Cargando…
Epidemiology of subpatent Plasmodium falciparum infection: implications for detection of hotspots with imperfect diagnostics
BACKGROUND: At the local level, malaria transmission clusters in hotspots, which may be a group of households that experience higher than average exposure to infectious mosquitoes. Active case detection often relying on rapid diagnostic tests for mass screen and treat campaigns has been proposed as...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3701503/ https://www.ncbi.nlm.nih.gov/pubmed/23815811 http://dx.doi.org/10.1186/1475-2875-12-221 |
_version_ | 1782275652453400576 |
---|---|
author | Mosha, Jacklin F Sturrock, Hugh JW Greenhouse, Bryan Greenwood, Brian Sutherland, Colin J Gadalla, Nahla Atwal, Sharan Drakeley, Chris Kibiki, Gibson Bousema, Teun Chandramohan, Daniel Gosling, Roly |
author_facet | Mosha, Jacklin F Sturrock, Hugh JW Greenhouse, Bryan Greenwood, Brian Sutherland, Colin J Gadalla, Nahla Atwal, Sharan Drakeley, Chris Kibiki, Gibson Bousema, Teun Chandramohan, Daniel Gosling, Roly |
author_sort | Mosha, Jacklin F |
collection | PubMed |
description | BACKGROUND: At the local level, malaria transmission clusters in hotspots, which may be a group of households that experience higher than average exposure to infectious mosquitoes. Active case detection often relying on rapid diagnostic tests for mass screen and treat campaigns has been proposed as a method to detect and treat individuals in hotspots. Data from a cross-sectional survey conducted in north-western Tanzania were used to examine the spatial distribution of Plasmodium falciparum and the relationship between household exposure and parasite density. METHODS: Dried blood spots were collected from consenting individuals from four villages during a survey conducted in 2010. These were analysed by PCR for the presence of P. falciparum, with the parasite density of positive samples being estimated by quantitative PCR. Household exposure was estimated using the distance-weighted PCR prevalence of infection. Parasite density simulations were used to estimate the proportion of infections that would be treated using a screen and treat approach with rapid diagnostic tests (RDT) compared to targeted mass drug administration (tMDA) and Mass Drug Administration (MDA). RESULTS: Polymerase chain reaction PCR analysis revealed that of the 3,057 blood samples analysed, 1,078 were positive. Mean distance-weighted PCR prevalence per household was 34.5%. Parasite density was negatively associated with transmission intensity with the odds of an infection being subpatent increasing with household exposure (OR 1.09 per 1% increase in exposure). Parasite density was also related to age, being highest in children five to ten years old and lowest in those > 40 years. Simulations of different tMDA strategies showed that treating all individuals in households where RDT prevalence was above 20% increased the number of infections that would have been treated from 43 to 55%. However, even with this strategy, 45% of infections remained untreated. CONCLUSION: The negative relationship between household exposure and parasite density suggests that DNA-based detection of parasites is needed to provide adequate sensitivity in hotspots. Targeting MDA only to households with RDT-positive individuals may allow a larger fraction of infections to be treated. These results suggest that community-wide MDA, instead of screen and treat strategies, may be needed to successfully treat the asymptomatic, subpatent parasite reservoir and reduce transmission in similar settings. |
format | Online Article Text |
id | pubmed-3701503 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-37015032013-07-05 Epidemiology of subpatent Plasmodium falciparum infection: implications for detection of hotspots with imperfect diagnostics Mosha, Jacklin F Sturrock, Hugh JW Greenhouse, Bryan Greenwood, Brian Sutherland, Colin J Gadalla, Nahla Atwal, Sharan Drakeley, Chris Kibiki, Gibson Bousema, Teun Chandramohan, Daniel Gosling, Roly Malar J Research BACKGROUND: At the local level, malaria transmission clusters in hotspots, which may be a group of households that experience higher than average exposure to infectious mosquitoes. Active case detection often relying on rapid diagnostic tests for mass screen and treat campaigns has been proposed as a method to detect and treat individuals in hotspots. Data from a cross-sectional survey conducted in north-western Tanzania were used to examine the spatial distribution of Plasmodium falciparum and the relationship between household exposure and parasite density. METHODS: Dried blood spots were collected from consenting individuals from four villages during a survey conducted in 2010. These were analysed by PCR for the presence of P. falciparum, with the parasite density of positive samples being estimated by quantitative PCR. Household exposure was estimated using the distance-weighted PCR prevalence of infection. Parasite density simulations were used to estimate the proportion of infections that would be treated using a screen and treat approach with rapid diagnostic tests (RDT) compared to targeted mass drug administration (tMDA) and Mass Drug Administration (MDA). RESULTS: Polymerase chain reaction PCR analysis revealed that of the 3,057 blood samples analysed, 1,078 were positive. Mean distance-weighted PCR prevalence per household was 34.5%. Parasite density was negatively associated with transmission intensity with the odds of an infection being subpatent increasing with household exposure (OR 1.09 per 1% increase in exposure). Parasite density was also related to age, being highest in children five to ten years old and lowest in those > 40 years. Simulations of different tMDA strategies showed that treating all individuals in households where RDT prevalence was above 20% increased the number of infections that would have been treated from 43 to 55%. However, even with this strategy, 45% of infections remained untreated. CONCLUSION: The negative relationship between household exposure and parasite density suggests that DNA-based detection of parasites is needed to provide adequate sensitivity in hotspots. Targeting MDA only to households with RDT-positive individuals may allow a larger fraction of infections to be treated. These results suggest that community-wide MDA, instead of screen and treat strategies, may be needed to successfully treat the asymptomatic, subpatent parasite reservoir and reduce transmission in similar settings. BioMed Central 2013-07-01 /pmc/articles/PMC3701503/ /pubmed/23815811 http://dx.doi.org/10.1186/1475-2875-12-221 Text en Copyright © 2013 Mosha 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 Mosha, Jacklin F Sturrock, Hugh JW Greenhouse, Bryan Greenwood, Brian Sutherland, Colin J Gadalla, Nahla Atwal, Sharan Drakeley, Chris Kibiki, Gibson Bousema, Teun Chandramohan, Daniel Gosling, Roly Epidemiology of subpatent Plasmodium falciparum infection: implications for detection of hotspots with imperfect diagnostics |
title | Epidemiology of subpatent Plasmodium falciparum infection: implications for detection of hotspots with imperfect diagnostics |
title_full | Epidemiology of subpatent Plasmodium falciparum infection: implications for detection of hotspots with imperfect diagnostics |
title_fullStr | Epidemiology of subpatent Plasmodium falciparum infection: implications for detection of hotspots with imperfect diagnostics |
title_full_unstemmed | Epidemiology of subpatent Plasmodium falciparum infection: implications for detection of hotspots with imperfect diagnostics |
title_short | Epidemiology of subpatent Plasmodium falciparum infection: implications for detection of hotspots with imperfect diagnostics |
title_sort | epidemiology of subpatent plasmodium falciparum infection: implications for detection of hotspots with imperfect diagnostics |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3701503/ https://www.ncbi.nlm.nih.gov/pubmed/23815811 http://dx.doi.org/10.1186/1475-2875-12-221 |
work_keys_str_mv | AT moshajacklinf epidemiologyofsubpatentplasmodiumfalciparuminfectionimplicationsfordetectionofhotspotswithimperfectdiagnostics AT sturrockhughjw epidemiologyofsubpatentplasmodiumfalciparuminfectionimplicationsfordetectionofhotspotswithimperfectdiagnostics AT greenhousebryan epidemiologyofsubpatentplasmodiumfalciparuminfectionimplicationsfordetectionofhotspotswithimperfectdiagnostics AT greenwoodbrian epidemiologyofsubpatentplasmodiumfalciparuminfectionimplicationsfordetectionofhotspotswithimperfectdiagnostics AT sutherlandcolinj epidemiologyofsubpatentplasmodiumfalciparuminfectionimplicationsfordetectionofhotspotswithimperfectdiagnostics AT gadallanahla epidemiologyofsubpatentplasmodiumfalciparuminfectionimplicationsfordetectionofhotspotswithimperfectdiagnostics AT atwalsharan epidemiologyofsubpatentplasmodiumfalciparuminfectionimplicationsfordetectionofhotspotswithimperfectdiagnostics AT drakeleychris epidemiologyofsubpatentplasmodiumfalciparuminfectionimplicationsfordetectionofhotspotswithimperfectdiagnostics AT kibikigibson epidemiologyofsubpatentplasmodiumfalciparuminfectionimplicationsfordetectionofhotspotswithimperfectdiagnostics AT bousemateun epidemiologyofsubpatentplasmodiumfalciparuminfectionimplicationsfordetectionofhotspotswithimperfectdiagnostics AT chandramohandaniel epidemiologyofsubpatentplasmodiumfalciparuminfectionimplicationsfordetectionofhotspotswithimperfectdiagnostics AT goslingroly epidemiologyofsubpatentplasmodiumfalciparuminfectionimplicationsfordetectionofhotspotswithimperfectdiagnostics |