Maass Saskia W M C, Roekaerts Paul M H J, Lancé Marcus D
Department of Intensive Care, Maastricht University Medical Centre, Maastricht, Netherlands.
Department of Intensive Care, Maastricht University Medical Centre, Maastricht, Netherlands.
J Cardiothorac Vasc Anesth. 2014 Jun;28(3):534-9. doi: 10.1053/j.jvca.2014.01.007. Epub 2014 Apr 16.
The aim of the present study was to compare 2 noninvasive cardiac output measurement methods with the continuous cardiac output thermodilution (CCO-TD) method.
A single-center prospective design.
A university hospital.
Fifty-three consecutive patients scheduled for elective, non-emergent cardiac surgery.
With each participant the cardiac output was measured using 3 methods: CCO-TD, the Endotracheal Cardiac Output Monitor (ECOM), and the Nexfin monitor.
Measurements were performed simultaneously at 7 time points: After induction, before cardiopulmonary bypass, after cardiopulmonary bypass, after protamine, after arrival in the intensive care unit, and before extubation on postoperative day 1. Statistical analysis was performed using Pearson's correlation, Bland-Altman, percent error, and polar plots. Compared to CCO-TD, ECOM showed significant correlation of R0.619 with a bias of -0.13 L/min (95% confidence interval -2.19-1.93 L/min), a percent error of 40%, and trending ability of 87% and 97% within 0.5 L/min and 1.0 L/min, respectively. The Nexfin monitor showed significant correlation of R0.535 with a bias of-0.35 L/min (95% confidence interval-3.36-2.66 L/min), a percent error of 58% and trending ability of 84% and 97% were within 0.5 L/min and 1.0 L/min limits of agreement.
Neither the ECOM nor the Nexfin had the ability to replace the thermodilution-based continuous cardiac output monitor. The ECOM did not have acceptable accuracy or trending ability and only could be utilized for intubated patients. The Nexfin lacked reliability and trending ability. Also, the Nexfin did not provide consistent results.
本研究旨在比较两种非侵入性心输出量测量方法与连续心输出量热稀释法(CCO-TD)。
单中心前瞻性设计。
大学医院。
53例连续安排进行择期非急诊心脏手术的患者。
对每位参与者使用三种方法测量心输出量:CCO-TD、气管内心输出量监测仪(ECOM)和Nexfin监测仪。
在7个时间点同时进行测量:诱导后、体外循环前、体外循环后、鱼精蛋白注射后、进入重症监护病房后以及术后第1天拔管前。使用Pearson相关性分析、Bland-Altman分析、百分比误差分析和极坐标图进行统计分析。与CCO-TD相比,ECOM显示出显著相关性,R为0.619,偏差为-0.13升/分钟(95%置信区间-2.19至1.93升/分钟),百分比误差为40%,在0.5升/分钟和1.0升/分钟范围内的趋势能力分别为87%和97%。Nexfin监测仪显示出显著相关性,R为0.535,偏差为-0.35升/分钟(95%置信区间-3.36至2.66升/分钟),百分比误差为58%,在0.5升/分钟和1.0升/分钟一致性界限内的趋势能力分别为84%和97%。
ECOM和Nexfin都没有能力取代基于热稀释法的连续心输出量监测仪。ECOM没有可接受的准确性或趋势能力,仅可用于插管患者。Nexfin缺乏可靠性和趋势能力。此外,Nexfin没有提供一致的结果。