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The clinical response of West Nile virus neuroinvasive disease to intravenous immunoglobulin therapy

The aim of the study was to determine whether intravenous gamma globulin (IVIG) treatment is effective in patients with West Nile Virus (WNV) neuroinvasive disease. We contacted hospital based infectious disease experts in Israeli hospitals to identify patients with WNV neuroinvasive disease who wer...

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Autores principales: Shimoni, Zvi, Bin, Hanna, Bulvik, Shlomo, Niven, Mark, Hazzan, Rawi, Mendelson, Ella, Froom, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3981344/
https://www.ncbi.nlm.nih.gov/pubmed/24765417
http://dx.doi.org/10.4081/cp.2012.e18
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author Shimoni, Zvi
Bin, Hanna
Bulvik, Shlomo
Niven, Mark
Hazzan, Rawi
Mendelson, Ella
Froom, Paul
author_facet Shimoni, Zvi
Bin, Hanna
Bulvik, Shlomo
Niven, Mark
Hazzan, Rawi
Mendelson, Ella
Froom, Paul
author_sort Shimoni, Zvi
collection PubMed
description The aim of the study was to determine whether intravenous gamma globulin (IVIG) treatment is effective in patients with West Nile Virus (WNV) neuroinvasive disease. We contacted hospital based infectious disease experts in Israeli hospitals to identify patients with WNV neuroinvasive disease who were treated with IVIG. The main outcome measure was neurological response after treatment. There were 12 patients who received IVIG and four improved within 48 h. Three patients died, 6 had partial recovery, and 3 recovered completely. Eleven of the 12 patients were infected with Israeli genotypes that are highly homologous to Europe/Africa viruses. The rapid response in some patients suggests that IVIG is effective, and might be used to treat patients with WNV neuroinvasive disease with IVIG.
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spelling pubmed-39813442014-04-24 The clinical response of West Nile virus neuroinvasive disease to intravenous immunoglobulin therapy Shimoni, Zvi Bin, Hanna Bulvik, Shlomo Niven, Mark Hazzan, Rawi Mendelson, Ella Froom, Paul Clin Pract Brief Report The aim of the study was to determine whether intravenous gamma globulin (IVIG) treatment is effective in patients with West Nile Virus (WNV) neuroinvasive disease. We contacted hospital based infectious disease experts in Israeli hospitals to identify patients with WNV neuroinvasive disease who were treated with IVIG. The main outcome measure was neurological response after treatment. There were 12 patients who received IVIG and four improved within 48 h. Three patients died, 6 had partial recovery, and 3 recovered completely. Eleven of the 12 patients were infected with Israeli genotypes that are highly homologous to Europe/Africa viruses. The rapid response in some patients suggests that IVIG is effective, and might be used to treat patients with WNV neuroinvasive disease with IVIG. PAGEPress Publications 2012-01-27 /pmc/articles/PMC3981344/ /pubmed/24765417 http://dx.doi.org/10.4081/cp.2012.e18 Text en ©Copyright Z. Shimoni et al., 2012 This work is licensed under a Creative Commons Attribution NonCommercial 3.0 License (CC BY-NC 3.0). Licensee PAGEPress, Italy
spellingShingle Brief Report
Shimoni, Zvi
Bin, Hanna
Bulvik, Shlomo
Niven, Mark
Hazzan, Rawi
Mendelson, Ella
Froom, Paul
The clinical response of West Nile virus neuroinvasive disease to intravenous immunoglobulin therapy
title The clinical response of West Nile virus neuroinvasive disease to intravenous immunoglobulin therapy
title_full The clinical response of West Nile virus neuroinvasive disease to intravenous immunoglobulin therapy
title_fullStr The clinical response of West Nile virus neuroinvasive disease to intravenous immunoglobulin therapy
title_full_unstemmed The clinical response of West Nile virus neuroinvasive disease to intravenous immunoglobulin therapy
title_short The clinical response of West Nile virus neuroinvasive disease to intravenous immunoglobulin therapy
title_sort clinical response of west nile virus neuroinvasive disease to intravenous immunoglobulin therapy
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3981344/
https://www.ncbi.nlm.nih.gov/pubmed/24765417
http://dx.doi.org/10.4081/cp.2012.e18
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