Coagulation parameters were analyzed using a Sysmex CS-2400 coagulation analyzer (Sysmex Corporation, Kobe, Japan). D-dimer testing was performed using a latex-enhanced photometric immunoassay (Siemens, Marburg, Germany) and the result was expressed in μg/ml FEU. The laboratory reference interval was 0–0.5 μg/ml FEU. The PT testing was performed using Thromborel S and the APTT testing was performed using Actin FSL, both from Siemens. The laboratory reference interval for PT and APTT was 10–13 s and 20–31 s, respectively.
Latex enhanced photometric immunoassay
Manufactured by Siemens
Sourced in Germany, Japan
Latex-enhanced photometric immunoassay is a laboratory equipment used for the quantitative determination of analytes in biological samples. It utilizes the principles of antigen-antibody reactions and photometric detection to measure the concentration of target analytes.
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Lab products found in correlation
2 protocols using latex enhanced photometric immunoassay
1
Coagulation Biomarker Analysis
2
Adverse Outcomes in COVID-19: D-dimer and FBG
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In total, 2469 patients had laboratory examinations within 24 hours of admission and were categorized into either the normal (<0.50 mg/L) or the high (≥0.50 mg/L) D-dimer group according to the laboratory reference. D-dimer was determined on CS5100 automatic coagulation analyzer (Sysmex, Kobe, Japan) by using a latex-enhanced photometric immunoassay (Siemens, Marburg, Germany).12 (link) And to specifically assess the combined effects of FBG and D-dimer on adverse in-hospital outcomes, we also divided the patients into two groups with a cut point of 7.00 mmol/L. FBG test was conducted by a laboratory plasma measurement.
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