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Determination of the Plasmodium vivax relapse pattern in Camopi, French Guiana
BACKGROUND: Malaria is a major public health problem in French Guiana, where Plasmodium vivax has become the dominant malaria species since 2000. As in others endemic areas, it is important to specify the pattern of vivax malaria relapses and to try to discriminate efficiently re-infections from rel...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2793261/ https://www.ncbi.nlm.nih.gov/pubmed/19961585 http://dx.doi.org/10.1186/1475-2875-8-278 |
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author | Hanf, Matthieu Stéphani, Aurélia Basurko, Célia Nacher, Mathieu Carme, Bernard |
author_facet | Hanf, Matthieu Stéphani, Aurélia Basurko, Célia Nacher, Mathieu Carme, Bernard |
author_sort | Hanf, Matthieu |
collection | PubMed |
description | BACKGROUND: Malaria is a major public health problem in French Guiana, where Plasmodium vivax has become the dominant malaria species since 2000. As in others endemic areas, it is important to specify the pattern of vivax malaria relapses and to try to discriminate efficiently re-infections from relapses. METHODS: This study was conducted in children born between January 1, 2001 and December 31, 2008 in Camopi, an Amerindian village located in the Amazon forest (n = 325), using an open cohort design. Primary and secondary attack rates of P. vivax were calculated using survival analysis. With the difference between the primary and secondary rates, this study aimed to estimate indirectly P. vivax relapse rate and evaluate its time evolution. RESULTS: Of the 1042 malaria attacks recorded, 689 (66%) were due to P. vivax (without mixed infection). One hundred and fifty one children had their primary attack with P. vivax and 106 had their two first attacks with P. vivax. In the absence of primaquine treatment, it was shown that P. vivax relapses mainly occurred during the first three months after the first attack. Thirty percent of children never had a relapse, 42% had a relapse before the first month after primary attack, 59% before the second month and 63% before the third month. CONCLUSION: This study confirmed that the relapse pattern in Camopi was compatible with the pattern described for the P. vivax Chesson (tropical) strain. In addition, due to the relapse rate time evolution, a simple arbitrary classification rule could be constructed: before 90 days after the primary attack, the secondary attack is a relapse; after 90 days, it is a re-infection. Adapted management of malaria cases based on these results could be devised. |
format | Text |
id | pubmed-2793261 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27932612009-12-15 Determination of the Plasmodium vivax relapse pattern in Camopi, French Guiana Hanf, Matthieu Stéphani, Aurélia Basurko, Célia Nacher, Mathieu Carme, Bernard Malar J Research BACKGROUND: Malaria is a major public health problem in French Guiana, where Plasmodium vivax has become the dominant malaria species since 2000. As in others endemic areas, it is important to specify the pattern of vivax malaria relapses and to try to discriminate efficiently re-infections from relapses. METHODS: This study was conducted in children born between January 1, 2001 and December 31, 2008 in Camopi, an Amerindian village located in the Amazon forest (n = 325), using an open cohort design. Primary and secondary attack rates of P. vivax were calculated using survival analysis. With the difference between the primary and secondary rates, this study aimed to estimate indirectly P. vivax relapse rate and evaluate its time evolution. RESULTS: Of the 1042 malaria attacks recorded, 689 (66%) were due to P. vivax (without mixed infection). One hundred and fifty one children had their primary attack with P. vivax and 106 had their two first attacks with P. vivax. In the absence of primaquine treatment, it was shown that P. vivax relapses mainly occurred during the first three months after the first attack. Thirty percent of children never had a relapse, 42% had a relapse before the first month after primary attack, 59% before the second month and 63% before the third month. CONCLUSION: This study confirmed that the relapse pattern in Camopi was compatible with the pattern described for the P. vivax Chesson (tropical) strain. In addition, due to the relapse rate time evolution, a simple arbitrary classification rule could be constructed: before 90 days after the primary attack, the secondary attack is a relapse; after 90 days, it is a re-infection. Adapted management of malaria cases based on these results could be devised. BioMed Central 2009-12-04 /pmc/articles/PMC2793261/ /pubmed/19961585 http://dx.doi.org/10.1186/1475-2875-8-278 Text en Copyright ©2009 Hanf 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 | Research Hanf, Matthieu Stéphani, Aurélia Basurko, Célia Nacher, Mathieu Carme, Bernard Determination of the Plasmodium vivax relapse pattern in Camopi, French Guiana |
title | Determination of the Plasmodium vivax relapse pattern in Camopi, French Guiana |
title_full | Determination of the Plasmodium vivax relapse pattern in Camopi, French Guiana |
title_fullStr | Determination of the Plasmodium vivax relapse pattern in Camopi, French Guiana |
title_full_unstemmed | Determination of the Plasmodium vivax relapse pattern in Camopi, French Guiana |
title_short | Determination of the Plasmodium vivax relapse pattern in Camopi, French Guiana |
title_sort | determination of the plasmodium vivax relapse pattern in camopi, french guiana |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2793261/ https://www.ncbi.nlm.nih.gov/pubmed/19961585 http://dx.doi.org/10.1186/1475-2875-8-278 |
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