Abstract | OBJECTIVE: STUDY DESIGN: We conducted a secondary analysis of a 3-arm double-blind randomized trial of different dose regimens of oxytocin to prevent uterine atony after vaginal delivery. The primary outcome was uterine atony or hemorrhage requiring treatment. In all, 21 potential risk factors were evaluated. Logistic regression was used to identify independent risk factors using 2 complementary predefined model selection strategies. RESULTS: Among 1798 women randomized to 10, 40, or 80 U of prophylactic oxytocin after vaginal delivery, treated uterine atony occurred in 7%. Hispanic (odds ratio [OR], 2.1; 95% confidence interval [CI], 1.3-3.4), non-Hispanic white (OR, 1.6; 95% CI, 1.0-2.5), preeclampsia (OR, 3.2; 95% CI, 2.0-4.9), and chorioamnionitis (OR, 2.8; 95% CI, 1.6-5.0) were consistent independent risk factors. Other risk factors based on the specified selection strategies were obesity, induction/augmentation of labor, twins, hydramnios, anemia, and arrest of descent. Amnioinfusion appeared to be protective against uterine atony (OR, 0.53; 95% CI, 0.29-0.98). CONCLUSION:
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Authors | Luisa A Wetta, Jeff M Szychowski, Samantha Seals, Melissa S Mancuso, Joseph R Biggio, Alan T N Tita |
Journal | American journal of obstetrics and gynecology
(Am J Obstet Gynecol)
Vol. 209
Issue 1
Pg. 51.e1-6
(Jul 2013)
ISSN: 1097-6868 [Electronic] United States |
PMID | 23507549
(Publication Type: Journal Article, Randomized Controlled Trial)
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Copyright | Copyright © 2013 Mosby, Inc. All rights reserved. |
Chemical References |
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Topics |
- Adult
- Delivery, Obstetric
(adverse effects)
- Double-Blind Method
- Female
- Humans
- Logistic Models
- Oxytocics
(administration & dosage)
- Oxytocin
(administration & dosage)
- Postpartum Hemorrhage
(drug therapy, etiology, prevention & control)
- Pregnancy
- Risk Factors
- Uterine Inertia
(drug therapy, etiology, prevention & control)
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