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Consistency Analysis of 3 Detection Systems for Measuring Serum C-Reactive Protein
Xueyan Chen1, Chuanyihong Huang1, Weichuan Zhong1
1Department of Clinical Laboratory, The People's Hospital of Longhua Shenzhen, Shenzhen, Guangdong, China (mainland).
This study compared three C-reactive protein (CRP) detection systems. The Mindray BC-5390 and BC-6800 showed consistent CRP measurements, while the Johnson Vitros5600 had deviations.
Area of Science:
- Clinical chemistry
- Laboratory diagnostics
- Biomedical instrumentation
Background:
- C-reactive protein (CRP) is a crucial biomarker in clinical diagnostics.
- Variability in CRP measurements across different analytical platforms necessitates consistency evaluation.
- Turbidimetry is a common method for serum CRP detection.
Purpose of the Study:
- To assess the inter-instrument consistency of serum C-reactive protein (CRP) measurements.
- To compare CRP detection using Mindray BC-5390, Mindray BC-6800, and Johnson Vitros5600 systems.
- To evaluate the interchangeability of Mindray BC-5390 and BC-6800 for routine blood tests.
Main Methods:
- Comparative analysis of CRP measurements from 847 patients.
- Utilized turbidimetric assays on Mindray BC-5390, Mindray BC-6800, and Johnson Vitros5600 analyzers.
- Employed Pearson correlation, Passing-Bablok, and weighted Deming analyses for consistency assessment.
Main Results:
- Significant differences in CRP values were observed among the three tested instruments (P<0.001).
- Mindray BC-5390 demonstrated high consistency with both BC-6800 (R=0.994) and Vitros5600 (R=0.983).
- A constant deviation was noted between BC-6800 and Vitros5600 CRP measurements (R=0.994); BC-5390 and BC-6800 were interchangeable for routine blood tests.
Conclusions:
- The Mindray BC-5390, BC-6800, and Johnson Vitros5600 exhibit varying levels of consistency for CRP detection.
- The BC-5390 and BC-6800 analyzers are interchangeable for routine blood tests.
- Findings provide valuable reference data for selecting appropriate CRP detection instruments in clinical settings.
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