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临床试验/NCT06730919
NCT06730919已完成不适用

Risk Factors for Postpartum Hemorrhage After Cesarean Delivery in Women With Systemic Autoimmune Disease: A Multicenter Retrospective Study

RenJi Hospital5 个研究点 分布在 1 个国家目标入组 1,000 人开始时间: 2019年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
1,000
试验地点
5
主要终点
The incidence of PPH

研究概览

简要总结

Postpartum hemorrhage (PPH) is the most significant leading cause of pregnancy-related mortality in high-risk cesarean delivery women. Systemic autoimmune diseases are associated with adverse pregnancy outcomes (APOs), including PPH, preeclampsia, thromboembolism, abortion, and intrauterine growth restriction. The incidence of PPH in women with systemic lupus erythematosus (SLE) has been reported to be as high as 34%. However, few studies have investigated PPH risk factors in pregnant women with systemic autoimmune disease. Therefore, the purpose of this study is to investigate the incidence and related risk factors of PPH in pregnant women with systemic autoimmune disease, and to provide the latest evidence for further study on prevention of PPH in women at high risk of PPH.

详细描述

The worldwide estimated cumulative prevalence of autoimmune disease is approximately 5%. Studies are often limited by small sample sizes and focused on a specific autoimmune disease such as SLE and antiphospholipid syndrome (APS), which is characterized by the production of autoantibodies leading to inflammation of multiple organs. Systemic autoimmune diseases are associated with APOs, including increased cesarean delivery rates, PPH, preeclampsia, thromboembolism, abortion, premature delivery, and intrauterine growth restriction. Preeclampsia is the most commonly reported complication in patients with SLE and is also a high risk factor for PPH. The incidence of PPH in women with SLE has been reported to be as high as 34%. Antiphospholipid antibodies (APLAs) are often present in SLE and APS patients, which predict serious perinatal complications and are associated with the risk of thrombosis. APLAs are detected not only in SLE and APS but also in other connective tissue diseases such as systemic sclerosis (SSc), Sjögren's syndrome (SS), rheumatoid arthritis (RA), and undifferentiated connective tissue disease (UCTD). Women with positive APLAs during pregnancy usually receive antithrombotic therapy to reduce the incidence of fetal loss, which may increase the risk of PPH, but existing research evidence is insufficient. PPH increases the need for blood transfusion and related complications and is a significant clinical and socio-economic problem. The aim of this study is to investigate the incidence and related risk factors of PPH in pregnant women with systemic autoimmune disease, and to provide the latest evidence for further study on prevention of PPH in women at high risk of PPH.

The investigators will review patients who underwent cesarean delivery in five hospitals between June 2019 and June 2024. The complication of pregnancy, placental function, estimated blood loss 24h postoperatively, blood transfusion 3d postpartum, additional uterotonics, other surgical intervention for PPH and APOs will be recorded. The group of patients included in the analysis for risk factors associated with PPH consisted of those who with systemic autoimmune disease.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Gestational period was ≥ 28 week;
  • Delivered by cesarean delivery;
  • With systemic autoimmune diseases (SLE, APS, SSc, SS,RA, UCTD)

排除标准

  • Intrauterine fetal death
  • Hemorrhagic disease, significant prenatal bleeding
  • Missing clinical information

结局指标

主要结局

The incidence of PPH

时间窗: From skin incision to 1day after surgery

PPH is defined as estimated blood loss ≥1000 mL within 24 h after cesarean delivery.

次要结局

  • Estimated blood loss within 1day after surgery(From skin incision to 1day after surgery)
  • The volume of blood transfusion within 3days after surgery and complications(From skin incision to 3days after surgery)
  • Whether additional uterotonics are needed(From the delivery of placenta until 3 days postoperatively.)
  • Whether other surgical intervention for PPH are needed(From the delivery of placenta until 3 days postoperatively.)
  • Maternal and neonatal mortality 42d after cesarean delivery(From skin incision to 42 days after surgery.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (5)

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