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Leontine Alkema

Publications and source records attributed to Leontine Alkema.

23 records · Page 2Linked to original sources

Global Estimation of Neonatal Mortality using a Bayesian Hierarchical Splines Regression Model

In recent years, much of the focus in monitoring child mortality has been on assessing changes in the under-five mortality rate (U5MR). However, as the U5MR decreases, the share of neonatal deaths (within the first month) tends to increase, warranting increased efforts in monitoring this indicator in addition to the U5MR. A Bayesian splines regression model is presented for estimating neonatal mortality rates (NMR) for all countries. In the model, the relationship between NMR and U5MR is assessed and used to inform estimates, and spline regression models are used to capture country-specific trends. As such, the resulting NMR estimates incorporate trends in overall child mortality while also capturing data-driven trends. The model is fitted to 195 countries using the database from the United Nations Interagency Group for Child Mortality Estimation, producing estimates from 1990, or earlier if data are available, until 2015. The results suggest that, above a U5MR of 34 deaths per 1000 live births, at the global level, a 1 per cent increase in the U5MR leads to a 0.6 per cent decrease in the ratio of NMR to U5MR. Below a U5MR of 34 deaths per 1000 live births, the proportion of deaths under-five that are neonatal is constant at around 54 per cent. However, the relationship between U5MR and NMR varies across countries. The model has now been adopted by the United Nations Inter-agency Group for Child Mortality Estimation.

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A Bayesian approach to the global estimation of maternal mortality

The maternal mortality ratio (MMR) is defined as the number of maternal deaths in a population per 100,000 live births. Country-specific MMR estimates are published on a regular basis by the United Nations Maternal Mortality Estimation Inter-agency Group (UN MMEIG) to track progress in reducing maternal deaths and to evaluate regional and national performance related to Millennium Development Goal (MDG) 5, which calls for a 75% reduction in the MMR between 1990 and 2015. Until 2014, the UN MMEIG used a multilevel regression model for producing estimates for countries without sufficient data from vital registration systems. While this model worked well in the past to assess MMR levels for countries with limited data, it was deemed unsatisfactory for final MDG 5 reporting for countries where longer time series of observations had become available because by construction, estimated trends in the MMR were covariate-driven only and did not necessarily track data-driven trends. We developed a Bayesian maternal mortality estimation model, which extends upon the UN MMEIG multilevel regression model. The new model assesses data-driven trends through the inclusion of an ARIMA time series model that captures accelerations and decelerations in the rate of change in the MMR. Varying reporting and data quality issues are accounted for in source-specific data models. The revised model provides data-driven estimates of MMR levels and trends and will be used for MDG 5 reporting for all countries.

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Global estimation of child mortality using a Bayesian B-spline Bias-reduction model

Estimates of the under-five mortality rate (U5MR) are used to track progress in reducing child mortality and to evaluate countries' performance related to Millennium Development Goal 4. However, for the great majority of developing countries without well-functioning vital registration systems, estimating the U5MR is challenging due to limited data availability and data quality issues. We describe a Bayesian penalized B-spline regression model for assessing levels and trends in the U5MR for all countries in the world, whereby biases in data series are estimated through the inclusion of a multilevel model to improve upon the limitations of current methods. B-spline smoothing parameters are also estimated through a multilevel model. Improved spline extrapolations are obtained through logarithmic pooling of the posterior predictive distribution of country-specific changes in spline coefficients with observed changes on the global level. The proposed model is able to flexibly capture changes in U5MR over time, gives point estimates and credible intervals reflecting potential biases in data series and performs reasonably well in out-of-sample validation exercises. It has been accepted by the United Nations Inter-agency Group for Child Mortality Estimation to generate estimates for all member countries.

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Bayesian Population Projections for the United Nations

The United Nations regularly publishes projections of the populations of all the world's countries broken down by age and sex. These projections are the de facto standard and are widely used by international organizations, governments and researchers. Like almost all other population projections, they are produced using the standard deterministic cohort-component projection method and do not yield statements of uncertainty. We describe a Bayesian method for producing probabilistic population projections for most countries which are projections that the United Nations could use. It has at its core Bayesian hierarchical models for the total fertility rate and life expectancy at birth. We illustrate the method and show how it can be extended to address concerns about the UN's current assumptions about the long-term distribution of fertility. The method is implemented in the R packages bayesTFR, bayesLife, bayesPop and bayesDem.

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Probabilistic projections of HIV prevalence using Bayesian melding

The Joint United Nations Programme on HIV/AIDS (UNAIDS) has developed the Estimation and Projection Package (EPP) for making national estimates and short-term projections of HIV prevalence based on observed prevalence trends at antenatal clinics. Assessing the uncertainty about its estimates and projections is important for informed policy decision making, and we propose the use of Bayesian melding for this purpose. Prevalence data and other information about the EPP model's input parameters are used to derive a probabilistic HIV prevalence projection, namely a probability distribution over a set of future prevalence trajectories. We relate antenatal clinic prevalence to population prevalence and account for variability between clinics using a random effects model. Predictive intervals for clinic prevalence are derived for checking the model. We discuss predictions given by the EPP model and the results of the Bayesian melding procedure for Uganda, where prevalence peaked at around 28% in 1990; the 95% prediction interval for 2010 ranges from 2% to 7%.

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