Modern longitudinal studies collect feature data at many timepoints, often of the same order of sample size. Such studies are typically affected by {dropout} and positivity violations. We tackle these problems by generalizing effects of recent incremental interventions (which shift propensity scores rather than set treatment values deterministically) to accommodate multiple outcomes and subject dropout. We give an identifying expression for incremental intervention effects when dropout is conditionally ignorable (without requiring treatment positivity), and derive the nonparametric efficiency bound for estimating such effects. Then we present efficient nonparametric estimators, showing that they converge at fast parametric rates and yield uniform inferential guarantees, even when nuisance functions are estimated flexibly at slower rates. We also study the variance ratio of incremental intervention effects relative to more conventional deterministic effects in a novel infinite time horizon setting, where the number of timepoints can grow with sample size, and show that incremental intervention effects yield near-exponential gains in statistical precision in this setup. Finally we conclude with simulations and apply our methods in a study of the effect of low-dose aspirin on pregnancy outcomes.
翻译:现代纵向研究在许多时间点收集地貌数据,往往按相同的抽样大小顺序收集。这类研究通常受到{漏出}和反正现象的影响。我们解决这些问题的方法是,通过推广最近递增干预措施(即改变偏向分数,而不是确定治疗值)的影响,以适应多重结果和学科辍学。我们提出在有条件地忽略辍学时递增干预效应的表示(不要求治疗相对性),并得出非对称效率,以估计这种效应。然后我们提出有效的非参数估测器,表明它们会以快速的参数率趋同,并产生统一的精度保障,即使对妨害功能的估计较慢。我们还研究在新的无限时间范围环境中,递增干预效应与较常规的确定性效应的差异比率,因为在这一范围中,定时点的数量可以随着抽样规模的增加而增加,并表明递增干预效应在统计精确度方面产生近乎极限的增益。最后,我们用模拟和运用了方法研究低剂量阿斯匹灵对怀孕结果的影响。