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Published on: January 17, 2019
The association between 17-hydroxyprogesterone caproate use and postpartum hemorrhage
Emily S Miller1, Allie Sakowicz1, Archana Roy1
1Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Recent 17α-hydroxyprogesterone caproate (17P) use before delivery does not increase postpartum hemorrhage risk. This study found no significant association between 17P administration and postpartum bleeding in women at risk for preterm birth.
Area of Science:
- Obstetrics and Gynecology
- Maternal-Fetal Medicine
- Pharmacology
Background:
- 17α-hydroxyprogesterone caproate (17P) is used to prevent recurrent preterm birth.
- The potential association between recent 17P administration and postpartum hemorrhage (PPH) requires investigation.
Purpose of the Study:
- To determine if 17P administration within seven days of delivery is linked to an increased risk of PPH.
- To analyze the safety profile of 17P concerning postpartum bleeding.
Main Methods:
- Retrospective cohort study of 221 women receiving 17P for preterm birth prevention (2010-2014).
- Women were grouped based on 17P administration within seven days of delivery.
- Bivariable and multivariable analyses were performed to assess PPH risk, adjusting for confounders.
Main Results:
- Of 221 women, 93 (42%) received 17P within seven days of delivery; 18 (7.8%) experienced PPH.
- No significant difference in PPH frequency was observed between groups (9.7% vs. 7.0%, p=0.478).
- Adjusted analysis showed no increased PPH risk (aOR 2.9, 95% CI 0.5-15.8).
Conclusions:
- Recent administration of 17P for preterm birth prevention is not associated with an increased risk of postpartum hemorrhage.
- Findings suggest 17P is safe concerning postpartum bleeding complications.
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