Duke Electronic Health Records Study Design Workshop (EHR-SDW) 2024

Electronic poster for the Duke Electronic Health Records Study Design Workshop taking place December 2-6, 2024. Detailed information on the poster is contained in the body of the webpage.

Duke AI Health is pleased to announce the Duke Electronic Health Records Study Design Workshop (EHR-SDW) 2024. The workshop will be offered in December as a virtual five-day class that provides foundational lectures and hands-on studios on the fundamentals of working with and designing EHR-based studies.

The EHR-SDW is targeted toward individuals interested in learning about how to work with and conduct studies using edata from electronic health records (EHRs). EHR data are a widely available form of real-world data that are being used in different types of studies, spanning clinical trials, comparative effectiveness, risk prediction, population health, and more. The EHR-SDW will introduce learners to the components of EHR data and in considerations for designing effective studies. In addition to didactic lectures, participants will get hands-on experience in working with publicly available tools to facilitate EHR studies (e.g., RxNorm, CCS codes, geocoding), as well as feedback on effective study designs.

This course will be conducted virtually via Zoom.

The course builds upon Dr. Benjamin Goldstein’s and Dr. Jillian Hurst’s prior experience with the Spring 2022 course on clinical research with EHRs and is the third offering of this course. Drs. Goldstein and Hurst are currently developing plans for learning opportunities in 2025.

To register for the EHR-SDW, please visit  https://events.duke.edu/ehr-sdw-2024

To request consideration for a scholarship, please visit https://duke.qualtrics.com/jfe/form/SV_a3Fs9TyyK82Bkr4

The deadline for registration is  Thursday, November 21, 2024.

Who Should Attend

The EHR-SDW is intended for participants working with (or interested in working with) EHR data in academic, industrial, or government settings for research or professional purposes. Previous experience with or direct access to EHR data is not required.

Recent years have seen a tremendous growth in the use of EHR data by academic researchers, biomedical companies, and government bodies to provide insight into how health care is provided in a real-world context. The breadth of EHR data makes it suitable for designing and conducting clinical trials, performing comparative effectiveness studies, developing clinical prediction tools, and performing public health surveillance.

While powerful, EHR data also come with a number of embedded challenges that require thoughtful study design. This course will introduce the components of EHR data, discuss its inherent challenges, and go over different study designs that one may want to conduct with EHR data.

The EHR-SDW is designed to provide value to participants with various backgrounds. Those new to EHR data will develop an appreciation for how EHR data can be used to enhance various types of studies. Participants with experience using EHR data will develop deeper appreciation for the subtleties of different study designs.

The 5-day workshop will combine foundations lectures with hands-on studios allowing participants to engage directly with experienced practitioners. After the introductory first data, each day will focus on a specific study design that uses EHR data:

  • Randomized Studies
  • Observational Studies
  • Prediction Studies
  • Population Health Studies

Each day will be broken into a didactic morning session and group-based afternoon session. The morning session will consist of lectures by experts in conducting the types of studies discussed. Topics will cover rationale for the type of studies, how and why to leverage EHR data into the study, and caveats to consider when using designing studies that use EHR data.

The afternoon session will allow participants to gain experience designing the discussed study topic. An experienced practitioner will walk through a design plan for the study under discussion. Participants will then be divided into small groups (via Zoom Breakout Rooms) and will work through vignettes to design their own studies. The groups will reconvene at the end to present their designs and receive feedback.

At the end of the EHR-SDW, each participant will have a deeper understanding of various types of studies one can conduct with EHR data and the challenges and solutions for how to design appropriate studies.

Curriculum

Morning sessions will be led by clinical and methodological faculty from Duke University with hands-on experience designing and conducting EHR studies in both academic and industry settings. Afternoon workshops will be led by practicing biostatisticians experienced in conducting the discussed studies.

Individual course themes for each day are provided below:

Introduction to Electronic Health Record (EHR) Data
Monday, December 2, 2024 (9:00 AM – 4:00 PM Eastern time) 

  • Introduction to EHR systems and EHR data
  • EHR data that are used for clinical research
  • Differences between structured and unstructured data
  • Privacy concerns with EHR data
  • Potential challenges and biases associated with EHR data
  • Afternoon Studio: Hands on working with ontology systems (RxCUI, CCS) to assist EHR based studies

Pragmatic and Randomized Clinical Trials
Tuesday, December 3, 2024 (9:00 AM – 4:00 PM Eastern time) 

  • EHR systems and EHR data to promote population health
  • Defining target populations and catchments
  • Identifying and mitigating biases in epidemiologic and population health studies
  • Linking social and environmental data with EHR data
  • Afternoon Studio: Population health design

Pragmatic and Randomized Clinical Trials
Wednesday, December 4, 2024 (9:00 AM – 4:00 PM Eastern time) 

  • Using EHR data to design clinical trials
  • Identifying patients for clinical trials
  • Pragmatic trials
  • Afternoon Studio: Randomized study design

Comparative Effectiveness Studies
Thursday, December 5, 2024 (9:00 AM – 4:00 PM Eastern time) 

  • Principles of clinical prediction studies
  • Handling diverse and longitudinal predictor variables
  • Design prediction models for implementation
  • Algorithmic bias and fairness
  • Afternoon Studio: Clinical prediction design

Clinical Prediction Studies
Friday, December 6, 2022 (9:00 AM – 4:00 PM Eastern time) 

  • Principles of observational studies and comparative effectiveness research (CER)
  • Confounding and selection bias
  • Propensity scores
  • Afternoon Studio: Observational study design

A final wrap-up will be conducted at the end of the Friday studio.

Instructors

The course will be taught by an experienced group of methodological and clinical investigators from Duke University experienced in using EHR data for academic, industry, and government projects.

  • Dr. Benjamin Goldstein, Associate Professor of Biostatistics and Bioinformatics
            • Meaningful use of EHR data for clinical research; biases in EHR data
            • Course co-creator, Day 5 presenter
    Dr. Jillian Hurst, Assistant Professor of Pediatrics
              • Use of real-world data for pediatric studies; training of clinician scholars
              • Course co-creator, Day 1 presenter
    Dr. Amanda Brucker, Biostatistician, BERD Core
              • Use of EHR data for clinical research studies
              • Day 1 presenter
    Dr. Nrupen Bhavsar, Associate Professor of Medicine
              • EHR data to study chronic disease; incorporation of geospatial data in EHR studies
              • Day 3 presenter
    Dr. Deepshikha Ashana, Assistant Professor of Medicine
              • Social drivers of health; health policy
              • Day 3 presenter
    Dr. Frank Rockhold, Professor of Biostatistics & Bioinformatics
              • Pragmatic clinical trials in cardiology
              • Day 2 presenter
    Ms. Hillary Mulder, Senior Biostatistician, Duke Clinical Research Institute
              • Pragmatic clinical trials in cardiology
              • Day 2 presenter
    • Ms. Congwen Zhao, Biostatistician, BERD Core
              • Use of EHR data for predictive modelling
              • Day 5 presenter
    Ms. Sophia Bessias, Data Scientist, Health AI Evaluation & Governance
              • Evaluation of clinical decision support tools
              • Day 5 presenter
    • Dr. Laine Thomas, Professor of Biostatistics and Bioinformatics
              • Observational data studies; causal inference
              • Day 4 presenter
    Dr. Karen Chiswell, Statistical Scientist, Duke Clinical Research Institute
              • Use of real-world data for observational studies
              • Day 4 presenter

Program Details

Location, Registration, and Cost

The registration fee for the EHR-SDW is $400. We are able to offer a set number of seats at a discount for members of nonprofit organizations ($150) and current students with a valid ID at Duke or other universities ($50). All fees are payable through the registration site.

All fees are non-refundable. Once we reach maximum registration, we will maintain a waitlist and will contact those on the waitlist as spots become available. We also have a small number of scholarships available for those who would be otherwise unable to join.

Each participant will receive a personal link for the virtual webinars, which will be held live and provide opportunities for questions and engagement with each lecturer. We strongly encourage live participation during all sessions across the 5 days, but every participant will also have access to the video recordings of lectures to use for their personal reference.