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Nicholas P. Jewell

Publications and source records attributed to Nicholas P. Jewell.

7 recordsLinked to original sources

Doubly Robust Machine Learning for Population Size Estimation with Missing Covariates: Application to Gaza Conflict Mortality

Population size estimation from capture-recapture data is central for studying hard-to-reach populations, incorporating auxiliary covariates to account for heterogeneous capture probabilities and recapture dependencies. However, missing attributes pose a critical methodological challenge due to reluctance to share sensitive information, data collection limitations, and imperfect record linkage. Existing approaches either ignore missingness or rely on a priori imputation, potentially introducing substantial bias. In this work, we develop a novel nonparametric estimation framework using a Missing at Random assumption to identify capture probabilities under missing covariates. Using semiparametric efficiency theory, we construct one-step estimators that combine efficiency, robustness, and finite-sample validity: they approximately achieve the nonparametric efficiency bound, accommodate flexible machine learning methods through a doubly robust structure, and provide approximately valid inference for any sample size. Simulations demonstrate substantial improvements over naive imputation approaches, with our doubly robust ML estimators maintaining valid inference even at high missingness rates where competing methods fail. We apply our methodology to re-estimate mortality in the Gaza Strip from October 7, 2023, to June 30, 2024, using three-list capture-recapture data with missing demographic information. Our approach yields more conservative yet precise estimates compared to previous methods, indicating the true death toll exceeds official statistics by approximately 26%. Our framework provides practitioners with principled tools for handling incomplete data in conflict settings and other applications with hard-to-reach populations.

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Investigating symptom duration using current status data: a case study of post-acute COVID-19 syndrome

For infectious diseases, characterizing symptom duration is of clinical and public health importance. Symptom duration may be assessed by surveying infected individuals and querying symptom status at the time of survey response. For example, in a SARS-CoV-2 testing program at the University of Washington, participants were surveyed at least $28$ days after testing positive and asked to report current symptom status. This study design yielded current status data: outcome measurements for each respondent consisted only of the time of survey response and a binary indicator of whether symptoms had resolved by that time. Such study design benefits from limited risk of recall bias, but analyzing the resulting data necessitates tailored statistical tools. Here, we review methods for current status data and describe a novel application of modern nonparametric techniques to this setting. The proposed approach is valid under weaker assumptions compared to existing methods, allows use of flexible machine learning tools, and handles potential survey nonresponse. From the university study, under an assumption that the survey response time is conditionally independent of symptom resolution time within strata of measured covariates, we estimate that 19% of participants experienced ongoing symptoms 30 days after testing positive, decreasing to 7% at 90 days. We assess the sensitivity of these results to deviations from conditional independence, finding the estimates to be more sensitive to assumption violations at 30 days compared to 90 days. Female sex, fatigue during acute infection, and higher viral load were associated with slower symptom resolution.

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Test-Negative Designs with Multiple Testing Sources

Test-negative designs (TNDs), a form of case-cohort study, are widely used to evaluate infectious disease interventions, notably for influenza and, more recently, COVID-19 vaccines. TNDs rely on recruiting individuals who are tested for the disease of interest and comparing test-positive and test-negative individuals by exposure status (e.g., vaccination). Traditionally, TND studies focused on symptomatic individuals to minimize confounding from healthcare-seeking behavior. However, during outbreaks such as COVID-19 and Ebola, testing also occurred for asymptomatic individuals (e.g., through contact tracing), introducing potential bias when combining symptomatic and asymptomatic cases. Motivated by a trial evaluating an Ebola virus disease (EVD) vaccine, we study a specific version of this ``multiple reasons for testing" problem. In this setting, symptomatic individuals were tested under the standard TND approach, while asymptomatic close contacts of test-positive cases were also tested. We propose a simple method to estimate the common vaccine efficacy across these groups and assess whether efficacy differs by recruitment pathway. Although the EVD trial ended early due to the cessation of the outbreak, the proposed methodology remains relevant for future vaccine trials with similar designs.

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Randomization Inference for Cluster-Randomized Test-Negative Designs with Application to Dengue Studies: Unbiased estimation, Partial compliance, and Stepped-wedge design

In 2019, the World Health Organization identified dengue as one of the top ten global health threats. For the control of dengue, the Applying Wolbachia to Eliminate Dengue (AWED) study group conducted a cluster-randomized trial in Yogyakarta, Indonesia, and used a novel design, called the cluster-randomized test-negative design (CR-TND). This design can yield valid statistical inference with data collected by a passive surveillance system and thus has the advantage of cost-efficiency compared to traditional cluster-randomized trials. We investigate the statistical assumptions and properties of CR-TND under a randomization inference framework, which is known to be robust and efficient for small-sample problems. We find that, when the differential healthcare-seeking behavior comparing intervention and control varies across clusters (in contrast to the setting of Dufault and Jewell, 2020 where the differential healthcare-seeking behavior is constant across clusters), current analysis methods for CR-TND can be biased and have inflated type I error. We propose the log-contrast estimator that can eliminate such bias and improve precision by adjusting for covariates. Furthermore, we extend our methods to handle partial intervention compliance and a stepped-wedge design, both of which appear frequently in cluster-randomized trials. Finally, we demonstrate our results by simulation studies and re-analysis of the AWED study.

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Doubly robust capture-recapture methods for estimating population size

Estimation of population size using incomplete lists (also called the capture-recapture problem) has a long history across many biological and social sciences. For example, human rights and other groups often construct partial and overlapping lists of victims of armed conflicts, with the hope of using this information to estimate the total number of victims. Earlier statistical methods for this setup either use potentially restrictive parametric assumptions, or else rely on typically suboptimal plug-in-type nonparametric estimators; however, both approaches can lead to substantial bias, the former via model misspecification and the latter via smoothing. Under an identifying assumption that two lists are conditionally independent given measured covariate information, we make several contributions. First, we derive the nonparametric efficiency bound for estimating the capture probability, which indicates the best possible performance of any estimator, and sheds light on the statistical limits of capture-recapture methods. Then we present a new estimator, and study its finite-sample properties, showing that it has a double robustness property new to capture-recapture, and that it is near-optimal in a non-asymptotic sense, under relatively mild nonparametric conditions. Next, we give a method for constructing confidence intervals for total population size from generic capture probability estimators, and prove non-asymptotic near-validity. Finally, we study our methods in simulations, and apply them to estimate the number of killings and disappearances attributable to different groups in Peru during its internal armed conflict between 1980 and 2000.

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Interval censored recursive forests

We propose the interval censored recursive forests (ICRF) which is an iterative tree ensemble method for interval censored survival data. This nonparametric regression estimator makes the best use of censored information by iteratively updating the survival estimate, and can be viewed as a self-consistent estimator with convergence monitored using out-of-bag samples. Splitting rules optimized for interval censored data are developed and kernel-smoothing is applied. The ICRF displays the highest prediction accuracy among competing nonparametric methods in most of the simulations and in an applied example to avalanche data. An R package icrf is available for implementation.

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On a general structure for hazard-based regression models: an application to population-based cancer research

The proportional hazards model represents the most commonly assumed hazard structure when analysing time to event data using regression models. We study a general hazard structure which contains, as particular cases, proportional hazards, accelerated hazards, and accelerated failure time structures, as well as combinations of these. We propose an approach to apply these different hazard structures, based on a flexible parametric distribution (Exponentiated Weibull) for the baseline hazard. This distribution allows us to cover the basic hazard shapes of interest in practice: constant, bathtub, increasing, decreasing, and unimodal. In an extensive simulation study, we evaluate our approach in the context of excess hazard modelling, which is the main quantity of interest in descriptive cancer epidemiology. This study exhibits good inferential properties of the proposed model, as well as good performance when using the Akaike Information Criterion for selecting the hazard structure. An application on lung cancer data illustrates the usefulness of the proposed model.

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