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Resistance of infection by Plasmodium vivax to chloroquine in Bolivia
BACKGROUND: Chloroquine (CQ) over three days plus primaquine (PQ) for seven days is the treatment of choice of infections by Plasmodium vivax in Bolivia, where 95% of the cases of malaria are attributed to this species. The aim of this study was to evaluate the therapeutic efficacy of CQ in this set...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4488061/ https://www.ncbi.nlm.nih.gov/pubmed/26126708 http://dx.doi.org/10.1186/s12936-015-0774-4 |
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author | Añez, Arletta Moscoso, Manuel Laguna, Ángel Garnica, Cecilia Melgar, Viviana Cuba, Mauren Gutierrez, Sonia Ascaso, Carlos |
author_facet | Añez, Arletta Moscoso, Manuel Laguna, Ángel Garnica, Cecilia Melgar, Viviana Cuba, Mauren Gutierrez, Sonia Ascaso, Carlos |
author_sort | Añez, Arletta |
collection | PubMed |
description | BACKGROUND: Chloroquine (CQ) over three days plus primaquine (PQ) for seven days is the treatment of choice of infections by Plasmodium vivax in Bolivia, where 95% of the cases of malaria are attributed to this species. The aim of this study was to evaluate the therapeutic efficacy of CQ in this setting. METHODS: Patients in the Amazon region of northern Bolivia, were included in the study from May to November 2011 and the therapeutic efficacy of CQ was evaluated over a 28-day follow-up period. Patients with P. vivax mono-infection received 25 mg/Kg body weight of CQ over three days. The concentrations of CQ + desethylchloroquine (DCQ) in blood were determined at days 7 and 28 of follow up; at follow-up and on the day of treatment failure was administered PQ. RESULTS: One hundred patients fulfilled the inclusion criteria, two were lost to follow up and another two were later excluded for protocol violation. Of the 96 patients who completed the follow up 10 showed TF; one presented continued parasitaemia until day 7 of follow up, three on day 21 and six on day 28 of follow up. The geometric mean of CQ + DCQ on day 7 was 321.7 ng/ml (range 197–535 ng/ml). In six patients with TF the CQ + DCQ concentrations in blood on the day of TF were >100 ng/ml. The rate of resistance was 6.5%. CONCLUSION: The present study demonstrates the presence of resistance to CQ in the treatment of malaria by P. vivax in the Amazon region of Bolivia. New clinical trials are needed to establish alternative treatments against these parasites in this region of South America. |
format | Online Article Text |
id | pubmed-4488061 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44880612015-07-03 Resistance of infection by Plasmodium vivax to chloroquine in Bolivia Añez, Arletta Moscoso, Manuel Laguna, Ángel Garnica, Cecilia Melgar, Viviana Cuba, Mauren Gutierrez, Sonia Ascaso, Carlos Malar J Research BACKGROUND: Chloroquine (CQ) over three days plus primaquine (PQ) for seven days is the treatment of choice of infections by Plasmodium vivax in Bolivia, where 95% of the cases of malaria are attributed to this species. The aim of this study was to evaluate the therapeutic efficacy of CQ in this setting. METHODS: Patients in the Amazon region of northern Bolivia, were included in the study from May to November 2011 and the therapeutic efficacy of CQ was evaluated over a 28-day follow-up period. Patients with P. vivax mono-infection received 25 mg/Kg body weight of CQ over three days. The concentrations of CQ + desethylchloroquine (DCQ) in blood were determined at days 7 and 28 of follow up; at follow-up and on the day of treatment failure was administered PQ. RESULTS: One hundred patients fulfilled the inclusion criteria, two were lost to follow up and another two were later excluded for protocol violation. Of the 96 patients who completed the follow up 10 showed TF; one presented continued parasitaemia until day 7 of follow up, three on day 21 and six on day 28 of follow up. The geometric mean of CQ + DCQ on day 7 was 321.7 ng/ml (range 197–535 ng/ml). In six patients with TF the CQ + DCQ concentrations in blood on the day of TF were >100 ng/ml. The rate of resistance was 6.5%. CONCLUSION: The present study demonstrates the presence of resistance to CQ in the treatment of malaria by P. vivax in the Amazon region of Bolivia. New clinical trials are needed to establish alternative treatments against these parasites in this region of South America. BioMed Central 2015-07-01 /pmc/articles/PMC4488061/ /pubmed/26126708 http://dx.doi.org/10.1186/s12936-015-0774-4 Text en © Añez et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Añez, Arletta Moscoso, Manuel Laguna, Ángel Garnica, Cecilia Melgar, Viviana Cuba, Mauren Gutierrez, Sonia Ascaso, Carlos Resistance of infection by Plasmodium vivax to chloroquine in Bolivia |
title | Resistance of infection by Plasmodium vivax to chloroquine in Bolivia |
title_full | Resistance of infection by Plasmodium vivax to chloroquine in Bolivia |
title_fullStr | Resistance of infection by Plasmodium vivax to chloroquine in Bolivia |
title_full_unstemmed | Resistance of infection by Plasmodium vivax to chloroquine in Bolivia |
title_short | Resistance of infection by Plasmodium vivax to chloroquine in Bolivia |
title_sort | resistance of infection by plasmodium vivax to chloroquine in bolivia |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4488061/ https://www.ncbi.nlm.nih.gov/pubmed/26126708 http://dx.doi.org/10.1186/s12936-015-0774-4 |
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