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Reliability of cardiac output measurements using LiDCOrapid™ and FloTrac/Vigileo™ across broad ranges of cardiac output values

机译:使用LiDCOrapid™和FloTrac / Vigileo™在广泛的心输出量值范围内进行心输出量测量的可靠性

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摘要

Knowing a patient’s cardiac output (CO) could contribute to a safe, optimized hemodynamic control during surgery. Precise CO measurements can serve as a guide for resuscitation therapy, catecholamine use, differential diagnosis, and intervention during a hemodynamic crisis. Despite its invasiveness and intermittent nature, the thermodilution technique via a pulmonary artery catheter (PAC) remains the clinical gold standard for CO measurements. LiDCOrapid™ (LiDCO, London, UK) and FloTrac/Vigileo™ (Edwards Lifesciences, Irvine, CA) are less invasive continuous CO monitors that use arterial waveform analysis. Their calculations are based on arterial waveform characteristics and do not require calibration. Here, we evaluated LiDCOrapid™ and FloTrac/Vigileo™ during off-pump coronary artery bypass graft (OPCAB) and living-donor liver transplantation (LDLT) surgery. This observational, single-center study included 21 patients (11 OPCAB and 10 LDLT). We performed simultaneous measurements of CO at fixed sampling points during surgery using both devices (LiDCOrapid™ version 1.04-b222 and FloTrac/Vigileo™ version 3.02). The thermodilution technique via a PAC was used to obtain the benchmark data. LiDCOrapid™ and FloTrac/Vigileo™ were used in an uncalibrated fashion. We analyzed the measured cardiac index using a Bland–Altman analysis (the method of variance estimates recovery), a polar plot method (half-moon method), a 4-quadrant plot and compared the widths of the limits of agreement (LOA) using an F test. One OPCAB patient was excluded because of the use of an intra-aortic balloon pumping during surgery, and 20 patients (10 OPCAB and 10 LDLT) were ultimately analyzed. We obtained 149 triplet measurements with a wide range of cardiac index. For the FloTrac/Vigileo™, the bias and percentage error were −0.44 L/min/m2 and 74.4 %. For the LiDCOrapid™, the bias and percentage error were −0.38 L/min/m2 and 53.5 %. The polar plot method showed an angular bias (FloTrac/Vigileo™ vs. LiDCOrapid™: 6.6° vs. 5.8°, respectively) and radial limits of agreement (−63.9 to 77.1 vs. −41.6 to 53.1). A 4-quadrant plot was used to obtain concordance rates (FloTrac/Vigileo™ vs. PAC and LiDCOrapid™ vs. PAC: 84.0 and 92.4 %, respectively). We could compare CO measurement devices across broad ranges of CO and SVR using LDLT and OPCAB surgical patients. An F test revealed no significant difference in the widths of the LoA for both devices when sample sizes capable of detecting a more than two-fold difference were used. We found that both devices tended to underestimate the calculated CIs when the CIs were relatively high. These proportional bias produced large percentage errors in the present study.
机译:了解患者的心输出量(CO)可有助于在手术过程中进行安全,优化的血液动力学控制。精确的一氧化碳测量可以作为复苏疗法,儿茶酚胺的使用,鉴别诊断和在血流动力学危机期间进行干预的指南。尽管具有侵入性和间歇性,但通过肺动脉导管(PAC)进行的热稀释技术仍然是CO测量的临床金标准。 LiDCOrapid™(英国伦敦的LiDCO)和FloTrac / Vigileo™(加利福尼亚州尔湾的Edwards Lifesciences)是使用动脉波形分析的侵入性较小的连续CO监测器。他们的计算基于动脉波形特征,不需要校准。在这里,我们在非体外循环冠状动脉搭桥术(OPCAB)和活体供肝移植(LDLT)手术期间评估了LiDCOrapid™和FloTrac / Vigileo™。这项观察性,单中心研究包括21例患者(11例OPCAB和10例LDLT)。我们使用两种设备(LiDCOrapid™版本1.04-b222和FloTrac / Vigileo™版本3.02)在手术期间的固定采样点同时测量CO。使用通过PAC的热稀释技术获得基准数据。 LiDCOrapid™和FloTrac / Vigileo™以未经校准的方式使用。我们使用Bland–Altman分析(方差估计回收率的方法),极坐标图方法(半月方法),四象限图分析了测得的心脏指数,并使用以下方法比较了协议限度(LOA)的宽度: F测试。一名OPCAB患者被排除在外,因为在手术期间使用了主动脉内球囊抽吸,最终对20例患者(10例OPCAB和10 LDLT)进行了分析。我们获得了149种三联体测量值,具有广泛的心脏指数。对于FloTrac / Vigileo™,偏差和百分比误差为-0.44 L / min / m 2 和74.4%。对于LiDCOrapid™,偏差和百分比误差分别为-0.38 L / min / m 2 和53.5%。极坐标图方法显示了角度偏差(FloTrac / Vigileo™与LiDCOrapid™:分别为6.6°与5.8°)和一致的径向极限(-63.9至77.1与-41.6至53.1)。使用四象限图获得一致性率(FloTrac / Vigileo™对PAC和LiDCOrapid™对PAC:分别为84.0%和92.4%)。我们可以比较使用LDLT和OPCAB手术患者的广泛CO和SVR范围内的CO测量设备。当使用能够检测到两倍以上差异的样本量时,F测试表明两种设备的LoA宽度均无显着差异。我们发现,当CI相对较高时,两种设备都倾向于低估计算出的CI。这些比例偏差在本研究中产生了很大的百分比误差。

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