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Bayesian spatial analysis of a national urinary schistosomiasis questionnaire to assist geographic targeting of schistosomiasis control in Tanzania, East Africa

dc.contributor.authorBrooker, S
dc.contributor.authorNyandindi, U
dc.contributor.authorFenwick, A
dc.contributor.authorBlair, L
dc.contributor.authorClements, Archie
dc.date.accessioned2015-12-13T22:29:00Z
dc.date.issued2008
dc.date.updated2015-12-11T08:44:58Z
dc.description.abstractSpatial modelling was applied to self-reported schistosomiasis data from over 2.5 million school students from 12,399 schools in all regions of mainland Tanzania. The aims were to derive statistically robust prevalence estimates in small geographical units (wards), to identify spatial clusters of high and low prevalence and to quantify uncertainty surrounding prevalence estimates. The objective was to permit informed decision-making for targeting of resources by the Tanzanian national schistosomiasis control programme. Bayesian logistic regression models were constructed to investigate the risk of schistosomiasis in each ward, based on the prevalence of self-reported schistosomiasis and blood in urine. Models contained covariates representing climatic and demographic effects and random effects for spatial clustering. Degree of urbanisation, median elevation of the ward and median normalised difference vegetation index (NDVI) were significantly and negatively associated with schistosomiasis prevalence. Most regions contained wards that had >95% certainty of schistosomiasis prevalence being >10%, the selected threshold for bi-annual mass chemotherapy of school-age children. Wards with >95% certainty of schistosomiasis prevalence being >30%, the selected threshold for annual mass chemotherapy of school-age children, were clustered in north-western, south-western and south-eastern regions. Large sample sizes in most wards meant raw prevalence estimates were robust. However, when uncertainties were investigated, intervention status was equivocal in 6.7-13.0% of wards depending on the criterion used. The resulting maps are being used to plan the distribution of praziquantel to participating districts; they will be applied to prioritising control in those wards where prevalence was unequivocally above thresholds for intervention and might direct decision-makers to obtain more information in wards where intervention status was uncertain.
dc.identifier.issn0020-7519
dc.identifier.urihttp://hdl.handle.net/1885/74473
dc.publisherElsevier
dc.sourceInternational Journal for Parasitology
dc.subjectKeywords: albendazole; praziquantel; Bayesian analysis; chemotherapy; data set; decision making; disease control; disease prevalence; geographical region; health risk; hemoparasite; questionnaire survey; schistosomiasis; spatial analysis; student; Africa; article; Bayesian modelling; CAR model; Disease control; Haematuria; Questionnaire; Schistosoma haematobium; Schistosomiasis; Spatial analysis; Tanzania
dc.titleBayesian spatial analysis of a national urinary schistosomiasis questionnaire to assist geographic targeting of schistosomiasis control in Tanzania, East Africa
dc.typeJournal article
local.bibliographicCitation.issue3-4
local.bibliographicCitation.lastpage415
local.bibliographicCitation.startpage401
local.contributor.affiliationClements, Archie, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationBrooker, S, Loondon School of Hygiene and Tropical Medicine
local.contributor.affiliationNyandindi, U, Ministry of Health
local.contributor.affiliationFenwick, A, Imperial College London
local.contributor.affiliationBlair, L, Imperial College London
local.contributor.authoruidClements, Archie, u5611518
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor111706 - Epidemiology
local.identifier.ariespublicationU3488905xPUB4141
local.identifier.citationvolume38
local.identifier.doi10.1016/j.ijpara.2007.08.001
local.identifier.scopusID2-s2.0-38949141203
local.type.statusPublished Version

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