Semi-parametric sensitivity analysis for trials with irregular and informative assessment times

被引:1
|
作者
Smith, Bonnie B. [1 ]
Gao, Yujing [2 ]
Yang, Shu [2 ]
Varadhan, Ravi [3 ]
Apter, Andrea J. [4 ]
Scharfstein, Daniel O [5 ]
机构
[1] Department of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore,MD,21205, United States
[2] Department of Statistics, North Carolina State University, Raleigh,NC,27695, United States
[3] Department of Oncology, Johns Hopkins School of Medicine, Baltimore,MD,21205, United States
[4] Pulmonary Allergy Critical Care Division, Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia,PA,19104, United States
[5] Department of Population Health Sciences, University of Utah School of Medicine, Salt Lake City,UT,84108, United States
关键词
Diseases - Inverse problems;
D O I
10.1093/biomtc/ujae154
中图分类号
学科分类号
摘要
Many trials are designed to collect outcomes at or around pre-specified times after randomization. If there is variability in the times when participants are actually assessed, this can pose a challenge to learning the effect of treatment, since not all participants have outcome assessments at the times of interest. Furthermore, observed outcome values may not be representative of all participants' outcomes at a given time. Methods have been developed that account for some types of such irregular and informative assessment times; however, since these methods rely on untestable assumptions, sensitivity analyses are needed. We develop a sensitivity analysis methodology that is benchmarked at the explainable assessment (EA) assumption, under which assessment and outcomes at each time are related only through data collected prior to that time. Our method uses an exponential tilting assumption, governed by a sensitivity analysis parameter, that posits deviations from the EA assumption. Our inferential strategy is based on a new influence function-based, augmented inverse intensity-weighted estimator. Our approach allows for flexible semiparametric modeling of the observed data, which is separated from specification of the sensitivity parameter. We apply our method to a randomized trial of low-income individuals with uncontrolled asthma, and we illustrate implementation of our estimation procedure in detail. © 2024 The Author(s).
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