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超声稀释技术在婴幼儿心输出量测量和分流检测中的验证。

Validation of an ultrasound dilution technology for cardiac output measurement and shunt detection in infants and children.

机构信息

1Department of Anesthesia and Intensive Care, Children's Hospital, Pediatric Intensive Care Unit, University Hospital of Lund, Lund, Sweden. 2Department of Pediatric Cardiac Surgery, Children's Hospital, University Hospital of Lund, Lund, Sweden.

出版信息

Pediatr Crit Care Med. 2014 Feb;15(2):139-47. doi: 10.1097/PCC.0000000000000053.

Abstract

OBJECTIVE

To validate cardiac output measurements by ultrasound dilution technology (COstatus monitor) against those obtained by a transit-time ultrasound technology with a perivascular flow probe and to investigate ultrasound dilution ability to estimate pulmonary to systemic blood flow ratio in children.

DESIGN

Prospective observational clinical trial.

SETTING

Pediatric cardiac operating theater in a university hospital.

MATERIAL AND METHODS

In 21 children (6.1 ± 2.6 kg, mean ± SD) undergoing heart surgery, cardiac output was simultaneously recorded by ultrasound dilution (extracorporeal arteriovenous loop connected to existing arterial and central venous catheters) and a transit-time ultrasound probe applied to the ascending aorta, and when possible, the main pulmonary artery. The pulmonary to systemic blood flow ratio estimated from ultrasound dilution curve analysis was compared with that estimated from transit-time ultrasound technology.

RESULTS

Bland-Altman analysis of the whole cohort (90 pairs, before and after surgery) showed a bias between transit-time ultrasound (1.01 ± 0.47 L/min) and ultrasound dilution technology (1.03 ± 0.51 L/min) of -0.02 L/min, limits of agreement -0.3 to 0.3 L/min, and percentage error of 31%. In children with no residual shunts, the bias was -0.04 L/min, limits of agreement -0.28 to 0.2 L/min, and percentage error 19%. The pooled co efficient of variation was for the whole cohort 3.5% (transit-time ultrasound) and 6.3% (ultrasound dilution), and in children without shunt, it was 2.9% (transit-time ultrasound) and 4% (ultrasound dilution), respectively. Ultrasound dilution identified the presence of shunts (pulmonary to systemic blood flow ≠ 1) with a sensitivity of 100% and a specificity of 92%. Mean pulmonary to systemic blood flow ratio by transit-time ultrasound was 2.6 ± 1.0 and by ultrasound dilution 2.2 ± 0.7 (not significant).

CONCLUSION

The COstatus monitor is a reliable technique to measure cardiac output in children with high sensitivity and specificity for detecting the presence of shunts.

摘要

目的

验证超声稀释技术(COstatus 监测仪)测量心输出量与经血管内超声探头的瞬态时间超声技术的相关性,并探讨超声稀释技术在儿童肺循环与体循环血流量比值中的估计能力。

设计

前瞻性观察性临床试验。

地点

大学医院小儿心脏手术室。

材料和方法

在 21 例(6.1 ± 2.6 kg,均值 ± 标准差)接受心脏手术的儿童中,通过超声稀释(连接到现有动脉和中心静脉导管的体外动静脉环)和应用于升主动脉(并在可能时应用于主肺动脉)的瞬态时间超声探头同时记录心输出量。从超声稀释曲线分析估计的肺循环与体循环血流量比值与从瞬态时间超声技术估计的比值进行比较。

结果

对整个队列(90 对,手术前后)进行 Bland-Altman 分析显示,瞬态时间超声(1.01 ± 0.47 L/min)与超声稀释技术(1.03 ± 0.51 L/min)之间的偏差为 -0.02 L/min,一致性界限为 -0.3 至 0.3 L/min,百分比误差为 31%。在无残余分流的儿童中,偏差为 -0.04 L/min,一致性界限为 -0.28 至 0.2 L/min,百分比误差为 19%。整个队列的总变异系数为 3.5%(瞬态时间超声)和 6.3%(超声稀释),无分流儿童的变异系数分别为 2.9%(瞬态时间超声)和 4%(超声稀释)。超声稀释技术可以检测到分流(肺循环与体循环血流量≠1),灵敏度为 100%,特异性为 92%。通过瞬态时间超声的平均肺循环与体循环血流量比值为 2.6 ± 1.0,通过超声稀释的为 2.2 ± 0.7(无统计学差异)。

结论

COstatus 监测仪是一种可靠的技术,可以测量儿童的心输出量,具有高灵敏度和特异性,可用于检测分流的存在。

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