Combining Incomplete Observational and Randomized Data for Heterogeneous Treatment Effects
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融合不完整观测数据与随机试验数据估计异质性处理效应AI 解读 ↓
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Data from observational studies (OSs) is widely available and readily obtainable yet frequently contains confounding biases. On the other hand, data derived from randomized controlled trials (RCTs) helps to reduce these biases; however, it is expensive to gather, resulting in a tiny size of randomized data. For this reason, effectively fusing observational data and randomized data to better estimate heterogeneous treatment effects (HTEs) has gained increasing attention. However, existing methods for integrating observational data with randomized data must require \textit{complete} observational data, meaning that both treated subjects and untreated subjects must be included in OSs. This prerequisite confines the applicability of such methods to very specific situations, given that including all subjects, whether treated or untreated, in observational studies is not consistently achievable. In our paper, we propose a resilient approach to \textbf{C}ombine \textbf{I}ncomplete \textbf{O}bservational data and randomized data for HTE estimation, which we abbreviate as \textbf{CIO}. The CIO is capable of estimating HTEs efficiently regardless of the completeness of the observational data, be it full or partial. Concretely, a confounding bias function is first derived using the pseudo-experimental group from OSs, in conjunction with the pseudo-control group from RCTs, via an effect estimation procedure. This function is subsequently utilized as a corrective residual to rectify the observed outcomes of observational data during the HTE estimation by combining the available observational data and the all randomized data. To validate our approach, we have conducted experiments on a synthetic dataset and two semi-synthetic datasets.
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Population-level heterogeneity is ubiquitous in biomedical data, where differences across demographic or clinical subgroups can substantially alter risk patterns. For example, in intensive care unit (ICU) studies, the mortality risk associated with specific admission diagnoses can vary across ethnic groups. Existing approaches for detecting risk heterogeneity are often sensitive to baseline model misspecification and regularization bias, both of which commonly arise in…
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非精确匹配何时能在无需调整的情况下保证平衡与有效推断?
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