Breaking Down the Barriers to Optimal Diabetes Outcomes: Considerations for GLP-1 Agonists
Program Overview/Statement of Need:
The most recent State of Health Care Quality Report, published by the National Committee for Quality Assurance (NCQA), indicated that only 43.2% of patients with diabetes had good HbA1c control (<7%), while 61.3% had an HbA1c of <8% and 28.5% had poor control (HbA1c >9%). Additional data show that many patients who reach their glycemic goal do not maintain it. Patients must become "partners in care," but more direction is needed to help clinicians successfully engage their patients.
Breaking Down the Barriers to Optimal Diabetes Outcomes: Considerations for GLP-1 Agonists will guide internists, PCPs, nurses, pharmacists, NPs, and PAs through the practical application of up-to-date information in T2DM management and best practices to break down barriers preventing patients from reaching HbA1c goals. Clinicians will gain an improved understanding of the place of GLP-1 agonists in the treatment armamentarium; will be better able to differentiate the GLP-1 agonists currently available, including safety and efficacy profiles and injection delivery methods.
Target Audience: This activity is intended for internists, PCPs, nurses, pharmacists, NPs, and PAs involved in the management of patients with T2DM.
After completion of this activity, participants should be able to:
DISCLOSURE POLICY STATEMENT
- Describe the relationships between glycemia and diabetes complications
- Consider the HbA1c-lowering properties of GLP-1 agonists with their impacts on T2DM pathophysiology, CV risk factors, and hypoglycemic risk when individualizing treatment strategies for diabetic patients to reach target goals
- Develop strategies to attain glycemic control throughout the life cycle of T2DM
- Promote a collaborative approach to T2DM management, empowering the patient through individualized patient education to address and break down barriers for optimal outcomes, including adherence and injection-related barriers
Potomac Center for Medical Education (PCME) adheres to the policies and guidelines, including the Standards for Commercial Support, set forth to providers by the Accreditation Council for Continuing Medical Education (ACCME) and all other professional organizations, as applicable, stating those activities where continuing education credits are awarded must be balanced, independent, objective, and scientifically rigorous.
All persons in a position to control the content of a continuing medical education program provided by PCME are required to disclose any relevant financial relationships with any commercial interest to PCME as well as to learners. All conflicts are identified and resolved by PCME in accordance with the Standards for Commercial Support in advance of delivery of the activity to learners.
The content of this activity was vetted by an external medical reviewer to assure objectivity and that the activity is free of commercial bias. Faculty Disclosures
The faculty reported the following relevant financial relationships that they or their spouse/partner have with commercial interests: Zachary T. Bloomgarden, MD, MACE: Consultant/Advisor:
AstraZeneca, Johnson & Johnson, Merck, Novartis, Novo Nordisk; Speaker:
AstraZeneca, Boehringer Ingelheim, Johnson & Johnson, Merck, Novo Nordisk, Santaris Pharma; Stockholder:
Baxter International, CVS Caremark, Novartis, Roche Holdings, St. Jude Medical Ellen H. Miller, MD
Non-faculty content contributors and/or reviewers reported the following relevant financial relationships that they or their spouse/partner have with commercial interests: Carole Drexel, PhD; Blair St. Amand; Jay Katz, CCMEP; Ashley Marostica, Joshua Kilbridge:
Nothing to disclose DISCLAIMER
The contents of some CME/CE activities may contain discussions of non-approved or off-label uses of some agents mentioned. Please consult the prescribing information for full disclosure of approved uses. PHYSICIAN CREDIT DESIGNATION
The Potomac Center for Medical Education designates this enduring activity for a maximum of 1.0 AMA PRA Category 1 Credit
™. Physicians should only claim credit commensurate with the extent of their participation in the activity.
For questions regarding CME credit, the post-test, or evaluation, please email firstname.lastname@example.org. ACCREDITATION
This activity has been planned and implemented in accordance with the accreditation requirements and policies of the Accreditation Council for Continuing Medical Education through the joint providership of the Potomac Center for Medical Education and Rockpointe. The Potomac Center for Medical Education is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians.
This continuing medical education activity is jointly provided by the Potomac Center for Medical Education and Rockpointe. COMMERCIAL SUPPORT
This activity is supported by an educational grant from AstraZeneca. HOW TO RECEIVE CREDIT
By reviewing the course content and successfully completing the post-test and evaluation, physicians are entitled to receive 1.0 AMA PRA category 1 Credit
™. Statement of credit will be available to print from your user history page.
COURSE VIEWING REQUIREMENTS
- Read the learning objectives and faculty disclosures.
- Participate in the activity.
- Complete the post-test and activity evaluation.
- Physicians who successfully complete the post-test and evaluation will receive CME credit. You must score 80% or higher on the post-test to receive credit for this activity.
- All other participants who successfully complete the post-test and evaluation will receive a certificate of participation.
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