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Vmax encore 229

Manufactured by BD
Sourced in United States

The Vmax Encore 229 is a laboratory equipment designed for performing spectrophotometric measurements. It features a wavelength range of 190 to 1100 nanometers and can accommodate various sample types. The device is intended for use in research and analytical applications, providing accurate and reliable absorbance data.

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9 protocols using vmax encore 229

1

Comprehensive Pulmonary Function Assessment

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Spirometry, whole‐body plethysmography, and single‐breath diffusion capacity for carbon monoxide were assessed using a pulmonary function testing system (Vmax Encore 229 with V62J Autobox; CareFusion, Yorba Linda, USA) according to standard procedures (Graham et al., 2019 (link); Macintyre et al., 2005 (link)). Pulmonary function measurements were expressed in absolute and percent predicted values (Crapo et al., 1982 (link); Quanjer et al., 2012 (link)). Blood hemoglobin concentration ([Hb]) was determined (HemoCue, Helsingborg, Sweden) to correct diffusion capacity measures. Measures of pulmonary function were performed in order to ensure that male and female participants were comparable.
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2

Pulmonary Gas Exchange Measurement

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Pulmonary gas exchange and ventilation were measured breath‐by‐breath using a calibrated, computer‐based system (Vmax Encore 229, CareFusion, Yorba Linda, CA). Both gas and volume calibrations were calibrated prior to each exercise testing session. Oxygen and carbon dioxide were calibrated using a two‐point calibration with atmospheric air and a known gas mixture (16% oxygen, 4% carbon dioxide). Volume calibration was completed with a 3 L volume syringe in accordance to the specifications outlined by the manufacture. Pulmonary gas exchange was measured continuously.
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3

Pulmonary Gas Exchange Measurement

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Pulmonary gas exchange was measured breath-by-breath using a calibrated, computer-based system (Vmax Encore 229, CareFusion, Yorba Linda, CA) as discussed previously [11 (link)]. Pulmonary oxygen uptake ( V˙O2 ) was measured continuously. Participants were outfitted with a 4 lead electrocardiogram for the measurements of HR throughout exercise.
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4

Inspiratory Muscle Function and Pulmonary Testing

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Participants reported to the laboratory on two separate occasions separated by at least 48 h. Participants were instructed to avoid caffeine for 8 h and exercise for 24 h prior to each testing session. Session 1 involved anthropometric measurements and pulmonary function tests (Vmax Encore 229 with V62J Autobox; CareFusion, CA, USA), which were performed in accordance with standard recommendations (Miller et al., 2005 (link); Wanger et al., 2005 (link)). Inspiratory muscle strength was measured using a semi‐occluded mouthpiece connected to a calibrated differential pressure transducer (DP15‐34; Validyne Engineering, CA, USA) as recommended (Laveneziana et al., 2019 (link)). Pulmonary function and inspiratory muscle strength results were presented in absolute units and as a percentage of predicted values (Black & Hyatt, 1969 (link); Gutierrez et al., 2004 (link); Tan et al., 2011 (link)). Participants were then familiarized with the scales used to record dyspnea during IPTL as well as the IPTL protocol itself. Session 2 was the primary testing session where participants engaged in IPTL until task failure. Diaphragm contractile function and voluntary activation were measured during session 2 only.
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5

Incremental Cycle Exercise Testing Protocols

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Spirometry and plethysmography were performed using a commercially available system (Vmax Encore 229, V62J Autobox; CareFusion) according to standard recommendations. The incremental cycle test to exhaustion was performed on an electromagnetically braked ergometer. Participants began at a work rate of 80 W (women) or 120 W (men) and work increased every 2 min by 20 W for both sexes until volitional exhaustion. Flows, volume, and esophageal pressures (balloon‐tipped catheter) were obtained using previously described methods (Dominelli et al., 2015). Following exercise, subjects completed forced vital capacity (FVC) maneuvers to ensure forced expired volume in 1 s (FEV1) was not reduced during exercise. All raw data collected on the first day of testing were recorded at 200 Hz continuously using a 16‐channel analog‐to‐digital data acquisition system (PowerLab/16SP model ML 795, ADIinstrument, Colorado Springs, CO) and stored on a personal computer for analysis.
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6

Metabolic and Ventilatory Responses Measurement

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Standard metabolic and ventilatory responses were measured breath-by-breath using a metabolic cart (Vmax Encore 229; CareFusion, Yorba Linda, CA). In the younger subjects, heart rate (HR) was measured using a telemetric system (Polar T34; Polar Electro, Kempele, Finland). In the older subjects, HR was measured using a 12-lead electrocardiogram (Cardiosoft Diagnostics System v6.71; GE Healthcare, Mississauga, Canada).
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7

Comprehensive Pulmonary Function Assessment

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Spirometry, whole-body plethysmography, single-breath diffusing capacity for carbon monoxide, maximum voluntary ventilation, as well as maximum inspiratory and expiratory pressures were assessed using a commercially available system (Vmax Encore 229, V62J Autobox; CareFusion, Yorba Linda, CA) according to standard recommendations ( [27] [28] [29] [30] ). Pulmonary function measurements were expressed in absolute values and as a percentage of predicted values ( 8, 9, 21 ).
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8

Lung Function Assessments in Patients

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Patients performed spirometry, plethysmography, 12-s maximal voluntary ventilation, and single-breath diffusing capacity of the lungs for carbon monoxide (DLCO), according to established guidelines [8] [9] [10] . Values were measured using a commercially available system (Vmax Encore 229, V62J Autobox; CareFusion, Yorba Linda, CA, USA) and expressed as a percentage of predicted values [11, 12] .
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9

Cardiorespiratory Responses During Exercise

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Standard cardiorespiratory responses were measured on a breath-by-breath basis at rest and during exercise (Vmax Encore 229; CareFusion). This metabolic cart has not been validated with an FIO 2 of 0.60; therefore, differences in gas exchange parameters (i.e. oxygen consumption and carbon dioxide production) and gas exchange-derived parameters (i.e. ventilatory equivalents and the respiratory exchange ratio) were not compared between conditions (Visits 3 and 4). Flow was calibrated using a 3-L calibration syringe connected to the breathing apparatus and using the appropriate gas mixture from the Douglas bag at a wide range of flow rates. The inflection point in tidal volume relative to minute ventilation (VT/V′E) was determined for each patient by examining 30-s averaged data throughout incremental exercise (Visit 2). The time at which the corresponding VT was achieved during Visits 3 and 4, if at all, was also identified using the 30-s averaged data from those visits. Arterial oxygen saturation was estimated via finger pulse oximetry (Radical-7 Pulse CO Oximeter; Masimo Corp., Irvine, CA, USA). Heart rate was recorded using 12-lead electrocardiography.
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