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Reflotron desktop analyzer

Manufactured by Roche
Sourced in United Kingdom

The Reflotron Desktop Analyzer is a compact, automated clinical chemistry analyzer designed for in-vitro diagnostic testing. The device performs rapid analysis of a variety of analytes from small sample volumes, enabling quick and efficient results in a clinical setting.

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Lab products found in correlation

2 protocols using reflotron desktop analyzer

1

Anthropometric and Metabolic Measurements

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All study‐related measurements were performed between 8 and 11 AM following a 12‐hr overnight fast, which included refraining from alcohol or caffeine.
Standard anthropometric measures of height and weight were recorded to determine body mass index (BMI = weight/height2). Systolic blood pressure (SBP), diastolic blood pressure (DBP) and heart rate (HR) were measured using an automatic BP monitor (UA‐767; A&D Instruments Ltd, Oxford, UK) to determine mean arterial pressure (MAP = 2/3 DBP + 1/3 SBP). IOP readings were obtained using noncontact tonometry (Pulsair; Keeler Ltd, UK) to determine ocular perfusion pressure (OPP = 2/3 MAP – IOP).
In addition, blood and plasma samples drawn from the antecubital fossa vein were assessed immediately for fasting glucose (GLUC), triglycerides (TG), total cholesterol (CHOL) and high‐density lipoprotein cholesterol (HDL‐c) using the Reflotron Desktop Analyzer (Roche Diagnostics, UK). Low‐density lipoprotein cholesterol (LDL‐c) values were calculated as per the Friedewald equation (Friedewald et al. 1972).
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2

Cardiovascular Disease Risk Assessment

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Blood and plasma samples drawn from the antecubital fossa vein were assessed immediately for fasting glucose (GLUC), triglycerides (TG), total cholesterol (T-CHOL), high-density lipoprotein cholesterol (HDL-C) and glycated haemoglobin (HbA1c) using the Reflotron Desktop Analyzer (Roche Diagnostics, Welwyn Garden City, UK). Low-density lipoprotein cholesterol (LDL-C) values were calculated as per the Friedewald equation [15 (link)].
These variables, in addition to the above parameters, were used to calculate the Framingham Risk Score (FRS) for each individual [16 (link)]. Absolute CVD risk percentage over 10 years was classified as low risk (<10%), intermediate risk (10–20%) and high risk (>20%) [17 (link)].
Additional set of urine samples were also collected and sent to the pathology unit for assessment of albumin/creatinine ratio (ACR).
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