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The Bristol third stage trial: active versus physiological management of third stage of labour.

机译:布里斯托尔第三阶段试验:第三阶段的主动管理与生理管理。

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摘要

OBJECTIVE--To compare the effects on fetal and maternal morbidity of routine active management of third stage of labour and expectant (physiological) management, in particular to determine whether active management reduced incidence of postpartum haemorrhage. DESIGN--Randomised trial of active versus physiological management. Women entered trial on admission to labour ward with allocation revealed just before vaginal delivery. Five months into trial high rate of postpartum haemorrhage in physiological group (16.5% v 3.8%) prompted modification of protocol to exclude more women and allow those allocated to physiological group who needed some active management to be switched to fully active management. Sample size of 3900 was planned, but even after protocol modification a planned interim analysis after first 1500 deliveries showed continuing high postpartum haemorrhage rate in physiological group and study was stopped. SETTING--Maternity hospital. PARTICIPANTS--Of 4709 women delivered from 1 January 1986 to 31 January 1987, 1695 were admitted to trial and allocated randomly to physiological (849) or active (846) management. Reasons for exclusion were: refusal, antepartum haemorrhage, cardiac disease, breech presentation, multiple pregnancy, intrauterine death, and, after May 1986, ritodrine given two hours before delivery, anticoagulant treatment, and any condition needing a particular management of third stage. INTERVENTIONS--All but six women allocated to active management actually received it, having prophylactic oxytocic, cord clamping before placental delivery, and cord traction; whereas just under half those allocated to physiological management achieved it. A fifth of physiological group received prophylactic oxytocic, two fifths underwent cord traction and just over half clamping of the cord before placental delivery. ENDPOINT--Reduction in incidence of postpartum haemorrhage from 7.5% under physiological management to 5.0% under active management. MEASUREMENTS AND MAIN RESULTS--Incidence of postpartum haemorrhage was 5.9% in active management group and 17.9% in physiological group (odds ratio 3.13; 95% confidence interval 2.3 to 4.2), a contrast reflected in other indices of blood loss. In physiological group third stage was longer (median 15 min v 5 min) and more women needed therapeutic oxytocics (29.7% v 6.4%). Apgar scores at one and five minutes and incidence of neonatal respiratory problems were not significantly different between groups. Babies in physiological group weighed mean of 85 g more than those in active group. When women allocated to and receiving active management (840) were compared with those who actually received physiological management (403) active management still produced lower rate of postpartum haemorrhage (odds ratio 2.4;95% CI1.6 to 3.7). CONCLUSIONS--Policy of active management practised in this trial reduces incidence of postpartum haemorrhage, shortens third stage, and results in reduced neonatal packed cell volume.
机译:目的-比较第三阶段常规主动管理和预期(生理)管理对胎儿和产妇发病的影响,特别是确定主动管理是否能降低产后出血的发生率。设计-主动管理与生理管理的随机对照试验。妇女进入产房接受审判,并在阴道分娩前发现分配情况。进入试用期五个月后,生理学组较高的产后出血率(16.5%vs 3.8%)促使对治疗方案进行了修改,以排除更多女性,并允许分配给需要积极管理的生理学组的女性转为完全积极管理。计划中的样本量为3900,但即使在方案修改后,在生理学组中的前1500次分娩后,计划中的中期分析仍显示持续高的产后出血率,并且研究被停止。地点-妇产医院。参加者-在1986年1月1日至1987年1月31日分娩的4709名妇女中,有1695名被纳入试验,并随机分配到生理(849)或主动(846)治疗。排除的原因是:拒绝,产前出血,心脏病,臀位,多胎妊娠,子宫内死亡,以及1986年5月以后,分娩前两小时给予利多君,抗凝治疗以及需要特殊治疗的第三阶段疾病。干预措施-除了六名被分配到积极管理的妇女以外,其他所有妇女实际上都接受了这种治疗,包括预防性催产素,胎盘分娩前的脐带夹紧和脐带牵引。而分配给生理管理者的比例不到一半。生理组的五分之一接受了预防性催产药,五分之二的人接受了脐带牵引,胎盘分娩前将脐带夹住了一半以上。终点-产后出血的发生率从生理管理下的7.5%降低到主动管理下的5.0%。测量和主要结果-积极管理组产后出血的发生率为5.9%,生理学组为17.9%(几率为3.13; 95%的置信区间为2.3至4.2),这一差异反映在其他失血指数中。在生理学组中,第三阶段的时间更长(中位数为15分钟v 5分钟),更多的女性需要治疗性催产药(29.7%v 6.4%)。两组之间的一分钟和五分钟的Apgar评分和新生儿呼吸问题的发生率无显着差异。生理组的婴儿比活动组的婴儿平均重85 g。将分配并接受积极管理的妇女(840名)与实际接受生理管理的妇女(403名)进行比较,积极管理仍然产生较低的产后出血率(比值比为2.4; 95%CI1.6至3.7)。结论-该试验中实行的积极管理政策可降低产后出血的发生率,缩短第三阶段并减少新生儿的充盈细胞体积。

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