Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, University of Utah Health, Salt Lake City, Utah, USA.
Division of Maternal-Fetal Medicine, Intermountain Healthcare, Salt Lake City, Utah, USA.
J Ultrasound Med. 2024 Nov;43(11):2153-2162. doi: 10.1002/jum.16546. Epub 2024 Aug 7.
Our objective was to determine the feasibility and interobserver reliability of umbilical cord and placental arteriolar flow assessment in low-risk pregnancies near term.
This was a prospective pilot study in low-risk pregnancies at 36 weeks with anterior placentas. We excluded any with an indication for antenatal testing or delivery before 39 weeks. Each participant underwent two ultrasounds by different examiners, which included arterial and venous velocimetry at three cord sites (fetal, free loop, and placental) in addition to maternal and fetal placental arterioles. The interobserver reliability was quantified using the Pearson correlation coefficient with that of standard clinical parameters serving as a benchmark for interpretation.
Among 53 participants scanned at 35-37 weeks, the mean examination duration was 20.5 ± 4.2 minutes. Ascertainment success was high for measures at the free loop, placental cord insertion, and fetal placental arterioles (range 90.6%-99.1%) and was lower at the fetal cord insertion and maternal spiral arterioles (range 47.2%-87.7%). Interobserver reliability estimates for free-loop systolic/diastolic and pulsatility index ranged from 0.38 to 0.44. Interobserver reliability for experimental parameters varied by measurement site, and all were poor at the fetal insertion and in placental arterioles. Parameters had significant variation across cord sites (range 4.3%-21.7%).
In our cohort, flow assessments of the free loop, placental insertion, and placental arterioles are feasible, but interrater reliability varies by measurement type and cord site. Future studies are needed to establish feasibility and reliability in nonanterior placentation and to assess clinical relevance.
本研究旨在确定在接近足月的低危妊娠中评估脐带和胎盘小动脉血流的可行性和观察者间可靠性。
这是一项在有前位胎盘的低危妊娠中进行的前瞻性试点研究,纳入标准为妊娠 36 周且无产前检查或 39 周前分娩的指征。每位患者均由两位不同的检查者进行两次超声检查,包括三个脐带部位(胎儿、游离环和胎盘)的动脉和静脉血流速度,以及母体和胎儿胎盘小动脉。观察者间可靠性通过 Pearson 相关系数进行量化,并以标准临床参数作为解释的基准。
在 35-37 周扫描的 53 名患者中,平均检查时间为 20.5±4.2 分钟。游离环、胎盘脐带插入处和胎儿胎盘小动脉的测量值获取成功率较高(范围为 90.6%-99.1%),而胎儿脐带插入处和母体螺旋小动脉的成功率较低(范围为 47.2%-87.7%)。游离环收缩/舒张和搏动指数的观察者间可靠性估计值范围为 0.38 至 0.44。实验参数的观察者间可靠性因测量部位而异,在胎儿插入处和胎盘小动脉处均较差。各脐带部位的参数差异较大(范围为 4.3%-21.7%)。
在我们的研究中,游离环、胎盘插入处和胎盘小动脉的血流评估是可行的,但观察者间的可靠性因测量类型和脐带部位而异。未来的研究需要确定在前置胎盘和评估临床相关性中评估可行性和可靠性。