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Severe falciparum malaria in young children of the Kassena-Nankana district of northern Ghana

STUDY DESIGN: Severe falciparum malaria in children was studied as part of the characterization of the Kassena-Nankana District Ghana for future malaria vaccine trials. Children aged 6–59 months with diagnosis suggestive of acute disease were characterized using the standard WHO definition for sever...

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Autores principales: Oduro, Abraham R, Koram, Kwadwo A, Rogers, William, Atuguba, Frank, Ansah, Patrick, Anyorigiya, Thomas, Ansah, Akosua, Anto, Francis, Mensah, Nathan, Hodgson, Abraham, Nkrumah, Francis
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1950879/
https://www.ncbi.nlm.nih.gov/pubmed/17662142
http://dx.doi.org/10.1186/1475-2875-6-96
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author Oduro, Abraham R
Koram, Kwadwo A
Rogers, William
Atuguba, Frank
Ansah, Patrick
Anyorigiya, Thomas
Ansah, Akosua
Anto, Francis
Mensah, Nathan
Hodgson, Abraham
Nkrumah, Francis
author_facet Oduro, Abraham R
Koram, Kwadwo A
Rogers, William
Atuguba, Frank
Ansah, Patrick
Anyorigiya, Thomas
Ansah, Akosua
Anto, Francis
Mensah, Nathan
Hodgson, Abraham
Nkrumah, Francis
author_sort Oduro, Abraham R
collection PubMed
description STUDY DESIGN: Severe falciparum malaria in children was studied as part of the characterization of the Kassena-Nankana District Ghana for future malaria vaccine trials. Children aged 6–59 months with diagnosis suggestive of acute disease were characterized using the standard WHO definition for severe malaria. RESULTS: Of the total children screened, 45.2% (868/1921) satisfied the criteria for severe malaria. Estimated incidence of severe malaria was 3.4% (range: 0.4–8.3%) cases per year. The disease incidence was seasonal: 560 cases per year, of which 70.4% occurred during the wet season (June-October). The main manifestations were severe anaemia (36.5%); prolonged or multiple convulsions (21.6%); respiratory distress (24.4%) and cerebral malaria (5.4%). Others were hyperpyrexia (11.1%); hyperparasitaemia (18.5%); hyperlactaemia (33.4%); and hypoglycaemia (3.2%). The frequency of severe anaemia was 39.8% in children of six to 24 months of age and 25.9% in children of 25–60 months of age. More children (8.7%) in the 25–60 months age group had cerebral malaria compared with 4.4% in the 6–24 months age group. The overall case fatality ratio was 3.5%. Cerebral malaria and hyperlactataemia were the significant risk factors associated with death. Severe anaemia, though a major presentation, was not significantly associated with risk of death. CONCLUSION: Severe malaria is a frequent and seasonal childhood disease in northern Ghana and maybe an adequate endpoint for future malaria vaccine trials.
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spelling pubmed-19508792007-08-24 Severe falciparum malaria in young children of the Kassena-Nankana district of northern Ghana Oduro, Abraham R Koram, Kwadwo A Rogers, William Atuguba, Frank Ansah, Patrick Anyorigiya, Thomas Ansah, Akosua Anto, Francis Mensah, Nathan Hodgson, Abraham Nkrumah, Francis Malar J Research STUDY DESIGN: Severe falciparum malaria in children was studied as part of the characterization of the Kassena-Nankana District Ghana for future malaria vaccine trials. Children aged 6–59 months with diagnosis suggestive of acute disease were characterized using the standard WHO definition for severe malaria. RESULTS: Of the total children screened, 45.2% (868/1921) satisfied the criteria for severe malaria. Estimated incidence of severe malaria was 3.4% (range: 0.4–8.3%) cases per year. The disease incidence was seasonal: 560 cases per year, of which 70.4% occurred during the wet season (June-October). The main manifestations were severe anaemia (36.5%); prolonged or multiple convulsions (21.6%); respiratory distress (24.4%) and cerebral malaria (5.4%). Others were hyperpyrexia (11.1%); hyperparasitaemia (18.5%); hyperlactaemia (33.4%); and hypoglycaemia (3.2%). The frequency of severe anaemia was 39.8% in children of six to 24 months of age and 25.9% in children of 25–60 months of age. More children (8.7%) in the 25–60 months age group had cerebral malaria compared with 4.4% in the 6–24 months age group. The overall case fatality ratio was 3.5%. Cerebral malaria and hyperlactataemia were the significant risk factors associated with death. Severe anaemia, though a major presentation, was not significantly associated with risk of death. CONCLUSION: Severe malaria is a frequent and seasonal childhood disease in northern Ghana and maybe an adequate endpoint for future malaria vaccine trials. BioMed Central 2007-07-27 /pmc/articles/PMC1950879/ /pubmed/17662142 http://dx.doi.org/10.1186/1475-2875-6-96 Text en Copyright © 2007 Oduro 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
Oduro, Abraham R
Koram, Kwadwo A
Rogers, William
Atuguba, Frank
Ansah, Patrick
Anyorigiya, Thomas
Ansah, Akosua
Anto, Francis
Mensah, Nathan
Hodgson, Abraham
Nkrumah, Francis
Severe falciparum malaria in young children of the Kassena-Nankana district of northern Ghana
title Severe falciparum malaria in young children of the Kassena-Nankana district of northern Ghana
title_full Severe falciparum malaria in young children of the Kassena-Nankana district of northern Ghana
title_fullStr Severe falciparum malaria in young children of the Kassena-Nankana district of northern Ghana
title_full_unstemmed Severe falciparum malaria in young children of the Kassena-Nankana district of northern Ghana
title_short Severe falciparum malaria in young children of the Kassena-Nankana district of northern Ghana
title_sort severe falciparum malaria in young children of the kassena-nankana district of northern ghana
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1950879/
https://www.ncbi.nlm.nih.gov/pubmed/17662142
http://dx.doi.org/10.1186/1475-2875-6-96
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