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产时非侵入性电生理监测:一项前瞻性观察研究。

Intrapartum non-invasive electrophysiological monitoring: A prospective observational study.

机构信息

Department of Obstetrics and Gynecology, Máxima Medical Center, Veldhoven, The Netherlands.

Eindhoven MedTech Innovation Center (e/MTIC), Eindhoven, The Netherlands.

出版信息

Acta Obstet Gynecol Scand. 2020 Oct;99(10):1387-1395. doi: 10.1111/aogs.13873. Epub 2020 May 17.

Abstract

INTRODUCTION

Doppler ultrasound cardiotocography is a non-invasive alternative that, despite its poor specificity, is often first choice for intrapartum monitoring. Doppler ultrasound suffers from signal loss due to fetal movements and is negatively correlated with maternal body mass index (BMI). Reported accuracy of fetal heart rate monitoring by Doppler ultrasound varies between 10.6 and 14.3 bpm and reliability between 62.4% and 73%. The fetal scalp electrode (FSE) is considered the reference standard for fetal monitoring but can only be applied after membranes have ruptured with sufficient cervical dilatation and is sometimes contra-indicated. A non-invasive alternative that overcomes the shortcomings of Doppler ultrasound, providing reliable information on fetal heart rate, could be the answer. Non-invasive fetal electrocardiography (NI-fECG) uses a wireless electrode patch on the maternal abdomen to obtain both fetal and maternal heart rate signals as well as an electrohysterogram. We aimed to validate a wireless NI-fECG device for intrapartum monitoring in term singleton pregnancies, by comparison with the FSE.

MATERIAL AND METHODS

We performed a multicenter cross-sectional observational study at labor wards of 6 hospitals located in the Netherlands, Belgium, and Spain. Laboring women with a healthy singleton fetus in cephalic presentation and gestational age between 36 and 42 weeks were included. Participants received an abdominal electrode patch and FSE after written informed consent. Accuracy, reliability, and success rate of fetal heart rate readings were determined, using FSE as reference standard. Analysis was performed for the total population and measurement period as well as separated by labor stage and BMI class (≤30 and >30 kg/m ).

RESULTS

We included a total of 125 women. Simultaneous registrations with NI-fECG and FSE were available in 103 women. Overall accuracy is -1.46 bpm and overall reliability 86.84%. Overall success rate of the NI-fECG is around 90% for the total population as well as for both BMI subgroups. Success rate dropped to 63% during second stage of labor, similar results are found when looking at the separate BMI groups.

CONCLUSIONS

Performance measures of the NI-fECG device are good in the overall group and the separate BMI groups. Compared with Doppler ultrasound performance measures from the literature, NI-fECG is a more accurate alternative. Especially, when women have a higher BMI, NI-fECG performs well, resembling FSE performance measures.

摘要

简介

多普勒超声胎心监护是一种非侵入性的替代方法,尽管其特异性较差,但通常是分娩期间监测的首选方法。多普勒超声会因胎儿运动而导致信号丢失,并且与母体体重指数(BMI)呈负相关。通过多普勒超声报告的胎儿心率监测的准确性在 10.6 至 14.3 bpm 之间变化,可靠性在 62.4%至 73%之间变化。胎儿头皮电极(FSE)被认为是胎儿监测的参考标准,但只能在胎膜破裂且宫颈充分扩张后应用,有时也会出现禁忌证。一种可以克服多普勒超声缺点的非侵入性替代方法,为胎儿心率提供可靠信息,可能是答案。非侵入性胎儿心电图(NI-fECG)使用贴在母亲腹部的无线电极贴片来获得胎儿和母亲的心率信号以及电子宫图。我们旨在通过与 FSE 比较,验证一种用于足月单胎妊娠分娩期间监测的无线 NI-fECG 设备。

材料和方法

我们在荷兰、比利时和西班牙的 6 家医院的产房进行了一项多中心横断面观察性研究。纳入了具有健康单胎、头位和 36 至 42 周妊娠的孕妇。参与者在书面知情同意后接受腹部电极贴片和 FSE。使用 FSE 作为参考标准,确定胎儿心率读数的准确性、可靠性和成功率。分析针对总人群和测量期进行,以及按劳动阶段和 BMI 类别(≤30 和>30 kg/m )进行分层。

结果

我们共纳入了 125 名女性。103 名女性同时进行了 NI-fECG 和 FSE 记录。总体准确性为-1.46 bpm,总体可靠性为 86.84%。总体而言,NI-fECG 的成功率在总人群中以及在两个 BMI 亚组中均约为 90%。第二产程的成功率降至 63%,当分别观察 BMI 亚组时,结果相似。

结论

NI-fECG 设备的性能指标在总人群和单独的 BMI 组中均良好。与文献中的多普勒超声性能指标相比,NI-fECG 是一种更准确的替代方法。特别是当女性 BMI 较高时,NI-fECG 表现良好,类似于 FSE 的性能指标。

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