Harmonization of units and reference intervals of plasma proteins: state of the art from an External Quality Assessment Scheme

Author:

Secchiero Sandra1,Sciacovelli Laura2ORCID,Plebani Mario23ORCID

Affiliation:

1. Centre of Biomedical Research – Department of Laboratory Medicine , University-Hospital of Padova , Via Giustiniani, 2 , 35128 Padova , Italy , Phone: +39-049-821-4490, Fax: +39-049-821-7916

2. Centre of Biomedical Research , University-Hospital of Padova , Padova , Italy

3. Department of Laboratory Medicine , University-Hospital of Padova , Padova , Italy

Abstract

Abstract Background: The need to harmonize laboratory information is particularly intense in the field of plasma proteins, considering their clinical impact and relevance in monitoring diseases. Methods: We evaluated units and reference intervals (RIs) utilized by participants of the External Quality Assessment Scheme (EQAS) for plasma proteins of the Centre of Biomedical Research. Moreover, we evaluated inter-laboratory analytical variability from 2001 to 2017. Results: The census of participants’ units employed in 2017 showed that for albumin (ALB), ~66% of laboratories still used dL instead of L, and for most other proteins, ~70% still expressed the results in mg/dL. Laboratories primarily used the RIs reported in the packaging inserts of their analytical systems, but for each protein, there was a wide variability of RIs, also among laboratories using the same analytical method. Mean CVs% of the 13 certified proteins in the last five EQA cycles ranged from 3.8% of haptoglobin (HPT) to 12.4% of α1-antitrypsin (AAT) and decreased from 2001 to 2017 for most of them, in particular for C3, ALB, α2-macroglobulin (A2M), HPT and transferrin (TRF). Conclusions: In the face of a reduction in inter-laboratory variability for a lot of proteins, there has not been a substantial change in the units and in the RIs used by the participants. To change old habits is difficult and requires coordination and collaboration. The EQAS plays an important role in the assessment and monitoring of all elements that contribute to the formulation of laboratory information and may be useful to contribute to their harmonization.

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

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