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Sensitivity of fever for diagnosis of clinical malaria in a Kenyan area of unstable, low malaria transmission

BACKGROUND: Malaria in highland areas of Kenya affects children and adults. Local clinicians include symptoms other than fever when screening for malaria because they believe that fever alone does not capture all cases of malaria. METHODS: Individuals who presented to dispensaries in a highland Keny...

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Autores principales: Mutanda, Albino L, Cheruiyot, Priscah, Hodges, James S, Ayodo, George, Odero, Wilson, John, Chandy C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4021053/
https://www.ncbi.nlm.nih.gov/pubmed/24885660
http://dx.doi.org/10.1186/1475-2875-13-163
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author Mutanda, Albino L
Cheruiyot, Priscah
Hodges, James S
Ayodo, George
Odero, Wilson
John, Chandy C
author_facet Mutanda, Albino L
Cheruiyot, Priscah
Hodges, James S
Ayodo, George
Odero, Wilson
John, Chandy C
author_sort Mutanda, Albino L
collection PubMed
description BACKGROUND: Malaria in highland areas of Kenya affects children and adults. Local clinicians include symptoms other than fever when screening for malaria because they believe that fever alone does not capture all cases of malaria. METHODS: Individuals who presented to dispensaries in a highland Kenya site of low, unstable malaria transmission from 2007–2011 with 1 or more of 11 symptoms were tested by microscopy for malaria. Clinical malaria was defined as asexual Plasmodium falciparum infection on peripheral blood smear in an individual with any screening symptom. Asymptomatic P. falciparum infection was assessed in a cohort at ten time points to determine the extent to which symptomatic episodes with parasitaemia might be attributable to baseline (asymptomatic) parasitaemia in the community. RESULTS: 3,420 individuals were screened for malaria, 634 < 5 years of age and 2,786 ≥ 5 years of age. For the diagnosis of clinical malaria, the symptom of fever had a sensitivity and specificity of 88.9% and15.4% in children <5 years, and 55.8% and 54.4% in children ≥5 years, respectively. Adding the symptom of headache increased sensitivity to 94. 4% in children <5 years and 96.8% in individuals ≥5 years, but decreased specificity to 9.9% and 11.6%, respectively, and increased the number of individuals who would be tested by 6% and 92%, respectively. No combination of symptoms improved upon the presence fever or headache for detection of clinical malaria. In the cohort of asymptomatic individuals, P. falciparum parasitaemia was infrequent (0.1%). CONCLUSION: In areas of low, unstable malaria transmission, fever is a sensitive indicator of clinical malaria in children <5 years, but not in older children and adults. Adding headache to fever as screening symptom increases sensitivity of detection in individuals ≥5 years old at the cost of decreased specificity. Screening for symptoms in addition to fever may be required to accurately capture all cases of clinical malaria in individuals ≥5 years old in areas of low malaria transmission.
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spelling pubmed-40210532014-05-16 Sensitivity of fever for diagnosis of clinical malaria in a Kenyan area of unstable, low malaria transmission Mutanda, Albino L Cheruiyot, Priscah Hodges, James S Ayodo, George Odero, Wilson John, Chandy C Malar J Research BACKGROUND: Malaria in highland areas of Kenya affects children and adults. Local clinicians include symptoms other than fever when screening for malaria because they believe that fever alone does not capture all cases of malaria. METHODS: Individuals who presented to dispensaries in a highland Kenya site of low, unstable malaria transmission from 2007–2011 with 1 or more of 11 symptoms were tested by microscopy for malaria. Clinical malaria was defined as asexual Plasmodium falciparum infection on peripheral blood smear in an individual with any screening symptom. Asymptomatic P. falciparum infection was assessed in a cohort at ten time points to determine the extent to which symptomatic episodes with parasitaemia might be attributable to baseline (asymptomatic) parasitaemia in the community. RESULTS: 3,420 individuals were screened for malaria, 634 < 5 years of age and 2,786 ≥ 5 years of age. For the diagnosis of clinical malaria, the symptom of fever had a sensitivity and specificity of 88.9% and15.4% in children <5 years, and 55.8% and 54.4% in children ≥5 years, respectively. Adding the symptom of headache increased sensitivity to 94. 4% in children <5 years and 96.8% in individuals ≥5 years, but decreased specificity to 9.9% and 11.6%, respectively, and increased the number of individuals who would be tested by 6% and 92%, respectively. No combination of symptoms improved upon the presence fever or headache for detection of clinical malaria. In the cohort of asymptomatic individuals, P. falciparum parasitaemia was infrequent (0.1%). CONCLUSION: In areas of low, unstable malaria transmission, fever is a sensitive indicator of clinical malaria in children <5 years, but not in older children and adults. Adding headache to fever as screening symptom increases sensitivity of detection in individuals ≥5 years old at the cost of decreased specificity. Screening for symptoms in addition to fever may be required to accurately capture all cases of clinical malaria in individuals ≥5 years old in areas of low malaria transmission. BioMed Central 2014-04-30 /pmc/articles/PMC4021053/ /pubmed/24885660 http://dx.doi.org/10.1186/1475-2875-13-163 Text en Copyright © 2014 Mutanda 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
Mutanda, Albino L
Cheruiyot, Priscah
Hodges, James S
Ayodo, George
Odero, Wilson
John, Chandy C
Sensitivity of fever for diagnosis of clinical malaria in a Kenyan area of unstable, low malaria transmission
title Sensitivity of fever for diagnosis of clinical malaria in a Kenyan area of unstable, low malaria transmission
title_full Sensitivity of fever for diagnosis of clinical malaria in a Kenyan area of unstable, low malaria transmission
title_fullStr Sensitivity of fever for diagnosis of clinical malaria in a Kenyan area of unstable, low malaria transmission
title_full_unstemmed Sensitivity of fever for diagnosis of clinical malaria in a Kenyan area of unstable, low malaria transmission
title_short Sensitivity of fever for diagnosis of clinical malaria in a Kenyan area of unstable, low malaria transmission
title_sort sensitivity of fever for diagnosis of clinical malaria in a kenyan area of unstable, low malaria transmission
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4021053/
https://www.ncbi.nlm.nih.gov/pubmed/24885660
http://dx.doi.org/10.1186/1475-2875-13-163
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