首页> 外文期刊>BMC Pregnancy and Childbirth >Protocol for a randomised controlled trial of fetal scalp blood lactate measurement to reduce caesarean sections during labour: the Flamingo trial [ACTRN12611000172909]
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Protocol for a randomised controlled trial of fetal scalp blood lactate measurement to reduce caesarean sections during labour: the Flamingo trial [ACTRN12611000172909]

机译:胎儿头皮血乳酸测量以减少分娩时剖腹产的随机对照试验方案:火烈鸟试验[ACTRN12611000172909]

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Background The rate of caesarean sections around the world is rising each year, reaching epidemic proportions. Although many caesarean sections are performed for concerns about fetal welfare on the basis of abnormal cardiotocography, the majority of babies are shown to be well at birth, meaning that the operation, with its inherent short and long term risks, could have been avoided without compromising the baby’s health. Previously, fetal scalp blood sampling for pH estimation was performed in the context of an abnormal cardiotocograph, to improve the identification of babies in need of expedited delivery. This test has largely been replaced by lactate measurement, although its validity is yet to be established through a randomised controlled trial. This study aims to test the hypothesis that the performance of fetal scalp blood lactate measurement for women in labour with an abnormal cardiotocograph will reduce the rate of birth by caesarean section from 38?% to 25?% (a 35?% relative reduction). Methods/Design Prospective unblinded randomised controlled trial conducted at a single tertiary perinatal centre. Women labouring with a singleton fetus in cephalic presentation at 37 or more weeks’ gestation with ruptured membranes and with an abnormal cardiotocograph will be eligible. Participants will be randomised to one of two groups: fetal monitoring by cardiotocography alone, or cardiotocography augmented by fetal scalp blood lactate analysis. Decisions regarding the timing and mode of delivery will be made by the treating team, in accordance with hospital protocols. The primary study endpoint is caesarean section with secondary outcomes collected from maternal, fetal and neonatal clinical course and morbidities. A cost effectiveness analysis will also be performed. A sample size of 600 will provide 90?% power to detect the hypothesised difference in the proportion of women who give birth by caesarean section. Discussion This world-first trial is adequately powered to determine the impact of fetal scalp blood lactate measurement on rates of caesarean section. Preventing unnecessary caesarean sections will reduce the health and financial burdens associated with this operation, both in the index and any future pregnancies. Trial registration Australian New Zealand Clinical Trials Registry ACTRN12611000172909
机译:背景技术全世界剖腹产的比率每年都在上升,达到流行病的比例。尽管由于心电图检查异常而进行了许多剖宫产手术,以担心胎儿的健康,但大多数婴儿的出生状况良好,这意味着可以避免手术,因为这种手术具有内在的短期和长期风险,而不会影响其安全性。婴儿的健康。以前,在心脏心电图仪异常的情况下进行胎儿头皮血液采样以进行pH估算,以提高对需要快速分娩的婴儿的识别能力。尽管尚未通过随机对照试验确定其有效性,但该测试已被乳酸测量所取代。这项研究的目的是检验以下假设:对心电图检查异常的产妇进行胎头血乳酸检测,可使剖腹产的出生率从38%降低至25%(相对降低35%)。方法/设计在单个三级围产期中心进行的前瞻性无盲随机对照试验。妊娠37周或以上且胎膜破裂且心动图异常的头胎表现为单胎胎儿的妇女将符合资格。参与者将被随机分为两组之一:仅通过心动描记术进行胎儿监护,或通过胎儿头皮血液乳酸分析进行增强的心动描记术。有关分娩时间和方式的决定将由治疗团队根据医院的规程做出。主要研究终点为剖腹产,并从孕产妇,胎儿和新生儿的临床病程和发病率中收集次级结果。还将进行成本效益分析。 600个样本的样本将提供90%的功效,以检测通过剖腹产分娩的妇女比例中的假设差异。讨论该世界上第一个试验足以确定胎儿头皮血液乳酸测定对剖宫产率的影响。预防不必要的剖腹产将减少与该手术相关的健康和财务负担,无论是在指数还是将来的怀孕方面。试验注册澳大利亚新西兰临床试验注册中心ACTRN12611000172909

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