Verification of the Analytical Performance of the Serum Lipoprotein (a) Assay on the Abbott Alinity ci®: Experience of the Biochemistry Laboratory at Mohammed VI University Hospital of Oujda

The verification of analytical methods, as required by the ISO 15189 standard, allows for the evaluation and comparison of a method’s performance against predefined analytical objectives. This study focuses on verifying the assay of Lipoprotein (a) on the Abbott® Alinity analyzer, contributing to accreditation and quality improvement in the laboratory. The assay was performed using immunoturbidimetry. The evaluation of analytical performance (repeatability and intermediate precision) was conducted using two quality control levels, with results analyzed via BYG Informatique software. The obtained results show satisfactory repeatability with CV1 = 1.16% and CV2 = 0.44%. Intra-laboratory reproducibility is also satisfactory, with CV1 = 2.16% and CV2 = 1.29%, in line with the manufacturer's specifications.

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Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2025-03-30
DOI
https://doi.org/10.5281/zenodo.16926683
Primary Topic
Theoretical and Computational Physics
Type
article
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article

Verification of the Analytical Performance of the Serum Lipoprotein (a) Assay on the Abbott Alinity ci®: Experience of the Biochemistry Laboratory at Mohammed VI University Hospital of Oujda

Zenodo (CERN European Organization for Nuclear Research)
Theoretical and Computational Physics
article

Verification of the Analytical Performance of the Serum Lipoprotein (a) Assay on the Abbott Alinity ci®: Experience of the Biochemistry Laboratory at Mohammed VI University Hospital of Oujda

article en

Abstract

The verification of analytical methods, as required by the ISO 15189 standard, allows for the evaluation and comparison of a method’s performance against predefined analytical objectives. This study focuses on verifying the assay of Lipoprotein (a) on the Abbott® Alinity analyzer, contributing to accreditation and quality improvement in the laboratory. The assay was performed using immunoturbidimetry. The evaluation of analytical performance (repeatability and intermediate precision) was conducted using two quality control levels, with results analyzed via BYG Informatique software. The obtained results show satisfactory repeatability with CV1 = 1.16% and CV2 = 0.44%. Intra-laboratory reproducibility is also satisfactory, with CV1 = 2.16% and CV2 = 1.29%, in line with the manufacturer's specifications.

Zenodo (CERN European Organization for Nuclear Research)
Mohamed I University (MA)
Openalex Percentile: Top 42%
Theoretical and Computational Physics
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