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Advia 2400 system

Manufactured by Siemens

The Advia 2400 system is a fully automated clinical chemistry analyzer designed for high-volume laboratory testing. It offers automated sample processing, reagent handling, and result reporting capabilities. The system is capable of performing a wide range of routine clinical chemistry tests, including tests for liver function, kidney function, and metabolic markers. The Advia 2400 system is designed to provide accurate and reliable results to support clinical decision-making.

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Lab products found in correlation

3 protocols using advia 2400 system

1

Analyzing HIL Index in Patient Admissions

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In August 2012, three HIL index results were analyzed according to patient-admission type, age, sex, and proportion of HIL alert indices. The HIL data obtained from the Advia 2400 system (Siemens Healthcare Diagnostics) were combined with those from the Modular DPE system (Roche Diagnostics), because the analytes were measured in the Advia 2400 system (Siemens Healthcare Diagnostics) using Roche reagents.
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2

Automated Serum Interference Detection

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The HIL index was measured automatically by the ADVIA-2400 system (Siemens Healthcare Diagnostics). The HIL index were measured automatically by the ADVIA-2400 system (Siemens Healthcare Diagnostics). The serum HIL index feature of the ADVIA-2400 chemistry system can detect and produce a qualitative estimate absorbance value of three sets of wavelengths: hemolysis (λ1 = 571 nm, λ2 = 596 nm), lipemia (λ1 = 658 nm, λ2 = 694 nm), and icterus (λ1 = 478 nm, λ2 = 505 nm) [11 (link)]. The concentration ranges of HIL index value were set as follows: hemoglobin, < 45 mg/dL (-), 45–140 mg/dL (+), 140–235 mg/dL (++), 235–445 mg/dL (+++) and > 445 mg/dL (++++); lipemia, < 120 mg/dL (-), 120~245 mg/dL (+), 245~495 mg/dL (++), 495–995 mg/dL (+++) and > mg/dL 995 (++++); icterus, < 1.60 mg/dL (-), 1.60–6.50 mg/dL (+), 6.50–15.0 mg/dL (++), 15.0–28.0 mg/dL (+++) and > 28.0 mg/dL (++++). Clinical and Laboratory Standards Institute (CLSI) document C56A guides the use of serum indices to measure HIL interference and recommends the selection of assay-specific HIL cut-offs, above which HIL interferences will affect results. The HIL index in the study is defined as the lowest concentrations of HIL that interfere with chemical analyses, yielding a bias >10%.
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3

Plasma ELA Measurement and Lipid Profile Analysis

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Peripheral venous blood was drawn from all subjects in the early morning after hospitalization and stored in EDTA anticoagulation vacuum tubes. Plasma samples were immediately centrifuged at 3000 g for 10 min and kept at -80℃ for measurement.
The plasma ELA concentration was measured using an enzyme-linked immunosorbent assay kit (S-1508.0001, Peninsula Laboratories International, San Carlos, CA) following the protocol. The kit used a double-antibody sandwich enzyme-linked immunosorbent assay to determine the level of ELA in the samples.
Serum triglycerides (TG), total cholesterol (TC), high- density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), lipoprotein a [LP(a)], and indexes of liver and renal function were measured using Siemens-ADVIA 2400 system. Serum cTnI levels were detected by chemiluminescence immunoassay. CK-MB and BNP were measured by chemiluminescence assay.
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