Team-based Care for Patients with Type 2 Diabetes


Team-based Care for Patients with Type 2 Diabetes

Topic: Endocrinology
Relevant Terms: Type 2 diabetes; insulin therapy
Primary Audience: Endocrinologists, primary care physicians, and other members of the care team involved in the management of patients with T2DM, including endocrinology and primary care nurse practitioners (NPs), physician assistants (PAs), and nurses
Launch Date: 21-Dec-17
Credits: AMA PRA Category 1 Credit
1 CDR continuing professional education unit
Expiration Date: 21-Dec-18
Curriculum Name: Evolving Paradigms for Insulin Therapy of Type 2 Diabetes

Learning Objectives

After completing this activity, the participant will demonstrate the ability to:

  1. Describe the benefits and risks of currently approved insulin therapies for the management of T2DM.
  2. Incorporate insulin into the management of patients with T2DM who do not achieve glycemic control.
  3. Intensify insulin therapy for patients with T2DM who do not achieve glycemic goals with initial insulin therapy.
  4. Summarize the current evidence-based practice guidelines for the management of T2DM.
  5. Develop strategies to overcome patient-related adherence barriers to the use of insulin in patients with T2DM.


    Neda Laiteerapong, MD, MS, FACP
    Assistant Professor, Section of General Internal Medicine
    Associate Director, Center for Translational and Policy Research of Chronic Diseases
    Co-Director of Research Writing Workshop
    The University of Chicago Pritzker School of Medicine
    Chicago, IL
    Louis H. Philipson, MD, PhD
    Professor of Medicine
    Director, Kovler Diabetes Center
    The University of Chicago Pritzker School of Medicine
    Chicago, IL
    Amy Hess-Fischl, MS, RDN, LDN, BC-ADM, CDE 
    Certified Diabetes Educator, Nutrition Specialist, Program Coordinator
    Kovler Diabetes Center
    The University of Chicago Pritzker School of Medicine
    Chicago, IL

    As a provider accredited by the ACCME, The University of Chicago Pritzker School of Medicine, asks everyone who is in a position to control the content of an education activity to disclose all relevant financial relationships with any commercial interest. This includes any entity producing, marketing, re-selling, or distributing health care goods or services consumed by, or used on, patients. The ACCME defines "relevant financial relationships" as financial relationships in any amount occurring within the past 12 months including financial relationships of a spouse or life partner that could create a conflict of interest. Mechanisms are in place to identify and resolve any potential conflict of interest prior to the start of the activity. 

    Dr. Philipson discloses that he has received grant/research support from Johnson & Johnson, Novo Nordisk, and Xoma. He has served as a consultant for Calico and Neurotronic, and has served on a speakers bureau for Merck.

    Dr. Laiteerapong has no conflicts of interest to disclose.

    Ms. Hess-Fischl has no conflicts of interest to disclose.

    Mahira Zec Bonomo, University of Chicago, Director for CME, has nothing to disclose. 
    Joshua Kilbridge, medical writer, has nothing to disclose. 
    Kathleen Hines, MCM Education VP, Editorial Services, has nothing to disclose. 
    Terry Ann Glauser, MD, MPH, MCM Education VP, Medical Affairs, has nothing to disclose. 

    Faculty members are required to inform the audience when they are discussing off-label or unapproved uses of devices or drugs. Devices or drugs that are still undergoing clinical trials are identified as such and should not be portrayed as standard, accepted therapy. Please consult full prescribing information before using any product mentioned in this activity. If using products in an investigational, off-label manner, it is the responsibility of the prescribing physician to monitor the medical literature to determine recommended dosages and uses of the drugs. Neither the publisher nor the providers promote the use of any agent outside of approved labeling.

    Credit Statements
    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 Chicago Pritzker School of Medicine and MCM Education in collaboration with RealCME. The University of Chicago Pritzker School of Medicine is accredited by the ACCME to provide continuing medical education for physicians. 

    The University of Chicago Pritzker School of Medicine designates this enduring material for a maximum of 1.0 AMA PRA Category 1 CreditTM. Physicians should claim only the credit commensurate with the extent of their participation in the activity. 

    Nurses and other health care professionals will receive a Certificate of Participation. For information on the applicability and acceptance of Certificates of Participation for educational activities certified for AMA PRA Category 1 CreditTM from organizations accredited by the ACCME, please consult your professional licensing board.

    Commission on Dietetic Registration (CDR) - Provider Name: University of Chicago, Activity #138105 approved for 1.0 CPEUs.

    Commercial Support Statements
    This activity is supported by independent educational grants from Novo Nordisk Inc. and Sanofi US, and Boehringer Ingelheim Pharmaceuticals, Inc. and Lilly USA, LLC.

    ©2017 MCM Education. All rights reserved. None of the contents may be reproduced in any form without prior written permission from the publisher. The opinions expressed in this educational activity are those of the faculty and do not necessarily reflect the opinions or recommendations of their affiliated institutions, the publisher, the University of Chicago Pritzker School of Medicine, Novo Nordisk Inc., Sanofi US, Boehringer Ingelheim Pharmaceuticals, Inc., or Lilly USA, LLC. Any medications, diagnostic procedures, or treatments discussed by the program presenters should not be used by clinicians or other health care professionals without first evaluating their patients' conditions, considering possible contraindications or risks, reviewing any applicable manufacturer’s product information, and comparing any therapeutic approach with the recommendations of other authorities. 

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