Placenta ACCRETA
PROFESSIONAL
RESOURCES

 
Placenta accreta delivery in 2016, photo used with permission courtesy of the Belgum Family

Placenta accreta delivery in 2016, photo used with permission courtesy of the Belgum Family

 

National Accreta Foundation helps connect the placenta accreta interest community with data driven content of value:

 
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JOINT ACOG & SMFM OBSTETRIC CARE CONSENSUS #7: Placenta Accreta Spectrum (RELEASED DECEMBER 2018)

Obstetric Care Consensus #7 is the latest placenta accreta professional consensus document released jointly by The American College of Obstetricians and Gynecologists and Society for Maternal-Fetal Medicine and endorsed by The Society of Gynecologic Oncology. This document replaces previously published ACOG Committee Opinion No. 529 (July 2012) and SMFM Clinical Guideline #1 (November 2010).

 
 
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Society for maternal-fetal medicine accreta Patient Safety checklists

Did you know SMFM has checklist resources for managing placenta accreta, increta and percreta?

 

Materials to Share with patients

Download and print our free accreta cards to give to patients to point them to our patient resources. Our patient stories, support groups and other content of value can help them navigate their accreta experience. We also have educational rack cards and postcards available with a donation.

 
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PAN-AMERICAN SOCIETY FOR THE PLACENTA ACCRETA SPECTRUM (PAS2)

PAS2 is an independent society made up of obstetricians, maternal-fetal medicine (MFM) specialists, gynecologic oncologists, anesthesiologists, and more. Become a member and join their mission to reduce the morbidity and mortality of Placenta Accreta Spectrum.

 

PATIENT REPRESENTATION

Patient Speakers and Advocates are critical members of any maternal health quality improvement initiative. Contact us to be matched with a patient story, speaker or perspective to help your team to take action to improve maternal health.

 

ACCRETA EXPERIENCES SERIES

In our “Accreta Experiences,” series, National Accreta Foundation features articles written by survivors in their own words to share their placenta accreta experiences and learnings. Read these articles to gain insight into the patient experience of placenta accreta and direct your patients to our site to join the community.

 

LET’S COLLABORATE

We are an organization of accreta survivors dedicated to using our lived experiences to make change for future moms. We would love to contribute to your research or help you and your team understand and improve the placenta accreta patient experience at your hospital. You can even get your hospital involved in Accreta Awareness Month! Contact us to brainstorm how we can help.

 

MEDIA

National Accreta Foundation has worked with numerous media outlets to bring attention to placenta accreta, cesarean overuse, and United States maternal mortality and morbidity.

 

EVENTS

National Accreta Foundation attends and speaks at events to improve maternal health. Come see our work and meet us in person.

 

Donate

National Accreta Foundation is entirely volunteer staffed and donation funded. If you find our content of value, please consider making a tax-deductible donation to help our cause.

 
 

National Accreta Foundation is a non-profit 501(c)(3) organization dedicated to placenta accreta advocacy. Content on this site is provided for informational purposes only and is not meant to substitute for the advice provided by your own physician or other medical professional, please see our medical disclaimer here. National Accreta Foundation is entirely volunteer staffed and donation funded, if you find our content of value, please consider making a tax-deductible donation to help us continue this work.