Achieving Euglycemic Levels and Minimizing the Impact of Dysmetabolic Risk Factors in Diabetes Management: A Primary Perspective

Please review the CE/CME information below, and click “continue” to view the activity.


Intended Audience

This activity was developed for primary care clinicians (PCCs)—family physicians, internists, general practitioners, and CDE-RNs—who are interested in diabetes management.


Statement of Need

The presence of overweight or obesity in individuals increases the risk of cardiovascular disease and diabetes.1 Studies demonstrate that weight loss, reduction in glycosylated hemoglobin (A1C) levels, and management of cardiovascular risk factors (dyslipidemia and hypertension) of diabetes are critical elements in reducing overall morbidity and mortality.2-4 This activity highlights the importance of intensive risk factor management for patients with diabetes, as reflected in the recent national guidelines for obesity (NHLBI), cholesterol (NCEP-ATP III), hypertension (JNC VII), and diabetes (ADA). Optimum management of diabetes depends on a comprehensive approach to treatment by health-care providers. Because PCCs are first to treat and educate patients with diabetes, it is important that they are aware of evolving treatment options for diabetes to improve patient outcomes. This program will highlight the importance of PCCs as the first line of care in managing dysmetabolic risk factors and type 2 diabetes and their role in effective patient education and follow-up to improve treatment outcomes.


References
1. NHLBI Obesity Education Initiative. The practical guide: identification, evaluation, and treatment of overweight and obesity in adults. Bethesda, MD: National Heart, Lung, and Blood Institute; 2000. NIH publication 00-4084.
2. UK Prospective Diabetes Study (UKPDS) Group. Effect of intensive blood-glucose control with metformin on complications in overweight patients with type 2 diabetes (UKPDS 34). Lancet. 1998;352(9131):854-865.
3. ADVANCE Collaborative Group. Intensive blood glucose control and vascular outcomes in patients with type 2 diabetes. N Engl J Med. 2008;358(24):2560-2572.
4. Lean ME, Powrie JK, Anderson AS, Garthwaite PH. Obesity, weight loss and prognosis in type 2 diabetes. Diabet Med. 1990;7(3):228-233.


Learning Objectives

Accreditation and Certification
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 Annenberg Center for Health Sciences at Eisenhower and CogniMed Inc. The Annenberg Center is accredited by the ACCME to provide continuing medical education for physicians.

The Annenberg Center designates this educational activity for a maximum of 1 AMA PRA Category 1 Credit™. Physicians should only claim credit commensurate with the extent of their participation in the activity.

There is no charge for this activity. Statements of Credit will be provided by mail following activity participation and upon completion and electronic submission of the posttest and evaluation form to CogniMed Inc. A link to the evaluation form is available upon completion of the activity. Please allow 4 to 6 weeks for the delivery of your statement.


Faculty

Robert R. Henry, MD
Chairperson
Professor of Medicine
Division of Endocrinology and Metabolism
University of California, San Diego
Chief, Section of Endocrinology, Metabolism
 & Diabetes
Director, Center for Metabolic Research
VA Medical Center
San Diego, California

Robert J. Chilton, DO, FACC
Professor of Medicine
Department of Medicine
Division of Cardiology
Director of Cardiac Catheterization
Audie Murphy VA
University of Texas Health Science Center at
  San Antonio
San Antonio, Texas

Catherine L. Martin, MS, APRN, BC-ADM, CDE
Clinical Study Coordinator
Division of Metabolism, Endocrinology,
  and Diabetes
University of Michigan Health System
Ann Arbor, Michigan
Frank Svec, MD, PhD
Clinical Professor of Medicine
Section of Endocrinology
Louisiana State University Health Sciences Center
New Orleans, Louisiana

Disclosure Declaration
It is the policy of the Annenberg Center to ensure fair balance, independence, objectivity, and scientific rigor in all programming. All faculty participating in sponsored activities are expected to identify and reference off-label product use and disclose any significant relationships with those supporting the activity or any others whose products or services are discussed.

In accordance with the Accreditation Council for Continuing Medical Education standards, parallel documents from other accrediting bodies, and Annenberg Center policy, the following disclosures have been made:

Annenberg Center for Health Sciences
All staff at the Annenberg Center for Health Sciences at Eisenhower have nothing to disclose.
CogniMed Inc.
All staff at CogniMed Inc. have nothing to disclose.

Robert R. Henry, MD
Dr Henry receives research support from Amylin Pharmaceuticals, Inc.; Biodel Inc.; Bristol-Myers Squibb Company; Daiichi Sankyo, Inc.; Eli Lilly and Company; GlaxoSmithKline; Keryx Biopharmaceuticals, Inc.; Lifescan, Inc.; Merck & Co., Inc.; Novartis; Novo Nordisk; Roche; and Veralight, Inc. He is a consultant for Amylin Pharmaceuticals, Inc.; AstraZeneca; Bristol-Myers Squibb Company; Daiichi Sankyo Inc.; DiObex, Inc.; Eli Lilly and Company; GlaxoSmithKline; Isis Pharmaceuticals, Inc.; Merck & Co., Inc.; Novartis; Novo Nordisk; Roche; Sanofi-Aventis; and Takeda Pharmaceuticals Company Limited. He also serves on the speakers bureaus of Amylin Pharmaceuticals, Inc.; Eli Lilly and Company; GlaxoSmithKline; Merck & Co., Inc.; Novo Nordisk; Sanofi-Aventis; and Takeda Pharmaceuticals Company Limited. He is a stockholder in DiObex, Inc.; GlaxoSmithKline; Merck & Co., Inc.; and Pfizer Inc.

Robert J. Chilton, DO, FACC
Dr Chilton has no interest or relationship to report.

Catherine L. Martin, MS, APRN, BC-ADM, CDE
Ms Martin serves on the speakers bureaus of Amylin Pharmaceuticals, Inc., and Eli Lilly and Company.

Frank Svec, MD, PhD
Dr Svec has no interest or relationship to report. 

The faculty have disclosed that there will be discussion about the use of products for non–FDA-approved indications.

The ideas and opinions presented in this educational activity are those of the faculty and do not necessarily reflect the views of the Annenberg Center and/or its agents. As in all educational activities, we encourage the practitioners to use their own judgment in treating and addressing the needs of each individual patient, taking into account that patient’s unique clinical situation. The Annenberg Center disclaims all liability and cannot be held responsible for any problems that may arise from participating in this activity or following treatment recommendations presented.

 This activity is supported by an independent educational grant provided by

This activity is an enduring material and consists of a Web posting. Successful completion is achieved by viewing the material, reflecting on its implications in your practice, and completing the assessment component.

The estimated time to complete this activity is 1 hour.

This activity was originally released November 14, 2008, and is eligible for credit through November 14, 2009.