Session Details

AM7: Causal Inference and Causal Diagrams in Medical Decision Making and Big Real World Data
(Event: 17th Biennial European Conference (ESMDM) - Leiden, The Netherlands)

Jun 10, 2018 9:00AM - Jun 10, 2018 12:30PM
Session Type: Short Course- AM 1/2 Day

Description
Background
One of the most important tasks of decision makers is to derive causal interpretations using both statistical analyses of original datasets and decision analysis. Often an intervention, action or risk factor is modeled to have a "causal effect" on one or more model parameters (e.g., probability, rate, or mean of outcome). Therefore, both the biostatistician and the decision analyst need tools to check: (1) when effect estimates have a causal interpretation and when they do not; and (2) the appropriate methods to derive causal effects instead of merely statistical associations.
Course Type
Half Day
Course Level
Intermediate
Format Requirements
The course will consist of lectures, exercises drawn from the published literature and interactive discussion. The intended audience includes researchers from all substance matter fields, statisticians, epidemiologists, and decision analysts interested either in methods of causal analysis or causal interpretation of results based on the underlying method. Requirements: Basic knowledge in epidemiologic methods (confounding).
Overview
This course will provide an introduction to the principles of causation and causal diagrams, with focus on Directed Acyclic Graphs (DAG) and a brief introduction to methods for causal inference including multivariate analysis, g-formula, marginal structural models with inverse probability of treatment weighting, and structural nested models with g-estimation (lecture - exercises - discussion). We will use the "target trial" concept and a counterfactual approach with "replicates" to apply causal methods to big real world datasets. The objectives of this course are to draw and interpret causal diagrams, to decide which biostatistical/epidemiological methods must be used in different situations to derive causal effect parameters, to understand causal modeling, and to be able to apply these methods in large real world data. Published cardiovascular, HIV, nutrition and obstetrics examples will be used to: *** Adjust for compliance in randomized clinical trials, where both "intention to treat" and "per protocol" analyses can fail to yield the true causal intervention effect; *** Assess the "fallibility of estimating direct effects" (i.e., adjusting for intermediate steps); *** Adjust for time-independent confounders in observational studies (i.e., confounder affects both risk factor and disease), where standard stratification, regression analysis or propensity score methods yield valid causal effects if all confounders are measured, and *** Adjust for time-dependent confounding in observational studies (i.e., the confounder simultaneously acts as an intermediate step in the causal chain between risk factor and disease), where standard regression analysis fails and "causal methods" such as marginal structural models or g-estimation must be used.
Description & Objectives
The Objectives of this course are:

(1) to define causal interventions and actions, draw and interpret causal diagrams, and apply the rules of causal diagrams to distinguish causal from non-causal statistical associations.

(2) to decide which biostatistical/epidemiological methods must be used in different situations to derive causal effect parameters.

(3) to use causal diagrams to estimate the direction of bias in "non-causal" models.

(4) to understand the conceptual approaches of causal modeling

(5) to know how these methods are applied in big real world data

Published cardiovascular, HIV, cancer, nutrition and obstetrics examples will be used to:

  • Adjust for compliance in randomized clinical trials, where both "intention to treat" and "per protocol" analyses can fail to yield the true causal intervention effect;
  • Assess the “fallibility of estimating direct effects” (i.e., adjusting for intermediate steps);
  • Adjust for time-independent confounders in observational studies (i.e., confounder affects both risk factor and disease), where standard stratification, regression analysis, propensity score methods and matching/balancing approaches yield valid causal effects if all confounders are measured;
  • Adjust for time-dependent confounding in observational studies (i.e., the confounder simultaneously acts as an intermediate step in the causal chain between risk factor and disease), where standard regression analysis fails and "causal methods" such as marginal structural models or g-estimation must be used; and

Assess unmeasured confounding

Course Director
  • Uwe Siebert
    • UMIT, Dept. of Public Health, Health Services Research & HTA / Harvard Univ., Dept. Health Policy & Management, Institute for Technology Assessment
Course Faculty
  • Felicitas Kuehne
    • Department of Public Health, Health Services Research and Health Technology Assessment, UMIT - University for Health Sciences, Medical Informatics and Technology

  

Session Fees
Fee TypeMember FeeNon-Member Fee
This session is free
Early: $158.00 $216.00
Regular: $158.00 $216.00
Late: $173.00 $241.00
This session is free
Early: $80.00 $80.00
Regular: $80.00 $80.00
Late: $91.00 $91.00

 

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