A Review of Causal Inference Methods for Estimating the Effects of Exposure Change when Incident Exposure Is Unobservable

被引:0
作者
Liu, Fangyu [1 ,2 ]
Duchesneau, Emilie D. [3 ]
Lund, Jennifer L. [4 ]
Jackson, John W. [1 ,2 ,5 ]
机构
[1] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD 21205 USA
[2] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Biostat, Baltimore, MD 21205 USA
[3] Wake Forest Sch Med, Dept Epidemiol & Prevent, Div Publ Hlth Sci, Winston Salem, NC USA
[4] Univ North Carolina Chapel Hill, Gillings Sch Global Publ Hlth, Dept Epidemiol, Chapel Hill, NC USA
[5] Johns Hopkins Bloomberg Sch Publ Hlth, Ctr Drug Safety & Effectiveness, Baltimore, MD USA
关键词
Target trial emulation; Exposure change; Sequential conditional mean model; Time-dependent matching; Inverse probability weighting; Parametric g-formula; INVERSE PROBABILITY WEIGHTS; MARGINAL STRUCTURAL MODELS; DOUBLY ROBUST ESTIMATION; PROPENSITY-SCORE; TARGET TRIAL; G-COMPUTATION; RISK;
D O I
10.1007/s40471-024-00343-5
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Purpose of ReviewResearch questions on exposure change and health outcomes are both relevant to clinical and policy decision making for public health. Causal inference methods can help investigators answer questions about exposure change when the first or incident exposure is unobserved or not well defined. This review aims to help researchers conceive of helpful causal research questions about exposure change and understand various statistical methods for answering these questions to promote wider adoption of causal inference methods in research on exposure change outside the field of pharmacoepidemiology.Recent FindingsEpidemiologic studies examining exposure changes face challenges that can be addressed by causal inference methods, including target trial emulation. However, their application outside the field of pharmacoepidemiology is limited.SummaryIn this review, we (a) illustrate considerations in defining an exposure change and defining the total and joint effects of an exposure change, (b) provide practical guidance on trial emulation design and data set-up for statistical analysis, (c) demonstrate four statistical methods that can estimate total and/or joint effects (structural conditional mean models, time-dependent matching, inverse probability weighting, and the parametric g-formula), and (d) compare the advantages and limitations of these statistical methods.
引用
收藏
页码:185 / 198
页数:14
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