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Rapid lab 865

Manufactured by Bayer
Sourced in Germany

The Rapid Lab 865 is a compact, automated clinical chemistry analyzer designed for in-vitro diagnostic testing. It is capable of performing a range of common clinical chemistry tests, including tests for metabolic disorders, diabetes, and other medical conditions. The Rapid Lab 865 is intended for use in medical laboratories and healthcare settings.

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4 protocols using rapid lab 865

1

Integrative Acid-Base Assessment Protocol

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The pH and PCO2 were measured by blood gas analysis (Rapid Lab 865, Bayer Diagnostics, Tarrytown, NY, USA, at 37°C). Actual bicarbonate and base excess values were calculated according to the recommendations of the National Committee for Clinical Laboratory standards. Serum sodium, chloride, albumin and lactate concentrations were measured using central chemical analyzers (Roche Modular P800 Module, Roche Diagnostics, Indianapolis, IN, USA). We calculated the relative plasma volume changes in percentage from (Hb0/Hb90)–((1-Hct90/1-Hct0)), in which Hb is haemoglobin and Hct haematocrit, measured at 0 min and 90 min (Sysmex SE-9000, Sysmex Corporation, Kobe, Japan) [29 (link)]. We calculated, in each patient, the sodium chloride concentration difference as a measure of apparent strong ion difference and the corrected anion gap as a measure of strong ion gap [3 (link),4 (link),28 (link)]. The anion gap (AG) was calculated from sodium minus chloride and bicarbonate concentrations and the corrected AG from AG + (0.25 x (45-[albumin in g/L]))–(lactate in mmol/L) to estimate unmeasured, non-lactic acid, anions. Hence, we integratively used physochemical (according to Stewart) and Henderson-Hasselbalch principles to assess acid base status [2 (link),5 (link)].
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2

Comprehensive Pulmonary Function Assessment

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The following pulmonary function tests (PFT Masterscreen; Jaeger, Hoechberg, Germany) were performed using standard methodologies that included spirometry, plethysmography, and measurement of the diffusion capacity of the lung for carbon monoxide (DLco).[11 (link)12 (link)13 (link)] Arterial blood gas (ABG) values (Rapid Lab 865; Bayer, Plymouth, UK) were obtained to determine the partial pressure of oxygen (PaO2), the partial pressure of carbon dioxide (PaCO2), and oxygen saturation (SaO2). After the PFTs and ABG sampling, patients were asked to perform a six-minute walk test (6MWT) in accordance with ATS guidelines.[14 (link)] Oxygen saturation (SpO2) was recorded at the beginning and end of the six-minute walk. At the end of the test, the total distance walked in meters was documented.
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3

Continuous Hemodynamic Monitoring in CPR

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The primary outcome was ETCO2 values, which were determined every 30 s by averaging the ETCO2 values for the preceding 30 s interval. Aortic and RA pressures were continuously monitored (CS/3 CCM; Datex-Ohmeda, Helsinki, Finland), and the data were transferred to a personal computer using S/5 Collect (Datex-Ohmeda, Helsinki, Finland). Coronary perfusion pressure (CPP) was calculated by subtracting the end-diastolic RA pressure from the simultaneous end-diastolic aortic pressure. Aortic systolic pressure, aortic diastolic pressure, and CPP were sampled at 30 s intervals by averaging pressures from five consecutive compressions. CBF was continuously monitored, and its value was sampled every 30 s. Arterial blood gases (Rapidlab 865; Bayer Health Care, Fernwald, Germany) were measured at the pre-arrest baseline and end of each ventilation type.
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4

Hepatic Devascularization Biomarker Monitoring

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Blood samples were obtained hourly following hepatic devascularization. Blood ammonia (NH3), glucose (GLU), albumin (ALB), creatinine (CR), calcium (CA), blood urea nitrogen (BUN), aspartate aminotransferase (AST), alanine aminotransferase (ALT), total bilirubin (TBIL), lactate dehydrogenase (LDH) and alkaline phosphatase (ALP) were determined using an automatic biochemical analyzer (Dri-chem 3000, Fujifilm, Japan). Blood electrolytes and pH levels were measured using an arterial blood gas analyzer (Rapidlab 865, Bayer, Germany), and activated clotting times (ACT) were determined using a whole blood coagulation system (Hemochron, ITC, USA).
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