Using Events From Dropouts in Nonparametric Survival Function Estimation With Application to Incubation of AIDS
利用退出研究后的事件估计非参数生存函数:艾滋病潜伏期应用AI 解读 ↓
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利用退出研究后的事件估计非参数生存函数:艾滋病潜伏期应用AI 解读 ↓
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Often postdropout responses (PDR) in study dropouts are identified from death/disease registries or other medical records. If ail dropout is random, then use of postdropout responses while censoring other subjects at date of dropout (CDO/PDR) will bias nonparametric survival probability estimates downward. Censoring all individuals at the last date of study contact, ignoring postdropout information (CDO) will produce unbiased nonparametric survival estimates. As onset of the response sometimes incapacitates the individual, preventing further study participation, dropout is often positively correlated with response. In this case CDO/PDR tends to prevent nonparametric survival overestimation but could lead to underestimation. When all of the responses in dropouts are identified, then regardless of dropout cause, use of all postdropout information, together with censoring all other subjects at time of analysis (CTA/PDR) will produce unbiased minimum variance estimates. We analyze the bias properties of nonparametric survival estimates produced using CDO/PDR, CDO, and CTA/PDR censoring mechanisms under various causes of study dropout and degrees of postdropout response recovery. The goal is to identify which of these censoring methods best incorporates postdropout information. Postdropout information may create interval-censored data. To facilitate statistical analysis of such data, the likelihood function is formulated in terms of the hazard. This results in computationally simple nonparametric estimates and covariances for interval-censored and left-truncated data. An application to estimation of acquired immune deficiency (AIDS)-free time after human immunodeficiency virus (HIV)-1 seroconversion using data from a long-term cohort study with considerable dropout is presented. Upper and lower bound estimates for AIDS-free survival probabilities derived using CDO and CDO/PDR are shown to be quite close when compared to the underlying variance of these estimates.
Principal stratification (PS) is a commonly used approach for understanding the mechanisms through which a treatment affects an outcome. The goal of this work is to extend the PS framework to studies with continuous treatments, which introduces a number of both challenges and opportunities in terms of defining causal effects and performing inference. This manuscript provides multiple key methodological contributions: 1) we introduce principal causal estimands for continuous…
We develop a semiparametric continuous time inferential framework for testing cumulative treatment effects, including both immediate and carryover effects. The latent state process is modeled by an ordinary differential equation (ODE) whose drift depends on state and treatment, while the observed data are noisy measurements of this latent state at irregular, multi resolution time points. We define the average treatment effect (ATE) as the difference of expected cumulative…
We study inference for continuous linear functionals of solutions to ill-posed inverse problems, including Euclidean parameters arising in nonparametric instrumental variables, proximal causal inference, and shadow-variable models. Although pointwise root-$n$ inference is possible under standard conditions, we show that this need not translate into locally reliable inference. Under a model imposing only minimal regularity conditions, the target is Hellinger discontinuous…
Motivation: Mediation analysis is an important tool for elucidating causal mechanisms in biomedical research and has recently gained increasing attention in microbiome studies. Motivated by a microbiome study of acute myeloid leukemia (AML) patients, we investigate whether the effect of induction chemotherapy intensity on infection status is mediated through gut microbial taxa. This problem poses substantial methodological challenges due to the high dimensionality, zero…
We study difference-in-differences designs in which all units are initially untreated and later receive heterogeneous, strictly positive treatment doses. When quasi-untreated units receive doses close to zero, a difference-in-difference estimand using those units as the control group identifies a weighted average treatment effect per unit of treatment, under a parallel-trends assumption. We develop a nonparametric estimator and bias-corrected confidence intervals for this…
伪面板事件研究:可信应用的计量经济学基础
Event studies with panel data are widely used to estimate treatment effects. With repeated cross-sections, future treatment dates are unobserved for untreated individuals. Pseudo-panel event studies impute pre-treatment outcomes of the treated using matched untreated individuals. This paper establishes identification in such designs and characterizes bias when identification conditions fail. I show that the pseudo-panel regression is equivalent to weighted least squares with…