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Bayesian spatio-temporal modeling of mortality in relation to malaria incidence in Western Kenya

INTRODUCTION: The effect of malaria exposure on mortality using health facility incidence data as a measure of transmission has not been well investigated. Health and demographic surveillance systems (HDSS) routinely capture data on mortality, interventions and other household related indicators, of...

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Detalles Bibliográficos
Autores principales: Khagayi, Sammy, Amek, Nyaguara, Bigogo, Godfrey, Odhiambo, Frank, Vounatsou, Penelope
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5509217/
https://www.ncbi.nlm.nih.gov/pubmed/28704417
http://dx.doi.org/10.1371/journal.pone.0180516
Descripción
Sumario:INTRODUCTION: The effect of malaria exposure on mortality using health facility incidence data as a measure of transmission has not been well investigated. Health and demographic surveillance systems (HDSS) routinely capture data on mortality, interventions and other household related indicators, offering a unique platform for estimating and monitoring the incidence-mortality relationship in space and time. METHODS: Mortality data from the HDSS located in Western Kenya collected from 2007 to 2012 and linked to health facility incidence data were analysed using Bayesian spatio-temporal survival models to investigate the relation between mortality (all-cause/malaria-specific) and malaria incidence across all age groups. The analysis adjusted for insecticide-treated net (ITN) ownership, socio-economic status (SES), distance to health facilities and altitude. The estimates obtained were used to quantify excess mortality due to malaria exposure. RESULTS: Our models identified a strong positive relationship between slide positivity rate (SPR) and all-cause mortality in young children 1–4 years (HR = 4.29; 95% CI: 2.78–13.29) and all ages combined (HR = 1.55; 1.04–2.80). SPR had a strong positive association with malaria-specific mortality in young children (HR = 9.48; 5.11–37.94), however, in older children (5–14 years), it was associated with a reduction in malaria specific mortality (HR = 0.02; 0.003–0.33). CONCLUSION: SPR as a measure of transmission captures well the association between malaria transmission intensity and all-cause/malaria mortality. This offers a quick and efficient way to monitor malaria burden. Excess mortality estimates indicate that small changes in malaria incidence substantially reduce overall and malaria specific mortality.