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Table 1 Comparison of CDS, Return of Results and Educational Strategies for IGNITE Projects

From: The IGNITE network: a model for genomic medicine implementation and research

Site/Project

Characteristics of CDS

Return of results

Educational strategies

Duke University: Implementation, Adoption and Utility of Family History in Diverse Care Settings

• Open source (OpenCDS)

• Bidirectional

• Based on HL7 Virtual Medical Record standard

• Epic-based system

• Directly to patients and providers via CDS within the EHR

• English and Spanish language versions of FHH software

• Printed and web based materials

• Patient workbook and instructions for capturing FHH

• Patient report for FHH results

Indiana University - INGenious: INdiana Genomics Implementation: an Opportunity for the UnderServed

• Eskenazi home-grown EHR system

• Automated identification and randomization of patients

• Capture of genetic variant data and reporting into EHR

• Automatic alerts

• Links to guidelines and supporting evidence for patients with pharmacogenomic results

• Directly to providers via CDS within the EHR

• Personal engagement with Eskenazi patient representative organization

• Print materials in language-appropriate form in clinics

Icahn School of Medicine at Mount Sinai - Genetic testing to Understand and Address Renal Disease Disparities (GUARDD)

• Epic-based system that incorporates CLIPMERGE

• Alert-based informed message for provider that integrates EHR and allele data

• Based on HL7 standards

• Integrated with Redcap

• CDS alert includes link to provider and patient education materials

• Directly to providers via CDS within the EHR

• To patients by research staff trained by genetic counselors

• Genetic counselor available for consultation with patients or research staff

• Print materials (low-literacy, culturally appropriate, co-developed with community leaders and APOL1-positive patients) provided to patients at return of result and available for download by clinicians

University of Florida – UF Health Personalized Medicine Program

• Epic-based system

• Alert-based informed message for provider that integrates EHR and allele data

• Integrated with Redcap

• CDS alert includes link to patient education materials

• Directly to providers via CDS within the EHR

• Print and online materials for patients and clinicians

• Continuing education and academic courses for health care professionals and students

University of Maryland - Genomic Diagnosis and Personalized Therapy for Highly Penetrant Genetic Diabetes

• Epic-based system

• Interface of screening tool and algorithm with EHR to produce alert for testing

• Integration of actionable result report into EHR

• Genetic result-based diagnosis/treatment recommendation alerts

• Direct communication of results to patients and entry into medical record

• Customized materials provided to patients for communicating with other family members

• If a variant of unknown significance is found, patients will be informed and invited to participate in additional research

• In-person throughout the study process (e.g., patient informed consent conducted by genetic counselor and research coordinator)

• For patients with a pathogenic variant, study team and provider will discuss implications

• Print materials also provided to patients throughout study

Vanderbilt University - Integrated, Individualized and Intelligent Prescribing (I3P) Network

• Multiple EHR systems (Epic, Veterans Affairs CPRS, McKesson, home-grown)

• Bidirectional

• Based on HL7 standards

• Incorporates newly developed HL7 genomic data standard

• Include interpretative recommendations

• Link out to external information sources (e.g., MyCancerGenome.org)

• Passive and active alerts

• Directly to providers via CDS within the EHR

• Print and online materials for patients and clinicians

• Integrated with CDS

• Provider focus groups

  1. CDS clinical decision support, HL7 health level-7, EHR electronic health record, FHH family health history, CPRS computerized patient record system