Evidence map›Paper›PMID 42325296›Full record

ArticleInfectious diseases & immunity2024

Identifying Malaria Hotspots Regions in Ghana Using Bayesian Spatial and Spatiotemporal Models.

Abdul-Karim Iddrisu, Dominic Otoo, Gordon Hinneh, Yakubu Dekongmene Kanyiri, Kanimam Yaaba Samuel, Cecilia Kubio, Francis Balungnaa Dhari Veriegh

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Article in Infectious diseases & immunity, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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0cells of the map it votes in
4citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Abdul-Karim IddrisuDepartment of Mathematics and Statistics, University of Energy and Natural Resources, Sunyani 233, Ghana.
Dominic OtooDepartment of Mathematics and Statistics, University of Energy and Natural Resources, Sunyani 233, Ghana.
Gordon HinnehDepartment of Mathematics and Statistics, University of Energy and Natural Resources, Sunyani 233, Ghana.
Yakubu Dekongmene KanyiriDepartment of Statistical Service, Ghana Statistical Service, Bono Region, Sunyani 233, Ghana.
Kanimam Yaaba SamuelDepartment of Mathematics and ICT, Gambaga College of Education, Sunyani 233, Ghana.
Cecilia KubioHuman Resources Division, University of Energy and Natural Resources, Sunyani 233, Ghana.
Francis Balungnaa Dhari VerieghDepartment of Biological Science, University of Energy and Natural Resources, Sunyani 233, Ghana.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Malaria remains a significant public health concern in Ghana, with varying risk levels across different geographical areas. Malaria affects millions of people each year and imposes a substantial burden on the health care system and population. Accurate risk estimation and mapping are crucial for effectively allocating resources and implementing targeted interventions to identify regions with disease hotspots. This study aimed to identify regions exhibiting elevated malaria risk so that public health interventions can be implemented, and to identify malaria risk predictors that can be controlled as part of public health interventions for malaria control. Methods: The data on laboratory-confirmed malaria cases from 2015 to 2021 were obtained from the Ghana Health Service and Ghana Statistical Service. We studied the spatial and spatiotemporal patterns of the relative risk of malaria using Bayesian spatial and spatiotemporal models. The malaria risk for each region was mapped to visually identify regions with malaria hotspots. Clustering and heterogeneity of disease risks were established using correlated and uncorrelated structures via the conditional autoregressive and Gaussian models, respectively. Parameter estimates from the marginal posterior distribution were estimated within the Integrated Nested Laplace Approximation using the R software. Results: The spatial model indicated an increased risk of malaria in the North East, Bono East, Ahafo, Central, Upper West, Brong Ahafo, Ashanti, and Eastern regions. The spatiotemporal model results highlighted an elevated malaria risk in the North East, Upper West, Upper East, Savannah, Bono East, Central, Bono, and Ahafo regions. Both spatial and spatiotemporal models identified the North East, Upper West, Bono East, Central, and Ahafo Regions as hotspots for malaria risk. Substantial variations in risk were evident across regions ( Conclusions: Malaria risk was clustered and varied among regions in Ghana. There are many regions in Ghana that are hotspots for malaria risk, and climate and economic factors have no significant influence on malaria risk. This study could provide information on malaria transmission patterns in Ghana, and contribute to enhance the effectiveness of malaria control strategies.

Indexed as

Bayesian modelingConditional auto-regressiveDisease hotspotIntegrated Nested Laplace ApproximationMalariaSpatial and spatiotemporal models

Identifiers

PMID42325296
PMCPMC13277526

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.