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. 2024 Oct;21(5):623-635.
doi: 10.1177/17407745241243308. Epub 2024 Apr 28.

Causal interpretation of the hazard ratio in randomized clinical trials

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Causal interpretation of the hazard ratio in randomized clinical trials

Michael P Fay et al. Clin Trials. 2024 Oct.

Abstract

Background: Although the hazard ratio has no straightforward causal interpretation, clinical trialists commonly use it as a measure of treatment effect.

Methods: We review the definition and examples of causal estimands. We discuss the causal interpretation of the hazard ratio from a two-arm randomized clinical trial, and the implications of proportional hazards assumptions in the context of potential outcomes. We illustrate the application of these concepts in a synthetic model and in a model of the time-varying effects of COVID-19 vaccination.

Results: We define causal estimands as having either an individual-level or population-level interpretation. Difference-in-expectation estimands are both individual-level and population-level estimands, whereas without strong untestable assumptions the causal rate ratio and hazard ratio have only population-level interpretations. We caution users against making an incorrect individual-level interpretation, emphasizing that in general a hazard ratio does not on average change each individual's hazard by a factor. We discuss a potentially valid interpretation of the constant hazard ratio as a population-level causal effect under the proportional hazards assumption.

Conclusion: We conclude that the population-level hazard ratio remains a useful estimand, but one must interpret it with appropriate attention to the underlying causal model. This is especially important for interpreting hazard ratios over time.

Keywords: Causal inference; clinical trial; estimand; hazard ratio; proportional hazards model; survival analysis.

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Conflict of interest statement

Declaration of conflicting interestsThe author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Figures

Figure 1.
Figure 1.
Example 1: Potential outcome bivariate distribution, F, plotted in the form of its bivariate probability mass function, f. Darker values have more mass.
Figure 2.
Figure 2.
Example 1: Potential outcome survival curves.
Figure 3.
Figure 3.
Example 1: Potential outcome probability mass functions.
Figure 4.
Figure 4.
Example 1: Potential outcome hazard curves.
Figure 5.
Figure 5.
Example 1: Hazard ratio estimands over time, except θCoxHB(t) is estimated from a simulated study with n=10,000 with the end of study censoring changing such that τ=t.
Figure 6.
Figure 6.
Example 2: Vaccine example based on a mixture of 4 exponential curves, with hazard rates from Table 1.

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