Zhu Haiyan, Lu Danni, Branch D Ware, Troendle James, Tang Yingcai, Bernitz Stine, Zamora Javior, Betran Ana Pilar, Zhou Yingchun, Zhang Jun
Key Laboratory of Advanced Theory and Application in Statistics and Data Science - MOE, School of Statistics, East China Normal University, Shanghai, China.
Ministry of Education-Shanghai Key Laboratory of Children's Environmental Health, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Am J Obstet Gynecol. 2024 Feb;230(2):247.e1-247.e9. doi: 10.1016/j.ajog.2023.07.054. Epub 2023 Aug 3.
Previous studies reported conflicting results on the relationship between oxytocin use for labor augmentation and the risk of postpartum hemorrhage, probably because it is rather challenging to disentangle oxytocin use from labor dystocia.
This study aimed to investigate the independent association between oxytocin use for augmentation and the risk of postpartum hemorrhage by using advanced statistical modeling to control for labor patterns and other covariates.
We used data from 20,899 term, cephalic, singleton pregnancies of patients with spontaneous onset of labor and no previous cesarean delivery from Intermountain Healthcare in Utah in the Consortium on Safe Labor. Presence of postpartum hemorrhage was identified on the basis of a clinical diagnosis. Propensity scores were calculated using a generalized linear mixed model for oxytocin use for augmentation, and covariate balancing generalized propensity score was applied to obtain propensity scores for the duration and total dosage of oxytocin augmentation. A weighted generalized additive mixed model was used to depict dose-response curves between the duration and total dosage of oxytocin augmentation and the outcomes. The average treatment effects of oxytocin use for augmentation on postpartum hemorrhage and estimated blood loss (mL) were assessed by inverse probability weighting of propensity scores.
The odds of both postpartum hemorrhage and estimated blood loss increased modestly when the duration and/or total dosage of oxytocin used for augmentation increased. However, in comparison with women for whom oxytocin was not used, oxytocin augmentation was not clinically or statistically significantly associated with estimated blood loss (6.5 mL; 95% confidence interval, 2.5-10.3) or postpartum hemorrhage (adjusted odds ratio, 1.02; 95% confidence interval, 0.82-1.24) when rigorously controlling for labor pattern and potential confounders. The results remained consistent regardless of inclusion of women with an intrapartum cesarean delivery.
The odds of postpartum hemorrhage and estimated blood loss increased modestly with increasing duration and total dosage of oxytocin augmentation. However, in comparison with women for whom oxytocin was not used and after controlling for potential confounders, there was no clinically significant association between oxytocin use for augmentation and estimated blood loss or the risk of postpartum hemorrhage.
既往研究报告了缩宫素用于引产与产后出血风险之间相互矛盾的结果,这可能是因为将缩宫素的使用与产程异常区分开来颇具挑战性。
本研究旨在通过运用先进的统计模型来控制产程模式及其他协变量,探讨缩宫素用于引产与产后出血风险之间的独立关联。
我们使用了来自犹他州山间医疗保健机构的20899例足月、头位、单胎妊娠患者的数据,这些患者自发临产且既往无剖宫产史,数据来自安全分娩联盟。产后出血的存在依据临床诊断确定。使用广义线性混合模型计算缩宫素用于引产的倾向评分,并应用协变量平衡广义倾向评分来获得缩宫素引产持续时间和总剂量的倾向评分。使用加权广义相加混合模型来描绘缩宫素引产持续时间和总剂量与结局之间的剂量反应曲线。通过倾向评分的逆概率加权评估缩宫素用于引产对产后出血和估计失血量(毫升)的平均治疗效果。
当用于引产的缩宫素持续时间和/或总剂量增加时,产后出血和估计失血量的几率均适度增加。然而,与未使用缩宫素的女性相比,在严格控制产程模式和潜在混杂因素后,缩宫素引产与估计失血量(6.5毫升;95%置信区间,2.5 - 10.3)或产后出血(校正比值比,1.02;95%置信区间,0.82 - 1.24)在临床或统计学上均无显著关联。无论是否纳入产时剖宫产的女性,结果均保持一致。
随着缩宫素引产持续时间和总剂量的增加,产后出血和估计失血量的几率适度增加。然而,与未使用缩宫素的女性相比,在控制潜在混杂因素后,缩宫素用于引产与估计失血量或产后出血风险之间无临床显著关联。