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i-STAT便携式临床分析仪的分析评估及非实验室医护人员的使用

Analytical evaluation of i-STAT Portable Clinical Analyzer and use by nonlaboratory health-care professionals.

作者信息

Jacobs E, Vadasdi E, Sarkozi L, Colman N

机构信息

Department of Pathology, Mount Sinai School of Medicine, New York, NY 10029-6574.

出版信息

Clin Chem. 1993 Jun;39(6):1069-74.

PMID:8504539
Abstract

We evaluated the performance of the i-STAT Portable Clinical Analyzer, a hand-held instrument that, with its current cartridge, analyzes for electrolytes, urea nitrogen, glucose, and hematocrit in approximately 60 microL of whole blood in approximately 90 s. Accuracy, imprecision, and linearity studies were performed with aqueous controls and standards and by split-sample analysis. Intrarun imprecision (CV) ranged from 0.34% to 3.97%. Total imprecision over a 2-month period ranged from 0.42% to 4.83%, with urea nitrogen and glucose analyses generating the higher values. Patients' results from the Portable Clinical Analyzer correlated well with those obtained for whole blood or plasma by the Nova Stat Profile 5, the Beckman Synchron CX3, or the Technicon H1 Hematology Analyzer, with Sylx values < 0.2 mmol/L for potassium; < 1.5 mmol/L for sodium, glucose, and urea nitrogen; < 2.4 mmol/L for chloride, and < 2.4% for hematocrit. We also ascertained imprecision and accuracy of the system placed in a cardiothoracic intensive-care unit and operated by nurses. There were no significant differences in either the imprecision or accuracy of the system in this setting. We conclude that operator technique is not a factor in the analytical performance of the system and that it can be used by nonlaboratorians with a high degree of confidence that reliable results will be obtained.

摘要

我们评估了i-STAT便携式临床分析仪的性能,这是一种手持式仪器,使用其当前的检测卡,可在约90秒内对约60微升全血中的电解质、尿素氮、葡萄糖和血细胞比容进行分析。采用水性对照品和标准品并通过拆分样本分析进行了准确性、不精密度和线性研究。批内不精密度(CV)范围为0.34%至3.97%。在2个月期间的总不精密度范围为0.42%至4.83%,其中尿素氮和葡萄糖分析的数值较高。便携式临床分析仪检测的患者结果与通过Nova Stat Profile 5、贝克曼Synchron CX3或Technicon H1血液分析仪对全血或血浆检测获得的结果相关性良好,钾的Sylx值<0.2 mmol/L;钠、葡萄糖和尿素氮的Sylx值<1.5 mmol/L;氯的Sylx值<2.4 mmol/L,血细胞比容的Sylx值<2.4%。我们还确定了放置在心胸重症监护病房并由护士操作的该系统的不精密度和准确性。在这种情况下,该系统的不精密度或准确性均无显著差异。我们得出结论,操作人员技术不是该系统分析性能的影响因素,非实验室人员可以高度自信地使用该系统并获得可靠结果。

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