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William S. Weintraub

Publications and source records attributed to William S. Weintraub.

2 recordsLinked to original sources

An Efficient Approach for Optimizing the Cost-effective Individualized Treatment Rule Using Conditional Random Forest

Evidence from observational studies has become increasingly important for supporting healthcare policy making via cost-effectiveness (CE) analyses. Similar as in comparative effectiveness studies, health economic evaluations that consider subject-level heterogeneity produce individualized treatment rules (ITRs) that are often more cost-effective than one-size-fits-all treatment. Thus, it is of great interest to develop statistical tools for learning such a cost-effective ITR (CE-ITR) under the causal inference framework that allows proper handling of potential confounding and can be applied to both trials and observational studies. In this paper, we use the concept of net-monetary-benefit (NMB) to assess the trade-off between health benefits and related costs. We estimate CE-ITR as a function of patients' characteristics that, when implemented, optimizes the allocation of limited healthcare resources by maximizing health gains while minimizing treatment-related costs. We employ the conditional random forest approach and identify the optimal CE-ITR using NMB-based classification algorithms, where two partitioned estimators are proposed for the subject-specific weights to effectively incorporate information from censored individuals. We conduct simulation studies to evaluate the performance of our proposals. We apply our top-performing algorithm to the NIH-funded Systolic Blood Pressure Intervention Trial (SPRINT) to illustrate the CE gains of assigning customized intensive blood pressure therapy.

stat.ME↗

An integrated approach to simulating the vulnerable atherosclerotic plaque

Analyses of individual atherosclerotic plaques are mostly descriptive, relying -- for example -- on histological classification by spectral analysis of ultrasound waves or staining and observing particular cellular components. Such passive methods have proved useful for characterizing the structure and vulnerability of plaques but have little quantitative predictive power. In this viewpoint article, we propose an integrated quantitative framework to understand the evolution of plaque. The main approach is to use Partial Differential Equations (PDEs) with macrophages, necrotic cells, oxidized lipids, oxygen concentration and PDGF as primary variables coupled to a biomechanical model to describe vessel growth. The model is deterministic, providing mechanical, morphological, and histological characteristics of an atherosclerotic vessel at any desired future time point. We discuss the pros and cons of such a model, how such a model can provide insight to the clinician, and potentially guide therapy. Finally, we use our model to create computer-generated animations of a plaque evolution that are in qualitative agreement with serial ultrasound images published by Kubo et al. (2010) and hypothesize possible atherogenic mechanisms.

q-bio.TO↗