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Engstr m carestation

Manufactured by GE Healthcare
Sourced in United States

The Engström Carestation is a ventilator system designed for critical care and anesthesia applications. It provides ventilation support and monitoring capabilities to assist healthcare professionals in patient care. The Engström Carestation is engineered to deliver precise and reliable respiratory support to patients.

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8 protocols using engstr m carestation

1

Non-Invasive Ventilation Management

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NIMV was performed with the ICU ventilation device (Engström Carestation, GE Healthcare) in NIMV mode using a facemask. Continuous positive airway pressure (CPAP) or bilevel positive airway pressure modes were used during NIMV. For the NIMV-treated patients under bilevel positive airway pressure mode, inspiratory positive airway pressure was initially set as 7 cm H2O and the expiratory positive airway pressure as 3 to 4 cm H2O in order to improve patient compliance, and later increased incrementally by 1 to 2 cm H2O to the target 6 to 8 mL/kg of tidal volume. Under the CPAP mode, the initial pressure was set as 7 cm H2O. Pressure and FiO2 changes were based on the blood gas, saturation, and respiratory distress symptoms of the patients.
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2

Anesthetized Pig Ventilation Model

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Pigs were anesthetized with propofol and fentanyl, tracheotomized and mechanically ventilated in volume-controlled mode, with constant inspiratory flow, VT 10 mL · kg-1, inspired fraction of oxygen (FiO2) 0.21, zero end-expiratory pressure, and RR adjusted to achieve normocapnia using Engström Carestation® ventilator (General Electric Healthcare, Madison, WI, USA). Muscle relaxation was obtained with pancuronium bromide. Right jugular vein was cannulated with a 3-lumen 8.5-Fr catheter for drug administration. Carotid artery was cannulated with an 8.5 Fr catheter. FiO2 was increased to 1 at the end of animal preparation.
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3

Anesthetized Rat Model for Continuous Monitoring

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Adult male Sprague-Dawley rats were anesthetized in inhalation chamber with Sevoflurane (Sevorane®; Abbott, France) and then with 80 mg/kg of intraperitoneal pentobarbital sodium (Pentobarbital sodique; Ceva, France). After catheterization of the right femoral vein (Insyte-22-gauge), anesthesia was maintained by continuous intravenous infusion of pentobarbital sodium at 1 mL/h (14 mg/kg/h). Analgesia was performed with intraperitoneal xylazine (10 mg/kg, Rompun 2%®; Bayer, Germany). The right femoral artery was catheterized (Insyte-24-gauge) for continuous arterial pressure monitoring and blood withdrawal. A tracheostomy was performed (Insyte-16-gauge) and animals were mechanically ventilated with room air in prone position (Engström Carestation®; General Electric, USA; tidal volume 6-8 mL/kg, respiratory rate 60 per minute, and positive expiratory pressure [PEP] 3 cm H2O).
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4

Validating BENGI's Tidal Volume Accuracy

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To determine the BENGI’s accuracy at measuring VT, the BENGI and computer flow sensor were connected in-line in series between a mechanical ventilator (Engström Carestation™, General Electric Healthcare, Chicago, IL) and the test lung. The ventilator was set in mandatory volume control ventilation, and breaths were delivered to the test lung at a constant respiratory rate (10 breaths/min) and varying inspiratory times (tinsp = 0.5, 1.0, and 2.0 s) and tidal volumes (VT = 300 to 900 mL in 50 mL increments). Flow measurements from at least 10 consecutive respiratory cycles were captured with the computer flow sensor. The flow waveform was analyzed with custom code written in Python (version 3.7.2, Python Software Foundation, Beaverton, Oregon, United States) to determine inspiratory start and end times and calculate VT. The onboard, real-time calculation of VT by the BENGI was sent to the computer at end inspiratory time via USB transmission. The computer and BENGI calculated VTs were matched based upon end inspiration times, and the measurement differences in VT were analyzed by Bland–Altman plot analysis.
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5

Indirect Calorimetry for Metabolic Assessment

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A calorimeter module (Engström Carestation, General Electric, Madison, WI) was used for indirect calorimetry. The module consists of a fast differential paramagnetic oxygen analyzer, an infrared analyzer for carbon dioxide, and a pneumotachograph to measure the inspired and expired volumes. The pneumotachograph and gas sampling ports were connected to a disposable connector, placed between the Y-piece of the ventilator circuit and the endotracheal tube. The signals from the pneumotachograph and gas analyzers were synchronized for breath-by-breath data on gas exchange. Under each condition, the data were collected for 30 min with the first 10 min being discarded for analysis purposes. We consider the steady state to be the point after 5 consecutive minutes measurement when VCO2 and VO2 vary by ±10%. During the last 5 min of each steady state, the following data were recorded: VCO2, VO2, EE, and respiratory quotient (RQ).
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6

Decremental PEEP Trial in Ventilated Patients

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All patients received pressure‐controlled ventilation (PCV) (Engström Carestation, GE Healthcare, Madison, WI, USA) as this is the standard of care in our hospital. The inspiratory pressure above PEEP (Pinsp) was tailored to reach a tidal volume of 8 ± 2 ml/kg predicted body weight, and remained unchanged during the entire PEEP trial. In addition, FiO2 was set to achieve a PaO2 of 8–12 kPa. First baseline measurements were performed, after which a recruitment maneuver (RM) was performed using a peak inspiratory pressure (PIP) of 40 cmH2O with 20 cmH2O PEEP for 30–40 s, during which the respiratory cycle continued, to continue gas exchange. A PEEP of 15 cmH2O was applied for 15 min to achieve a steady‐state situation, by means of a stable carbon dioxide volume (VCO2) signal for at least 10 min. Steady state was based on VCO2 as this is the main parameter in the formula to calculate EELV,4 which is integrated in the Engström Care station. The first PEEP level was set to 15 cmH2O to avoid peak inspiratory pressures above 30 cmH2O. Thereafter, a decremental PEEP trial was performed from 15 to 0 cmH2O PEEP in steps of 5 cmH2O. Each PEEP level was applied for 10–20 min, depending on the hemodynamics and respiratory stability of patient.
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7

Recruitment Maneuver and PEEP Titration

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A 16-electrode silicon belt (EIT evaluation kit 2, Dräger, Lübeck, Germany) was placed around the patient’s thoracic cage between the 6th and 7th intercostal spaces [16 (link)]. Patients were ventilated with pressure-controlled ventilation (PCV) (Engström Carestation, GE Healthcare, Madison, WI, USA) and, throughout the entire study period, the inspiratory pressure above PEEP, the Inspiration/expiration (I/E) ratio, frequency and inspired oxygen fraction (FiO2) remained unchanged.
In this study we performed a recruitment maneuver in which mechanical ventilation was continued with a pressure amplitude of 20 cm H2O while PEEP was rapidly increased from 5 to 20 cm H2O in incremental steps of 5 cm H2O: thus, a peak pressure of 40 cm H2O for a 40-s period, as long as blood pressure remained stable. Thereafter, PEEP was decreased to 15 cm H2O and the pressure amplitude was decreased from 20 to 10 cm H2O. A PEEP level of 15 cm H2O was applied for 15 minutes to achieve a steady state. Thereafter, a decremental PEEP trial was performed from 15 to 0 cm H2O PEEP in steps of 5 cm H2O. Each PEEP level was applied for 10 to 20 minutes (depending on hemodynamic stability and blood gas analyses). At the end of each PEEP step, EIT, PaO2/FiO2 ratio and dynamic compliance (tidal volume divided by pressure above PEEP) were calculated.
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8

Porcine Model for Hemodynamic Monitoring

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Anesthesia was induced and maintained through continuous infusion of propofol and fentanyl, with atracurium used intravenously solely to facilitate endotracheal intubation. Basic monitoring, including pulse oximetry (Radical 7; Masimo, Irvine, CA, USA) and invasive blood pressure (S/5, GE-Datex-Ohmeda; Chalfont, St. Giles, United Kingdom), was performed. Animals were ventilated using pressure-controlled ventilation-volume guaranteed mode (PCV-VG) (Engström Carestation; GE healthcare, Chalfont, St Giles, Buckinghamshire, UK) with a tidal volume of 6–8 ml kg−1, a positive end-expiratory pressure (PEEP) of 5 mbar, fraction of inspired oxygen (FiO2) of 0.4, and respiratory rate adjusted to the end-tidal CO2.
Seldinger’s technique was employed for femoral vascular access after ultrasound-guided puncture to place a central venous line, a venous introducer for a pulmonary artery catheter, and an arterial introducer for a pulse contour cardiac output catheter (PiCCO; Pulsion Medical, Munich, Germany). The data from all devices were continuously monitored and stored. Balanced electrolyte fluid (BEL, Sterofundin; Braun, Melsungen, Germany) was administered at a rate of 5 ml−1 kg−1.
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