SearcharxivSearch

arXiv subjects

Martin Hazelton

Publications and source records attributed to Martin Hazelton.

2 recordsLinked to original sources

Causal inference for spatiotemporal point processes in the presence of outcome spillover and carryover

We develop a framework for causal inference with continuous spatiotemporal point-process outcomes under cell-level interventions and outcome spillover. Potential outcomes are indexed by full treatment allocations, and the observed post-treatment process is represented as an unlabelled superposition of latent control and treatment components. On the observed design support, expected post-treatment event counts in any spacetime region under a given treatment allocation are identified under consistency, exchangeability, and positivity; off-support contrasts are identified relative to a regime-stable structural point-process model. Estimation is likelihood-based and implemented with stochastic EM. To understand when this is feasible, we analyse a predictable blockwise hard-EM surrogate and show nonasymptotic contraction of estimation error to a statistical floor governed by locally ambiguous regions. This yields plug-in guarantees for cell-level and global causal functionals, and clarifies the additional array conditions needed for unnormalised growing-window contrasts. The framework covers history dependent spatiotemporal point processes including Poisson and Hawkes models, with applications to settings such as epidemiology, seismology, and finance. We provide an application assessing the causal effect of injecting wastewater into the ground on seismic activity in Oklahoma.

stat.ME

Bayesian Inference for Population Attributable Measures from Under-identified Models

Population attributable risk (PAR) is used in epidemiology to predict the impact of removing a risk factor from the population. Until recently, no standard approach for calculating confidence intervals or the variance for PAR was available in the literature. Pirikahu et al. (2016) outlined a fully Bayesian approach to provide credible intervals for the PAR from a cross-sectional study, where the data was presented in the form of a 2 x 2 table. However, extensions to cater for other frequently used study designs were not provided. In this paper we provide methodology to calculate credible intervals for the PAR for case-control and cohort studies. Additionally, we extend the cross-sectional example to allow for the incorporation of uncertainty that arises when an imperfect diagnostic test is used. In all these situations the model becomes over-parameterised, or non-identifiable, which can result in standard "off-the-shelf" Markov chain Monte Carlo updaters taking a long time to converge or even failing altogether. We adapt an importance sampling methodology to overcome this problem, and propose some novel MCMC samplers that take into consideration the shape of the posterior ridge to aid in the convergence of the Markov chain.

stat.ME