This activity is intended for healthcare providers delivering care to women and their families.
After completing this activity, the participant should be better able to:
1. Explain the post partum screening protocols used to diagnose diabetes
2. Define the plasma glucose values necessary to diagnose prediabetes and diabetes
Estimated time to complete activity: 0.25 hours
Susan J. Gross, MD, FRCSC, FACOG, FACMG
President and CEO, The ObG Project
Postgraduate Institute for Medicine (PIM) requires faculty, planners, and others in control of educational content to disclose all their financial relationships with ineligible companies. All identified conflicts of interest (COI) are thoroughly vetted and mitigated according to PIM policy. PIM is committed to providing its learners with high quality accredited continuing education activities and related materials that promote improvements or quality in healthcare and not a specific proprietary business interest of an ineligible company.
The PIM planners and others have nothing to disclose. The OBG Project planners and others have nothing to disclose.
Faculty: Susan J. Gross, MD, receives consulting fees from Cradle Genomics, and has financial interest in The ObG Project, Inc.
Planners and Managers: The PIM planners and managers, Trace Hutchison, PharmD, Samantha Mattiucci, PharmD, CHCP, Judi Smelker-Mitchek, MBA, MSN, RN, and Jan Schultz, MSN, RN, CHCP have nothing to disclose.
Fees for participating and receiving CME credit for this activity are as posted on The ObG Project website. During the period from Jan 25 2022 through Jan 25 2024, participants must read the learning objectives and faculty disclosures and study the educational activity.
If you wish to receive acknowledgment for completing this activity, please complete the test and evaluation. Upon registering and successfully completing the test with a score of 100% and the activity evaluation, your certificate will be made available immediately.
In support of improving patient care, this activity has been planned and implemented by the Postgraduate Institute for Medicine and The ObG Project. Postgraduate Institute for Medicine is jointly accredited by the Accreditation Council for Continuing Medical Education (ACCME), the Accreditation Council for Pharmacy Education (ACPE), and the American Nurses Credentialing Center (ANCC), to provide continuing education for the healthcare team.
Postgraduate Institute for Medicine designates this enduring material for a maximum of 0.25 AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
The maximum number of hours awarded for this Continuing Nursing Education activity is 0.2 contact hours.
While there is controversy as to how best to screen for gestational diabetes mellitus (GDM) during pregnancy, all professional groups recommend screening during the postpartum period following GDM for prediabetes or diabetes at 4 to 12 weeks postpartum. Historically, two options, fasting plasma glucose (FPG) and the 2-hour oral glucose tolerance test (OGTT), have been used. However ACOG, citing the Fifth International Workshop on Gestational Diabetes, recommends the 2-hour OGTT, which should include FPG as well, to improve sensitivity:
Up to 1/3 of women who had GDM during their pregnancy will have impaired glucose metabolism or diabetes at postpartum screening, and up to 70% may develop diabetes later in life. Even if screening is negative at the postpartum visit, the ADA and ACOG recommend assessing glycemic status every 1 to 3 years and counseling patients regarding diet and/or exercise as needed. Follow-up screening is particularly advantageous for those women considering future pregnancies as it gives an opportunity for preconception counseling and management prior to the next pregnancy.
ACOG Practice Bulletin No.190: Gestational Diabetes Mellitus
WPSI: Screening for Diabetes Mellitus After Pregnancy
SMFM Special Statement: Quality metric on the rate of postpartum diabetes screening after pregnancies with gestational diabetes mellitus
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This educational activity may contain discussion of published and/or investigational uses of agents that are not indicated by the FDA. The planners of this activity do not recommend the use of any agent outside of the labeled indications.
The opinions expressed in the educational activity are those of the faculty and do not necessarily represent the views of the planners. Please refer to the official prescribing information for each product for discussion of approved indications, contraindications, and warnings.
Participants have an implied responsibility to use the newly acquired information to enhance patient outcomes and their own professional development. The information
presented in this activity is not meant to serve as a guideline for patient management. Any procedures, medications, or other courses of diagnosis or treatment discussed or suggested in this activity should not be used by clinicians without evaluation of their patient’s conditions and possible contraindications and/or dangers in use, review of any applicable manufacturer’s product information, and comparison with recommendations of other authorities.
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