Reassessing Preterm Birth Prevention After the Withdrawal of 17-α Hydroxyprogesterone Caproate
- PMID: 37441790
- DOI: 10.1097/AOG.0000000000005290
Reassessing Preterm Birth Prevention After the Withdrawal of 17-α Hydroxyprogesterone Caproate
Abstract
The U.S. Food and Drug Administration has recently withdrawn approval for 17-α hydroxyprogesterone caproate for prevention of recurrent preterm birth, and recent studies have called into question benefits of the pessary in the setting of a short cervix. Obstetric health care professionals are once again left with limited remaining options for preterm birth prevention. This narrative review summarizes the best current evidence on the use of vaginal progesterone, low-dose aspirin, and cerclage for the prevention of preterm birth; attempts to distill possible lessons learned from studies of progesterone and pessary, as well as their implementation into practice; and highlights areas where inroads into preterm birth prevention may be possible outside of the progesterone-aspirin-cerclage paradigm.
Copyright © 2023 by the American College of Obstetricians and Gynecologists. Published by Wolters Kluwer Health, Inc. All rights reserved.
Conflict of interest statement
Financial Disclosure The author did not report any potential conflicts of interest.
References
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- Society for Maternal-Fetal Medicine.SMFM special statement: response to the Food and Drug Administration's withdrawal of 17-alpha hydroxyprogesterone caproate. Accessed May 23, 2003. https://smfm.org/publications/467-smfm-special-statement-response-to-the...
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