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Evaluation of a new pediatric continuous oximetry catheter.

机译:新型儿科连续血氧定量导管的评估。

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摘要

PURPOSE: : To evaluate the accuracy of central venous oxygen saturation recordings from a new in-line pediatric oximetry catheter. DESIGN: : Prospective, observational study. STUDY POPULATION: : Eighteen pediatric patients who needed central venous access for monitoring and/or treatment between January 2006 and June 2006 in the pediatric intensive care unit of the Hospital for Sick Children in Toronto, Canada. METHODS AND MAIN RESULTS: : Measurements were done at the baseline and then every 4-8 hrs. The monitor was calibrated in vivo at the baseline and then daily. In vitro calibration of the monitor was also performed in the last five patients. The hemoglobin value was updated when there was a significant change. The maximum duration of sampling was 72 hrs (if indicated). There were 131 measurements in 17 patients; each subject had a different number of paired measurements (median 5). Three patients were excluded due to violation of the protocol, and 113 measurements were left in analysis. The mean difference of catheter value from the laboratory value was -1.01 (median 0). The interquartile range was 5. The difference of both methods was evenly distributed as per a Bland-Altman plot, with one patient's data lying outside of the comparable limits of +/-1.96 sd from the mean differences. The relationship of the difference between the catheter data and the lab data to the independent variables (age, weight, gender, catheter tip, diagnosis, and signal quality index) was estimated by using the multiple regression analysis (version 9.1, SAS Institute, Cary, NC). All variables were eliminated. The Pearson correlation coefficient between lab-mixed venous oxygen saturation and oximetry catheter readings for measurements was 0.88. CONCLUSION: : In this limited number of patients, use of the PediaSat venous oximetry catheter was safe and had good agreement with co-oximetry-measured values.
机译:目的::评估从新的在线儿科血氧饱和度导管中心静脉血氧饱和度记录的准确性。设计::前瞻性观察研究。研究人群:2006年1月至2006年6月之间,加拿大多伦多病童医院儿科重症监护病房需要监测和/或治疗的18名儿科患者。方法和主要结果:在基线进行测量,然后每4-8小时进行一次。监测仪在基线进行体内校准,然后每天校准。最后五名患者也进行了监护仪的体外校准。当发生显着变化时,将更新血红蛋白值。最长采样时间为72小时(如果有指示)。在17例患者中进行了131次测量。每个受试者的配对测量数均不同(中位数为5)。由于违反协议,三名患者被排除在外,分析中还剩下113个测量值。导管值与实验室值的平均差为-1.01(中位数0)。四分位间距为5。两种方法的差异均按照Bland-Altman图均匀分布,一名患者的数据超出了平均差异的+/- 1.96 sd的可比范围。使用多元回归分析(9.1版,SAS Institute,Cary)估算导管数据和实验室数据之间的差异与自变量(年龄,体重,性别,导管尖端,诊断和信号质量指数)之间的关系。 ,NC)。消除了所有变量。实验室混合的静脉血氧饱和度与用于测量的血氧饱和度导管读数之间的皮尔逊相关系数为0.88。结论:在这一有限的患者中,使用PediaSat静脉血氧饱和度测定导管是安全的,并且与血氧饱和度测定值具有良好的一致性。

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