Cargando…

Occurrence of hemolytic anemia in patients with GBS treated with high-dose IVIg

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 ex...

Descripción completa

Detalles Bibliográficos
Autores principales: Nguyen, Thy P., Biliciler, Suur, Wahed, Amer, Sheikh, Kazim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4268039/
https://www.ncbi.nlm.nih.gov/pubmed/25520957
http://dx.doi.org/10.1212/NXI.0000000000000050
Descripción
Sumario: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.