Elevating Patient Care: Early Detection and Evidence-Based Pharmacotherapy for Postpartum Depression in Primary Care

To participate in this activity, please:

Postpartum depression, or depression in women within 12 months of giving birth, is common. It affects one-quarter of these women, which is why current recommendations are to begin screening for depression during pregnancy. Left un- and under-treated, the mother, newborn, and family are at risk for relationship problems, psychiatric illness, and other consequences. In this 1-hour, case-based activity, developed by family medicine and mental health clinicians, team-based screening recommendations, along with strategies for overcoming barriers in diagnosis, are applied to primary care practice. The risks and benefits of treatment, including nonpharmacologic and pharmacologic options, such as selective serotonin reuptake inhibitors and neuroactive steroid gamma-aminobutyric acid A receptor positive modulators, are discussed, to enable the development of a personalized care plan using a collaborative care model.

Course Credit:

1 AMA PRA Category 1 CreditTM
1 ANCC Contact Hour
1 CA-BRN Contact Hour
0.5 Pharmacology Hours

Dates:

Opens: 2024-05-24
Closes: 2025-05-24

Target Audience:

This activity was developed for primary care physicians and advanced practice providers.

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

Accreditation

In support of improving patient care, Annenberg Center for Health Sciences at Eisenhower (Annenberg Center) 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.

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

Annenberg Center for Health Sciences at Eisenhower designates this enduring activity for a maximum of 1 ANCC contact hour, including 0.5 pharmacology hours.

Provider is approved by the California Board of Registered Nursing, Provider #13664, for 1 contact hour.
To receive credit for education contact hours outside of the state of California, please check with your state board of registered nursing for reciprocity.

Additional Content Planners

Amber Lambert, MSN, FNP-C, DNP (Nurse Reviewer)
No significant relationships to disclose.

Kam A. Newman, MD (Peer Reviewer)
No significant relationships to disclose.

Sunali Wadehra, MD (Medical Writer)
No significant relationships to disclose.

Annenberg Center for Health Sciences

Staff at the Annenberg Center for Health Sciences at Eisenhower have no relevant financial relationships to disclose.

All of the financial relationships listed for these individuals have been mitigated.

    Presenting Faculty

  • Anita H. Clayton, MD

    Wilford W. Spradlin Professor and Chair
    Department of Psychiatry and Neurobehavioral Sciences
    Professor, Clinical Obstetrics and Gynecology
    University of Virginia School of Medicine
    Charlottesville, Virginia

  • Sarah Nagle-Yang, MD

    Vice Chair for Quality
    Deputy Executive Director, Colorado Center for Women's Behavioral Health
    Associate Professor of Psychiatry
    University of Colorado School of Medicine
    Aurora, Colorado

  • Barbara P. Yawn, MD

    Adjunct Professor
    University of Minnesota
    Department of Family and Community Health
    Minneapolis, Minnesota

Learning Objectives

  • Demonstrate effective screening techniques for identifying women at high risk of depression during pregnancy and postpartum utilizing validated measures in a live meeting setting
  • Engage in interactive discussions on tailoring evidence-based pharmacotherapy for patients with postpartum depression (PPD) during live sessions.
  • Practice collaborative approaches with patients experiencing PPD to facilitate the initiation and adjustment of antidepressant therapy to attain treatment objectives within a live meeting environment.
  • Evaluate the safety and effectiveness of medications prescribed for PPD in a dynamic, real-time context.

Faculty Disclosures

Anita H. Clayton, MD

Advisory Board and Consultant: AbbVie, Biogen, Brii Biosciences, Fabre-Kramer, Initiator Pharma, Janssen Research & Development, LLC, Mind Cure Health, Ovoca Bio plc, Praxis Precision Medicines, PureTech Health, Reunion Neuroscience, Inc. (formerly Field Trip Health), S1 Biopharma, Sage Therapeutics, Sirtsei Pharmaceuticals, Inc., Takeda/Lundbeck, Vella Bioscience, Inc., WCG MedAvante-ProPhase

Research Support: Daré Bioscience, Janssen, Neumora Therapeutics, Otsuka, Praxis Precision Medicines, Relmada Therapeutics, Inc., Sage Therapeutics

Royalties/Copyright: Ballantine Books/Random House, Changes in Sexual Functioning Questionnaire, Guilford Publications

Shares/Restricted Stock Units: Euthymics, Mediflix LLC, S1 Biopharma


Sarah Nagle-Yang, MD

No relationships to disclose.

Barbara P. Yawn, MD

No relationships to disclose.