Department of Anesthesiology and Perioperative Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan.
Department of Anesthesiology and Perioperative Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan.
J Cardiothorac Vasc Anesth. 2023 Jul;37(7):1143-1151. doi: 10.1053/j.jvca.2023.03.019. Epub 2023 Mar 17.
The clinical use of less-invasive devices that calculate the cardiac output from arterial pressure waveform is increasing. The authors aimed to evaluate the accuracy and characteristics of the systemic vascular resistance index (SVRI) of the cardiac index measured by 2 less-invasive devices, fourth-generation FloTrac (CI) and LiDCOrapid (CI), compared with the intermittent thermodilution technique, using a pulmonary artery catheter (CI).
This was a prospective observational study.
This study was conducted at a single university hospital.
Twenty-nine adult patients undergoing elective cardiac surgery.
Elective cardiac surgery was used as an intervention.
Hemodynamic parameters, CI, CI, and CI, were measured after the induction of general anesthesia, at the start of cardiopulmonary bypass, after completion of weaning from cardiopulmonary bypass, 30 minutes after weaning, and at sternal closure (135 measurements in total). The CI and CI had moderate correlations with CI (r = 0.62 and 0.58, respectively). Compared with CI CI and CI had a bias of -0.73 and -0.61 L/min/m, limit of agreement of -2.14-to-0.68 L/min/m and -2.42-to-1.20 L/min/m, and percentage error of 39.9% and 51.2%, respectively. Subgroup analysis for evaluating SVRI characteristics showed that the percentage errors of CI and CI were 33.9% and 54.5% in low SVRI (<1,200 dyne×s/cm/m), 37.6% and 47.9% in moderate SVRI (1,200-1,800 dyne×s/cm/m), 49.3% and 50.6% in high SVRI (>1,800 dyne·s/cm/m), respectively.
The accuracy of CI or CI was not clinically acceptable for cardiac surgery. Fourth-generation FloTrac was unreliable in high SVRI. LiDCOrapid was inaccurate across a broad range of SVRI, and minimally affected by SVRI.
越来越多的临床医生使用基于动脉压力波形计算心输出量的微创设备。作者旨在评估两种微创设备(第四代 FloTrac [CI] 和 LiDCOrapid [CI])测量的系统血管阻力指数(SVRI)与肺动脉导管(CI)间歇性热稀释技术测量的 CI 的准确性和特征。
这是一项前瞻性观察性研究。
本研究在一家大学医院进行。
29 名接受择期心脏手术的成年患者。
使用择期心脏手术作为干预措施。
全麻诱导后、体外循环开始时、体外循环脱机完成后、脱机 30 分钟后和胸骨关闭时(共 135 次测量)测量血流动力学参数、CI、CI 和 CI。CI 与 CI 具有中度相关性(r=0.62 和 0.58)。与 CI 相比,CI 和 CI 的偏差分别为-0.73 和-0.61 L/min/m,一致性界限为-2.14 至 0.68 L/min/m 和-2.42 至 1.20 L/min/m,误差百分比分别为 39.9%和 51.2%。评估 SVRI 特征的亚组分析表明,在低 SVRI(<1,200 dyne×s/cm/m)时,CI 和 CI 的误差百分比分别为 33.9%和 54.5%,在中 SVRI(1,200-1,800 dyne×s/cm/m)时为 37.6%和 47.9%,在高 SVRI(>1,800 dyne·s/cm/m)时为 49.3%和 50.6%。
CI 或 CI 的准确性在心脏手术中不能被临床接受。第四代 FloTrac 在高 SVRI 时不可靠。LiDCOrapid 在广泛的 SVRI 范围内不准确,并且受 SVRI 的影响最小。