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Published on: March 22, 2022
Different Analytical Modes on Automatic Hematology Analyzers for Testing Quality Control Materials and Commutability
Bingshuang Ren1, Ya Cheng1, Hongping Ba1
1Department of Clinical Laboratory, Wuhan Center for Clinical Laboratory, Wuhan, China.
International Journal of Laboratory Hematology
|July 22, 2026
Summary
Quality control materials for hematology analyzers show variable performance. Differences in sampling and measurement modes, and matrix effects impact results, affecting diagnostic accuracy.
Area of Science:
- Clinical Hematology
- Analytical Chemistry
- Laboratory Medicine
Background:
- Accurate complete blood count (CBC) results are crucial for diagnosing and monitoring hematological disorders.
- Automated hematology analyzers require robust quality control (QC) for reliable CBC results.
- The commutability of commercial hematology QC materials (HQCM) and the impact of analytical modes are not fully understood.
Purpose of the Study:
- To evaluate the analytical performance of two HQCM brands (Bioyuan and XC).
- To assess the commutability of these HQCMs across two different hematology analyzers (Sysmex XN-1000 and Mindray BC-6800 Plus).
- To investigate the influence of measurement and sampling modes on QC results.
Main Methods:
- Systematic comparison of results between QC and patient sample measurement modes.
- Comparison of manual and autoloader sampling modes on the Mindray analyzer.
- Commutability assessment using clinical patient samples as a reference.
Main Results:
- Differences between QC and sample modes were analyzer and parameter-specific (e.g., WBC, HCT, MCV on Sysmex).
- Manual vs. autoloader sampling on the Mindray analyzer caused significant parameter differences.
- Neither HQCM brand was universally commutable for key parameters (WBC, RBC, HGB, PLT), especially at extreme concentrations, indicating matrix effects.
Conclusions:
- Analytical variables (sampling, measurement modes) and material-dependent matrix effects significantly influence QC results and interpretation.
- Laboratories need to standardize protocols and carefully select QC materials for reliable hematology testing and quality assurance.
- Further research is needed for developing more commutable reference materials and multicenter validation.
