Effect of improved uterotonic availability on postpartum hemorrhage and maternal morbidity after vaginal delivery, review of a single-center quality-improvement initiative.
Danielle L Chirumbole, Towana Sims, Stacie Denning, Sheena Glover, Lauren Shubert, Michael Jochum, Celeste Green, Courtney Thompson, Adewunmi Babalola, Tara Barrick, Sharon Burks, Manisha Gandhi, Christina Davidson
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Abstract
Introduction: After implementation of a hemorrhage risk stratification system and management bundle in 2019, our hospital demonstrated a reduction in hemorrhage-related severe maternal morbidity (SMM-H). We then noted a plateau in postpartum hemorrhage (PPH) rates and a gradual increase in SMM-H after 2020, with the majority of PPH after vaginal deliveries (VDs) occurring in those deemed low-risk. Consequently, we implemented a strategy to improve the availability of second-line uterotonics in the delivery room regardless of PPH risk. The objective of this study is to evaluate the effect of this intervention on rates of PPH and SMM-H after VDs.
Methods: Through this quality improvement (QI) initiative, we aimed to improve injectable uterotonic availability and use at time of delivery. Our primary outcome measures were rate of PPH and SMM-H in VD. We reviewed all deliveries from the 16 months before and after this intervention (April 2023-July 2024, September 2024-December 2025). Deliveries from August 2024 were excluded to allow for washout. Chi-square was used to determine statistical significance.
Results: There were 5365 VDs included in the pre-intervention group with 63.6% designated low-risk for PPH and 4768 included in the post-intervention group with 62.4% designated low-risk. There was no difference in VD PPH pre- versus post-intervention (6.33% vs. 6.61%, p = 0.61). Similarly, there was no significant change in VD SMM-H (22.9% vs. 25.6%, p = 0.40). The rates of PPH and SMM-H in low-risk VD patients were 5.7% and 18.6% pre-intervention compared to 6.1% and 18.8% post-intervention. These differences were not statistically significant. Low-risk patients comprised 57.5% of VDs with PPH after the intervention. Of VDs requiring second-line uterotonics, misoprostol was the most common first agent prior to the intervention (60%) versus methylergonovine after (45%), which was statistically different from prior (p < 0.0001).
Conclusion: Improving second-line uterotonic availability in the delivery room did not improve VD PPH rates or SMM-H but did change second-line uterotonic choice.
导语:2019年,我院实施出血风险分层和管理捆绑后,出血相关重症孕产妇发病率(SMM-H)明显降低。然后我们注意到,产后出血(PPH)率在2020年后趋于平稳,SMM-H逐渐增加,阴道分娩(VDs)后的PPH大部分发生在那些被认为是低风险的人群中。因此,我们实施了一项策略,以提高产房中二线子宫强子术的可用性,而不考虑PPH风险。本研究的目的是评估这种干预对VDs后PPH和SMM-H发生率的影响。方法:通过质量改进(QI)计划,旨在提高可注射子宫强张剂的可及性和分娩时的使用。我们的主要结局指标是VD患者PPH和SMM-H的比率。我们回顾了干预前后16个月(2023年4月- 2024年7月,2024年9月- 2025年12月)的所有交付情况。2024年8月以后的交付被排除在外,以允许淘汰。采用卡方法确定统计学显著性。结果:干预前组有5365名vd,其中63.6%为PPH低风险,干预后组有4768名vd,其中62.4%为低风险。干预前与干预后VD PPH无差异(6.33% vs. 6.61%, p = 0.61)。同样,VD SMM-H无显著变化(22.9% vs. 25.6%, p = 0.40)。干预前低危VD患者PPH和SMM-H的发生率分别为5.7%和18.6%,干预后分别为6.1%和18.8%。这些差异没有统计学意义。低危患者占干预后PPH的VDs的57.5%。在需要二线子宫强张的VDs中,米索前列醇是干预前最常见的第一种药物(60%),而干预后甲基麦草碱(45%),这与干预前有统计学差异(p)。结论:改善产房二线子宫强张的可用性并不能改善VD PPH率或SMM-H,但确实改变了二线子宫强张的选择。