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Ca 7000 system coagulation analyzer

Manufactured by Sysmex
Sourced in Japan

The CA-7000 System is a coagulation analyzer manufactured by Sysmex. It is designed to perform automated coagulation tests, including prothrombin time (PT), activated partial thromboplastin time (APTT), and other coagulation-related assays. The CA-7000 System is capable of processing multiple samples simultaneously and provides consistent and reliable results for clinical diagnostic purposes.

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2 protocols using ca 7000 system coagulation analyzer

1

Evaluating Hepatic Disease Severity

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Relevant demographic and clinical data were obtained from medical records. Routine biochemical tests including alanine aminotransferase (ALT), aspartate aminotransferase (AST), total protein, albumin, creatinine, total bilirubin, blood urea nitrogen, and HDL‐C were measured in a Hitachi 7600 Analyzer. Routine blood tests including monocytes and hemoglobin were measured in a Sysmex XE‐2100 Analyzer. Coagulation indices including international normalized ratio (INR) were measured in a Sysmex CA‐7000 System Coagulation Analyzer. Baseline MHR was calculated as monocytes (×109/L) divided by HDL‐C (mmol/L). Hepatic disease severity was evaluated by the Model for End‐Stage Liver Disease (MELD) score as previously described.18
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2

COVID-19 Biomarker Profiling in Blood

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Venous blood samples (4 mL) were obtained from all persons who tested positive to a COVID-19 PCR test and were divided into two aliquots: one aliquot was anticoagulated and divided into two test tubes. The first one was for hematological examinations of total leucocytes count (WBCs) using a Hema Screen 18-Automated Haematology Analyser (Hospitex Diagnostics, Sesto Fiorentino, Italy). The second test tube contained plasma separated for d-dimer with an Sysmex® CA-7000 system coagulation analyzer (Sysmex, Kobe, Japan), and detection of hs-C- reactive protein (CRP) with a Hitachi Model 7600 Series Automatic Analyzer (Hitachi High Technologies Corporation, Hitachi, Japan). The kits used in the experiments were d-dimer PLUS (Siemens Healthcare Diagnostics Products GmbH) and reagent kit for hs-CRP test (latex agglutination assay). Their reference values were 0.1417 (90% CL 0.00–0.55) µg/mL for d-dimer, and < 6 mg/L for hs-CRP, respectively.
From other aliquots of blood, samples could clot, and sera were then separated by centrifugation (3,500 rpm, 20 min, 25 °C) and stored at −20 °C for later biochemical determinations (serum creatinine and lactate dehydrogenase (LDH)). Plasma levels of total cholesterol, LDL-C, HDL-C, triacyclglycerols, and phospholipids were estimated using Synchron cx5 autoanalyzer (Beckman, USA) and calculated with the Friedewald formula.
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