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Active management of the third stage of labour with and without controlled cord traction: A randomised, controlled, non-inferiority trial

机译:积极管理第三阶段的劳动力,无控制线牵引:随机,受控,非劣势试验

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摘要

Background: Active management of the third stage of labour reduces the risk of post-partum haemorrhage. We aimed to assess whether controlled cord traction can be omitted from active management of this stage without increasing the risk of severe haemorrhage. Methods: We did a multicentre, non-inferiority, randomised controlled trial in 16 hospitals and two primary healthcare centres in Argentina, Egypt, India, Kenya, the Philippines, South Africa, Thailand, and Uganda. Women expecting to deliver singleton babies vaginally (ie, not planned caesarean section) were randomly assigned (in a 1:1 ratio) with a centrally generated allocation sequence, stratified by country, to placental delivery with gravity and maternal effort (simplified package) or controlled cord traction applied immediately after uterine contraction and cord clamping (full package). After randomisation, allocation could not be concealed from investigators, participants, or assessors. Oxytocin 10 IU was administered immediately after birth with cord clamping after 1-3 min. Uterine massage was done after placental delivery according to local policy. The primary (non-inferiority) outcome was blood loss of 1000 mL or more (severe haemorrhage). The non-inferiority margin for the risk ratio was 1·3. Analysis was by modified intention-to-treat, excluding women who had emergency caesarean sections. This trial is registered with the Australian and New Zealand Clinical Trials Registry, ACTRN 12608000434392. Findings: Between June 1, 2009, and Oct 30, 2010, 12 227 women were randomly assigned to the simplified package group and 12 163 to the full package group. After exclusion of women who had emergency caesarean sections, 11 861 were in the simplified package group and 11 820 were in the full package group. The primary outcome of blood loss of 1000 mL or more had a risk ratio of 1·09 (95% CI 0·91-1·31) and the upper 95% CI limit crossed the pre-stated non-inferiority margin. One case of uterine inversion occurred in the full package group. Other adverse events were haemorrhage-related. Interpretation: Although the hypothesis of non-inferiority was not met, omission of controlled cord traction has very little effect on the risk of severe haemorrhage. Scaling up of haemorrhage prevention programmes for non-hospital settings can safely focus on use of oxytocin. Funding: United States Agency for International Development and UN Development Programme/UN Population Fund/WHO/World Bank Special Programme of Research, Development and Research Training in Human Reproduction, Department of Reproductive Health and Research.
机译:背景:第三阶段的积极管理降低了Partum Heatum Heatum的风险。我们旨在评估是否可以从该阶段的主动管理中省略受控绳牵引而不增加严重出血的风险。方法:我们在阿根廷,埃及,印度,肯尼亚,菲律宾,南非,泰国和乌干达和乌干达和乌干达和乌干达和乌干达的三个医院和两个主要医疗中心进行了多中心,非劣等,随机对照试验。期望将单身婴儿进行阴道(即,未计划的剖面部分)被随机分配(以1:1的比率为1:1的比例),其中由国家分层分层,以引力和母体努力(简化包装)或子宫收缩和帘线夹紧后立即施加控制的绳索牵引(全包装)。随机化后,无法从调查人员,参与者,评估员隐藏分配。催产素10 IU在出生后立即在1-3分钟后夹紧后施用。根据当地政策,胎盘交付后的子宫按摩完成。原发性(非较低)结果为1000毫升或更高(严重出血)的失血。风险比的非劣势余量为1·3。通过修改意向治疗,不包括有紧急剖腹产的妇女。该试验是澳大利亚和新西兰临床试验登记处的注册机构,ACTRN 12608000434392。调查结果:2009年6月1日至2010年10月30日,1227名妇女随机分配到简化的包装组和12 163到全套组。排除后有紧急剖腹产的妇女,11861在简化的包装组中,11820年在完整的包装组中。血液损失的主要结果为1000mL或更多的风险比为1·09(95%CI 0·91-1·31),95%CI极限越过预先说的非劣级边缘。在完整包组中发生了子宫倒置的一种情况。其他不良事件有关的血腥事件。解释:虽然不符合非劣等性的假设,但受控脐带牵引的遗漏对严重出血的风险影响很小。用于非医院环境的出血预防计划的扩大可以安全地关注使用催产素。资金:美国国际发展和联合国发展计划/联合国人民基金/世卫组织/世贸组织/世界银行的研究,开发和研究培训,人类繁殖,生殖健康和研究部。

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  • 来源
    《The Lancet》 |2012年第9827期|共7页
  • 作者单位

    UNDP/UNFPA/WHO/World Bank Special Programme of Research World Health Organization Department of;

    Department of Obstetrics and Gynaecology Faculty of Medicine Khon Kaen University Khon Kaen;

    UNDP/UNFPA/WHO/World Bank Special Programme of Research World Health Organization Department of;

    UNDP/UNFPA/WHO/World Bank Special Programme of Research World Health Organization Department of;

    Department of Obstetrics and Gynaecology Faculty of Medicine Assiut University Assiut Egypt;

    Department of Obstetrics and Gynaecology Philippine General Hospital University of the;

    Centro Rosarino de Estudios Perinatales Rosario Argentina;

    Department of Obstetrics and Gynaecology University of Nairobi Nairobi Kenya;

    UNDP/UNFPA/WHO/World Bank Special Programme of Research World Health Organization Department of;

    UNDP/UNFPA/WHO/World Bank Special Programme of Research World Health Organization Department of;

    UNDP/UNFPA/WHO/World Bank Special Programme of Research World Health Organization Department of;

    Women's and Children's Health Research Unit Jawaharlal Nehru Medical College Belgaum Karnataka;

    Harvard Medical School Boston MA United States;

    United States Agency for International Development Washington DC United States;

    Effective Care Research Unit Eastern Cape Department of Health Universities of Witwatersrand and;

    Department of Obstetrics and Gynaecology Philippine General Hospital University of the;

    Institute for Clinical Effectiveness and Health Policy Buenos Aires Argentina;

    San Raphael of St. Francis Hospital Nsambya Uganda;

    Effective Care Research Unit Eastern Cape Department of Health Universities of Witwatersrand and;

    United States Agency for International Development Washington DC United States;

    Department of Obstetrics and Gynaecology Center for Women's and Children's Health Research;

    London School of Hygiene and Tropical Medicine London United Kingdom;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 医药、卫生;
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