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Published on: December 9, 2015
Modelling the spatial variability and uncertainty for under-vaccination and zero-dose children in fragile settings
Victor A Alegana1, Johnson M Ticha2, Jason M Mwenda2
1WHO Regional Office for Africa, Brazzaville, Congo. aleganav@gmail.com.
Insights
This study mapped under-immunized and zero-dose children in Chad, revealing significant spatial variations in vaccination coverage. Identifying these vulnerable populations is crucial for improving childhood immunization programs and child health outcomes.
Area of Science:
- * Global Health
- * Epidemiology
- * Demography
Background:
- * Universal childhood vaccination is vital for child health and achieving sustainable development goals.
- * Identifying under-immunized and zero-dose children at a granular level is essential for targeted interventions.
Purpose of the Study:
- * To identify under-immunized and zero-dose children in Chad using fine-scale spatial modeling.
- * To estimate age-disaggregated populations and vaccination coverage at a 1km x 1km resolution.
Main Methods:
- * Utilized the most recent nationally representative household survey data from Chad.
- * Employed a Bayesian geostatistical framework to model population and vaccination coverage.
- * Adjusted models using parsimonious covariates for fine spatial resolution.
Main Results:
- * Estimated 312,723 zero-dose children (based on DTP1) in Chad.
- * Revealed significant spatial variation in the 12-23 month population, with a national mean of 18.6%.
- * Reported modelled birth coverage for BCG (49.0%), DTP1 (44.8%), DTP3 (24.7%), and MCV1 (47.0%).
Conclusions:
- * Fine-scale mapping identified substantial numbers of zero-dose children, highlighting inequities in vaccination access.
- * Improving routine immunization requires strengthening primary healthcare systems.
- * Acknowledged uncertainties in estimates, emphasizing the need for higher quality data and further investigation.
Abstract:
Universal access to childhood vaccination is important to child health and sustainable development. Here we identify, at a fine spatial scale, under-immunized children and zero-dose children. Using Chad, as an example, the most recent nationally representative household survey that included recommended vaccine antigens was assembled. Age-disaggregated population (12-23 months) and vaccination coverage were modelled at a fine spatial resolution scale (1km × 1 km) using a Bayesian geostatistical framework adjusting for a set of parsimonious covariates. There was a variation at fine spatial scale in the population 12-23 months a national mean of 18.6% (CrI 15.8%-22.6%) with the highest proportion in the South-East district of Laremanaye 20.0% (14.8-25.0). Modelled coverage at birth was 49.0% (31.2%-75.3%) for BCG, 44.8% (27.1-74.3) for DTP1, 24.7% (12.5-46.3) for DTP3 and 47.0% (30.6-71.0) for measles (MCV1). Combining coverage estimates with the modelled population at a fine spatial scale yielded 312,723 (Lower estimate 156055-409266) zero-dose children based on DTP1. Improving routine immunization will require investment in the health system as part of enhancing primary health care. The uncertainties in our estimates highlight areas that require further investigation and higher quality data to gain a better understanding of vaccination coverage.
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