Implementation of an oxytocin bolus protocol for cesarean delivery at a Texas level IV maternal center: a single-center retrospective study.

Q3 Medicine Baylor University Medical Center Proceedings Pub Date : 2025-01-02 eCollection Date: 2025-01-01 DOI:10.1080/08998280.2024.2446021
Brittany Hood, Emily E Sharpe, Carmen Gomez Fitzpatrick, Annarose Dement, Claudia Serrano, Jessica C Ehrig, Chandni Raiyani, Michael P Hokfamp
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Abstract

Objective: We hypothesized that patients who underwent cesarean delivery and received oxytocin boluses followed by an infusion would have a lower incidence of secondary uterotonic administration compared to patients who had an oxytocin infusion without boluses.

Methods: Patients who had cesarean deliveries at our hospital from September 1, 2021 through December 31, 2021 and from September 1, 2022 through December 31, 2022, corresponding to the oxytocin bolus and oxytocin infusion cohorts, respectively, were included. Patient demographic, physical, and clinical characteristic data were collected by a study investigator. Intramyometrial oxytocin, intramuscular methylergonovine, intramuscular carboprost tromethamine, and sublingual misoprostol were defined as secondary uterotonics.

Results: There were 266 and 283 patients in the oxytocin bolus and oxytocin infusion cohorts, respectively. The odds ratio for patients in the oxytocin bolus cohort receiving a secondary uterotonic was 0.25 (95% confidence interval 0.16, 0.41; P < 0.01).

Conclusion: Patients in the oxytocin bolus cohort were approximately 75% less likely to receive a secondary uterotonic agent compared to patients in the oxytocin infusion cohort. A limitation of this study was that we defined intramyometrial administration of oxytocin as a secondary uterotonic, and our results may not be generalizable to hospitals that do not use intramyometrial oxytocin.

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在德克萨斯州四级产妇中心实施剖宫产催产素丸方案:一项单中心回顾性研究
目的:我们假设剖宫产后接受催产素注射后再输注的患者与不输注催产素的患者相比,继发性子宫扩张的发生率较低。方法:选取2021年9月1日至2021年12月31日、2022年9月1日至2022年12月31日在我院剖宫产的患者,分别对应于催产素丸组和催产素输注组。研究人员收集了患者的人口学、生理和临床特征数据。子宫内膜内注射催产素、肌内注射甲基麦角碱、肌内注射卡前列素、丙二胺和舌下注射米索前列醇被定义为继发性子宫强直。结果:催产素丸组266例,催产素输注组283例。催产素丸组患者接受二次子宫扩张的优势比为0.25(95%可信区间0.16,0.41;结论:与催产素输注组相比,催产素注射组患者接受二次子宫扩张药物的可能性约低75%。本研究的一个局限性是,我们将子宫内膜内注射催产素定义为继发性子宫张力,我们的结果可能无法推广到不使用子宫内膜内注射催产素的医院。
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