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Treatment of imported severe malaria with artesunate instead of quinine - more evidence needed?

Rapid and fast acting anti-malarials are essential to treat severe malaria. Quinine has been the only option for parenteral therapy until recently. While current evidence shows that intravenous artesunate is more effective than quinine in treating severe malaria in endemic countries, some questions...

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Autores principales: Cramer, Jakob P, López-Vélez, Rogelio, Burchard, Gerd D, Grobusch, Martin P, de Vries, Peter J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3224352/
https://www.ncbi.nlm.nih.gov/pubmed/21899729
http://dx.doi.org/10.1186/1475-2875-10-256
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author Cramer, Jakob P
López-Vélez, Rogelio
Burchard, Gerd D
Grobusch, Martin P
de Vries, Peter J
author_facet Cramer, Jakob P
López-Vélez, Rogelio
Burchard, Gerd D
Grobusch, Martin P
de Vries, Peter J
author_sort Cramer, Jakob P
collection PubMed
description Rapid and fast acting anti-malarials are essential to treat severe malaria. Quinine has been the only option for parenteral therapy until recently. While current evidence shows that intravenous artesunate is more effective than quinine in treating severe malaria in endemic countries, some questions remain regarding safety profiles and drug resistance. For imported severe malaria, additional unanswered questions are related to generalizability of the findings from endemic countries and to legal aspects, as there is no Good Manufacturing Practice-conform drug available yet. Here, the implications of existing evidence for the treatment of imported severe malaria are discussed.
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spelling pubmed-32243522011-11-27 Treatment of imported severe malaria with artesunate instead of quinine - more evidence needed? Cramer, Jakob P López-Vélez, Rogelio Burchard, Gerd D Grobusch, Martin P de Vries, Peter J Malar J Commentary Rapid and fast acting anti-malarials are essential to treat severe malaria. Quinine has been the only option for parenteral therapy until recently. While current evidence shows that intravenous artesunate is more effective than quinine in treating severe malaria in endemic countries, some questions remain regarding safety profiles and drug resistance. For imported severe malaria, additional unanswered questions are related to generalizability of the findings from endemic countries and to legal aspects, as there is no Good Manufacturing Practice-conform drug available yet. Here, the implications of existing evidence for the treatment of imported severe malaria are discussed. BioMed Central 2011-09-07 /pmc/articles/PMC3224352/ /pubmed/21899729 http://dx.doi.org/10.1186/1475-2875-10-256 Text en Copyright ©2011 Cramer et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Commentary
Cramer, Jakob P
López-Vélez, Rogelio
Burchard, Gerd D
Grobusch, Martin P
de Vries, Peter J
Treatment of imported severe malaria with artesunate instead of quinine - more evidence needed?
title Treatment of imported severe malaria with artesunate instead of quinine - more evidence needed?
title_full Treatment of imported severe malaria with artesunate instead of quinine - more evidence needed?
title_fullStr Treatment of imported severe malaria with artesunate instead of quinine - more evidence needed?
title_full_unstemmed Treatment of imported severe malaria with artesunate instead of quinine - more evidence needed?
title_short Treatment of imported severe malaria with artesunate instead of quinine - more evidence needed?
title_sort treatment of imported severe malaria with artesunate instead of quinine - more evidence needed?
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3224352/
https://www.ncbi.nlm.nih.gov/pubmed/21899729
http://dx.doi.org/10.1186/1475-2875-10-256
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