Performance evaluation of alternate ESR measurement method using BC-780 automated hematology analyzer: a comparison study with the Westergren reference method

Author:

Prompetchara Eakachai1ORCID,Parnsamut Chalisa1,Wangviwat Nathawit2,Pitakpolrat Patrawadee1,Chaiwong Kwanlada2,Limpornpukdee Orakarn1,Tanticharoenkarn Surapat2,Ketloy Chutitorn1

Affiliation:

1. Department of Laboratory Medicine, Faculty of Medicine , Chulalongkorn University , Bangkok , Thailand

2. Division of Laboratory Medicine, King Chulalongkorn Memorial Hospital , Bangkok , Thailand

Abstract

Abstract Objectives Implementation of alternate erythrocyte sedimentation rate (ESR) measurement method is increasing worldwide due to its various advantages. In this study, we aim to evaluate the analytical performance of the BC-780 automated hematology analyzer in measurement of ESR value. Methods Analyzer performance including precision study, carryover, sample stability and potential interferences are examined. Samples with ESR values spanning the whole analytical ESR range are included for method comparison study. Samples with different hematocrit (Hct) and mean corpuscular volume (MCV) values are also analyzed and compared with the results obtained from the Westergren reference method. Results Precisions and carryover results are consistent with the manufacturers’ claim. ESR values do not change significantly in the samples stored at 2–8 °C for 24 h (h) or at room temperature (RT) for 8 h, but significantly decreased (p<0.001) when stored at RT for 24 h. Significant increase in ESR value is documented in samples that are hemolyzed (hemoglobin concentration ranged from 1.28–6.01 g/L) (p=0.010) or lipemic (triglyceride above 4.75 mmol/L) (p=0.001). Method comparison study yields a proportional difference with a regression equation=3.08+ 0.98x. Bland–Altman analysis shows a mean absolute bias of 3.12 mm. The obtained absolute mean biases are below 5 mm in all analytical categories except for the group where MCV>100 fL. Conclusions Most tested parameters met the manufacturer’s specifications and were comparable to the reference method. Despite the presence of positive bias, it falls within acceptable criteria. Extensive validation against potential interferences such as hemolysis/lipemia is still necessary in future.

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

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