Sameshima Hiroshi, Ikenoue Tsuyomu
Perinatal Center and Department of Obstetrics and Gynecology, Miyazaki Medical College, University of Miyazaki, Kihara, Kiyotake, Miyazaki, Japan.
Am J Perinatol. 2005 Jan;22(1):19-23. doi: 10.1055/s-2004-837272.
We evaluated the clinical significance of late decelerations (LD) of intrapartum fetal heart rate (FHR) monitoring to detect low pH (< 7.1) in low-risk pregnancies. We selected two secondary and two tertiary-level institutions where 10,030 women delivered. Among them, 5522 were low-risk pregnancies. The last 2 hours of FHR patterns before delivery were interpreted according to the guidelines of the National Institute of Child Health and Human Development. The correlation between the incidence of LD (occasional, < 50%; recurrent, > or = 50%) and severity (reduced baseline FHR accelerations and variability) of LD, and low pH (< 7.1) were evaluated. Statistical analyses included a contingency table with chi2 and the Fisher test, and one-way analysis of variance with the Bonferroni/Dunn test. In the 5522 low-risk pregnancies, 301 showed occasional LD and 99 showed recurrent LD. Blood gases and pH values deteriorated as the incidence of LD increased and as baseline accelerations or variability was decreased. Positive predictive value for low pH (< 7.1) was exponentially elevated from 0% at no deceleration, 1% in occasional LD, and > 50% in recurrent LD with no baseline FHR accelerations and reduced variability. In low-risk pregnancies, information on LD combined with acceleration and baseline variability enables us to predict the potential incidence of fetal acidemia.
我们评估了产时胎儿心率(FHR)监测中晚期减速(LD)对于检测低风险妊娠中低pH值(<7.1)的临床意义。我们选择了两家二级医疗机构和两家三级医疗机构,共有10,030名妇女在这些机构分娩。其中,5522例为低风险妊娠。分娩前最后2小时的FHR模式根据美国国家儿童健康与人类发展研究所的指南进行解读。评估了LD的发生率(偶发,<50%;反复出现,>或=50%)与LD的严重程度(基线FHR加速和变异性降低)以及低pH值(<7.1)之间的相关性。统计分析包括使用卡方检验和Fisher检验的列联表,以及使用Bonferroni/Dunn检验的单因素方差分析。在5522例低风险妊娠中,301例出现偶发LD,99例出现反复LD。随着LD发生率的增加以及基线加速或变异性的降低,血气和pH值恶化。低pH值(<7.1)的阳性预测值从无减速时的0%、偶发LD时的1%以及反复LD且无基线FHR加速和变异性降低时的>50%呈指数级升高。在低风险妊娠中,关于LD以及加速和基线变异性的信息使我们能够预测胎儿酸血症的潜在发生率。