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Validation of a noninvasive blood pressure monitoring device in pediatric intensive care patients

机译:小儿重症监护患者无创血压监测设备的验证

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The purpose of the study was to evaluate the performance and to define limitations of a noninvasive blood pressure monitoring device in the critically ill pediatric population. Measurements were collected simultaneously with those from an arterial line by a computer interfaced with the noninvasive blood pressure monitoring system and the patient's monitor. Patients were included in the study if they were between the ages of 1 month and 18 years with wrist circumferences of ≥ 10 centimeters and an arterial line in place. Comparison analysis was performed via bias and precision plots of the blood pressure and heart rate data in addition to calculation of Pearson correlation coefficients and concordance correlation coefficients. Twenty patients had blood pressure and heart rate monitored by a noninvasive blood pressure monitor for 30 minutes per patient. Data collection resulted in 2015 data points for each blood pressure and heart rate for comparison of both methods. Concordance correlation coefficients were the following: systolic blood pressure 0.93, diastolic 0.93, mean 0.94, and heart rate 0.85. Our study showed good agreement between the methods in the critically ill, pediatric population with a wrist circumference limitation defined at ≥ 11 centimeters.
机译:该研究的目的是评估危重儿科患者的性能并确定无创血压监测设备的局限性。通过与无创血压监测系统和患者监护仪接口的计算机,与动脉管线同时采集测量值。如果患者年龄在1个月至18岁之间,且手腕周长≥10厘米,并且有动脉线,则将其纳入研究。除了计算皮尔逊相关系数和一致性相关系数外,还通过血压和心率数据的偏差图和精度图进行比较分析。 20名患者通过无创血压监测仪对每位患者进行了30分钟的血压和心率监测。数据收集得出了每种血压和心率的2015年数据点,用于两种方法的比较。一致性相关系数如下:收缩压0.93,舒张压0.93,平均值0.94,心率0.85。我们的研究表明,在手腕周长限制在≥11厘米的危重儿科人群中,这些方法之间具有很好的一致性。

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