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Vitros 950

Manufactured by Ortho Clinical Diagnostics
Sourced in United States, Japan

The Vitros 950 is a clinical chemistry analyzer designed for in vitro diagnostic testing. It is capable of performing a variety of routine and specialty tests on patient samples. The Vitros 950 utilizes a unique slide technology to provide accurate and reliable results. Its core function is to analyze and measure different analytes in biological samples, such as blood or urine, to aid in the diagnosis and management of various medical conditions.

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10 protocols using vitros 950

1

Assessing Diabetes Risk Factors

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The primary cross-sectional outcomes in this analysis were fasting glucose, homeostatic model assessments of beta cell function (HOMA-β) and insulin resistance (HOMA-IR), and hemoglobin A1c (A1c). Fasting glucose and insulin concentrations were measured on a Vitros 950 or 250 Ortho-Clinical Diagnostics analyzer using standard procedures that met the College of American Pathologists accreditation requirement (Carpenter et al., 2004 (link)). A HPLC system (Tosoh Corp) was used to measure A1c. Insulin resistance and β-cell function were estimated using the following formula: HOMA-IR = (fasting plasma glucose [millimoles per liter] × fasting plasma insulin [milliunits per milliliter]) / 22.5 and HOMA-β = (20 × fasting plasma insulin) / (fasting plasma glucose − 3.5)% (Matthews et al., 1985 (link)). The primary longitudinal outcome was incident diabetes developed by Exam 3 among those free of diabetes at Exam 1. Diabetes was defined as HbA1c ≥ 6.5 % (48 mmol/mol), fasting blood glucose ≥ 126 mg/dL, taking T2DM medications and/or with a self-reported physician diagnosis (American Diabetes Association, 2013 (link)). The time of incident diabetes was defined as the midpoint between the last examination without diabetes and the examination at which diabetes developed among persons without diabetes at baseline.
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2

Renal Function and Troponin Levels

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Blood samples were drawn on admission (Median time from symptom onset to blood sampling: 16 (8–20) hours), as previously described [5 (link)]. Creatinine levels were measured on a Vitros 950 analyzer (Ortho Clinical Diagnostics) and the glomerular filtration rate (eGFR) was estimated on the Chronic Kidney Disease (CKD) EPI formula [12 (link)]. Normal or weakly impaired renal function, moderate and severe renal dysfunction were defined as eGFR > 60 mL/min, 30–60 mL/min and < 30 mL/min respectively. Plasma troponin Ic peak was assessed by sampling every eight hours during the first two days after admission (Dimension Vista Intelligent Lab System, Siemens).
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3

Fasting Plasma Glucose Measurement Protocol

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At baseline, fasting plasma glucose was measured by the glucose oxidase colorimetric method using a Vitros 950 or 250 (Ortho Clinical Diagnostics analyzer; Ortho Clinical Diagnostics, Raritan, NJ, USA). Ideal glucose was defined as an untreated fasting plasma glucose of <100 mg/dL; intermediate glucose was defined as a fasting plasma glucose of 100–125 mg/dL untreated or if treated to goal (<100 mg/dL); and poor was defined as a fasting plasma glucose of ≥126 mg/dL [1 (link)].
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4

Plasma Cholesterol and Glucose Measurement

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The total cholesterol of plasma samples obtained from the mice was measured enzymatically using commercial kits (Wako Chemicals, Richmond, VA, USA). The plasma glucose concentration was measured using a laboratory blood glucose meter (Vitros 950; Ortho-Clinical Diagnostics, Raritan, NJ).
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5

Serum Electrolytes and Hormone Analysis

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Serum electrolytes and creatinine were measured using a Vitros 950 instrument (Ortho Clinical Diagnostics). PRA was measured using a radioimmunoassay for angiotensin I (Clinical Assays GammaCoat kit); the intra-assay coefficient of variation (CV) was 4.6%, and the interassay CV was 7.6%. (11 (link)) Aldosterone was also measured by radioimmunoassay (Diagnostic Products Corporation), and the intra-assay and interassay CVs were 5.4% and 13.1%, respectively.
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6

Fasting Glucose Measurement and Categorization

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At baseline, fasting plasma glucose was measured by the glucose oxidase colorimetric method using a Vitros 950 or 250 (Ortho Clinical Diagnostics analyzer; Ortho Clinical Diagnostics, Raritan, NJ). Ideal glucose was defined as an untreated fasting plasma glucose of <100 mg/dl; intermediate glucose was defined as a fasting plasma glucose of 100–125 mg/dL untreated or if treated to goal with anti-hyperglycemic medications (<100 mg/dL); and poor was defined as a fasting plasma glucose of ≥126 mg/dL [6] (link).
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7

Incident Diabetes Mellitus Assessment

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At baseline, fasting plasma glucose was measured by the glucose oxidase colorimetric method using a Vitros 950 or 250 (Ortho Clinical Diagnostics analyzer; Ortho Clinical Diagnostics, Raritan, NJ), and at visits 2 and 3, it was measured using a Roche Modular P Chemistry analyzer (Roche Diagnostics, Indianapolis, IN). Glycated hemoglobin was measured using a Tosoh high‐performance liquid chromatography system (Tosoh Corporation, Tokyo, Japan). We defined type 2 diabetes mellitus as having either: (1) fasting glucose ≥126 mg/dL; (2) glycated hemoglobin ≥6.5%; (3) use of diabetes mellitus medication; or (4) a physician diagnosis of the condition. We assessed incident type 2 diabetes mellitus at follow‐up visits 2 and 3. For each incident case of type 2 diabetes mellitus, time to event was considered as midpoint between last exam without diabetes mellitus and the exam at which diabetes mellitus developed. For participants who remained event free, follow‐up time was censored at their last available visit.
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8

Calcitonin Measurement Evolution for MTC

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Before 1997, both pentagastrin-stimulated calcitonin levels and basal serum calcitonin levels were measured by radioimmunoassay. After 1997, calcitonin levels were measured by immunoluminometric assay and since April 2006, an immunoradiometric assay (CisBio Bioassays) is used. The appropriate reference levels for each method were used to determine whether the calcitonin levels were normal or elevated.
During the study period, both serum Ca and/or serum ionized Ca (iCa) levels have been measured to evaluate occurrence of hypoparathyroidism after surgery. Serum Ca was measured until 2006 with a Vitros950 (Ortho clinical diagnostics), followed by DxC (UniCel 600 DxC ; Beckman Coulter) until 2012 and since then an AU5811 (Beckman Coulter). Since the introduction in 2003, iCa has been measured by an ion selective electrode on a blood gas analyzer. For both measurements, the laboratory units were consistent from 1993 onwards.
All patients were screened for RET mutation in the National laboratory for Genetics at the UMCU. PCR amplification followed by direct sequence analysis of exons 10–16 of the RET proto-oncogene was used to determine the exact type of mutation. RET mutation was thereafter confirmed on a DNA duplicate sample. The affected codon was used to stratify patients into 3 risk groups according to the 2015 ATA guidelines to define age-appropriate surgery.4 (link)
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9

Measuring GOT, GPT, and Triacylglycerol

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The method utilized for measuring the concentrations of glutamic oxaloacetic transaminase (GOT) and glutamic pyruvic transaminase (GPT) was described in a previous publication [18 (link)]. Triacylglycerol levels were measured using an automated blood analyzer (Vitros 950, Ortho Clinical Diagnostics Co., Tokyo, Japan). Three measurements were taken for each parameter, and the average value was calculated from each individual sample.
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10

Pulmonary Disease Risk Stratification

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Pulmonary disease-specific risk scores that employ PFT, the basic metabolic profile, and complete blood count were highly predictive of mortality and provided good discrimination of risk among subjects undergoing PFT. The IMRS was easy to compute using electronic medical records and relatively-inexpensive parameters. This simple tool provided clinically-relevant information in the form of prognostic clinical risk stratification in subjects being evaluated for pulmonary disease. components evaluated were hematocrit, hemoglobin, red blood cell count, mean corpuscular volume, RDW, platelet count, mean platelet volume, mean corpuscular hemoglobin, mean corpuscular hemoglobin concentration, and total white blood cell count. BMP testing used the Vitros 950 (Ortho Clinical Diagnostics, Rochester, New York) and its components included: sodium, potassium, chloride, bicarbonate, blood urea nitrogen, creatinine, glucose, and calcium. CBC and BMP data were extracted electronically from the Intermountain Healthcare electronic data warehouse, as were subject age and sex. Race data were available for 23% of subjects.
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