Safety of Internal Electronic Fetal Heart Rate Monitoring During Labor

Yiheng Liang, Yun Li, Chunhua Huang, Xiaohong Li, Qiaoqing Cai, Jiying Peng, S. Fan
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Abstract

Abstract Objective: To investigate the safety and efficacy of internal electronic fetal heart rate (FHR) monitoring during labor. Methods: This was a retrospective case-control study, which was an analysis of monitoring FHR with a fetal scalp electrode or a Doppler probe (94 pregnant women per group). In the internal monitoring group, when the opening of the uterine orifice was ≥3 cm, the fetal scalp electrode was placed after natural or artificial rupture of the membrane. FHR was simultaneously monitored using a Doppler probe. In the external monitoring group, continuous FHR monitoring was performed using an ultrasound Doppler transducer fixed on the maternal abdomen. The toco transducer was used to record uterine contractions. Pathological examination of the placenta was performed prospectively in 49 and 48 cases in the internal electronic FHR monitoring group and control group, respectively. Maternal-infant outcomes (e.g. fever, puerperal infection, puerperal morbidity, delivery mode, Apgar score, and scalp injury) were recorded. Umbilical artery blood was extracted for blood gas analysis. Differences between the two groups were compared using the paired t-test, χ2 test, Yates corrected χ2 test or Fisher exact test. Results: Non-statistically significant differences between the internal and external monitoring groups were observed in the incidence of neonatal acidosis (1/94 (1.06%) vs. 3/94 (3.19%), respectively; χ2 = 0.255, P = 0.613), cesarean section/operative vaginal delivery (8/94 (8.51%) vs. 15/94 (15.96%), respectively; χ2 = 2.427, P = 0.181), fever during labor (18/94 (19.15%) vs. 15/94 (15.96%), respectively; χ2 = 0.331, P = 0.565), puerperal morbidity (2/94 (2.13%) vs. 3/94 (3.19%), respectively; χ2 = 0.000, P = 1.000), chorioamnionitis (9/49 (18.37%) vs. 7/48 (14.58%), respectively; χ2 = 0.252, P = 0.616), and neonatal asphyxia (0/94 (0.00%) vs. 1/94 (1.06%), respectively; χ2 = 0.000, P = 1.000). There were no puerperal infections, neonatal scalp injuries, or scalp abscesses found in either group. Using the internal monitoring value as reference, the incidence of FHR false deceleration in external FHR monitoring was 20.21% (19/94 women). Conclusion: Internal FHR monitoring during labor does not increase the incidence of adverse perinatal outcomes. External monitoring was associated with FHR false decelerations.
分娩过程中胎儿心率内部电子监测的安全性
摘要目的:探讨产程胎儿内部电子心率(FHR)监测的安全性和有效性。方法:这是一项回顾性病例对照研究,分析了用胎儿头皮电极或多普勒探头监测FHR的情况(每组94名孕妇)。在内部监测组中,当子宫口开口≥3 在膜自然或人工破裂后放置胎儿头皮电极。同时使用多普勒探头监测FHR。在外部监测组中,使用固定在母体腹部的超声多普勒换能器进行连续FHR监测。生育酚传感器用于记录子宫收缩。分别在内部电子FHR监测组和对照组中对49例和48例胎盘进行了前瞻性的病理检查。记录母婴结局(如发烧、产褥感染、产褥发病率、分娩方式、阿普加评分和头皮损伤)。提取脐带动脉血进行血气分析。使用配对t检验、χ2检验、Yates校正χ2检验或Fisher精确检验比较两组之间的差异。结果:内部和外部监测组的新生儿酸中毒发生率差异无统计学意义(分别为1/94(1.06%)和3/94(3.19%);χ2 = 0.255,P = 0.613),剖宫产/阴道手术分娩(分别为8/94(8.51%)和15/94(15.96%);χ2 = 2.427,P = 0.181),产程发热(分别为18/94(19.15%)和15/94(15.96%);χ2 = 0.331,P = 产褥期发病率分别为2/94(2.13%)和3/94(3.19%);χ2 = 0.000,P = 1.000),绒毛膜羊膜炎(分别为9/49(18.37%)和7/48(14.58%);χ2 = 0.252,P = 0.616)和新生儿窒息(分别为0/94(0.00%)和1/94(1.06%);χ2 = 0.000,P = 1.000)。两组均未发现产褥期感染、新生儿头皮损伤或头皮脓肿。以内部监测值为参考,外部FHR监测中FHR假减速的发生率为20.21%(19/94名女性)。结论:产程内FHR监测不会增加围产期不良结局的发生率。外部监测与FHR假减速相关。
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