Institute of Anaesthesiology and Intensive Care Medicine, Triemli Hospital Zurich, Zurich, Switzerland.
Institute of Anaesthesiology, Kantonsspital Winterthur, Winterthur, Switzerland.
J Cardiothorac Vasc Anesth. 2018 Apr;32(2):715-722. doi: 10.1053/j.jvca.2017.09.006. Epub 2017 Sep 7.
The aim of this study was to analyze the accuracy, precision, and trending ability of the following 4 pulse wave analysis devices to measure continuous cardiac output: PiCCO ([PCCO]; Pulsion Medical System, Munich, Germany); LiDCO ([LCCO]; LiDCO Ltd, London, UK); FloTrac/Vigileo ([FCCO]; Edwards Lifesciences, Irvine, CA); and Nexfin ([NCCO]; BMEYE, Amsterdam, The Netherlands).
Prospective, observational clinical study.
Intensive care unit of a single-center, teaching hospital.
The study comprised 22 adult patients after elective coronary artery bypass surgery.
Three measurement cycles were performed in all patient durings their immediate postoperative intensive care stay before and after fluid loading. Hemodynamic measurements were performed 5 minutes before and immediately after the administration of 500 mL colloidal fluid over 20 minutes.
PCCO, LCCO, FCCO, and NCCO were assessed and compared with cardiac output derived from intermittent transpulmonary thermodilution (ICO). One hundred thirty-two matched sets of data were available for analysis. Bland-Altman analysis using linear mixed effects models with random effects for patient and trial revealed a mean bias ±2 standard deviation (%error) of -0.86 ± 1.41 L/min (34.9%) for PCCO-ICO, -0.26 ± 2.81 L/min (46.3%) for LCCO-ICO, -0.28 ± 2.39 L/min (43.7%) for FCCO-ICO, and -0.93 ± 2.25 L/min (34.6%) for NCCO-ICO. Bland-Altman plots without adjustment for repeated measurements and replicates yielded considerably larger limits of agreement. Trend analysis for all techniques did not meet criteria for acceptable performance.
All 4 tested devices using pulse wave analysis for measuring cardiac output failed to meet current criteria for meaningful and adequate accuracy, precision, and trending ability in cardiac output monitoring.
本研究旨在分析以下 4 种脉搏波分析设备测量连续心输出量的准确性、精密度和趋势能力:脉搏指示剂连续心输出量监测仪(PiCCO;德国慕尼黑脉搏医疗系统公司)、LiDCO 连续心输出量监测仪(LiDCO Ltd,英国伦敦)、FloTrac/Vigileo(FCCO;美国加利福尼亚州欧文市爱德华兹生命科学公司)和 Nexfin 脉搏容积波心排量监测仪(NCCO;荷兰阿姆斯特丹 BMEYE 公司)。
前瞻性、观察性临床研究。
单中心教学医院的重症监护病房。
本研究纳入 22 例择期冠状动脉旁路移植术后的成年患者。
在患者术后即刻的重症监护期间,所有患者均进行 3 次测量周期,在进行液体负荷前后进行。血流动力学测量在输注 500ml 胶体液 20 分钟前和给药后 5 分钟进行。
评估了 PiCCO、LiDCO、FCCO 和 NCCO,并将其与间歇经肺热稀释法(ICO)得出的心输出量进行比较。分析了 132 组匹配数据。使用具有患者和试验随机效应的线性混合效应模型进行 Bland-Altman 分析显示,PiCCO-ICO 的平均偏倚±2 个标准差(%误差)为-0.86±1.41L/min(34.9%),LiDCO-ICO 为-0.26±2.81L/min(46.3%),FCCO-ICO 为-0.28±2.39L/min(43.7%),NCCO-ICO 为-0.93±2.25L/min(34.6%)。未经重复测量和重复测量调整的 Bland-Altman 图产生了相当大的一致性界限。所有技术的趋势分析均不符合可接受性能的标准。
在测量心输出量方面,使用脉搏波分析的所有 4 种测试设备均未达到当前对心输出量监测有意义和足够准确性、精密度和趋势能力的标准。