Evidence map›Paper›PMID 37324112›Full record

ArticleBiochemia medica2023

Analytical verification of the Dymind D7-CRP automated analyser.

Merima Čolić, Bojana Magdić, Monika Kolundžić, Jasna Leniček Krleža

Abstract read
In one paragraph

Article in Biochemia medica, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Merima ČolićDepartment of Laboratory Diagnostics, Children's Hospital Zagreb, Zagreb, Croatia.
Bojana MagdićDepartment of Laboratory Diagnostics, Children's Hospital Zagreb, Zagreb, Croatia.
Monika KolundžićDepartment of Laboratory Diagnostics, Children's Hospital Zagreb, Zagreb, Croatia.
Jasna Leniček KrležaDepartment of Laboratory Diagnostics, Children's Hospital Zagreb, Zagreb, Croatia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The aim of this study was to perform a verification of the Dymind D7-CRP automated analyser and compare it with established analysers. Materials and methods: Analytical verification included estimation of repeatability, between run precision, within-laboratory precision, and bias in control samples with low, normal and high levels. The acceptance criteria for analytical verification were defined using the European Federation of Clinical Chemistry and Laboratory Medicine (EFLM) 2019 Biological Variation Database. Method comparison between the Dymind D7-CRP and the Sysmex XN1000 for haematological parameters and the Dymind D7-CRP and the Beckman Coulter AU680 for CRP values was performed on 40 patient samples. Results: Analytical verification criteria were adequately met with the exception of monocyte count for repeatability and within-laboratory precision (13.4% and 11.5%, respectively, acceptance criteria 10.1%) and measurement uncertainty (23.0, acceptance criteria 20.0%) at low level, eosinophil count for BIAS at the low level (37.7%, acceptance criteria 25.2%), basophil count (BAS) for BIAS at the high level (14.2%, acceptance criteria 10.9%), and mean platelet volume (MPV) for repeatability (4.2% and 6.8%), between run precision (2.2% and 4.7%), within-laboratory precision (4.0% and 7.3%) (acceptance criteria 1.7%), and measurement uncertainty (8.0 and 14.6%, acceptance criteria 3.4%) at both the low and high concentrations. Method comparison showed no clinically significant constant or proportional differences for all parameters except BAS and MPV. Conclusion: The analytical verification of the Dymind D7-CRP showed adequate analytical characteristics. The Dymind D7-CRP can be used interchangeably with the Sysmex XN-1000 for all parameters tested, except BAS and MPV, and with the Beckman Coulter AU-680 for the determination of CRP.

Indexed as

Mean Platelet VolumeHumansLeukocyte Countblood cell countC-reactive proteinhaematologyverification

Identifiers

PMID37324112
PMCPMC10231769

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