Fetal Medicine Unit, St George's University Hospitals NHS Foundation Trust, University of London, London, UK.
Vascular Biology Research Centre, Molecular and Clinical Sciences Research Institute, St George's University of London, London, UK.
Ultrasound Obstet Gynecol. 2019 Aug;54(2):232-238. doi: 10.1002/uog.20142. Epub 2019 Jul 11.
Maternal hemodynamics change significantly during Cesarean section complicated by massive hemorrhage or severe hypertensive disease. Cardiac output (CO) monitoring aids early, goal-directed hemodynamic therapy. The aim of this study was to record hemodynamic changes observed during Cesarean section in pregnancies at high risk of hemodynamic instability, using invasive (LiDCOrapid™) and non-invasive (NICOM®) devices, and to assess agreement between the two devices in measuring CO.
Simultaneous intraoperative hemodynamic measurements were taken using the LiDCOrapid and NICOM devices, following standardized techniques, in women at high risk of hemodynamic instability undergoing Cesarean section. Agreement in CO measurements between the two devices was assessed using Bland-Altman plots and the agreement:tolerability index (ATI). Agreement analyses were performed for repeated measures in subjects, using centiles.
From 10 women, 307 paired measurements were analyzed. Mean bias (defined as the mean difference in CO measurements between the LiDCOrapid and NICOM devices) was 3.05 (95% CI, 1.89 to 4.21) L/min. Limits of agreement ranged from -1.58 (95% CI, -4.47 to -0.14) to 7.68 (95% CI, 6.24 to 10.56) L/min. The resulting agreement interval was 9.26 L/min which returned an ATI of 2.3.
There are large mean differences between CO measurements obtained during Cesarean section using the LiDCOrapid and NICOM hemodynamic monitors in pregnant women at high risk of hemodynamic instability, indicating that they should not be considered interchangeable clinically. There is an unacceptably low level of agreement (ATI > 2) in CO measurements between the devices, conferring a high risk of clinical misclassification during massive hemorrhage. Copyright © 2018 ISUOG. Published by John Wiley & Sons Ltd.
在伴有大量出血或严重高血压疾病的剖宫产手术中,产妇的血液动力学会发生显著变化。心输出量(CO)监测有助于进行早期、以目标为导向的血液动力学治疗。本研究的目的是记录高危产妇在剖宫产手术中观察到的血液动力学变化,使用有创(LiDCOrapid™)和无创(NICOM®)设备,并评估两种设备在 CO 测量方面的一致性。
使用标准化技术,对高危血液动力学不稳定的剖宫产妇女进行术中同时进行 LiDCOrapid 和 NICOM 设备的血流动力学测量。使用 Bland-Altman 图和一致性:可容忍性指数(ATI)评估两种设备在 CO 测量方面的一致性。使用百分位数对受试者的重复测量进行一致性分析。
从 10 名女性中分析了 307 对测量值。平均偏差(定义为 LiDCOrapid 和 NICOM 设备之间 CO 测量值的平均差异)为 3.05(95%CI,1.89 至 4.21)L/min。一致性范围为-1.58(95%CI,-4.47 至-0.14)至 7.68(95%CI,6.24 至 10.56)L/min。由此产生的一致性区间为 9.26 L/min,对应的 ATI 为 2.3。
在高危产妇中,使用 LiDCOrapid 和 NICOM 血流动力学监测器在剖宫产手术中获得的 CO 测量值存在较大的平均差异,表明它们在临床上不能互换使用。两种设备之间的 CO 测量值一致性水平(ATI > 2)非常低,在大量出血期间存在临床分类错误的高风险。版权所有 © 2018 ISUOG。由 John Wiley & Sons Ltd 出版。