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Dxh 900 hematology analyzer

Manufactured by Beckman Coulter
Sourced in United States

The DxH 900 Hematology Analyzer is a laboratory instrument designed for the automated analysis of blood samples. It performs a comprehensive evaluation of various blood cell parameters, providing clinicians with critical data for diagnostic and treatment purposes. The DxH 900 utilizes advanced technology to deliver accurate and reliable results, supporting healthcare professionals in their clinical decision-making.

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5 protocols using dxh 900 hematology analyzer

1

Biomarker Profiling of Blood Samples

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Blood samples were collected and tested for creatinine, estimated glomerular filtration rate, complement component C3 (C3), complement component C4 (C4), c-reactive protein (CRP), and lactate dehydrogenase using serum. Samples for sC5b-9, factor H, factor I, and midkine were collected in 2 mL EDTA tubes and placed immediately on ice. These samples were separated by centrifugation at 3,000 rpm at 4°C and the plasma frozen at −70°C until the assay was performed. Plasma sC5b-9, factor I, and midkine were all measured using colourimetric ELISA (Microvue sC5b-9 Plus Enzyme Immunoassay Quidel Corporation; Hycult Biotech; Cellmid Ltd.) as per manufacturer’s instructions. Factor H was assayed via nephelometry using an in-house method adapted from Sofat et al. [8] (link) (Siemens BN2, Binding Site anti-fH). Haemoglobin was measured photometrically at 525 nm on the DxH 900 Hematology Analyzer (Beckman Coulter, Inc., Brea, CA, USA). The platelet count was derived from the Coulter principle, also on the DxH 900 Hematology Analyzer (Beckman Coulter, Inc., Brea, CA, USA). CD46 was analysed using whole blood via flow cytometry (Beckman Coulter Navios Flow Cytometer, Life Sciences, Indianapolis, USA).
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2

Automated Hematology and Biomarker Analysis

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CBC with MDW was measured using the DxH 900 hematology analyzer (Beckman Coulter, Brea, California, USA). MDW is simultaneously calculated as the standard deviation of a set of monocyte cell volume values during CBC. CRP and PCT were measured using the AU5800 chemistry analyzer (Beckman Coulter) and the UniCel® DxI 800 immunoassay analyzer (Beckman Coulter), respectively.
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3

Sepsis Evaluation and Management Protocol

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Age, sex, weight, vital signs, and hourly urine output were all recorded since admission. Patients were classified according to their underlying medical history, site of infection, and vasopressors use. Glasgow, SOFA, and APACHE II scores were used to assess patient admission. We evaluated septic shock, mechanical ventilation, renal replacement therapy, length of ICU stay, and mortality within 28 days in all patients. Tests such as complete blood count, ALT, AST, total bilirubin, albumin, IL-6, procalcitonin, lactate, mineral panel, blood gas, baseline creatinine, and thrombomodulin were tested immediately upon admission. For the thrombomodulin test (Abcam brand), the blood sample was taken into a serum separator tube. After the formation of a clot, the blood sample was centrifuged at 2000 rpm for 10 minutes, then stored at −20 degrees Celsius or lower, avoiding repeating freezing and thawing for patient samples, which were tested by ELISA technique. We used Cobas® 8000 modular analyzer series - Roche Diagnostic and DxH 900 hematology analyzer - Beckman Coulter. The tests were conducted at the Department of Biochemistry and Hematology and Blood Transfusion Center of Hue Central Hospital, Vietnam.
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4

Comprehensive Blood Analysis Protocol

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Neutrophils were counted in EDTA-anticoagulated blood on the DxH 900 Hematology Analyzer (DxH900, DxH800 Beckman Coulter, Japan). The concentration of Zinc (Zn) in serum was measured using the reference atomic absorption (AA) method (PinAAcle 900, PerkinElmer). Vitamin D was detected by electrochemiluminescence immunoassay (ECLIA) and albumin by immunoturbidimetric assay (COBAS 6000,8000 Roche, Switzerland) in serum. The parameters related to haemostasis were examined in plasma. The Clauss method determined the fibrinogen level, and the concentration of D-dimer, and vWF activity were measured using an immunoturbidimetric method (ACL TOP 350 CTS, ACL TOP 500 CTS Werfen, Spain). According to the manufacturer (Cloud-Clone Corp.), the ELISA test determined TF concertation.
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5

Hematological Evaluation of Rabbits

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At the end of the experiment, ten rabbits per group were randomly selected to pick up the blood samples from the ear vein following the method described in [31] . The blood samples were divided into two subsamples. The first one was collected in a clean centrifuge tube without anticoagulant for serum separation of serum. It was then centrifuged at 2000 gravity for 20 min and stored at -20 °C for biochemical analyses. The second subsample was collected in EDTAcontaining tubes and used to assess hematological variables in the whole blood. The collected whole blood was used for determining the hemoglobin (Hb), red blood cells (RBCs), hematocrit (Hct), mean corpuscular hemoglobin concentration (MCHC), mean cell volume (MCV), mean corpuscular hemoglobin (MCH), platelets, mean platelet volume (MPV), platelet distribution width (PDW), and white blood cells (WBCs) using DxH 900 Hematology Analyzer (C23653 -DxH 900-2, Beckman Coulter, USA).
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