CME Presentations




  • Shania Seibles, DO, JD, FACOOG

    Shania Seibles, DO, JD, FACOOG

    Shania Seibles, DO, JD, FACOOG

    Maternal Fetal Medicine Physician

    Shania J. Seibles, DO, JD is currently an active practicing Maternal Fetal Medicine specialist in Columbus, GA. She has special interests in medico-legal aspects of obstetric practice including contracts, medical malpractice, and ethical dilemmas. Dr. Seibles completed combined DO and JD degrees at the University of Medicine and Dentistry of New Jersey and Rutgers School of Law - Camden, respectively, in 2010. She then went on to complete residency in Obstetrics and Gynecology through Michigan State University College of Osteopathic Medicine at Beaumont Healthcare – Osteopathic Division, and fellowship in Maternal Fetal Medicine through Michigan State University College of Osteopathic Medicine - St Joseph Mercy Oakland Hospital in 2018.
  • Kristina Deligiannidis, MD

    Kristina Deligiannidis, MD

    Kristina Deligiannidis, MD

    Director, Women’s Behavioral Health

    Kristina Deligiannidis, MD is the Director of Women’s Behavioral Health at Zucker Hillside Hospital, Northwell Health and a Professor of Psychiatry, Molecular Medicine and Obstetrics and Gynecology at the Donald and Barbara Zucker School of Medicine at Hofstra/Northwell (New York, NY). As Director, she leads a clinical/translational research program and advises on policies and services promoting women’s behavioral health at Northwell Health. Dr. Deligiannidis is a nationally recognized leader in the field of perinatal depression and in therapeutics research. She has published over 60 manuscripts and has given over 200 oral presentations/research posters. Dr. Deligiannidis contributes to national scientific committees and gives scientific presentations nationally and internationally.

CME Information

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Getting Better at Diagnosing and Treating Postpartum Depression (PPD)

Jointly provided by Partners for Advancing Clinical Education (PACE) and PlatformQ Health Education, LLC in collaboration with Depression and Bipolar Support Alliance (DBSA), The Policy Center for Maternal Mental Health, and American College of Osteopathic Obstetricians and Gynecologists (ACOOG).


This activity is supported by an educational grant from Sage Therapeutics, Inc. and Biogen.


This activity was released on April 21, 2023 and is valid until April 21, 2024. Requests for credit must be made no later than April 21, 2024.


The educational design of this activity addresses the needs of OB-GYNs, maternal-fetal medicine specialists, psychiatrists, psychologists, primary care physicians, NPs, PAs, and mental-health specialists, and other clinicians involved in the management of patients with postpartum depression (PPD).


Postpartum depression (PPD) remains an under-screened and underdiagnosed condition that affects maternal and infant health, as well as the well-being and safety of the entire family. Clinicians should be aware of the social, environmental, and neurochemical factors that contribute to the development of PPD in order to reduce the time to screening, diagnosis, and treatment.

Join an expert OB-GYN and a psychiatrist for an in-depth discussion of the factors associated with increased risk for PPD, as well as those that lead to inequalities in screening and diagnosis. Strategies to improve screening and diagnosis of PPD, especially in high-risk groups, will be shared. Panelists will also explore the evolving therapeutic landscape for PPD, which has expanded beyond selective serotonin reuptake inhibitors (SSRIs) and serotonin and norepinephrine reuptake inhibitors (SNRIs) to include fast-acting and long-lasting neuroactive steroids.

Do you have patients at risk for or diagnosed with PPD who could benefit from education on symptoms, screening, and current and emerging treatment options? Direct your patients to to access the activity, “Is this Postpartum Depression (PPD)? Faster Recognition and Treatment of PPD.”


After completing this activity, the participant should be better able to:
  • Review factors associated with higher risk of PPD in women
  • Discuss strategies to navigate barriers to screening and diagnosis of PPD
  • Describe the limitations of traditional antidepressants in the treatment of PPD
  • Evaluate clinical data related to emerging neuroactive steroid agents for the treatment of PPD



In support of improving patient care, this activity has been planned and implemented by Partners for Advancing Clinical Education (PACE) and PlatformQ Health Education, LLC. PACE 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.


PACE designates this enduring material for a maximum of 1.0 AMA PRA Category 1 Credit™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.


This activity should take approximately 60 minutes to complete.


In order to receive credit for this activity, the participant must (1) read the target audience, learning objectives, and disclosure statements, (2) complete the educational activity online, and (3) complete the post-test and activity evaluation. To receive AMA PRA Category 1 Credits™, participants must receive a score of 75% on the post-test.


Participants will need a computer with a recent version of Adobe Flash installed, as well as an internet connection sufficient for streaming media.


There is no fee for this educational activity.


PACE requires instructors, planners, managers, and other individuals who are in a position to control the content of this activity to disclose all financial relationships they may have with ineligible companies. All relevant financial relationships are thoroughly vetted and mitigated according to PACE policy. PACE is committed to providing learners with high-quality accredited CE activities and related materials that promote improvements or quality in healthcare and not a specific proprietary business interest of an ineligible company.

The faculty reported the following relevant financial relationships or relationships to products or devices they have with ineligible companies related to the content of this educational activity:

Faculty Conflicts of Interest
Shania J. Seibles, DO, JD
Maternal Fetal Medicine Physician
No relevant financial relationships to disclose
Kristina Deligiannidis, MD
Director, Women’s Behavioral Health
Zucker Hillside Hospital
Northwell Health
Professor of Psychiatry
Molecular Medicine and Obstetrics & Gynecology
Donald and Barbara Zucker School or Medicine at Hofstra/Northwell
Consultant, Advisor, Speaker: Brii Biosciences, Gerbera Therapeutics, GH Research, Neuroscience Software, Reunion Neuroscience, Sage Therapeutics, Inc.

Researcher: National Institutes of Health, Premier Healthcare, Sage Therapeutics, Inc., Woebot Health

The PACE planners and others have no relevant financial relationship(s) to disclose with ineligible companies. The PlatformQ Health Education, LLC planners and others have no relevant financial relationship(s) to disclose with ineligible companies.


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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