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仪器实验室ACL TOP新型分析前模块的技术评估:推进止血检测自动化

Technical evaluation of the novel preanalytical module on instrumentation laboratory ACL TOP: advancing automation in hemostasis testing.

作者信息

Lippi Giuseppe, Ippolito Luigi, Favaloro Emmanuel J

机构信息

1Laboratory of Clinical Chemistry and Hematology, Department of Laboratory Medicine, Academic Hospital of Parma, Parma, Italy.

出版信息

J Lab Autom. 2013 Oct;18(5):382-90. doi: 10.1177/2211068213491747. Epub 2013 Jun 4.

Abstract

Automation in hemostasis testing is entering an exciting and unprecedented phase. This study was planned to assess the performance of the new preanalytical module on the hemostasis testing system Instrumentation Laboratory ACL TOP. The evaluation included interference studies to define reliable thresholds for rejecting samples with significant concentrations of interfering substances; within-run imprecision studies of plasma indices on four different interference degrees for each index; comparison studies with reference measures of hemolysis index, bilirubin, and triglycerides on clinical chemistry analyzers; and calculation of turnaround time with and without automatic performance of preanalytical check. The upper limits for sample rejection according to our interference studies were 3.6 g/L for hemoglobin, 13.6 mg/dL for bilirubin, and 1454 mg/dL for triglycerides. We found optimal precision for all indices (0.6% to 3.1% at clinically relevant thresholds) and highly significant correlations with reference measures on clinical chemistry analyzers (from 0.985 to 0.998). The limited increase of turnaround time (i.e., +3% and +5% with or without cap-piercing), coupled with no adjunctive costs over performance of normal coagulation assays, contribute to make the automatic check of plasma indices on ACL TOP a reliable and practical approach for improving testing quality and safeguarding patient safety.

摘要

止血检测自动化正进入一个令人兴奋且前所未有的阶段。本研究旨在评估止血检测系统仪器实验室ACL TOP上新型分析前模块的性能。评估包括干扰研究,以确定拒绝含有高浓度干扰物质样本的可靠阈值;对每个指标在四种不同干扰程度下血浆指标的批内不精密度研究;与临床化学分析仪上溶血指数、胆红素和甘油三酯参考测量值的比较研究;以及分析前检查自动执行和不自动执行情况下周转时间的计算。根据我们的干扰研究,样本拒收的上限为血红蛋白3.6 g/L、胆红素13.6 mg/dL和甘油三酯1454 mg/dL。我们发现所有指标均具有最佳精密度(在临床相关阈值下为0.6%至3.1%),并且与临床化学分析仪上的参考测量值具有高度显著的相关性(从0.985至0.998)。周转时间的有限增加(即带帽穿刺和不带帽穿刺分别增加3%和5%),再加上与正常凝血检测相比没有额外成本,使得在ACL TOP上自动检测血浆指标成为提高检测质量和保障患者安全的可靠且实用的方法。

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