SCouT:通过时空变换器实现可操作医疗保健的合成反制造

Bhishma Dedhia, Roshini Balasubramanian, N. Jha
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引用次数: 1

摘要

合成控制方法开创了一类强大的数据驱动技术,用于从供体单位估计单位的反事实真实性。其核心是,该技术涉及一个拟合在干预前时期的线性模型,该模型结合捐赠者的结果来产生反事实。然而,使用时间不可知权重对每个时间实例的空间信息进行线性组合,无法捕捉重要的单元间和单元内时间上下文以及真实数据的复杂非线性动态。相反,我们提出了一种在干预开始前使用局部时空信息的方法,作为估计反事实序列的一种有前途的方法。为此,我们提出了一个Transformer模型,该模型利用特定的位置嵌入、修改的解码器注意力掩码和一个新颖的预训练任务来执行时空序列到序列建模。我们在合成数据上的实验证明了我们的方法在典型的小供体池设置中的有效性及其对噪声的鲁棒性。我们还通过模拟全州范围的公共卫生政策来评估其有效性,模拟哮喘药物的计算机试验来支持随机对照试验,以及对弗里德里希共济失调患者的医疗干预来改善临床决策并促进个性化治疗,从而在人群和患者层面产生可操作的医疗见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SCouT: Synthetic Counterfactuals via Spatiotemporal Transformers for Actionable Healthcare
The Synthetic Control method has pioneered a class of powerful data-driven techniques to estimate the counterfactual reality of a unit from donor units. At its core, the technique involves a linear model fitted on the pre-intervention period that combines donor outcomes to yield the counterfactual. However, linearly combining spatial information at each time instance using time-agnostic weights fails to capture important inter-unit and intra-unit temporal contexts and complex nonlinear dynamics of real data. We instead propose an approach to use local spatiotemporal information before the onset of the intervention as a promising way to estimate the counterfactual sequence. To this end, we suggest a Transformer model that leverages particular positional embeddings, a modified decoder attention mask, and a novel pre-training task to perform spatiotemporal sequence-to-sequence modeling. Our experiments on synthetic data demonstrate the efficacy of our method in the typical small donor pool setting and its robustness against noise. We also generate actionable healthcare insights at the population and patient levels by simulating a state-wide public health policy to evaluate its effectiveness, an in silico trial for asthma medications to support randomized controlled trials, and a medical intervention for patients with Friedreich’s ataxia to improve clinical decision-making and promote personalized therapy.
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CiteScore
10.30
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