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Can the blood gas analyser results be believed? A prospective multicentre study comparing haemoglobin, sodium and potassium measurements by blood gas analysers and laboratory auto-analysers

机译:血气分析仪是否可以相信? 血气分析仪和实验室自动分析仪比较血红蛋白,钠和钾测量的预期多期面研究

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Blood gas analysers are point-of-care testing devices used in the management of critically ill patients. Controversy remains over the agreement between the results obtained from blood gas analysers and laboratory auto-analysers for haematological and biochemistry parameters. We conducted a prospective analytical observational study in five intensive care units in Western Australia, in patients who had a full blood count (FBC), urea, electrolytes and creatinine (UEC), and a blood gas performed within 1 h of each other during the first 24 h of their intensive care unit admission. The main outcome measure was to determine the agreement in haemoglobin, sodium, and potassium results between laboratory haematology and biochemistry auto-analysers and blood gas analysers. A total of 219 paired tests were available for haemoglobin and sodium, and 215 for potassium. There was no statistically significant difference between the results of the blood gas and laboratory auto-analysers for haemoglobin (mean difference -0.35 g/L, 95% confidence interval (CI) -1.20 to 0.51, P=0.425). Although the mean differences between the two methods were statistically significant for sodium (mean difference 1.49 mmol/L, 95% CI 1.23-1.76, P<0.0001) and potassium (mean difference 0.19 mmol/L, 95% CI 0.15-0.24, P<0.0001), the mean biases on the Bland-Altman plots were small and independent of the magnitude of the measurements. The two methods of measurement for haemoglobin, sodium and potassium agreed with each other under most clinical situations when their values were within or close to normal range suggesting that routine concurrent blood gas and formal laboratory testing for haemoglobin, sodium and potassium concentrations in the intensive care unit is unwarranted.
机译:血气分析仪是用于危重病患者的管理的护理点测试装置。争议仍然是从血气分析仪和实验室自动分析仪获得的结果之间的协议,用于血液化学和生物化学参数。我们在西澳大利亚的五个重症监护病房中进行了一项前瞻性分析观察研究,该研究在西澳大利亚患者中进行了全血统(FBC),尿素,电解质和肌酐(UEC),以及在彼此的1小时内进行的血气首先24小时的重症监护室入学。主要结果措施是确定血红蛋白,钠和钾的协议,从实验室血液学和生物化学自动分析仪和血气分析仪之间产生。血红蛋白和钠共有219个配对试验,215次获得钾。血液气体和实验室自动分析仪的结果没有统计学显着差异(平均差异-0.35g / L,95%置信区间(CI)-1.20至0.51,P = 0.425)。虽然两种方法之间的平均差异对于钠(平均差1.49mmol / L,95%Ci 1.23-1.76,P <0.0001)和钾(平均差异0.19mmol / L,95%CI 0.15-0.24,P <0.0001),Bland-Altman图上的平均偏差小并且与测量的幅度无关。血红蛋白,钠和钾的两种测量方法在大多数临床情况下彼此同意,当它们的值在正常范围内或接近正常范围内,表明常规并发血液和重症监护中的血红蛋白,钠和钾浓度的正式实验室试验单位是无理的。

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