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Mefloquine safety and tolerability in pregnancy: a systematic literature review
BACKGROUND: Control of malaria in pregnant women is still a major challenge as it constitutes an important cause of maternal and neonatal mortality. Mefloquine (MQ) has been used for malaria chemoprophylaxis in non-immune travellers for several decades and it constitutes a potential candidate for in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3942617/ https://www.ncbi.nlm.nih.gov/pubmed/24581338 http://dx.doi.org/10.1186/1475-2875-13-75 |
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author | González, Raquel Hellgren, Urban Greenwood, Brian Menéndez, Clara |
author_facet | González, Raquel Hellgren, Urban Greenwood, Brian Menéndez, Clara |
author_sort | González, Raquel |
collection | PubMed |
description | BACKGROUND: Control of malaria in pregnant women is still a major challenge as it constitutes an important cause of maternal and neonatal mortality. Mefloquine (MQ) has been used for malaria chemoprophylaxis in non-immune travellers for several decades and it constitutes a potential candidate for intermittent preventive treatment in pregnant women (IPTp). METHODS: The safety of MQ, including its safety in pregnancy, is controversial and a continuing subject of debate. Published studies which evaluated the use of MQ for malaria prevention or treatment in pregnant women and which reported data on drug tolerability and/or pregnancy outcomes have been reviewed systematically. RESULTS: Eighteen articles fitted the inclusion criteria, only one study was double-blind and placebo controlled. No differences were found in the risk of adverse pregnancy outcomes in women exposed to MQ compared to those exposed to other anti-malarials or to the general population. MQ combined with artesunate seems to be better tolerated than standard quinine therapy for treatment of non-severe falciparum malaria, but a MQ loading dose (10 mg/kg) is associated with more dizziness compared with placebo. When used for IPTp, MQ (15 mg/kg) may have more side effects than sulphadoxine- pyrimethamine. CONCLUSIONS: In the published literature there are no indications that MQ use during pregnancy carries an increased risk for the foetus. Ideally, the use of MQ to prevent malaria should be based on a risk-benefit analysis of adverse effects against the risk of acquiring the infection. For this purpose double-blinded randomized controlled trials in African pregnant women are much needed. |
format | Online Article Text |
id | pubmed-3942617 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39426172014-03-06 Mefloquine safety and tolerability in pregnancy: a systematic literature review González, Raquel Hellgren, Urban Greenwood, Brian Menéndez, Clara Malar J Research BACKGROUND: Control of malaria in pregnant women is still a major challenge as it constitutes an important cause of maternal and neonatal mortality. Mefloquine (MQ) has been used for malaria chemoprophylaxis in non-immune travellers for several decades and it constitutes a potential candidate for intermittent preventive treatment in pregnant women (IPTp). METHODS: The safety of MQ, including its safety in pregnancy, is controversial and a continuing subject of debate. Published studies which evaluated the use of MQ for malaria prevention or treatment in pregnant women and which reported data on drug tolerability and/or pregnancy outcomes have been reviewed systematically. RESULTS: Eighteen articles fitted the inclusion criteria, only one study was double-blind and placebo controlled. No differences were found in the risk of adverse pregnancy outcomes in women exposed to MQ compared to those exposed to other anti-malarials or to the general population. MQ combined with artesunate seems to be better tolerated than standard quinine therapy for treatment of non-severe falciparum malaria, but a MQ loading dose (10 mg/kg) is associated with more dizziness compared with placebo. When used for IPTp, MQ (15 mg/kg) may have more side effects than sulphadoxine- pyrimethamine. CONCLUSIONS: In the published literature there are no indications that MQ use during pregnancy carries an increased risk for the foetus. Ideally, the use of MQ to prevent malaria should be based on a risk-benefit analysis of adverse effects against the risk of acquiring the infection. For this purpose double-blinded randomized controlled trials in African pregnant women are much needed. BioMed Central 2014-02-28 /pmc/articles/PMC3942617/ /pubmed/24581338 http://dx.doi.org/10.1186/1475-2875-13-75 Text en Copyright © 2014 González 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 credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research González, Raquel Hellgren, Urban Greenwood, Brian Menéndez, Clara Mefloquine safety and tolerability in pregnancy: a systematic literature review |
title | Mefloquine safety and tolerability in pregnancy: a systematic literature review |
title_full | Mefloquine safety and tolerability in pregnancy: a systematic literature review |
title_fullStr | Mefloquine safety and tolerability in pregnancy: a systematic literature review |
title_full_unstemmed | Mefloquine safety and tolerability in pregnancy: a systematic literature review |
title_short | Mefloquine safety and tolerability in pregnancy: a systematic literature review |
title_sort | mefloquine safety and tolerability in pregnancy: a systematic literature review |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3942617/ https://www.ncbi.nlm.nih.gov/pubmed/24581338 http://dx.doi.org/10.1186/1475-2875-13-75 |
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