TY - JOUR
T1 - Fitting dynamic measles models to subnational case notification data from Ethiopia
T2 - Methodological challenges and key considerations
AU - Sbarra, Alyssa N.
AU - Haeuser, Emily
AU - Kidane, Samuel
AU - Abate, Andargie
AU - Abebe, Ayele M.
AU - Ahmed, Muktar
AU - Alemayehu, Tsegaye
AU - Amsalu, Erkihun
AU - Aravkin, Aleksandr Y.
AU - Asgedom, Akeza A.
AU - Bayleyegn, Nebiyou
AU - Dagnew, Mulat
AU - Demisse, Biniyam
AU - Etafa, Werku
AU - Fetensa, Getahun
AU - Gebremeskel, Teferi G.
AU - Geremew, Habtamu
AU - Gizaw, Abraham T.
AU - Hunde, Gamechu A.
AU - Meles, Hadush N.
AU - Migbar, Sibhat
AU - Nguyen, Jason Q.
AU - Nigussie, Eshetu
AU - Ramshaw, Rebecca E.
AU - Rolfe, Sam
AU - Sahiledengle, Biniyam
AU - Shalev, Noga
AU - Solomon, Yonatan
AU - Tesfaye, Latera
AU - Yesera, Gesila E.
AU - Jit, Mark
AU - Mosser, Jonathan F.
N1 - Publisher Copyright:
© 2025 Sbarra et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2025/4
Y1 - 2025/4
N2 - In many settings, ongoing measles transmission is maintained due to pockets of un- or under-vaccinated individuals even if the critical vaccination threshold is reached nationwide. Therefore, assessing the underlying gaps in measles susceptibility within a population is essential for vaccination programs and measles control efforts. Recently, there have been increased efforts to use geospatial and small area methods to estimate subnational measles vaccination coverage in high-burden settings, such as in Ethiopia. However, the distribution of remaining susceptible individuals, either unvaccinated or having never previously been infected, across age groups and subnational geographies is unknown. In this study, we developed a dynamic transmission model that incorporates geospatial estimates of routine measles vaccination coverage, available data on supplemental immunization activities, and reported cases to estimate measles incidence and susceptibility across time, age, and space. We use gridded population estimates and subnational estimates of routine and supplemental measles vaccination coverage. To account for mixing between age-groups, we used a synthetic contact matrix, and travel times via a friction surface were used in a modified gravity model to account for spatial movement. We explored model fitting using Ethiopia as a case study. To address data-related and statistical challenges, we investigated a range of model parameterization and possible fitting algorithms. The approach with the best performance was a model fitted to case notifications adjusted for case ascertainment by using maximum likelihood estimation with block coordinate descent. This strategy was chosen because many data observations (and likely presence of unquantified uncertainty) yielded a steep likelihood surface, which was challenging to fit using Bayesian approaches. We ran sensitivity analyses to explore variations in vaccine effectiveness and compared patterns of susceptibility across space, time, and age. Substantial heterogeneity in reported measles cases as well as susceptibility persists across ages and second-administrative units. These methods and estimates could contribute towards tailored subnational and local planning to reduce preventable measles burden. However, computational and data challenges would need to be addressed for these methods to be applied on a large scale.
AB - In many settings, ongoing measles transmission is maintained due to pockets of un- or under-vaccinated individuals even if the critical vaccination threshold is reached nationwide. Therefore, assessing the underlying gaps in measles susceptibility within a population is essential for vaccination programs and measles control efforts. Recently, there have been increased efforts to use geospatial and small area methods to estimate subnational measles vaccination coverage in high-burden settings, such as in Ethiopia. However, the distribution of remaining susceptible individuals, either unvaccinated or having never previously been infected, across age groups and subnational geographies is unknown. In this study, we developed a dynamic transmission model that incorporates geospatial estimates of routine measles vaccination coverage, available data on supplemental immunization activities, and reported cases to estimate measles incidence and susceptibility across time, age, and space. We use gridded population estimates and subnational estimates of routine and supplemental measles vaccination coverage. To account for mixing between age-groups, we used a synthetic contact matrix, and travel times via a friction surface were used in a modified gravity model to account for spatial movement. We explored model fitting using Ethiopia as a case study. To address data-related and statistical challenges, we investigated a range of model parameterization and possible fitting algorithms. The approach with the best performance was a model fitted to case notifications adjusted for case ascertainment by using maximum likelihood estimation with block coordinate descent. This strategy was chosen because many data observations (and likely presence of unquantified uncertainty) yielded a steep likelihood surface, which was challenging to fit using Bayesian approaches. We ran sensitivity analyses to explore variations in vaccine effectiveness and compared patterns of susceptibility across space, time, and age. Substantial heterogeneity in reported measles cases as well as susceptibility persists across ages and second-administrative units. These methods and estimates could contribute towards tailored subnational and local planning to reduce preventable measles burden. However, computational and data challenges would need to be addressed for these methods to be applied on a large scale.
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U2 - 10.1371/journal.pcbi.1012922
DO - 10.1371/journal.pcbi.1012922
M3 - Article
C2 - 40238774
AN - SCOPUS:105002794023
SN - 1553-734X
VL - 21
JO - PLoS computational biology
JF - PLoS computational biology
IS - 4 April
M1 - e1012922
ER -