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使用压力记录分析方法对不稳定患者的心指数进行验证。

Cardiac index validation using the pressure recording analytic method in unstable patients.

机构信息

Department of Anesthesia and Intensive Care, Università Vita-Salute San Raffaele, Milano, Italy.

出版信息

J Cardiothorac Vasc Anesth. 2010 Apr;24(2):265-9. doi: 10.1053/j.jvca.2009.09.019. Epub 2009 Dec 11.

Abstract

OBJECTIVE

The authors investigated the accuracy and precision of the pressure recording analytic method (PRAM) in cardiac index measurement compared with thermodilution in unstable patients, a setting in which minimally invasive monitoring devices often fail.

DESIGN

Criterion standard.

SETTING

Intensive care unit.

PATIENTS

Thirty-two consecutive patients with low cardiac output syndrome treated with an intra-aortic balloon pump and/or high doses of inotropic drugs but without atrial fibrillation were studied after cardiac surgery.

INTERVENTIONS

None. Pulmonary and radial artery catheters were already in situ for clinical reasons.

MEASUREMENTS AND MAIN RESULTS

Four patients (12.5%) were excluded from the study because of artifacts caused by under- or overdamping of the arterial pressure monitoring system. The authors performed 3 injections of the thermal indicator in 5 minutes through the pulmonary artery catheter. Mean cardiac index values of 12 consecutive beats were considered for the PRAM. A significant correlation was found between the cardiac index assessed by thermodilution and PRAM (r = 0.72, p < 0.001). The mean bias between the 2 techniques was 0.072 +/- 0.41 L/min/m(2) with lower and upper 95% limits of confidence of -0.089 and 0.233 L/min/m(2), respectively. The percentage error was 30%. Sufficient agreement between the two techniques was evidenced by the Bland-Altman plot with only two points above the limits of agreement.

CONCLUSIONS

This study showed that PRAM, a minimally invasive method for cardiac index assessment, is clinically useful even in unstable patients such as those receiving intra-aortic balloon pump and/or ongoing high doses of a inotropic drugs because of a low cardiac output syndrome but without atrial fibrillation.

摘要

目的

作者研究了压力记录分析方法(PRAM)在不稳定患者中心脏指数测量中的准确性和精密度,这些患者处于微创监测设备经常失败的环境中。

设计

标准对照。

设置

重症监护病房。

患者

32 例接受主动脉内球囊泵和/或大剂量正性肌力药物治疗但无房颤的低心输出综合征患者,这些患者均来自心脏手术后。

干预措施

无。出于临床原因,已经在肺动脉和桡动脉放置了导管。

测量和主要结果

由于动脉压力监测系统的欠阻尼或过阻尼导致 4 例患者(12.5%)被排除在研究之外。作者通过肺动脉导管在 5 分钟内进行了 3 次热指示剂注射。PRAM 考虑了 12 个连续心搏的平均心脏指数值。通过热稀释法评估的心脏指数与 PRAM 之间存在显著相关性(r = 0.72,p < 0.001)。两种技术之间的平均偏差为 0.072 +/- 0.41 L/min/m²,置信区间的下限和上限分别为 -0.089 和 0.233 L/min/m²。误差百分比为 30%。Bland-Altman 图表明两种技术之间具有足够的一致性,只有两个点超出了一致性界限。

结论

这项研究表明,PRAM 是一种评估心脏指数的微创方法,即使在接受主动脉内球囊泵和/或持续高剂量正性肌力药物治疗的不稳定患者(如因低心输出综合征但无房颤而接受治疗的患者)中,也具有临床应用价值。

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