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A Bayesian multinomial model to analyse spatial patterns of childhood co-morbidity in Malawi
Lawrence N Kazembe1, Jimmy J Namangale
1Applied Statistics and Epidemiology Research Unit, Mathematical Sciences Department, Chancellor College, University of Malawi, Zomba, Malawi. ikazembe@yahoo.com
Abstract:
Children in less developed countries die from relatively small number of infectious disease, some of which epidemiologically overlap. Using self-reported illness data from the 2000 Malawi Demographic and Health Survey, we applied a random effects multinomial model to assess risk factors of childhood co-morbidity of fever, diarrhoea and pneumonia, and quantify area-specific spatial effects. The spatial structure was modelled using the conditional autoregressive prior. Various models were fitted and compared using deviance information criterion. Inference was Bayesian and was based on Markov Chain Monte Carlo simulation techniques. We found spatial variation in childhood co-morbidity and determinants of each outcome category differed. Specifically, risk factors associated with child co-morbidity included age of the child, place of residence, undernutrition, bednet use and Vitamin A. Higher residual risk levels were identified in the central and southern-eastern regions, particularly for fever, diarrhoea and pneumonia; fever and pneumonia; and fever and diarrhoea combinations. This linkage between childhood health and geographical location warrants further research to assess local causes of these clusters. More generally, although each disease has its own mechanism, overlapping risk factors suggest that integrated disease control approach may be cost-effective and should be employed.
Insights
Childhood infectious diseases like fever, diarrhea, and pneumonia often co-occur in developing nations. Integrated disease control strategies may be cost-effective due to overlapping risk factors and spatial variations in Malawi.
Area of Science:
- Epidemiology
- Public Health
- Spatial Analysis
Background:
- Infectious diseases pose a significant threat to children in less developed countries.
- Co-morbidity of common childhood illnesses like fever, diarrhea, and pneumonia is a critical public health concern.
- Understanding the spatial distribution and risk factors of these co-morbidities is essential for effective intervention.
Purpose of the Study:
- To assess risk factors associated with childhood co-morbidity of fever, diarrhea, and pneumonia in Malawi.
- To quantify area-specific spatial effects on these co-morbidities.
- To evaluate the effectiveness of integrated disease control approaches.
Main Methods:
- Utilized self-reported illness data from the 2000 Malawi Demographic and Health Survey.
- Applied a random effects multinomial model with a conditional autoregressive prior for spatial modeling.
- Employed Bayesian inference with Markov Chain Monte Carlo simulation techniques.
- Compared various models using the deviance information criterion.
Main Results:
- Identified significant spatial variation in childhood co-morbidity patterns across Malawi.
- Determined that risk factors for each co-morbidity outcome category differed.
- Key risk factors for co-morbidity included child's age, residence, undernutrition, bednet use, and Vitamin A status.
- Highlighted elevated residual risk levels in central and southern-eastern regions for specific disease combinations.
Conclusions:
- Childhood infectious disease co-morbidity exhibits distinct spatial clustering and varying determinants.
- The linkage between geographical location and childhood health outcomes necessitates further local investigation.
- Overlapping risk factors suggest that integrated disease control strategies could be a cost-effective approach.
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