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雅培 Alinity 系统常见生化分析的儿科参考区间验证。

Pediatric reference interval verification for common biochemical assays on the Abbott Alinity system.

机构信息

CALIPER Program, Pediatric Laboratory Medicine, The Hospital for Sick Children, Toronto, ON, Canada.

Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada.

出版信息

Clin Chem Lab Med. 2021 May 19;59(9):1554-1562. doi: 10.1515/cclm-2021-0336. Print 2021 Aug 26.

Abstract

OBJECTIVES

The quality of clinical laboratory service depends on quality laboratory operations and accurate test result interpretation based on reference intervals (RIs). As new analytical systems continue to be developed and improved, previously established RIs must be verified. The Canadian Laboratory Initiative on Pediatric Reference Intervals (CALIPER) has established comprehensive RIs for many biomarkers on several analytical systems. Here, published CALIPER RIs for 28 chemistry assays on the Abbott ARCHITECT were assessed for verification on the newer Alinity system.

METHODS

An analytical validation was first completed to assess assay performance. CALIPER serum samples (100) were analyzed for 28 chemistry assays on the Alinity system. The percentage of results falling within published pediatric ARCHITECT reference and confidence limits was determined for each analyte. Based on Clinical and Laboratory Standards Institute (CLSI) guidelines, if ≥90% of test results fell within confidence limits of ARCHITECT assay RIs, they were considered verified.

RESULTS

Of the 28 assays assessed, 26 met the criteria for verification. Reference values for calcium and magnesium did not meet the criteria for verification with 87% and 35% falling within previously established ARCHITECT confidence limits, respectively. However, both assays could be verified using pediatric RIs provided in the Abbott Alinity package insert.

CONCLUSIONS

In this study, CALIPER ARCHITECT RIs were verified on the Alinity system for several chemistry assays. These data demonstrate excellent concordance for most assays between the Abbott ARCHITECT and Alinity systems and will assist in the implementation of the Alinity system in pediatric healthcare institutions.

摘要

目的

临床实验室服务的质量取决于质量实验室操作和基于参考区间(RIs)的准确测试结果解释。随着新的分析系统不断开发和改进,以前建立的 RIs 必须经过验证。加拿大儿科参考区间实验室倡议(CALIPER)已经为多个分析系统上的许多生物标志物建立了全面的 RIs。在这里,对 Abbott ARCHITECT 上的 28 项化学测定的已发表的 CALIPER RI 进行了评估,以验证较新的 Alinity 系统。

方法

首先完成分析验证以评估分析性能。对 Alinity 系统上的 28 项化学测定进行了 100 份 CALIPER 血清样本的分析。对于每个分析物,确定落在公布的儿科 ARCHITECT 参考和置信限内的结果百分比。根据临床和实验室标准协会(CLSI)指南,如果≥90%的测试结果落在 ARCHITECT 测定 RI 的置信限内,则认为它们已得到验证。

结果

在所评估的 28 项测定中,有 26 项符合验证标准。钙和镁的参考值不符合验证标准,分别有 87%和 35%的结果落在以前建立的 ARCHITECT 置信限内。但是,这两种测定都可以使用 Abbott Alinity 试剂盒插页中提供的儿科 RI 进行验证。

结论

在这项研究中,对 Alinity 系统上的几个化学测定进行了 CALIPER ARCHITECT RI 的验证。这些数据表明 Abbott ARCHITECT 和 Alinity 系统之间大多数测定的一致性非常好,这将有助于在儿科医疗机构中实施 Alinity 系统。

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