 5 days plasmapheresis. His workup revealed a negative viral panel,AChRAB,HIV,syphilis,dengue,Zika,lyme. Acetylcholine Receptor Blocking Antibody was present with 43% inhibition. Electromyography revealed absent F waves, which was suggestive of GBS, but there was no cytoalbuminologic dissociation in CSF and Anti-GQ1B and Anti-VGCC were negative.Pyridostigmine was added and there was improvement in strength. His stay was complicated by ventilator-associated pneumonia, was extubated on day18 and discharged on day 22. DISCUSSION: The annual incidence of MG is 1–2/100,000.Myasthenic Crisis (MC) is the initial presentation for 20% of patients with ⅓ of patients surviving. 21% have onset after 60 years and 30% of them develop some degree of bulbar/respiratory weakness.Average age of admission with MC is 59.MG shows a bimodal distribution, with the following male:female ratios:3:7 if 50 years. Variants of GBS may present similarly and should be evaluated for. MG is an autoimmune disorder affecting neuromuscular transmission. It is due to autoantibodies against acetylcholine receptors in the postsynaptic motor end-plate. MC is characterized by worsening weakness resulting in respiratory failure. Most patients have a predisposing factor that triggers MC, generally a respiratory infection. Immunoglobulins, plasma exchange, and steroids are the pillars of therapy. Today with the modern critical care mortality <5%. The decision to intubate this patient was made on bedside measures of respiratory function. Only 19% of patients have crisis starting with bulbar symptoms and 5% with weakness of respiratory muscles. Majority of patients begin with generalized weakness. Our patient is a young male who had rapid onset bulbar weakness. Elective intubation is recommended rather than emergently after respiratory collapse. If the suspicion is high, quick bedside tests like NIF should be done and patients promptly intubated. CONCLUSIONS: When respiratory failure is expected, bedside assessments can document weakness and indicate need for invasive ventilation prior to respiratory embarrassment. Reference #1: Berrouschot J, Baumann I, Kalischewski P, et al. Therapy of myasthenic crisis. Crit Care Med 1997; 25:1228. Reference #2: Alshekhlee A, Miles JD, Katirji B, Preston DC, Kaminski HJ. Incidence and mortality rates of myasthenia gravis and myasthenic crisis in US hospitals. Neurology 2009;72:1548-1554 DISCLOSURES: No relevant relationships by Raghav Chaudhary, source=Web Response No relevant relationships by Latoya Gayle, source=Web Response No relevant relationships by Philip Kanemo, source=Web Response No relevant relationships by Rikki Racela, source=Web Response No relevant relationships by Rani Sittol, source=Web Response