This complimentary CME educational activity is designed for all cardiology-focused physicians, nurses, NPs, academicians, pharmacists, researchers, investigators, and program directors managing, referring, and/or consulting on patients with atrial fibrillation, with a focus on stroke prevention. We welcome diabetes-focused clinicians with a medical and educational needs in the fields of diabetology, endocrinology, internal medicine, primary care, and other providers that are part of the multidisciplinary team caring for patients with these and related conditions, including:
Diabetologists
Endocrinologistss
Primary care physicians
Internal medicine specialists
Diabetic nurse practitioners NPsn
Related practitioners
Registration
Participation in this iQ&A interactive Medical Intelligence Zone for Type 2 Diabetes 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.
Method of Physician Participation Utilized in Learning Process
There are no fees for participating and receiving CME credit for this activity. During the period November 18, 2011 through November 18, 2013 participants must 1) read the learning objectives and faculty disclosures; 2) study the educational activity, and are expected to view all 86 segments totaling 2 hours and 20 minutes 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 4) print out CME certificate
Course Overview
In this web-based program, physicians will learn how recent advances in basic and clinical research have helped to advance the understanding of treatment advances in the management of Type 2 diabetes.
Release Date
November 18, 2011
Expiration Date
November 18, 2013
Accreditation Statement
This activity has been planned and implemented in accordance with the Essential Areas and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint sponsorship of the University of Massachusetts Medical School Office of Continuing Medical Education (UMMS-OCME) and CMEducation Resources, LLC. The UMMS-OCME is accredited by the ACCME to provide continuing medical education for physicians.
Credit Designation Statement
The University of Massachusetts Medical School designates this enduring activity for a maximum of 2.5 AMA PRA Category 1 Credits(s)™. Physicians should claim only credit commensurate with the extent of their participation in the activity.
Estimated Time to Complete Educational Activity
2.5 hours
Grantor Support
Supported by an educational grant from Bristol-Myers Squibb and AstraZeneca
Policy on Faculty & Provider Disclosure
It is the policy of the University of Massachusetts Medical School to ensure fair balance, independence, objectivity and scientific rigor in all activities. All faculty participating in CME activities sponsored by the University of Massachusetts Medical School are required to present evidence-based data, identify and reference off-label product use and disclose all relevant financial relationships with those supporting the activity or others whose products or services are discussed. Faculty disclosure will be provided in the activity materials.
Policy on Faculty & Provider Disclosure
It is the policy of the University of Massachusetts Medical School to ensure fair balance, independence, objectivity and scientific rigor in all activities. All faculty participating in CME activities sponsored by the University of Massachusetts Medical School are required to present evidence-based data, identify and reference off-label product use and disclose all relevant financial relationships with those supporting the activity or others whose products or services are discussed. Faculty disclosure will be provided in the activity materials.
Program Faculty and Disclosure
Clifford J. Bailey, PhD, FRCP, FRCPath
UK Diabetes Research
Aston Pharmacy School
School of Life and Health Sciences Triangle
Aston University
Birmingham , UK
Advisor or consultant: AstraZeneca Pharmaceuticals LP; Bristol-Myers Squibb Company; GlaxoSmithKline; Merck Sharp & Dohme Corp.; Novo Nordisk; sanofi-aventis; Takeda Pharmaceuticals North America, Inc.
George L. Bakris, MD, FAHA, FASN
Professor of Medicine
Director, Hypertensive Diseases Unit
University of Chicago School of Medicine
Chicago, Illinois
Consultant/Principal Investigator: Medtronic, Johnson & Johnson, Abbott, Takeda,
John Buse, MD, PhD
Director, Diabetes Care Center
Chief, Division of Endocrinology
Executive Associate Dean for Clinical Research
University of North Carolina School of Medicine
Chapel Hill, North Carolina
Served as a director, officer, partner, employee, advisor, consultant, or trustee for: Amylin Pharmaceutical, Inc. Andromeda, Bayhill Therapeutics, Biodel, Boehringer Ingelheim, Catabasis, Diartis, Elcelyx, Eli Lilly and Co., Exsulin, GI Dynamics, Halozyme, Inc., Hoffman-LaRoche Inc., Johnson & Johnson, Lexicon, LipoScience, Medtronic MiniMed, Inc., Merck, Metabolon, Novan, Novo Nordisk Pharmaceuticals, Inc., Osiris Therapeutics, Inc., Orexigen, Pfizer, Inc., sanofi-aventis, Tolerex, Transition Therapeutics, TransPharma
Professor Bernard H. Charbonnel, MD
Professor of Endocrinology and Metabolic Diseases
University of Nantes
Nantes, France
Advisor/Consultant: AstraZeneca Pharmaceuticals LP; Bristol-Myers Squibb Company; Boehringer Ingelheim Pharmaceuticals, Inc.; GlaxoSmithKline; Eli Lilly and Company; Merck Sharpe & Dohme Corp.; Novartis Pharmaceuticals Corporation; Novo Nordisk; Roche; sanofi-aventis; Takeda Pharmaceuticals North America, Inc.
Speaker: AstraZeneca Pharmaceuticals LP; Bristol-Myers Squibb Company; Boehringer Ingelheim Pharmaceuticals, Inc.; GlaxoSmithKline; Eli Lilly and Company; Merck Sharpe & Dohme Corp.; Novartis Pharmaceuticals Corporation; Novo Nordisk; Roche; sanofi-aventis; Takeda Pharmaceuticals North America, Inc.
Ralph A. DeFronzo, MD
Professor of Medicine
School of Medicine
Diabetes and Metabolic Disorders (DMD) Track
Diabetes Research Unit
Barter Research Unit, UTHSCSA
UTHSCSA Graduate School of Biomedical Sciences
San Antonio, Texas
Consultant: Amylin, Eli Lilly, Takeda, Bristol-Myers Squibb, Astra Zeneca, J&J, Novartis, Merck
Grants: Amylin, Eli Lilly, Takeda, Bristol-Myers Squibb
Professor Stefano Del Prato, MD
Department of Endocrinology and Metabolism
Section of Metabolic Disease and Diabetes
University of Pisa
Pisa, Italy
Research Support: Merck & Co., Inc.; Novo Nordisk; sanofi-aventis
Advisor/Consultant: Bristol-Myers Squibb Company; Merck & Co., Inc.; Novartis Pharmaceuticals Corporation; Novo Nordisk; Pfizer Inc.; Roche
Speaker: GlaxoSmithKline; sanofi-aventis
Vivian A. Fonseca, MD, FRCP
Professor of Medicine and Pharmacology
Tulis-Tulane Alumni Chair in Diabetes
Chief, Section of Endocrinology
Tulane University Health Sciences Center
New Orleans, Louisiana
Grants/Research Support: Daiichi Sankyo, Inc.; Eli Lilly and Company; Halozyme Therapeutics; Novo Nordisk; Pamlab, L.L.C.; Reata Pharmaceuticals, Inc.; sanofi-aventis
Advisor/Consultant: AstraZeneca Pharmaceuticals LP; Daiichi Sankyo, Inc.; Eli Lilly and Company; GlaxoSmithKline; Novo Nordisk; Pamlab, L.L.C.; sanofi-aventis; Takeda Pharmaceuticals North America, Inc.; XOMA (US) LLC
Professor Markolf Hanefeld, MD, PHD
Centre for Clinical Studies,
Dresden Technical University
Dresden, Germany
Nothing to disclose
Silvio E. Inzucchi, MD
Professor of Medicine (Endocrinology)
Clinical Director, Section of Endocrinology
Director, Yale Diabetes Center
Director, Endocrinology & Metabolism Fellowship
Director, Yale Affiliated Hospitals Program
New Haven, Connecticut
Lawrence A. Leiter, MD, FRCP(C), FACP?
Professor, Departments of Medicine and Nutritional Sciences
Head of the Division of Endocrinology and Metabolism
Director of the Lipid Clinic
Associate Director
Clinical Nutrition and Risk Factor Modification Centre
St. Michael’s Hospital
University of Toronto
Toronto, Ontario
Speaker/Advisory Board Honoraria: AstraZeneca Pharmaceuticals, Boehringer-Ingelheim GmbH, Eli Lilly and Company,
GlaxoSmithKline, Novartis AG, Novo Nordisk A/S, sanofi-aventis U.S. LLC., and Pfizer Inc.
Grants/Research Support/Consultant: AstraZeneca Pharmaceuticals, Eli Lilly and Company, GlaxoSmithKline,
Merck & Co., Inc., Novartis Pharmaceuticals, Novo Nordisk Pharmaceuticals Inc., Roche Pharmaceuticals, sanofi-aventis, Servier Pharmaceuticals.
Dr. Juris J. Meier, MD
St Josef-Hospital
Klinikum der Ruhr-Universität Bochum
Bochum, Germany
Nothing to disclose
Michael A. Nauck, MD
Head of Diabetes Center
Head Physician, Diabeteszentrum
Bad Lauterberg, Germany
Grants/Research Support: Amylin Pharmaceuticals, Bayer Vital, Berlin-Chemie/Menarini, Eli Lilly and Company, Novartis, Novo Nordisk, Probiodrug, Restoragen Inc., Sanofi-Aventis; Consultant: AstraZeneca, Bayer Vital, Berlin-Chemie/Menarini, Biovitrum, ConjuChem, Inc., Eli Lilly and Company, Hoffmann-La Roche, Merck & Co., Inc., MSD, Novartis, Novo Nordisk, Pfizer Inc., Probiodrug, Restoragen Inc., Sanofi-Aventis, Takeda Pharmaceuticals Inc.; Advisory Boards: Amylin Pharmaceuticals, ConjuChem, Inc., Eli Lilly and Company, GlaxoSmithKline, Hoffmann-La Roche, Novartis, Novo Nordisk, Probiodrug, Restoragen Inc., Sanofi-Aventis
Anne Peters, MD, FACP, CDE
Professor of Medicine
Director of the USC Clinical Diabetes Program
Director, USC Westside Center for Diabetes
Beverly Hills, California
Advisory Board: Amylin, Lilly, Novo Nordisk
Speaker’s Bureau: Amylin, Lilly, Novo Nordisk, Boehringer Ingelheim, Takeda, sanofi aventis
Steven Shoelson, MD
Section Head, Cellular & Molecular Physiology
Joslin Diabetes Center
Professor of Medicine
Harvard Medical School
Boston, Massachusetts
Nothing to disclose
Professor Krzysztof Strojek, MD
Department of Internal Diseases, Diabetology, and Nephrology
Medical University of Silesia
Katowice, Poland
Advisory Board: Eli Lilly and sanofi-aventis
Speaker Fees: Eli Lilly and sanofi-aventis
Alexander Turchin, MD, MS
Assistant Professor
Harvard Medical School
Brigham and Women's Hospital
Boston, Massachusetts
Nothing to disclose
Mark E. Williams, MD, FACP, FASN
Associate Professor of Medicine
Harvard Medical School
Co-Director of Dialysis
Beth Israel Deaconess Medical Center
Senior Staff Physician, Joslin Diabetes Center
Boston, Massachusetts
Consultant: sanofi-aventis
Vincent Woo, MD
Endocrinology Section
Department of Internal Medicine
University of Manitoba
Health Sciences Centre Diabetes Research Group
Winnipeg, Canada
Nothing to disclose
Carol Wysham, MD
Clinical Associate Professor of Medicine
University of Washington School of Medicine
Section Head, Rockwood Center for Diabetes and Endocrinology
Spokane, Washington
Advisory Board: Amylin, Eli Lilly, sanofi-aventis, Boehringer Ingelheim
Speaker: Amylin, Eli Lilly, sanofi-aventis, Boehringer Ingelheim, Merck, Novo Nordisk
Program Managers and Web Editor Disclosure Program Manager Gideon Bosker, MD has nothing to disclose.
Program Reviewers Denise Leary and Richard Aghababian, MD have nothing to disclose.
Educational Objectives
Upon completion of this activity, participants will be able to:
Explain interventions that currently are deployed for T2D and that have been shown to be helpful for glycemic regulation in T2D; and, the impact of successful glycemic management of T2D on microvascular and macrovascular complications.
Detail advances in therapeutic strategies based on new mechanisms, involving SGLT2 inhibitors (encoded by the SLC5A2 gene), and their impact on glucose homeostasis; and, the effects these agents may have on cardiometabolic markers, including lipids, insulin resistance, HA1c, glucose levels, and microvascular/macrovascular disease.
Describe the mechanisms underlying, and the clinical implications of, SGLT2 inhibition and its potential for shifting the glucose “reabsorption/excretion” threshold to the left, thereby introducing a physiological basis for reducing plasma glucose in patients with T2D.
Describe recent advances in our scientific understanding of mechanisms of action of targeted agents that affect glucose reabsorption in the kidney, the rationale for such agents, and
how their actions can produce improvements in HA1c target levels and other goals identified by such national organizations as ADA and AACE
Detail the relationship between T2DM and atherosclerosis, and how emerging therapies might affect signaling and inflammatory signals, including cytokines, inflammation, and insulin
resistance, and the vasculopathic cascade that characterizes T2DM and its adverse thrombovascular sequelae.
Apply evidence from landmark trials, national guidelines from the ADA and AACE to the clinical challenge of multidimensional therapeutic interventions for T2D; and understand how emerging therapies aimed at inhibiting glucose reabsorption in the kidney may one day play a role as monotherapy, or in combination with established agents for diabetes, for managing patients with T2D.
Stratify patient populations and clinical profiles with T2D that are likely to be the most suitable candidates for and respond optimally to treatment with drugs affecting renal-mediated
glucose homeostasis, including: Treatment-naïve, newly diagnosed patients with T2D; Patients with T2D on concomitant, first-line metformin or sulfonylurea treatment; Patients who are on incretin-based therapy; and Patients on insulin.
Understand the rationale, indications, sequencing, and combination strategies that can be deployed using a glucosuric agent in combination with established platform agents for T2D, including metformin, sulfonylureas, IBTs, and insulin.
Detail, based on well-conducted clinical studies, what the possible safety issues are, or might be, with agents that impair glucose reabsorption in the kidney, and how to manage such side effects, if they occur.
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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