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Published on: November 9, 2017
Occurrence of hemolytic anemia in patients with GBS treated with high-dose IVIg
Thy P Nguyen1, Suur Biliciler1, Amer Wahed1
1Departments of Neurology (T.P.N., S.B., K.S.) and Pathology (A.W.), University of Texas Health Science Center at Houston, TX.
Objective:
We describe an underrecognized side effect of high-dose IV immunoglobulin (IVIg), hemolytic anemia.
Background:
There are no established guidelines on treating patients with Guillain-Barré syndrome (GBS) who relapse or do not improve after a standard course of treatment (IVIg or plasma exchange). Some centers will opt for a second course of the initial treatment. There is an ongoing trial of a second course of IVIg in patients with severe GBS.
Methods:
We retrospectively reviewed 4 patients with severe GBS who received high-dose IVIg. One patient inadvertently received a high dose of IVIg for Miller Fisher syndrome. All patients received a total of at least 2 courses of the standard dose of IVIg (total >4 g/kg). We review their clinical course and side effects.
Results:
All patients with non-O blood types developed clinically significant hemolytic anemia requiring blood transfusion.
Conclusion:
Hemolytic anemia may limit doses of IVIg for treatment of severe GBS in patients with non-O blood types.
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