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Michelle Shardell

Publications and source records attributed to Michelle Shardell.

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A Novel Tool for Evaluating Effect Modification in Older Adults with ADRD Using Medicare Claims

Studying consequences following baseline exposures has become increasingly important for advancing comparative effectiveness research using real-world data. This case study evaluates the impact of hospital-acquired conditions (HAC) during hospitalization for hip fracture on post-discharge recovery trajectories among older adults living with Alzheimer Disease and Related Dementia, a population particularly vulnerable to high post-hospital mortality. To appropriately account for truncation of recovery trajectory due to death and to explore heterogeneity in effect modification by patient demographics, we introduce a novel pseudo data-based robust (PD-Robust) analysis strategy, accompanied by an R package and detailed usage guidance to inform real data analysis. Grounded in an interpretable estimand via principal stratification under principal ignorability and a structural working model, PD-Robust accommodates truncation by death, provides model diagnosis and robustness check against assumption violation, and facilitates the characterization of patient profiles among the principal stratum. Applied to Medicare claims data, where better recovery is defined as more days at home (DAH) over six months post-discharge, PD-Robust reveals heterogeneity in HAC effects, with males under the age of 85 years as a high-risk subgroup experiencing up to 23 fewer DAH, comparing HAC to no HAC. This exceeds the 8-day threshold regarded as clinically meaningful difference in DAH due to any exposure. Moreover, simulation studies further demonstrate that PD-Robust achieves low estimation bias and accurate statistical inference, supporting its utility in real-world data applications.

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Gerontologic Biostatistics 2.0: Developments over 10+ years in the age of data science

Background: Introduced in 2010, the sub-discipline of gerontologic biostatistics (GBS) was conceptualized to address the specific challenges in analyzing data from research studies involving older adults. However, the evolving technological landscape has catalyzed data science and statistical advancements since the original GBS publication, greatly expanding the scope of gerontologic research. There is a need to describe how these advancements enhance the analysis of multi-modal data and complex phenotypes that are hallmarks of gerontologic research. Methods: This paper introduces GBS 2.0, an updated and expanded set of analytical methods reflective of the practice of gerontologic biostatistics in contemporary and future research. Results: GBS 2.0 topics and relevant software resources include cutting-edge methods in experimental design; analytical techniques that include adaptations of machine learning, quantifying deep phenotypic measurements, high-dimensional -omics analysis; the integration of information from multiple studies, and strategies to foster reproducibility, replicability, and open science. Discussion: The methodological topics presented here seek to update and expand GBS. By facilitating the synthesis of biostatistics and data science in gerontology, we aim to foster the next generation of gerontologic researchers.

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Analyzing Risk Factors for Post-Acute Recovery in Older Adults with Alzheimer's Disease and Related Dementia: A New Semi-Parametric Model for Large-Scale Medicare Claims

Nearly 300,000 older adults experience a hip fracture every year, the majority of which occur following a fall. Unfortunately, recovery after fall-related trauma such as hip fracture is poor, where older adults diagnosed with Alzheimer's Disease and Related Dementia (ADRD) spend a particularly long time in hospitals or rehabilitation facilities during the post-operative recuperation period. Because older adults value functional recovery and spending time at home versus facilities as key outcomes after hospitalization, identifying factors that influence days spent at home after hospitalization is imperative. While several individual-level factors have been identified, the characteristics of the treating hospital have recently been identified as contributors. However, few methodological rigorous approaches are available to help overcome potential sources of bias such as hospital-level unmeasured confounders, informative hospital size, and loss to follow-up due to death. This article develops a useful tool equipped with unsupervised learning to simultaneously handle statistical complexities that are often encountered in health services research, especially when using large administrative claims databases. The proposed estimator has a closed form, thus only requiring light computation load in a large-scale study. We further develop its asymptotic properties that can be used to make statistical inference in practice. Extensive simulation studies demonstrate superiority of the proposed estimator compared to existing estimators.

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The Effect of Alcohol intake on Brain White Matter Microstructural Integrity: A New Causal Inference Framework for Incomplete Phenomic Data

Although substance use, such as alcohol intake, is known to be associated with cognitive decline during aging, its direct influence on the central nervous system remains incompletely understood. In this study, we investigate the influence of alcohol intake frequency on reduction of brain white matter microstructural integrity in the fornix, a brain region considered a promising marker of age-related microstructural degeneration, using a large UK Biobank (UKB) cohort with extensive phenomic data reflecting a comprehensive lifestyle profile. Two major challenges arise: 1) potentially nonlinear confounding effects from phenomic variables and 2) a limited proportion of participants with complete phenomic data. To address these challenges, we develop a novel ensemble learning framework tailored for robust causal inference and introduce a data integration step to incorporate information from UKB participants with incomplete phenomic data, improving estimation efficiency. Our analysis reveals that daily alcohol intake may significantly reduce fractional anisotropy, a neuroimaging-derived measure of white matter structural integrity, in the fornix and increase systolic and diastolic blood pressure levels. Moreover, extensive numerical studies demonstrate the superiority of our method over competing approaches in terms of estimation bias, while outcome regression-based estimators may be preferred when minimizing mean squared error is prioritized.

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