Double Machine Learning of Continuous Treatment Effects with General Instrumental Variables

arXiv stat.ML / 4/14/2026

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Key Points

  • The paper proposes a new identification framework for average dose-response functions for continuous treatments using instrumental variables to reduce bias from unobserved confounding.
  • It introduces a “uniform regular weighting function” and covers the treatment space with finitely many regions (open sets) to achieve local identification within each region.
  • For estimation, the authors develop an augmented inverse probability weighted score for continuous treatments with instruments under a debiased machine learning approach.
  • The work provides asymptotic theory for estimating the dose-response function via kernel regression or empirical risk minimization and includes guidance for adaptively learning the regular weighting functions from data.
  • The methods are evaluated through simulations and empirical studies to study finite-sample performance.

Abstract

Estimating causal effects of continuous treatments is a common problem in practice, for example, in studying average dose-response functions. Classical analyses typically assume that all confounders are fully observed, whereas in real-world applications, unmeasured confounding often persists. In this article, we propose a novel framework for the identification of average dose-response functions using instrumental variables, thereby mitigating bias induced by unobserved confounders. We introduce the concept of a uniform regular weighting function and consider covering the treatment space with a finite collection of open sets. On each of these sets, such a weighting function exists, allowing us to identify the average dose-response function locally within the corresponding region. For estimation, we propose an augmented inverse probability weighted score for continuous treatments with instrumental variables under a debiased machine learning framework, and provide practical guidance to adaptively establish regular weighting functions from the data. We further establish the asymptotic properties when the average dose-response function is estimated via kernel regression or empirical risk minimization. Finally, we conduct both simulation and empirical studies to assess the finite-sample performance of the proposed methods.