Atrioventricular conduction abnormalities are associated with poor outcome following intermittent umbilical cord occlusions in fetal sheep.

IF 3.5 2区 医学 Q1 OBSTETRICS & GYNECOLOGY
Juulia Lantto, Jonas Johnson, Heikki Huhta, Mervi Haapsamo, Panu Kiviranta, Kati Räsänen, Hanna-Marja Voipio, Sven-Erik Sonesson, Juha Voipio, Juha Räsänen, Ganesh Acharya
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引用次数: 0

Abstract

Introduction: Fetal arrhythmias have been described with intrapartum hypoxemia; however, they cannot be accurately diagnosed with currently used fetal heart rate (FHR) monitoring systems due to low resolution and signal averaging. We used a Holter device to record electrocardiogram (ECG) at 250 Hz in term sheep fetuses that developed severe metabolic acidosis induced by intermittent umbilical cord occlusions (UCOs), mimicking human labor contractions. We hypothesized that UCOs leading to worsening fetal metabolic acidosis provoke distinct fetal arrhythmias that could indicate impending fetal death.

Material and methods: Thirteen pregnant sheep (gestational age 133-135/145 days) were instrumented under general anesthesia. Three electrodes were placed on the fetal chest and connected to a Holter device for continuous ECG recording at a sampling rate of 250 Hz. The fetal axillary artery was catheterized and an inflatable occluder was placed around the umbilical cord. After a 4-5 day recovery, complete UCOs were induced by inflating the occluder for 1 min, followed by deflation for 2 min, until the fetal arterial pH dropped <7.0 and/or base excess (BE) <-16. Thereafter, an emergency cesarean section was performed to deliver the fetus.

Results: Eight sheep fetuses were included in the final analysis. All fetuses had normal baseline arterial blood gases and lactate values. During the first two UCOs, all fetuses demonstrated isolated benign arrhythmias. Three fetuses that developed severe metabolic acidosis after five UCOs showed persistent atrioventricular (AV) conduction abnormalities during the last UCO and its release, requiring cardiopulmonary resuscitation (CPR) at birth. One fetus with third-degree AV block had no detectable QRS complexes at birth, developed ventricular tachycardia and fibrillation (VT/VF) during CPR, and was successfully defibrillated. Five fetuses tolerated ≥10 UCOs before developing severe metabolic acidosis, and none of these showed any persistent AV-conduction abnormalities, though one fetus died after developing VT/VF after the 10th UCO.

Conclusions: Metabolic acidemia induced by intermittent UCOs in term sheep fetuses is associated with various arrhythmias, some of which may be life-threatening. Continuous intrapartum fetal ECG recording at a sample rate of ≥250 Hz coupled with a software capable of automatically detecting significant arrhythmias could enhance intrapartum fetal monitoring in the future.

房室传导异常与胎羊间歇性脐带闭塞后的不良预后相关。
胎儿心律失常已被描述为产时低氧血症;然而,由于分辨率低和信号平均,目前使用的胎儿心率(FHR)监测系统无法准确诊断。我们使用动态心电图仪记录了由间歇性脐带阻塞(UCOs)引起的严重代谢性酸中毒的足月羊胎儿的心电图(ECG),模仿人类的分娩收缩。我们假设UCOs导致胎儿代谢性酸中毒恶化,引起不同的胎儿心律失常,这可能表明胎儿即将死亡。材料与方法:13只孕羊(胎龄133 ~ 135/145天)全身麻醉。将三个电极置于胎儿胸部,连接到Holter装置上,以250 Hz的采样率连续记录心电图。胎儿腋窝动脉插管,在脐带周围放置充气式封堵器。恢复4-5天后,将封堵器充气1分钟,再充气2分钟,直至胎儿动脉pH下降,诱导完全uco。结果:8只羊胎儿纳入最终分析。所有胎儿的基线动脉血气和乳酸值均正常。在前两次uco期间,所有胎儿都表现出孤立的良性心律失常。在5次UCO后发生严重代谢性酸中毒的3例胎儿在最后一次UCO及其释放期间表现出持续性房室(AV)传导异常,需要在出生时进行心肺复苏(CPR)。一名患有三度房室传导阻滞的胎儿在出生时没有检测到QRS复合物,在心肺复苏术中出现室性心动过速和颤动(VT/VF),并成功除颤。5例胎儿耐受≥10次UCO后发生严重代谢性酸中毒,均未出现持续性av传导异常,但有1例胎儿在第10次UCO后发生VT/VF后死亡。结论:间断UCOs引起的足月羊胎儿代谢性酸血症与多种心律失常有关,其中一些心律失常可能危及生命。以≥250hz的采样率连续记录产时胎儿心电图,并结合能够自动检测显著心律失常的软件,可以在未来加强产时胎儿监护。
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来源期刊
CiteScore
8.00
自引率
4.70%
发文量
180
审稿时长
3-6 weeks
期刊介绍: Published monthly, Acta Obstetricia et Gynecologica Scandinavica is an international journal dedicated to providing the very latest information on the results of both clinical, basic and translational research work related to all aspects of women’s health from around the globe. The journal regularly publishes commentaries, reviews, and original articles on a wide variety of topics including: gynecology, pregnancy, birth, female urology, gynecologic oncology, fertility and reproductive biology.
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