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外科重症监护患者非侵入性血红蛋白监测的评估

Evaluation of Noninvasive Hemoglobin Monitoring in Surgical Critical Care Patients.

作者信息

Xu Tim, Yang Ting, Kim Joseph B, Romig Mark C, Sapirstein Adam, Winters Bradford D

机构信息

1Department of Anesthesiology and Critical Care Medicine, Johns Hopkins University School of Medicine, Johns Hopkins University, Baltimore, MD. 2Armstrong Institute for Patient Safety and Quality, Johns Hopkins University School of Medicine, Johns Hopkins University, Baltimore, MD.

出版信息

Crit Care Med. 2016 Jun;44(6):e344-52. doi: 10.1097/CCM.0000000000001634.

Abstract

OBJECTIVE

To assess the clinical utility of noninvasive hemoglobin monitoring based on pulse cooximetry in the ICU setting.

DESIGN AND SETTING

A total of 358 surgical patients from a large urban, academic hospital had the noninvasive hemoglobin monitoring pulse cooximeter placed at admission to the ICU. Core and stat laboratory hemoglobin measurements were taken at the discretion of the clinicians, who were blinded to noninvasive hemoglobin monitoring values.

MEASUREMENT AND MAIN RESULTS

There was a poor correlation between the 2,465 time-matched noninvasive hemoglobin monitoring and laboratory hemoglobin measurements (r = 0.29). Bland-Altman analysis showed a positive bias of 1.0 g/dL and limits of agreement of -2.5 to 4.6 g/dL. Accuracy was best at laboratory values of 10.5-14.5 g/dL and least at laboratory values of 6.5-8 g/dL. At hemoglobin values that would ordinarily identify a patient as requiring a transfusion (< 8 g/dL), noninvasive hemoglobin monitoring consistently overestimated the patient's true hemoglobin. When sequential laboratory values declined below 8 g/dL (n = 102) and 7 g/dL (n = 13), the sensitivity and specificity of noninvasive hemoglobin monitoring at identifying these events were 27% and 7%, respectively. At a threshold of 8 g/dL, continuous noninvasive hemoglobin monitoring values reached the threshold before the labs in 45 of 102 instances (44%) and at 7 g/dL, noninvasive hemoglobin monitoring did so in three of 13 instances (23%). Noninvasive hemoglobin monitoring minus laboratory hemoglobin differences showed an intraclass correlation coefficient of 0.47 within individual patients. Longer length of stay and higher All Patient Refined Diagnostic-Related Groups severity of illness were associated with poor noninvasive hemoglobin monitoring accuracy.

CONCLUSIONS

Although noninvasive hemoglobin monitoring technology holds promise, it is not yet an acceptable substitute for laboratory hemoglobin measurements. Noninvasive hemoglobin monitoring performs most poorly in the lower hemoglobin ranges that include commonly used transfusion trigger thresholds and is not consistent within individual patients. Further refinement of the signal acquisition and analysis algorithms and clinical reevaluation are needed.

摘要

目的

评估基于脉搏血氧饱和度仪的无创血红蛋白监测在重症监护病房(ICU)环境中的临床实用性。

设计与设置

来自一家大型城市学术医院的358例外科患者在入住ICU时放置了无创血红蛋白监测脉搏血氧饱和度仪。临床医生根据需要酌情进行核心和即时实验室血红蛋白测量,他们对无创血红蛋白监测值不知情。

测量与主要结果

2465次时间匹配的无创血红蛋白监测值与实验室血红蛋白测量值之间的相关性较差(r = 0.29)。Bland-Altman分析显示正偏差为1.0 g/dL,一致性界限为-2.5至4.6 g/dL。在实验室值为10.5 - 14.5 g/dL时准确性最佳,在实验室值为6.5 - 8 g/dL时准确性最差。在通常会确定患者需要输血的血红蛋白值(< 8 g/dL)时,无创血红蛋白监测持续高估患者的真实血红蛋白水平。当连续实验室值降至8 g/dL以下(n = 102)和7 g/dL以下(n = 13)时,无创血红蛋白监测识别这些事件的敏感性和特异性分别为27%和7%。在8 g/dL的阈值下,102例中有45例(44%)无创血红蛋白监测值先于实验室值达到阈值,在7 g/dL时情况是13例中有3例(23%)。无创血红蛋白监测值减去实验室血红蛋白值的差异在个体患者中的组内相关系数为0.47。住院时间延长和所有患者精细诊断相关组疾病严重程度较高与无创血红蛋白监测准确性差相关。

结论

尽管无创血红蛋白监测技术有前景,但它尚未成为实验室血红蛋白测量的可接受替代方法。无创血红蛋白监测在包括常用输血触发阈值的较低血红蛋白范围内表现最差,且在个体患者中不一致。需要进一步完善信号采集和分析算法以及进行临床重新评估。

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