- CME/CE Activities
- Methods for Insulin Delivery and Glucose Monitoring in Diabetes
This CME/CE activity is provided by PRIME Education, Inc. (PRIME®) and is accredited for a multi-disciplinary audience of health care practitioners. This activity is supported by contract number HHSA290201200021I from the Agency for Healthcare Research and Quality. User data collected through this activity will reside on PRIME's educational portal for use by AHRQ.
Methods for Insulin Delivery and Glucose Monitoring in Diabetes: A Summary of Comparative Effectiveness Review
- Program Overview
- Faculty Biographies
- Accreditation Statements
- Post-Test & Evaluation
Credit for this CME/CE activity has expired.
You can still access the program, but will not receive a certificate.
Tight glycemic control with intensive insulin therapy has been suggested to reduce the risk of long-term complications in several diabetes populations; however, such an approach can also be associated with risks and challenges.
The Agency for Healthcare Research and Quality (AHRQ) commissioned a comparative effectiveness review of published studies to assess whether the mode of insulin delivery and/or the mode of blood glucose monitoring improves glycemic control, clinical outcomes, hypoglycemia and quality of life in patients with type 1 diabetes, type 2 diabetes, and pre-existing diabetes in pregnancy. This journal article summarizes the evidence obtained from the AHRQ systematic review to assist healthcare professionals in making informed decisions regarding insulin delivery and glucose monitoring systems in patients with diabetes.
At the conclusion of this activity, the participant should be able to:
- Compare the benefits of insulin delivery systems in improving clinical outcomes, glycemic control, hypoglycemia and quality of life in diabetic patients receiving intensive insulin therapy
- Evaluate the differential effect of glucose monitoring approaches on the process measures, intermediate and clinical outcomes in diabetic patients receiving intensive insulin therapy
- Apply the AHRQ findings to guide effective, patient-centered clinical decisions
This CME activity is designed to meet the educational needs of physicians, pharmacists, nurses and case managers.
Method of Participation
To receive a certificate for this activity, you should:
- Complete the learner assessment pretest
- View the entire activity online
- Complete an online evaluation & post-test
- Print your certificate online
The estimated time to complete this activity, including review of the materials, is 1.0 hour.
Term of Approval
August 31, 2012 through September 30, 2013. Original release date: August 31, 2012.
Acknowledgement of Support
There is no fee for this CME/CE activity. This activity is sponsored by PRIME Education, Inc (PRIME®) and funded under contract HHSA290201200021I from the Agency for Healthcare Research and Quality (AHRQ), U.S. Department of Health and Human Services (HHS).
Faculty Biographies and Disclosures
Sherita Hill Golden, MD, MHS, FAHA
Associate Professor of Medicine and Epidemiology Director
Inpatient Diabetes Management Service Chairperson
JHH Glucose Management Committee
Division of Endocrinology and Metabolism Welch Center for Prevention, Epidemiology, and Clinical Research
Johns Hopkins University School of Medicine
Co-Investigator with the Johns Hopkins Evidence-Based Practice Center
Tamar Sapir, PhD
Director of Scientific Affairs
PRIME Education, Inc.
Michele B Kaufman, PharmD, CGP, RPh
President, PRN Communications Inc.
Editor, Pharmacovigilance Forum, P&T Journal
Touro College of Pharmacy
New York, NY
Heidi Wynn Maloni, PhD, ANP-BC, CNRN, MSCN
National Clinical Nursing Director
Department of Neurology
Multiple Sclerosis Center of Excellence, East
Veterans Affairs Medical Center
Trinity Nursing Program School of Professional Studies
Trinity Washington University
Clinical Preceptor and Instructor
Advanced Practice Programs
The Catholic University of America School of Nursing
Debbie DeMuria, PharmD, RPh
Consultant, Regulatory Affairs
Sherman Podolsky, MD
Department of Emergency Medicine
Albert Einstein Medical Center
Kathleen A Jarvis, MS, RN, CCM
Fort Lauderdale, FL
This program is no longer accredited.
|Faculty Name ||Advisory Board||Consultant||Grants / Research||Salary / Contractual||Supported Promotional Education||Stock / Shareholder||Other Financial Support|
|Sherita Hill Golden, MD, MHS, FAHA
|Tamar Sapir, PhD
|Michele B Kaufman, PharmD, CGP, RPh
|Heidi Wynn Maloni, PhD, ANP-BC, CNRN, MSCN
|Debbie DeMuria, PharmD, RPh
|Sherman Podolsky, MD
|Kathleen A Jarvis, MS, RN, CCM
|Chris R Prostko, PhD|
Scientific Program Director
|Lynn Goldenberg, RN, BSN|
Director of Accreditation & Compliance
PRIME Education Inc (PRIME®) endorses the standards of the ACCME, as well as those of the AANP, ANCC and ACPE, that require everyone in a position to control the content of a CME/CE activity to disclose all financial relationships with commercial interests that are related to the content of the CME/CE activity. CME/CE activities must be balanced, independent of commercial bias and promote improvements or quality in healthcare. All recommendations involving clinical medicine must be based on evidence accepted within the medical profession.
A conflict of interest is created when individuals in a position to control the content of CME/CE have a relevant financial relationship with a commercial interest which therefore may bias his/her opinion and teaching. This may include receiving a salary, royalty, intellectual property rights, consulting fee, honoraria, stocks or other financial benefits.
PRIME® willidentify, review and resolve all conflicts of interest that speakers, authors, course directors, planners, peer reviewers, or relevant staff disclose prior to an educational activity being delivered to learners. Disclosure of a relationship is not intended to suggest or condone bias in any presentation but is made to provide participants with information that might be of potential importance to their evaluation of a presentation. Disclosure information for speakers, authors, course directors, planners, peer reviewers, and/or relevant staff are provided with this activity.
Presentations that provide information in whole or in part related to non FDA approved uses of drugs and/or devices will disclose the unlabeled indications or the investigational nature of their proposed uses to the audience. Participants should refer to the official prescribing information for each product for discussion of approved indications, contraindications and warnings. Participants should verify all information and data before treating patients or employing any therapies prescribed in this educational activity. The opinions expressed in the educational activity are those of the presenting faculty and do not necessarily represent the views of PRIME®, the ACCME, AANP, ACPE, ANCC and other relevant accreditation bodies.
Content validation methods are consistently utilized by PRIME® to ensure that all program content is evidence-based, fair-balanced, and developed with scientific rigor and integrity. All clinical recommendations are based on evidence accepted within the medical profession. All scientific research referred to, reported or used to support a clinical recommendation conforms to accepted standards of experimental design, data collection and analysis. In addition to review of content by course directors and expert faculty, content is also validated through independent peer reviewers selected for their expertise in the content area, as well as their experience in the intended audience. All peer reviewers, planners, course directors, faculty and relevant staff utilized by PRIME® complete disclosures which are related to their role in the educational activity.
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Post-Test & Evaluation
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Clinician & Consumer Summaries on Insulin Delivery and Glucose Monitoring
Download these free summaries for your reference and/or patient handouts. You may also order bulk copies free of charge from the AHRQ Publication Clearinghouse below.