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Doubly robust dose-response estimation for continuous treatments via generalized propensity score augmented outcome regression

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 Added by Daniel Graham
 Publication date 2015
and research's language is English




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This paper constructs a doubly robust estimator for continuous dose-response estimation. An outcome regression model is augmented with a set of inverse generalized propensity score covariates to correct for potential misspecification bias. From the augmented model we can obtain consistent estimates of mean average potential outcomes for distinct strata of the treatment. A polynomial regression is then fitted to these point estimates to derive a Taylor approximation to the continuous dose-response function. The bootstrap is used for variance estimation. Analytical results and simulations show that our approach can provide a good approximation to linear or nonlinear dose-response functions under various sources of misspecification of the outcome regression or propensity score models. Efficiency in finite samples is good relative to minimum variance consistent estimators.



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261 - Keli Guo 2020
The research described herewith is to re-visit the classical doubly robust estimation of average treatment effect by conducting a systematic study on the comparisons, in the sense of asymptotic efficiency, among all possible combinations of the estimated propensity score and outcome regression. To this end, we consider all nine combinations under, respectively, parametric, nonparametric and semiparametric structures. The comparisons provide useful information on when and how to efficiently utilize the model structures in practice. Further, when there is model-misspecification, either propensity score or outcome regression, we also give the corresponding comparisons. Three phenomena are observed. Firstly, when all models are correctly specified, any combination can achieve the same semiparametric efficiency bound, which coincides with the existing results of some combinations. Secondly, when the propensity score is correctly modeled and estimated, but the outcome regression is misspecified parametrically or semiparametrically, the asymptotic variance is always larger than or equal to the semiparametric efficiency bound. Thirdly, in contrast, when the propensity score is misspecified parametrically or semiparametrically, while the outcome regression is correctly modeled and estimated, the asymptotic variance is not necessarily larger than the semiparametric efficiency bound. In some cases, the super-efficiency phenomenon occurs. We also conduct a small numerical study.
129 - Chuyun Ye , Keli Guo , Lixing Zhu 2020
In this paper, we apply doubly robust approach to estimate, when some covariates are given, the conditional average treatment effect under parametric, semiparametric and nonparametric structure of the nuisance propensity score and outcome regression models. We then conduct a systematic study on the asymptotic distributions of nine estimators with different combinations of estimated propensity score and outcome regressions. The study covers the asymptotic properties with all models correctly specified; with either propensity score or outcome regressions locally / globally misspecified; and with all models locally / globally misspecified. The asymptotic variances are compared and the asymptotic bias correction under model-misspecification is discussed. The phenomenon that the asymptotic variance, with model-misspecification, could sometimes be even smaller than that with all models correctly specified is explored. We also conduct a numerical study to examine the theoretical results.
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Understanding how treatment effects vary on individual characteristics is critical in the contexts of personalized medicine, personalized advertising and policy design. When the characteristics are of practical interest are only a subset of full covariate, non-parametric estimation is often desirable; but few methods are available due to the computational difficult. Existing non-parametric methods such as the inverse probability weighting methods have limitations that hinder their use in many practical settings where the values of propensity scores are close to 0 or 1. We propose the propensity score regression (PSR) that allows the non-parametric estimation of the heterogeneous treatment effects in a wide context. PSR includes two non-parametric regressions in turn, where it first regresses on the propensity scores together with the characteristics of interest, to obtain an intermediate estimate; and then, regress the intermediate estimates on the characteristics of interest only. By including propensity scores as regressors in the non-parametric manner, PSR is capable of substantially easing the computational difficulty while remain (locally) insensitive to any value of propensity scores. We present several appealing properties of PSR, including the consistency and asymptotical normality, and in particular the existence of an explicit variance estimator, from which the analytical behaviour of PSR and its precision can be assessed. Simulation studies indicate that PSR outperform existing methods in varying settings with extreme values of propensity scores. We apply our method to the national 2009 flu survey (NHFS) data to investigate the effects of seasonal influenza vaccination and having paid sick leave across different age groups.
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