Bias Reduction in Matched Observational Studies with Continuous Treatments: Calipered Non-Bipartite Matching and Bias-Corrected Estimation and Inference

Anthony Frazier, Siyu Heng, Wen Zhou
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Abstract

Matching is a commonly used causal inference framework in observational studies. By pairing individuals with different treatment values but with the same values of covariates (i.e., exact matching), the sample average treatment effect (SATE) can be consistently estimated and inferred using the classic Neyman-type (difference-in-means) estimator and confidence interval. However, inexact matching typically exists in practice and may cause substantial bias for the downstream treatment effect estimation and inference. Many methods have been proposed to reduce bias due to inexact matching in the binary treatment case. However, to our knowledge, no existing work has systematically investigated bias due to inexact matching in the continuous treatment case. To fill this blank, we propose a general framework for reducing bias in inexactly matched observational studies with continuous treatments. In the matching stage, we propose a carefully formulated caliper that incorporates the information of both the paired covariates and treatment doses to better tailor matching for the downstream SATE estimation and inference. In the estimation and inference stage, we propose a bias-corrected Neyman estimator paired with the corresponding bias-corrected variance estimator to leverage the information on propensity density discrepancies after inexact matching to further reduce the bias due to inexact matching. We apply our proposed framework to COVID-19 social mobility data to showcase differences between classic and bias-corrected SATE estimation and inference.
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在连续治疗的匹配观察研究中减少偏差:Calipered Non-Bipartite Matching 和偏差校正估计与推论
匹配是观察性研究中常用的因果推断框架。通过将治疗值不同但协变量值相同的个体配对(即精确配对),可以使用经典的内曼式(均值差)估计器和置信区间对样本平均治疗效果(SATE)进行一致的估计和推断。然而,在实践中通常存在不完全匹配的情况,这可能会对下游治疗效果的估计和推断造成很大偏差。已经提出了许多方法来减少二元治疗案例中的非精确匹配造成的偏差。然而,据我们所知,目前还没有任何工作系统地研究过连续治疗情况下的非精确匹配导致的偏差。为了填补这一空白,我们提出了一个减少连续治疗非精确匹配观察研究偏差的总体框架。在匹配阶段,我们提出了一个精心制定的卡尺,将配对协变量和治疗剂量的信息纳入其中,为下游的 SATE 估计和推断提供更好的尾匹配。在估计和推断阶段,我们提出了一个偏差校正的内曼估计器,并配以相应的偏差校正方差估计器,以利用不完全匹配后的倾向密度差异信息,进一步减少不完全匹配导致的偏差。我们将提出的框架应用于 COVID-19 社会流动性数据,以展示经典和偏差校正 SATE 估计和推断之间的差异。
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