剖宫产期间经历严重产后出血的妇女的产科干预和产妇发病率

K. Seligman, B. Ramachandran, Priya Hegde, E. Riley, Y. El‐Sayed, Lorene M. Nelson, A. Butwick
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引用次数: 0

摘要

与阴道分娩的妇女相比,剖宫产(CD)妇女的产后出血(PPH)导致严重的产妇发病率和死亡率。PPH的计划和管理根据PPH是发生在产前CD还是产时CD而有所不同。本研究调查了产前CD和产时CD人群中严重PPH后的血液制品利用率、医疗和手术干预率以及产妇发病率。该研究是对2002年至2012年在一家三级产科中心进行的剖宫产数据的回顾性分析。血液制品利用率是本研究的主要结果,其次是医疗和手术干预以及与出血相关的产妇发病率。研究人群被分为两个CD队列:产前CD和分娩时经历严重PPH的CD。如果记录的估计失血量(EBL)≥1500 mL,或者在CD期间或CD后48小时内进行了红细胞(RBC)输血,则确定患者患有严重PPH。血液成分使用,医疗和手术干预以及产妇发病率进行了回顾。采用STATA(统计软件包)12版进行统计学分析,P <0.05为差异有统计学意义。研究数据包括269名分娩前妇女和278名分娩时妇女。对于产前队列,148例(55%)患者术中或cd后48小时内输血。产前CD患者的发病率更高,包括子宫切除术(18%)和需要进ICU(16%)。对于伴有严重PPH的产前CD组,异常胎盘导致了72%的剖宫产子宫切除术和49%的ICU入院。在产时CD队列中,术中接受红细胞的妇女比例低于术后(分别为18.3%和43.9%);P < 0.001)。在本综述中,甲基麦角碱是两组中最常用的二线子宫强张剂。总之,在分娩前或分娩时发生严重PPH的妇女中,输血率相对较高。这一数据反映了目前在分娩前和分娩时发生严重PPH的妇女中输血和手术治疗的情况。对于比较不同PPH干预措施对产妇结局的影响,大型实用研究是必不可少的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Obstetric Interventions and Maternal Morbidity Among Women Who Experience Severe Postpartum Hemorrhage During Caesarean Delivery
Postpartum hemorrhage (PPH) causes severe maternal morbidity and mortality in women undergoing cesarean delivery (CD) compared to women undergoing vaginal delivery. The planning and management of PPH varies according to whether PPH occurs during prelabor CD or intrapartum CD. This study examined the rates of blood product utilization, medical and surgical intervention and maternal morbidity after severe PPH in the prelabor CD and intrapartum CD populations. The study was a retrospective analysis of data from cesarean deliveries at a tertiary obstetric center between 2002 and 2012. Rate of blood product utilization was the primary outcome of this study, and the secondary outcomes were medical and surgical interventions and hemorrhage-related maternal morbidity. The study population was divided into two CD cohorts: prelabor CD and intrapartum CD that experienced severe PPH. Patients were identified as suffering from severe PPH if the documented estimated blood loss (EBL) was ≥1500 mL or if a red blood cell (RBC) transfusion was administered during CD or within 48 h after CD. Blood component use, medical and surgical intervention and maternal morbidity were reviewed. Statistical analyses were performed using STATA (statistical software package) version 12 and a P <0.05 was considered statistically significant. The study data comprised of 269 prelabor women and 278 intrapartum CD women. For the prelabor cohort, RBC transfusion was used intraoperatively or within 48 h post-CD in 148 (55%) patients. Prelabor CD cases had higher rates of morbidity, including hysterectomy (18%) and the need for ICU admission (16%). For the prelabor CD group with severe PPH, abnormal placentation was contributing in 72% of cesarean hysterectomies and 49% of ICU admissions. In the intrapartum CD cohort, a lower proportion of women received RBCs during the intraoperative period compared to the postoperative period (18.3% vs. 43.9%, respectively; P < 0.001). In this review, methylergonovine was the most commonly used second line uterotonic in both groups. In conclusion, the transfusion rates were relatively high for women with severe PPH during prelabor or intrapartum CD. This data is reflective of current transfusion and surgical practices for management of severe PPH during prelabor and intrapartum CD. Large pragmatic studies are essential for comparing the effects of different PPH interventions on maternal outcomes.
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