Abou El Hassan Mohamed, Stoianov Alexandra, Araújo Petra A T, Sadeghieh Tara, Chan Man Khun, Chen Yunqi, Randell Edward, Nieuwesteeg Michelle, Adeli Khosrow
CALIPER Program, Department of Pediatric Laboratory Medicine, The Hospital of Sick Children, Toronto, ON, Canada; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada.
CALIPER Program, Department of Pediatric Laboratory Medicine, The Hospital of Sick Children, Toronto, ON, Canada.
Clin Biochem. 2015 Nov;48(16-17):1151-9. doi: 10.1016/j.clinbiochem.2015.05.002. Epub 2015 May 13.
The CALIPER program has established a comprehensive database of pediatric reference intervals using largely the Abbott ARCHITECT biochemical assays. To expand clinical application of CALIPER reference standards, the present study is aimed at transferring CALIPER reference intervals from the Abbott ARCHITECT to Beckman Coulter AU assays.
Transference of CALIPER reference intervals was performed based on the CLSI guidelines C28-A3 and EP9-A2. The new reference intervals were directly verified using up to 100 reference samples from the healthy CALIPER cohort.
We found a strong correlation between Abbott ARCHITECT and Beckman Coulter AU biochemical assays, allowing the transference of the vast majority (94%; 30 out of 32 assays) of CALIPER reference intervals previously established using Abbott assays. Transferred reference intervals were, in general, similar to previously published CALIPER reference intervals, with some exceptions. Most of the transferred reference intervals were sex-specific and were verified using healthy reference samples from the CALIPER biobank based on CLSI criteria. It is important to note that the comparisons performed between the Abbott and Beckman Coulter assays make no assumptions as to assay accuracy or which system is more correct/accurate.
The majority of CALIPER reference intervals were transferrable to Beckman Coulter AU assays, allowing the establishment of a new database of pediatric reference intervals. This further expands the utility of the CALIPER database to clinical laboratories using the AU assays; however, each laboratory should validate these intervals for their analytical platform and local population as recommended by the CLSI.
CALIPER项目利用雅培ARCHITECT生化检测方法建立了一个全面的儿科参考区间数据库。为了扩大CALIPER参考标准的临床应用,本研究旨在将CALIPER参考区间从雅培ARCHITECT检测方法转移至贝克曼库尔特AU检测方法。
CALIPER参考区间的转移是根据临床和实验室标准协会(CLSI)指南C28-A3和EP9-A2进行的。新的参考区间通过使用来自健康CALIPER队列的多达100份参考样本进行直接验证。
我们发现雅培ARCHITECT和贝克曼库尔特AU生化检测方法之间具有很强的相关性,这使得之前使用雅培检测方法建立的绝大多数(94%;32项检测中的30项)CALIPER参考区间能够被转移。一般来说,转移后的参考区间与之前公布的CALIPER参考区间相似,但也有一些例外。大多数转移后的参考区间是针对特定性别的,并根据CLSI标准使用来自CALIPER生物样本库的健康参考样本进行了验证。需要注意的是,在雅培和贝克曼库尔特检测方法之间进行的比较并未对检测准确性或哪个系统更正确/准确做出假设。
大多数CALIPER参考区间可转移至贝克曼库尔特AU检测方法,从而能够建立一个新的儿科参考区间数据库。这进一步扩大了CALIPER数据库对使用AU检测方法的临床实验室的效用;然而,每个实验室应按照CLSI的建议,针对其分析平台和当地人群对这些区间进行验证。