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Country-specific estimates of misclassification rates of computer-coded verbal autopsy algorithms
Sandipan Pramanik1, Emily Wilson2, Henry D Kalter2
1Department of Biostatistics, Johns Hopkins University, Baltimore, Maryland, USA spraman4@jhu.edu.
Accurate cause of death (COD) estimation is improved by a new framework that calibrates computer-coded verbal autopsy (CCVA) algorithms. This method accounts for country-specific misclassification rates, enhancing mortality surveillance accuracy.
Area of Science:
- Epidemiology
- Biostatistics
- Public Health
Background:
- Computer-coded verbal autopsy (CCVA) algorithms are crucial for determining cause of death (COD) and estimating cause-specific mortality fractions (CSMFs).
- Frequent COD misclassification by CCVA algorithms introduces bias into CSMF estimates.
- Existing VA-calibration frameworks may overlook systematic patterns and cross-country variations, limiting accuracy.
Purpose of the Study:
- To develop and validate a country-specific VA-calibration framework to reduce COD misclassification bias.
- To estimate and inventory CCVA algorithm misclassification rates across different countries and age groups.
- To improve the accuracy of population-level mortality estimates derived from verbal autopsy data.
Main Methods:
- Utilized CHAMPS (Child Health and Mortality Prevention Surveillance) data to estimate misclassification rates for three CCVA algorithms (Expert Algorithm VA, InSilicoVA, InterVA).
- Estimated rates for two age groups (neonates and children aged 1-59 months) across eight countries.
- Applied Mozambique-specific rates to calibrate VA-only data from the COMSA project.
Main Results:
- Country-specific models demonstrated a better fit to misclassification rates compared to homogeneous models, reducing average absolute loss significantly for both neonates and children.
- Consistent misclassification patterns were observed across CCVA algorithms, with systematic over- or underestimation of certain causes.
- Calibration of COMSA data led to notable shifts in neonatal and child CSMFs, including increases for sepsis/meningitis/infection and malaria, and decreases for intrapartum-related events, prematurity, and pneumonia.
Conclusions:
- An inventory of VA misclassification rates across age groups, algorithms, and countries is now available, enabling broader calibration of VA-only data.
- The study identified systematic algorithmic biases in CCVA, highlighting areas for future algorithm refinement.
- The integrated VA-calibration workflow, supported by open-source software, represents a significant advancement in improving the accuracy of mortality surveillance systems globally.
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