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Abstract Details

Patterns in Axonal and Demyelinating Subtypes of Guillain-Barré Syndrome
Neuromuscular and Clinical Neurophysiology (EMG)
Neuromuscular and Clinical Neurophysiology (EMG) Posters (7:00 AM-5:00 PM)
075

To analyze the incidence of axonal vs demyelinating Guillain-Barré Syndrome (GBS) subtypes presenting to an academic center.

GBS is an autoimmune disease caused by molecular mimicry, where pathogenic epitopes from an infection are similar or identical to nerve antigens, resulting in autoimmune injury like axonal degeneration and demyelination. The classic GBS subtype is acute inflammatory demyelinating polyneuropathy (AIDP), however, acute motor sensory axonal neuropathy (AMSAN) and acute motor axonal neuropathy (AMAN) have been well described.

In a retrospective analysis of all cases of GBS identified in a database search of our electronic medical record system, we collected a list of subjects. The cases were verified by inclusion criteria of at least 2 of the following: supportive findings on electromyography, albuminocytologic dissociation on cerebrospinal fluid, clinical criteria, positive antibodies, or responsive to treatment. It was hypothesized that the AIDP subtype would be more common than AMSAN or AMAN. Information from the workup, diagnosis, course, and treatment were analyzed.

45 cases of GBS (m:23, f:22) from 2006 - 2019 were identified. Age ranged from 19 to 86 years (M=57.3, SD=18.4), average length of hospitalization was 13 days, and 28.9% and 22.2% had preceding symptoms for respiratory and gastrointestinal infections, respectively. The most common presenting symptom was lower extremity weakness (91.1%), followed by upper extremity paresthesia (55.6%). Physical exam was most notable for lower extremity weakness (80%) and hyporeflexia or areflexia (82.2%). The most common GBS subtype was AIDP (55.6%), followed by AMSAN (26.7%), and AMAN (8.9%). 80% of patients received intravenous immunoglobulin therapy, 11.1% received plasmapheresis and 8.9% received both. There were no significant findings between sex, age, or GBS subtype with the variables in the study.

The most common subtype of GBS was AIDP, although the non-demyelinating forms were fairly common. There were no significant differences in clinical course among the subtypes.

Authors/Disclosures
Peter Q. Mai, MD (Barrow Neurological Institute)
PRESENTER
Dr. Mai has nothing to disclose.
Pravesh Saini, MD (LAC + USC Keck Medical Center) Dr. Saini has nothing to disclose.
Lawrence A. Zeidman, MD, FÂé¶¹´«Ã½Ó³»­ (Endeavor Health Northshore Department of Neurology) Dr. Zeidman has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Johnson & Johnson. Dr. Zeidman has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Argenx. Dr. Zeidman has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Pfizer. Dr. Zeidman has received personal compensation in the range of $10,000-$49,999 for serving as an Expert Witness for Smith Blake Hill LLC. The institution of Dr. Zeidman has received research support from Octapharma. Dr. Zeidman has received publishing royalties from a publication relating to health care.
Michael J. Schneck, MD, FÂé¶¹´«Ã½Ó³»­ (Loyola University Chicago, Stritch School of Medicine) An immediate family member of Dr. Schneck has received personal compensation for serving as an employee of Cellcarta. Dr. Schneck has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for HLT Medical. Dr. Schneck has received personal compensation in the range of $10,000-$49,999 for serving as an Expert Witness for Miscellaneous legal firms. Dr. Schneck has stock in Baxter Labs. The institution of Dr. Schneck has received research support from NIH.