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35 protocols using automated hematology analyzer

1

Hematological Analysis of EDTA Blood

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Hematological results of EDTA-anticoagulant-treated peripheral blood were
analyzed by automated hematology analyzer (Sysmex, Japan), and hemoglobin
components and levels were performed by using capillary electrophoresis (CE;
Serbia, Paris, France).
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2

Automated Hematological Hemoglobin Analysis

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Hemoglobin level of each blood sample in EDTA tube was determined using an automated hematological analyzer (Sysmex Automated Hematology Analyzer, Kobe, Japan, XP-300, model no.: AC580857).
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3

Serum 25(OH)D and Immunological Biomarkers

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Measurements of serum 25(OH)D were performed by the enzyme-linked immunosorbent assay ELISA using DIAsource 25OH vitamin D Total ELISA kit (Louvain-la Neuve, Belgium). The analysis kit detection limit was defined as the apparent concentration two standard deviations below the average OD at zero binding was 1,5 ng/mL. Analysis of data was performed according to vitamin D content: deficiency < 20 ng/ml (< 50 nmol/L), insufficiency 20–30 ng / ml (50–75 nmol/L), normal amount 30–50 ng/ml (75–125 nmol/L) [34 –37 ].
Blood eosinophils evaluation was performed with an automated hematology analyzer (Sysmex, Kobe, Japan).
Measurements of total IgE level in serum were performed by ELISA using commercial test kit (ELISA, Bio-Clin-Inc., St. Louis, USA).
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4

Serological and Biochemical Profiling for Liver Biopsy

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The routine laboratory tests were performed the day before liver biopsies. The serological markers of HBV were detected with ELISA kits (Abbott, Wiesbaden, Germany). The HBV DNA was quantified by real-time PCR (Applied Biosystems, Foster City, USA), with the detection limit 500 copies/ml. The parameters including ALT and AST were measured by automation biochemistry analyzer (Hitachi, Tokyo, Japan). Platelet count was detected with automated hematology analyzer (Sysmex, Kobe, Japan). The calculation formulas of APRI and FIB-4 as follows: (1) APRI= (AST/ULN of AST)/platelet count×100; (2) FIB-4= (age × AST)/ (platelet count × (ALT)1/2).
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5

Stroke Biomarkers and Outcomes

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The variables collected included demographics (age and gender), medical histories (hypertension, atrial fibrillation, diabetes, hyperlipidemia, and coronary heart diseases), the National Institute of Health Stroke Scale (NIHSS) score, the Alberta Stroke Program Early CT Score (ASPECTS), hemorrhagic transformation (30 (link)), reperfusion therapy method, and the Trial of Org 10172 in Acute Stroke Treatment (TOAST) classification (31 (link)). Successful recanalization after endovascular therapy was defined as a modified Thrombolysis in Cerebral Infarction grading system score of 2b or 3 (32 (link)). Blood samples were collected for laboratory measurements in the emergency department. White blood cell (WBC) counts, including absolute numbers of neutrophils were measured using an automated hematology analyzer (Sysmex, Kobe, Japan). Serum albumin levels were determined with an Olympus AU-5400 automatic analyzer (Olympus, Tokyo, Japan).
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6

Hematological Evaluation via Automated Analyzer

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Hematological parameters were determined with an automated hematology analyzer (Sysmex, Japan), and hemoglobin analysis was performed with either high-performance liquid chromatography (Bio-Rad, USA) or capillary electrophoresis (Sebia, France and Helena, USA).
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7

Routine Blood Test Protocol

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Peripheral venous blood samples were collected at the time of admission. Routine blood tests, including the counts of red and white blood cells (RBC and WBC), leukocyte subtypes, hematocrit (HCT), hemoglobin (Hb), and platelet (PLT), were performed using an automated hematology analyzer (Sysmex Corporation, Kobe, Japan).16 Collected laboratory data included PLT, LYM, and neutrophil counts (NEU), serum urea, creatinine (Cr) and albumin levels, erythrocyte sedimentation rate (ESR), and CRP.
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8

Comprehensive Hematological and Cytokine Analysis

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A total of 24 clinical hematological parameters were determined using an Automated Hematology Analyzer (Sysmex, Tokyo, Japan). The serum levels of four cytokines, including interleukin-1β (IL-1β), IL-6, IL-10, and tumor necrosis factor-α (TNF-α), were quantified using enzyme-linked immunosorbent assay (ELISA) kits (Cat. No. ml037361; Cat. No. ml064292; Cat. No. ml037371; Cat. No. ml002859; Shanghai Enzyme-linked Biotechnology Co., Ltd., Shanghai, China). The assay was conducted on 6 biological replicates per treatment group, with each measurement repeated 3 times (technical replicates).
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9

Hematological Analysis of Mice

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At the end of the experiment (21 days), whole blood was obtained from the orbit of mice. Red blood cell (RBC), hemoglobin (HGB), hematocrit (HCT), white blood cell (WBC), platelet (PLT), and neutrophil (NEUT) were subsequently measured with an automated hematology analyzer (Sysmex, Shanghai, China). Criteria for HAPC diagnosis: HGB ≥ 210 g/L [27 (link)].
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10

Blood Sampling and Biochemical Analysis

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Blood samples were taken at the beginning of the study and at the end of the 3rd month, following overnight fasting of at least 10 h, in the morning. A Sysmex automated hematology analyzer was used for the whole blood counts. HbA1c levels were determined by high-performance liquid chromatography with a TOSOH. Serum vitamin B12 level was studied with electrochemiluminescence immunoassay method (Beckman Coulter UniCel D×l 600).
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