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Chad Hazlett

Publications and source records attributed to Chad Hazlett.

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Post-treatment problems: What can we say about the effect of a treatment among sub-groups who (would) respond in some way?

Investigators are often interested in how a treatment affects an outcome for units responding to treatment in a certain way. We may wish to know the effect among units that, for example, meaningfully implemented an intervention, passed an attention check, or demonstrated some important mechanistic response. Simply conditioning on the observed value of the post-treatment variable introduces problematic biases. Further, the identification assumptions required of several existing strategies are often indefensible. We propose the Treatment Reactive Average Causal Effect (TRACE), which we define as the total effect of treatment in the group that, if treated, would realize a particular value of the relevant post-treatment variable. By reasoning about the effect among the "non-reactive" group, we can identify and estimate the range of plausible values for the TRACE. We demonstrate the use of this approach with three examples: (i) learning the effect of police-perceived race on police violence during traffic stops, a case where point identification may be possible; (ii) estimating effects of a community-policing intervention in Liberia, in communities that meaningfully implemented it, and (iii) studying how in-person canvassing affects support for transgender rights, among participants for whom the intervention would result in more positive feelings towards transgender people.

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Inference at the data's edge: Gaussian processes for modeling and inference under model-dependency, poor overlap, and extrapolation

Many inferential tasks involve fitting models to observed data and predicting outcomes at new covariate values, requiring interpolation or extrapolation. Conventional methods select a single best-fitting model, discarding fits that were similarly plausible in-sample but would yield sharply different predictions out-of-sample. Gaussian Processes (GPs) offer a principled alternative. Rather than committing to one conditional expectation function, GPs deliver a posterior distribution over outcomes at any covariate value. This posterior effectively retains the range of models consistent with the data, widening uncertainty intervals where extrapolation magnifies divergence. In this way, the GP's uncertainty estimates reflect the implications of extrapolation on our predictions, helping to tame the "dangers of extreme counterfactuals" (King & Zeng, 2006). The approach requires (i) specifying a covariance function linking outcome similarity to covariate similarity, and (ii) assuming Gaussian noise around the conditional expectation. We provide an accessible introduction to GPs with emphasis on this property, along with a simple, automated procedure for hyperparameter selection implemented in the R package gpss. We illustrate the value of GPs for capturing counterfactual uncertainty in three settings: (i) treatment effect estimation with poor overlap, (ii) interrupted time series requiring extrapolation beyond pre-intervention data, and (iii) regression discontinuity designs where estimates hinge on boundary behavior.

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Sensitivity of weighted least squares estimators to omitted variables

We introduce tools for assessing the sensitivity, to unobserved confounding, of a common estimator of causal effects that employs weights: the weighted linear regression of the outcome on the treatment and observed covariates. This estimator's bias is a function of two intuitive weighted partial $R^2$ values: (i) the proportion of weighted variance in the treatment that unobserved confounding explains given the covariates and (ii) the proportion of weighted variance in the outcome that unobserved confounding explains given the covariates and the treatment. Following previous work, we define sensitivity statistics for routine reporting, derive formal bounds on the strength of unobserved confounding with (multiples of) the strength of certain covariates, and propose adjusted inference procedures. A key choice we make is to examine only how the outcome model is influenced by unobserved confounding, instead of how the weights have been affected. One benefit of this choice is that our tools apply with any (non-negative) weights (e.g., inverse propensity score, matching, or covariate balancing). Another benefit is that we can rely on omitted variable bias approaches that impose no distributional assumptions on the data or unobserved confounding, and can address misspecification bias. The tools are available in the sensewls package for R.

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Inference with weights: Residualization produces short, valid intervals for varying estimands and varying resampling processes

Weighting procedures are used in observational causal inference to adjust for covariate imbalance within the sample. Common practice for inference is to estimate robust standard errors from a weighted regression of outcome on treatment. However, it is well known that weighting can inflate variance estimates, sometimes significantly, leading to standard errors and confidence intervals that are overly conservative. We instead examine and recommend the use of robust standard errors from a weighted regression that additionally includes the balancing covariates and their interactions with treatment. We show that these standard errors are more precise and asymptotically correct for weights that achieve exact balance under multiple common resampling frameworks, including design-based and model-based inference, as well as superpopulation sampling with a finite sample correction. Gains to precision can be quite significant when the balancing weights adjust for prognostic covariates. For procedures that balance only approximately or in expectation, such as inverse propensity weighting or approximate balancing weights, our proposed method improves precision by reducing residuals through augmentation with the parametric model. We demonstrate our approach through simulation and re-analysis of multiple empirical studies.

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Demystifying and avoiding the OLS "weighting problem": Unmodeled heterogeneity and straightforward solutions

Researchers frequently estimate treatment effects by regressing outcomes (Y) on treatment (D) and covariates (X). Even without unobserved confounding, the coefficient on D yields a conditional-variance-weighted average of strata-wise effects, not the average treatment effect. Scholars have proposed characterizing the severity of these weights, evaluating resulting biases, or changing investigators' target estimand to the conditional-variance-weighted effect. We aim to demystify these weights, clarifying how they arise, what they represent, and how to avoid them. Specifically, these weights reflect misspecification bias from unmodeled treatment-effect heterogeneity. Rather than diagnosing or tolerating them, we recommend avoiding the issue altogether, by relaxing the standard regression assumption of "single linearity" to one of "separate linearity" (of each potential outcome in the covariates), accommodating heterogeneity. Numerous methods--including regression imputation (g-computation), interacted regression, and mean balancing weights--satisfy this assumption. In many settings, the efficiency cost to avoiding this weighting problem altogether will be modest and worthwhile.

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Causal progress with imperfect placebo treatments and outcomes

In the quest to make defensible causal claims from observational data, it is sometimes possible to leverage information from "placebo treatments" and "placebo outcomes". Existing approaches employing such information focus largely on point identification and assume (i) "perfect placebos", meaning placebo treatments have precisely zero effect on the outcome and the real treatment has precisely zero effect on a placebo outcome; and (ii) "equiconfounding", meaning that the treatment-outcome relationship where one is a placebo suffers the same amount of confounding as does the real treatment-outcome relationship, on some scale. We instead consider an omitted variable bias framework, in which users can postulate ranges of values for the degree of unequal confounding and the degree of placebo imperfection. Once postulated, these assumptions identify or bound the linear estimates of treatment effects. Our approach also does not require using both a placebo treatment and placebo outcome, as some others do. While applicable in many settings, one ubiquitous use-case for this approach is to employ pre-treatment outcomes as (perfect) placebo outcomes, as in difference-in-difference. The parallel trends assumption in this setting is identical to the equiconfounding assumption, on a particular scale, which our framework allows the user to relax. Finally, we demonstrate the use of our framework with two applications and a simulation, employing an R package that implements these approaches.

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Kpop: A kernel balancing approach for reducing specification assumptions in survey weighting

With the precipitous decline in response rates, researchers and pollsters have been left with highly non-representative samples, relying on constructed weights to make these samples representative of the desired target population. Though practitioners employ valuable expert knowledge to choose what variables, $X$ must be adjusted for, they rarely defend particular functional forms relating these variables to the response process or the outcome. Unfortunately, commonly-used calibration weights -- which make the weighted mean $X$ in the sample equal that of the population -- only ensure correct adjustment when the portion of the outcome and the response process left unexplained by linear functions of $X$ are independent. To alleviate this functional form dependency, we describe kernel balancing for population weighting (kpop). This approach replaces the design matrix $\mathbf{X}$ with a kernel matrix, $\mathbf{K}$ encoding high-order information about $\mathbf{X}$. Weights are then found to make the weighted average row of $\mathbf{K}$ among sampled units approximately equal that of the target population. This produces good calibration on a wide range of smooth functions of $X$, without relying on the user to decide which $X$ or what functions of them to include. We describe the method and illustrate it by application to polling data from the 2016 U.S. presidential election.

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Real Effect or Bias? Best Practices for Evaluating the Robustness of Real-World Evidence through Quantitative Sensitivity Analysis for Unmeasured Confounding

The assumption of no unmeasured confounders is a critical but unverifiable assumption required for causal inference yet quantitative sensitivity analyses to assess robustness of real-world evidence remains underutilized. The lack of use is likely in part due to complexity of implementation and often specific and restrictive data requirements required for application of each method. With the advent of sensitivity analyses methods that are broadly applicable in that they do not require identification of a specific unmeasured confounder, along with publicly available code for implementation, roadblocks toward broader use are decreasing. To spur greater application, here we present a best practice guidance to address the potential for unmeasured confounding at both the design and analysis stages, including a set of framing questions and an analytic toolbox for researchers. The questions at the design stage guide the research through steps evaluating the potential robustness of the design while encouraging gathering of additional data to reduce uncertainty due to potential confounding. At the analysis stage, the questions guide researchers to quantifying the robustness of the observed result and providing researchers with a clearer indication of the robustness of their conclusions. We demonstrate the application of the guidance using simulated data based on a real-world fibromyalgia study, applying multiple methods from our analytic toolbox for illustration purposes.

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Kernel Balancing: A flexible non-parametric weighting procedure for estimating causal effects

In the absence of unobserved confounders, matching and weighting methods are widely used to estimate causal quantities including the Average Treatment Effect on the Treated (ATT). Unfortunately, these methods do not necessarily achieve their goal of making the multivariate distribution of covariates for the control group identical to that of the treated, leaving some (potentially multivariate) functions of the covariates with different means between the two groups. When these "imbalanced" functions influence the non-treatment potential outcome, the conditioning on observed covariates fails, and ATT estimates may be biased. Kernel balancing, introduced here, targets a weaker requirement for unbiased ATT estimation, specifically, that the expected non-treatment potential outcome for the treatment and control groups are equal. The conditional expectation of the non-treatment potential outcome is assumed to fall in the space of functions associated with a choice of kernel, implying a set of basis functions in which this regression surface is linear. Weights are then chosen on the control units such that the treated and control group have equal means on these basis functions. As a result, the expectation of the non-treatment potential outcome must also be equal for the treated and control groups after weighting, allowing unbiased ATT estimation by subsequent difference in means or an outcome model using these weights. Moreover, the weights produced are (1) precisely those that equalize a particular kernel-based approximation of the multivariate distribution of covariates for the treated and control, and (2) equivalent to a form of stabilized inverse propensity score weighting, though it does not require assuming any model of the treatment assignment mechanism. An R package, KBAL, is provided to implement this approach.

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