Translating Clinical Evidence for Sensor-Based Glucose Monitoring and Technological Innovations to the Front Lines of Clinical Practice

The Evolving Landscape of Sensor-Based Technology for Optimizing Clinical Outcomes Across the Comprehensive Spectrum of Type 1 and Type 2 Diabetes Care

Tadej Battelino, MD, PhD

Video

Translating Landmark Trials and Meta-Analyses Trials in CGM to the Front Lines of Diabetes Care: Focus on the Role of Sensor-Based Technology to Improve Time in Range and Interpretation of Ambulatory Glucose Profiles

Richard Bergenstal, MD

Video

Real World, Interactive Case Management Sessions with the Faculty: Clinical Decision-Making Using Sensor-Based Glucose Monitoring Technology Across the Full Spectrum of Diabetes Care

Ramzi Ajjan, MD, PhD

Click Here to Access Program Slides

Translating Clinical Evidence forSensor-Based Glucose Monitoring and Technological Innovations to the Front Lines of Clinical Practice

Program Medium

Internet-based program

Estimated Time to Complete Educational Activity

1.5 hours

Course Overview

In this web-based program, physicians will learn how recent developments in sensor-based continuous glucose monitoring have advanced the management of Type 1 and Type 2 diabetes.

Release Date

March 3, 2020

Expiration Date

March 3, 2022

Method of Physician Participation Utilized in Learning Process

There are no fees for participating and receiving CME credit for this activity. During the period March 3, 2020 to March 3, 2022 participants must:
1) read the learning objectives and faculty disclosures;
2) study the educational activity, and are expected to view all 3 segments totaling 1.5 hours to successfully complete the activity and earn CME credit;
3) register and complete the evaluation form and post-test;
4) score 100% on the post-test; and
5) print out your CME certificate.

Registration

Participation in this WebCAST is complimentary, and clinicians are invited to view this CME-certified program and/or share this invitation with other colleagues, departmental staff members, and healthcare professionals.

Grantor Support

Supported by an educational grant from Abbott.

Accreditation Statement

This activity has been planned and implemented in accordance with the accreditation requirements and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint providership of The University of Massachusetts Medical School and CMEducation Resources, LLC. The University of Massachusetts Medical School is accredited by the ACCME to provide continuing medical education for physician.

Credit Designation Statement

The University of Massachusetts Medical School designates this enduring material for a maximum of 1.5 AMA PRA Category 1 Credits(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.

Policy on Faculty & Provider Disclosure

The University of Massachusetts Medical School requires instructors, planners, managers and other individuals who are in a position to control the content of this activity to disclose any real or apparent conflict of interest (COI) they may have as related to the content of this activity. All identified COI are thoroughly vetted and resolved according to The University of Massachusetts Medical School policy. The existence or absence of COI for everyone in a position to control content will be disclosed to participants prior to the start of each activity.

Other Credits

American Nurses Credentialing Center (ANCC) accepts AMA PRA Category 1 Credits™ from organizations accredited by the ACCME.

American Academy of Nurse Practitioners (AANP) accepts AMA PRA Category 1 Credits™ from organizations accredited by the ACCME.

American Academy of Physician Assistants (AAPA) accepts certificates of participation for educational activities certified for AMA PRA Category 1 Credits™ from organizations accredited by the ACCM.

Program Faculty and Disclosure

Tadej Battelino, MD, PhD
Program Chair
Department of Pediatric Endocrinology, Diabetes and Metabolism
University Children's Hospital
University Medical Centre Ljubljana
Faculty of Medicine
University of Ljubljana
Ljubljana, Slovenia

Advisory Board: Novo Nordisk, Sanofi, Eli Lilly, Boehringer, Medtronic, DreaMed Diabetes and Bayer Health Care.
Speaker’s Bureau: Eli Lilly, Bayer, Novo Nordisk, Medtronic, Abbott, Sanofi and Roche
Stock: DreamMed Diabetes
Institutional research grant support: Abbott, Medtronic, Novo Nordisk, GluSense, Sanofi, Sandoz and Diamyd

Richard Bergenstal, MD
Executive Director
International Diabetes Center- Park Nicollet
Minneapolis, MN, USA

Clinical research support, scientific advisory board, or consultant: Abbott Diabetes Care, Ascenia, CeQur, Dexcom, Eli Lilly, Hygieia, Johnson & Johnson, Medtronic, Novo Nordisk, Onduo, Roche, Sanofi, Senseonics and United Healthcare

Ramzi Ajjan, MD, PhD
Professor of Metabolic Medicine
Consultant in Diabetes and Endocrinology
University of Leeds and Leeds Teaching Hospitals Trust
Leeds, United Kingdom

Consultant and Research Support: Abbott Diabetes Care

Educational Objectives

Upon completion of the proposed program activities, physicians will be able to:

Outline and discuss the evidentiary basis for senor/patch-based CGM technologies, and how to best Implement CGM-based technologies into their overall diabetes care plans for patients with T1D and T2D.
Analyze the rationale and evidence for recommending and facilitating adoption of technology-centric CGM monitoring and treatment plans using patch-and-reader-based technologies.
Compare and contrast available CGM-facilitating monitoring technologies and pair such technologies with optimal patient profiles.
Educate patients with diabetes about the rationale, evidence, and outcome- optimizing results associated with technology-based, patient-centric and physician-directed CGM monitoring strategies that can be used to effect optimal lifestyle, diet-, and pharmacology-based approaches to attaining guideline-based HA1c levels in patients with T1d and T2D.
Identify which patients with diabetes are ideal candidates for a technology-based, patient-directed glucose monitoring system.
Interpret and apply data and results from clinical trials and experts with experience in CGM-facilitating monitoring technologies to improve patient care, improve safety of drug therapy for T1D and T2D, detect and mitigate risk of hypoglycemia, improve patient- and physician-directed changes in antidiabetic therapy, reinforce the safe use of antidiabetic drugs, and facilitate patient-activated drug titration, glycemic monitoring and disease management.
Translate landmark clinical studies focused on CGM-based technologies to the front lines of clinical practice in the diabetes and primary care setting; and understand the translational implications of deploying sensor-based, CGM-based technologies as a foundational approach to improving outcomes in patients across the spectrum of diabetes.
Educate other clinical providers on the diabetes care team about the rationale, role, evidence, and outcome-enhancing results that are derived from employing technology-based CGM strategies—both patient- and physician-directed—across the broad spectrum of patients with diabetes.

Hardware and Software Requirements:

To participate in this program, viewers must have a PC or Macintosh computer that has active, ongoing internet access for the duration of the program, as well as a compatible Flash-viewer. An email address is required for registration, and a printer is required to print out the CME certificate.

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