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Abdulrahman A. Ahmed

Publications and source records attributed to Abdulrahman A. Ahmed.

5 recordsLinked to original sources

County-Level Heterogeneity in Opioid Harm Reduction and Treatment Effects: A Simulation Modeling Analysis

Opioid overdose deaths remain a severe public health crisis in the US, with heterogeneous burden across counties that differ in epidemic trajectory, baseline resources, and local context. While harm reduction through naloxone distribution and buprenorphine treatment are both evidence-based strategies, limited information on county-level effects hinders the ability of policymakers to prioritize resources across counties. We developed a simulation model of opioid use disorder (OUD), calibrated separately to six Pennsylvania counties spanning large urban (Allegheny, Philadelphia), intermediate-sized (Erie, Dauphin), and rural (Clearfield, Columbia) settings. We projected county-specific overdose mortality trajectories under three levels of increase in buprenorphine dispensing and naloxone distribution (10%, 20%, and 30% above each county's baseline), over a five-year horizon from 2025 to 2029. A 30% increase in naloxone distribution above observed county baseline levels was projected to reduce 2029 overdose deaths by approximately 70% (95% uncertainty interval, UI: 55-81%) in Allegheny County, 11% (95% UI:4-17%) in Erie County, and 28% (95% UI:2-64%) in Clearfield County. Projected reductions in overdose deaths from increasing buprenorphine were consistently smaller (10%-23%), except that in Erie buprenorphine produced larger projected reduction by 20% vs 11% for naloxone. Heterogeneity in naloxone responsiveness was strongly associated with each county's historical naloxone dispensing variability. The same proportional increase in naloxone distribution yields substantially different projected mortality reductions across counties depending on each county's baseline distribution history, a pattern invisible from mortality statistics alone. County-level context is important for informing harm reduction and treatment prioritization at the county level.

stat.AP↗

Computationally Efficient Estimation of Localized Treatment Effects for Multi-Level, Multi-Component Interventions to Address the Opioid Crisis

The opioid epidemic remains a major public health challenge in the United States, requiring a multi-pronged intervention approach to mitigate harms to communities. Given the heterogeneity of the epidemic, it is crucial for policymakers to understand localized treatment effects of different intervention components and utilize limited resources efficiently. While locally calibrated simulation models can project epidemic outcomes for any given intervention policy, collecting simulation results for all intervention combinations to estimate localized treatment effects for each community is impractical because the number of combinations grows exponentially with the number of interventions and the levels at which they are applied. To tackle this, we develop a two-stage metamodel framework with a two-step sequential design for efficient sampling. The metamodel consists of a response function linking health outcomes to each intervention component's treatment effect, and a Gaussian process regression (GPR) to learn spatial and socio-economic structures of the treatment effects based on locally-contextualized covariates. With two-step sequential sampling, we leverage spatial correlations and posterior uncertainty to sequentially sample the most informative counties and treatment conditions. We apply this framework to estimate the treatment effects of buprenorphine dispensing and naloxone distribution on overdose mortality rates using a calibrated agent-based opioid epidemic model in Pennsylvania counties. Our approach achieves less than 5% average relative error using fewer than 2% of the runs required for an exhaustive simulation. Our two-stage framework provides a computationally efficient approach to support policymakers, enabling an efficient evaluation of alternative resource-allocation strategies to mitigate the opioid epidemic in local communities.

stat.AP↗

Optimized Model Selection for Estimating Treatment Effects from Costly Simulations of the US Opioid Epidemic

Agent-based simulation with a synthetic population can help us compare different treatment conditions while keeping everything else constant within the same population (i.e., as digital twins). Such population-scale simulations require large computational power (i.e., CPU resources) to get accurate estimates for treatment effects. We can use meta models of the simulation results to circumvent the need to simulate every treatment condition. Selecting the best estimating model at a given sample size (number of simulation runs) is a crucial problem. Depending on the sample size, the ability of the method to estimate accurately can change significantly. In this paper, we discuss different methods to explore what model works best at a specific sample size. In addition to the empirical results, we provide a mathematical analysis of the MSE equation and how its components decide which model to select and why a specific method behaves that way in a range of sample sizes. The analysis showed why the direction estimation method is better than model-based methods in larger sample sizes and how the between-group variation and the within-group variation affect the MSE equation.

stat.ME↗

Inferring epidemic dynamics using Gaussian process emulation of agent-based simulations

Computational models help decision makers understand epidemic dynamics to optimize public health interventions. Agent-based simulation of disease spread in synthetic populations allows us to compare and contrast different effects across identical populations or to investigate the effect of interventions keeping every other factor constant between ``digital twins''. FRED (A Framework for Reconstructing Epidemiological Dynamics) is an agent-based modeling system with a geo-spatial perspective using a synthetic population that is constructed based on the U.S. census data. In this paper, we show how Gaussian process regression can be used on FRED-synthesized data to infer the differing spatial dispersion of the epidemic dynamics for two disease conditions that start from the same initial conditions and spread among identical populations. Our results showcase the utility of agent-based simulation frameworks such as FRED for inferring differences between conditions where controlling for all confounding factors for such comparisons is next to impossible without synthetic data.

cs.MA↗

Estimating Treatment Effects Using Costly Simulation Samples from a Population-Scale Model of Opioid Use Disorder

Large-scale models require substantial computational resources for analysis and studying treatment conditions. Specifically, estimating treatment effects using simulations may require a lot of infeasible resources to allocate at every treatment condition. Therefore, it is essential to develop efficient methods to allocate computational resources for estimating treatment effects. Agent-based simulation allows us to generate highly realistic simulation samples. FRED (A Framework for Reconstructing Epidemiological Dynamics) is an agent-based modeling system with a geospatial perspective using a synthetic population constructed based on the U.S. census data. Given its synthetic population, FRED simulations present a baseline for comparable results from different treatment conditions and treatment conditions. In this paper, we show three other methods for estimating treatment effects. In the first method, we resort to brute-force allocation, where all treatment conditions have an equal number of samples with a relatively large number of simulation runs. In the second method, we try to reduce the number of simulation runs by customizing individual samples required for each treatment effect based on the width of confidence intervals around the mean estimates. In the third method, we use a regression model, which allows us to learn across the treatment conditions such that simulation samples allocated for a treatment condition will help better estimate treatment effects in other conditions. We show that the regression-based methods result in a comparable estimate of treatment effects with less computational resources. The reduced variability and faster convergence of model-based estimates come at the cost of increased bias, and the bias-variance trade-off can be controlled by adjusting the number of model parameters (e.g., including higher-order interaction terms in the regression model).

cs.MA↗