The comparison between the results of turbidimetric method for C-Reactive Protein measurement using different instruments
ACTA PHARMACEUTICA SCIENCIA, cilt.62, sa.4, ss.778-792, 2024 (Scopus)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 62 Sayı: 4
- Basım Tarihi: 2024
- Doi Numarası: 10.23893/1307-2080.aps6251
- Dergi Adı: ACTA PHARMACEUTICA SCIENCIA
- Derginin Tarandığı İndeksler: Scopus, EMBASE
- Sayfa Sayıları: ss.778-792
- Açık Arşiv Koleksiyonu: AVESİS Açık Erişim Koleksiyonu
- İstanbul Medipol Üniversitesi Adresli: Evet
Özet
C-reactive protein (CRP) is considered a marker of chronic inflammation and also
a mediator of the atherosclerotic process. The purpose of this study is to compare
the results of three quantitative immunoturbidimetric method used to measure
CRP amounts in patient serum samples in a clinical laboratory. Freshly collected
patient serums (n=100) were analyzed with 2 different analyzer (Siemens Advia
1800 and Abbott Architect C 8000) and 3 different reagents (Siemens, Sentinel,
Archem). In order to determine whether they provide equivalent results in terms
of traceability, the EP09-A3 guideline was used, and comparisons were evaluated
within the scope of this standard. Limit of quantification (LoQ), Inter27 assay,
Intra-assay, precision studies have been done. The relationship between these
three reagents was determined by regression analysis and Bland Altman method. Regression coefficiencies between these three methods were found: ArchemSentinel r2
=0,9987, Archem – Siemens r2
=0,9986 and Sentinel – Siemens
r2
=0,9984. Regression equations between Archem-Sentinel y= - 0,1359+1.0035x,
between Archem- Siemens y= -0,02646+1,002x and between Sentinel – Siemens
y=0,1326+0,9978x were found. For the first time in the literature, our results indicated that these three immunoturbidimetric methods were compatible.