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Defining Childhood Severe Falciparum Malaria for Intervention Studies

BACKGROUND: Clinical trials of interventions designed to prevent severe falciparum malaria in children require a clear endpoint. The internationally accepted definition of severe malaria is sensitive, and appropriate for clinical purposes. However, this definition includes individuals with severe no...

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Autores principales: Bejon, Philip, Berkley, James A, Mwangi, Tabitha, Ogada, Edna, Mwangi, Isaiah, Maitland, Kathryn, Williams, Thomas, Scott, J. Anthony G, English, Mike, Lowe, Brett S, Peshu, Norbert, Newton, Charles R. J. C, Marsh, Kevin
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1949845/
https://www.ncbi.nlm.nih.gov/pubmed/17713980
http://dx.doi.org/10.1371/journal.pmed.0040251
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author Bejon, Philip
Berkley, James A
Mwangi, Tabitha
Ogada, Edna
Mwangi, Isaiah
Maitland, Kathryn
Williams, Thomas
Scott, J. Anthony G
English, Mike
Lowe, Brett S
Peshu, Norbert
Newton, Charles R. J. C
Marsh, Kevin
author_facet Bejon, Philip
Berkley, James A
Mwangi, Tabitha
Ogada, Edna
Mwangi, Isaiah
Maitland, Kathryn
Williams, Thomas
Scott, J. Anthony G
English, Mike
Lowe, Brett S
Peshu, Norbert
Newton, Charles R. J. C
Marsh, Kevin
author_sort Bejon, Philip
collection PubMed
description BACKGROUND: Clinical trials of interventions designed to prevent severe falciparum malaria in children require a clear endpoint. The internationally accepted definition of severe malaria is sensitive, and appropriate for clinical purposes. However, this definition includes individuals with severe nonmalarial disease and coincident parasitaemia, so may lack specificity in vaccine trials. Although there is no “gold standard” individual test for severe malaria, malaria-attributable fractions (MAFs) can be estimated among groups of children using a logistic model, which we use to test the suitability of various case definitions as trial endpoints. METHODS AND FINDINGS: A total of 4,583 blood samples were taken from well children in cross-sectional surveys and from 1,361 children admitted to a Kenyan District hospital with severe disease. Among children under 2 y old with severe disease and over 2,500 parasites per microliter of blood, the MAFs were above 85% in moderate- and low-transmission areas, but only 61% in a high-transmission area. HIV and malnutrition were not associated with reduced MAFs, but gastroenteritis with severe dehydration (defined by reduced skin turgor), lower respiratory tract infection (clinician's final diagnosis), meningitis (on cerebrospinal fluid [CSF] examination), and bacteraemia were associated with reduced MAFs. The overall MAF was 85% (95% confidence interval [CI] 83.8%–86.1%) without excluding these conditions, 89% (95% CI 88.4%–90.2%) after exclusions, and 95% (95% CI 94.0%–95.5%) when a threshold of 2,500 parasites/μl was also applied. Applying a threshold and exclusion criteria reduced sensitivity to 80% (95% CI 77%–83%). CONCLUSIONS: The specificity of a case definition for severe malaria is improved by applying a parasite density threshold and by excluding children with meningitis, lower respiratory tract infection (clinician's diagnosis), bacteraemia, and gastroenteritis with severe dehydration, but not by excluding children with HIV or malnutrition.
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spelling pubmed-19498452007-08-21 Defining Childhood Severe Falciparum Malaria for Intervention Studies Bejon, Philip Berkley, James A Mwangi, Tabitha Ogada, Edna Mwangi, Isaiah Maitland, Kathryn Williams, Thomas Scott, J. Anthony G English, Mike Lowe, Brett S Peshu, Norbert Newton, Charles R. J. C Marsh, Kevin PLoS Med Research Article BACKGROUND: Clinical trials of interventions designed to prevent severe falciparum malaria in children require a clear endpoint. The internationally accepted definition of severe malaria is sensitive, and appropriate for clinical purposes. However, this definition includes individuals with severe nonmalarial disease and coincident parasitaemia, so may lack specificity in vaccine trials. Although there is no “gold standard” individual test for severe malaria, malaria-attributable fractions (MAFs) can be estimated among groups of children using a logistic model, which we use to test the suitability of various case definitions as trial endpoints. METHODS AND FINDINGS: A total of 4,583 blood samples were taken from well children in cross-sectional surveys and from 1,361 children admitted to a Kenyan District hospital with severe disease. Among children under 2 y old with severe disease and over 2,500 parasites per microliter of blood, the MAFs were above 85% in moderate- and low-transmission areas, but only 61% in a high-transmission area. HIV and malnutrition were not associated with reduced MAFs, but gastroenteritis with severe dehydration (defined by reduced skin turgor), lower respiratory tract infection (clinician's final diagnosis), meningitis (on cerebrospinal fluid [CSF] examination), and bacteraemia were associated with reduced MAFs. The overall MAF was 85% (95% confidence interval [CI] 83.8%–86.1%) without excluding these conditions, 89% (95% CI 88.4%–90.2%) after exclusions, and 95% (95% CI 94.0%–95.5%) when a threshold of 2,500 parasites/μl was also applied. Applying a threshold and exclusion criteria reduced sensitivity to 80% (95% CI 77%–83%). CONCLUSIONS: The specificity of a case definition for severe malaria is improved by applying a parasite density threshold and by excluding children with meningitis, lower respiratory tract infection (clinician's diagnosis), bacteraemia, and gastroenteritis with severe dehydration, but not by excluding children with HIV or malnutrition. Public Library of Science 2007-08 2007-08-21 /pmc/articles/PMC1949845/ /pubmed/17713980 http://dx.doi.org/10.1371/journal.pmed.0040251 Text en © 2007 Bejon et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Bejon, Philip
Berkley, James A
Mwangi, Tabitha
Ogada, Edna
Mwangi, Isaiah
Maitland, Kathryn
Williams, Thomas
Scott, J. Anthony G
English, Mike
Lowe, Brett S
Peshu, Norbert
Newton, Charles R. J. C
Marsh, Kevin
Defining Childhood Severe Falciparum Malaria for Intervention Studies
title Defining Childhood Severe Falciparum Malaria for Intervention Studies
title_full Defining Childhood Severe Falciparum Malaria for Intervention Studies
title_fullStr Defining Childhood Severe Falciparum Malaria for Intervention Studies
title_full_unstemmed Defining Childhood Severe Falciparum Malaria for Intervention Studies
title_short Defining Childhood Severe Falciparum Malaria for Intervention Studies
title_sort defining childhood severe falciparum malaria for intervention studies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1949845/
https://www.ncbi.nlm.nih.gov/pubmed/17713980
http://dx.doi.org/10.1371/journal.pmed.0040251
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