Abstract

BackgroundCardiotocography is almost ubiquitous in its use in intrapartum care. Although it has been demonstrated that there is some benefit from continuous intrapartum fetal monitoring using cardiotocography, there is also an increased risk of caesarean section which is accompanied by short-term and long-term risks to the mother and child. There is considerable potential to reduce unnecessary operative delivery with up to a 60% false positive diagnosis of fetal distress using cardiotocography alone. ST analysis of the fetal electrocardiogram is a promising adjunct to cardiotocography alone, and permits detection of metabolic acidosis of the fetus, potentially reducing false positive diagnosis of fetal distress.MethodsThis study will be a single-centre, parallel-group, randomised controlled trial, conducted over 3 years. The primary hypothesis will be that the proportion of women with an emergency caesarean section on ST analysis will not equal that for women on cardiotocography monitoring alone. Participants will be recruited at the Women’s and Children’s Hospital, a high-risk specialty facility with approximately 5000 deliveries per annum. A total of 1818 women will be randomised to the treatment or conventional arm with an allocation ratio of 1:1, stratified by parity. The primary outcome is emergency caesarean section (yes/no). Statistical analysis will follow standard methods for randomised trials and will be performed on an intention-to-treat basis. Secondary maternal and neonatal outcomes will also be analysed. Additional study outcomes include psychosocial outcomes, patient preferences and cost-effectiveness.DiscussionApproximately 20% of Australian babies are delivered by emergency caesarean section. This will be the first Australian trial to examine ST analysis of the fetal electrocardiogram as an adjunct to cardiotocography as a potential method for reducing this proportion. The trial will be among the first to comprehensively examine ST analysis, taking into account the impact on psychosocial well-being as well as cost-effectiveness. This research will provide Australian evidence for clinical practice and guideline development as well as for policy-makers and consumers to make informed, evidence-based choices about care in labour.Trial registrationANZCTR, ACTRN1261800006268. Registered on 19 January 2018.

Highlights

  • Cardiotocography is almost ubiquitous in its use in intrapartum care

  • Approximately 20% of Australian babies are delivered by emergency caesarean section

  • Continuous CTG is one of the most common procedures undertaken during labour, with routine data collection and other reports from Australia, the setting for ST analysis (STan) Australian Randomised controlled Trial (START), showing that it is applied in 60–70% of all labours [2, 3]

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Summary

Methods

Hypotheses We believe that STan monitoring (cardiotocographic electronic fetal monitoring (CTG) plus analysis of the ST segment of the fetal electrocardiogram) of labouring women will result in a reduction in the proportion of emergency caesarean sections when compared with CTG monitoring alone, from 17% to 12%. Sample size Considering the results of our pilot study [25], current hospital rates for emergency caesarean section and electronic fetal monitoring, and the results of previous research [12], we powered the primary hypothesis on a reduction of emergency caesarean section from 17% to 12%, (i.e. a 5% absolute difference), with 80% power and a conservative two-sided α = 0.05 To detect this absolute difference between the treatment groups, a total sample size of 1634 women is required. Given a recruitment period of about 2 years, we estimated that it would be possible to consent 2588 women, of whom 1818 will be subsequently randomised This sample size would provide power to detect clinically meaningful differences in the secondary outcomes of interest. Results will be directly disseminated via the Women’s Healthcare Australasia Clinical Network

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