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Constructing Causal Diagrams for Common Perinatal Outcomes: Benefits, Limitations and Motivating Examples with Maternal Antidepressant Use in Pregnancy
Author(s) -
Bandoli Gretchen,
Palmsten Kristin,
Flores Katrina F.,
Chambers Christina D.
Publication year - 2016
Publication title -
paediatric and perinatal epidemiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.667
H-Index - 88
eISSN - 1365-3016
pISSN - 0269-5022
DOI - 10.1111/ppe.12302
Subject(s) - directed acyclic graph , covariate , confounding , observational study , medicine , causal inference , causal model , selection bias , pregnancy , econometrics , computer science , mathematics , pathology , algorithm , biology , genetics
Background Covariate selection to reduce bias in observational data analysis has primarily relied upon statistical criteria to guide researchers. This approach may lead researchers to condition on variables that ultimately increase bias in the effect estimates. The use of directed acyclic graphs ( DAG s) aids researchers in constructing thoughtful models based on hypothesised biologic mechanisms to produce the least biased effect estimates possible. Methods After providing an overview of different relations in DAG s and the prevailing mechanisms by which conditioning on variables increases or reduces bias in a model, we illustrate examples of DAG s for maternal antidepressants in pregnancy and four separate perinatal outcomes. Results By comparing and contrasting the diagrams for maternal antidepressant use in pregnancy and spontaneous abortion, major malformations, preterm birth, and postnatal growth, we illustrate the different conditioning sets required for each model. Moreover, we illustrate why it is not appropriate to condition on the same set of covariates for the same exposure and different perinatal outcomes. We further discuss potential selection biases, overadjustment of mediators on the causal path, and sufficient sets of conditioning variables. Conclusion In our efforts to construct parsimonious models that minimise confounding and selection biases, we must rely upon our scientific knowledge of the causal mechanism. By structuring data collection and analysis around hypothesised DAG s, we ultimately aim to validly estimate the causal effect of interest.

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