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Servo ventilator 300

Manufactured by Siemens
Sourced in Sweden

The Servo Ventilator 300 is a medical device designed to provide mechanical ventilation support. It is capable of assisting patients with their breathing by delivering controlled volumes of air or oxygen-enriched air. The device is designed to operate with a range of ventilation modes and settings to accommodate varying patient needs.

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10 protocols using servo ventilator 300

1

Acute Anesthesia and Mechanical Ventilation

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Control animals were acutely anesthetized with sodium pentobarbital (60 mg/kg body weight IP). MV animals were tracheostomized and mechanically ventilated with a pressure-controlled ventilator (Servo Ventilator 300, Siemens) for 12 hours as previously reported (19 (link)).
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2

Anesthesia and Ventilation in Swedish Landrace Pigs

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Five Swedish landrace pigs with a median weight of 63 (61–65) kg were fasted overnight with free access to water. Premedication was performed with an intramuscular injection of xylazine (Rompun® vet. 20 mg/ml; Bayer AG, Leverkusen, Germany; 2 mg/kg) mixed with ketamine (Ketaminol® vet. 100 mg/ml; Farmaceutici Gellini S.p.A., Aprilia, Italy; 20 mg/kg), and a peripheral intravenous access was established in the earlobe. The pigs were then transferred to the laboratory and placed in the supine position on the operating table. Anesthesia was induced with sodium thiopental (Pentothal; Abbott Laboratories, North Chicago, Illinois, USA) and pancuronium bromide (Pavulon; N.V. Organon, Oss, The Netherlands). Anesthesia was maintained with a ketamine (Ketaminol® vet), Midazolam (Midazolam Panpharma®, Oslo, Norway), and fentanyl (Leptanal®, Lilly, France) infusion. Fluid loss was compensated for by continuous infusion of Ringer’s solution. Mechanical ventilation was established with a Siemens-Elema ventilator (Servo Ventilator 300, Siemens, Solna, Sweden).
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3

Rapid Volume Challenge in Ventilated Patients

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This prospective study was conducted over an 11-month period (February -December
2012) in the Central medical-surgical intensive care unit of the Complexo
Hospitalar Santa Casa
. Ventilated patients (> 18 years of age) were
included when they presented with circulatory instability and required a rapid volume
challenge according to the attending physician. The physician’s decision was based on
the presence of clinical signs of acute circulatory failure (low blood pressure or
urine output, tachycardia, mottling), and/or clinical signs of organ dysfunction
(renal dysfunction, hyperlactacidemia).
Mechanical ventilation was performed in volume-controlled mode using a Servo
Ventilator 300 (Siemens, Sweden). The study required perfect adaptation of the
patient to the ventilator before starting the respiration cycle. All patients were in
supine position with the head elevated to 30º and with ventilatory parameters
adjusted to maintain a tidal volume of 6 - 10mL/kg and a positive end-expiratory
pressure (PEEP) of 5 - 0cmH2O. The Complexo Hospitalar Santa
Casa
Research Ethics Committee approved this study (nº
38077214.1.0000.5335 - Plataforma Brasil) without the need for a consent form.
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4

Anesthetic Protocol for Swedish Landrace Pigs

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Six Swedish landrace pigs with a mean weight of 61 ± 1.8 kg were fasted overnight with free access to water. Premedication was performed with an intramuscular injection of Xylazine (Rompun® vet. 20 mg/ml; Bayer AG, Leverkusen, Germany; 2 mg/kg) mixed with ketamine (Ketaminol® vet. 100 mg/ml; Farmaceutici Gellini S.p.A., Aprilia, Italy; 20 mg/kg) in their stables, and a peripheral iv access was established in the earlobe. The pig was then transferred to the laboratory and placed in supine position on the operating table. Oral intubation was performed using a 7.5 size endotracheal tube after anesthesia induction with sodium thiopental (Pentothal; Abbott Laboratories, North Chicago, IL, USA) and pancuronium bromide (Pavulon; N.V. Organon, Oss, the Netherlands). Anesthesia was maintained with a ketamine (Ketaminol® vet), midazolam (Midazolam Panpharma®, Oslo, Norway), and fentanyl (Leptanal®, Lilly, France) infusion. Fluid loss was compensated by continuous infusion of Ringer’s Acetate. Mechanical ventilation was established with a Siemens-Elema ventilator (Servo Ventilator 300, Siemens, Solna, Sweden).
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5

Porcine Model for Cardiac Surgery

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All animals were sedated with intramuscular ketamine and xylazine and intubated with a 4.5‐mm cuffed endotracheal tube. Each animal was ventilated at an inspired oxygen fraction of 0.21 and a rate of 12 to 15 breaths/min, by means of a volume‐control ventilator (Servo Ventilator 300; Siemens, New York, NY) to achieve a normal pH and arterial carbon dioxide tension of 35 to 40 mm Hg. Intravenous bolus injections of fentanyl and pancuronium via a peripheral intravenous line were administered before surgery. Anesthesia was maintained by a continuous infusion of fentanyl, midazolam, and pancuronium throughout the entire experiment. Heterologous blood was obtained from a donor Yorkshire pig with weight of 35 to 45 kg that had been anesthetized with telazol and xylazine. Under anesthesia an intravenous cannula was placed in each femoral vein to obtain the blood. Heparin was administered intravenously. The donated blood was used to prime the CPB circuits for the experimental animals.
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6

Perfusion of Lung Allografts for Transplantation

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Left atrial drainage cannula and main pulmonary artery inflow cannula (XVIVO Perfusion Inc.) as well as endotracheal tube were secured in the standard fashion (Figure 1A, B).11 (link) A PiCCO catheter (Pulsion Medical, Inc., Powell, OH) was placed through a hemostasis valve and floated into the pulmonary artery to assess for extravascular lung water (Figure 1C, D).
Allografts were perfused after staged rewarming as follows. According to standard perfusion techniques, lungs were ventilated (Servo Ventilator 300, Siemens, Munich, Germany) at a tidal volume of 8 ml/kg with a positive end-expiratory pressure of 5 cm H2O and a respiratory rate of 8 breaths/minute.11 (link) The perfusate flow rate was slowly increased to 40% of cardiac output as the lungs were rewarmed to 37°C over the 4 hour EVLP period.11 (link) Left atrial pressure was targeted to 5–8 mm Hg (via gravity drainage reservoir height) and pulmonary artery pressure was equal to the inflow pressure of the circuit.
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7

Mechanical Ventilation Animal Model

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Control animals were not exposed to MV and were acutely anesthetized with sodium pentobarbital (60 mg/kg body weight intraperitoneally). MV animals were tracheostomized and mechanically ventilated with a pressure-controlled ventilator (Servo Ventilator 300, Siemens) for 12 hours as previously reported [28 (link)]. The carotid artery was cannulated to permit the continuous measurement of blood pressure during the protocol. A venous catheter was inserted into the jugular vein for continuous infusion of sodium pentobarbital (~10 mg/kg/hr) and fluid replacement. Body temperature was maintained at ~37°C by use of a heating blanket and heart rate was monitored via lead II electrocardiograph.
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8

Mechanical Ventilation Monitoring and Maintenance

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Ventilator settings (Servo Ventilator 300, Siemens) were as follows: upper airway pressure limit: 20 cm H2O, typical pressure generation above PEEP: 6–9 cm H2O, respiratory rate: 80 breaths/min; and PEEP: 1 cm H2O. Animals were constantly monitored during MV. Continuing care included expressing the animals’ bladders, rotating the animals to prevent blood pooling, and suctioning the airway to prevent mucus plugs. At the start of MV, animals received an intramuscular injection of glycopyrrolate (0.08 mg/kg) to decrease airway mucus secretions during MV. Animals also received a maintenance dose of glycopyrrolate (0.04 mg/kg) every two hours. Body temperature was read by a rectal thermometer and maintained at 37°C by resting animals on a recirculating water blanket. Heart rate was monitored by electrocardiograph. Following the initiation of MV, the carotid artery was cannulated to measure blood pressure. Blood samples (~100 μL) were taken from this catheter to ensure blood gas homeostasis was maintained during MV. If blood gas parameters changed, either tidal volume and/or oxygen concentration of the inspired air was increased to return to homeostasis. To maintain a surgical plane of anesthesia, sodium pentobarbital diluted in saline was constantly infused into a catheter in the jugular vein (~10 mg/kg/hr).
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9

Ventilator Setup for Respiratory Care

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We used a ventilator (Servo-300 ventilator, Siemens Elema, Solna, Sweden) with a humidifier and a disposable circuit (DAR Neonatal, Medtronic, Dublin, Ireland) which were configured based on the manufacturer’s recommendation (Fig. 4).
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10

Pulmonary Vasodilation Measurement Protocol

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The thromboxane A2-mimetic 9,11-dideoxy-9α, 11α-methanoepoxy PGF, U46619 (Cayman Chemical, MI, USA), was supplied in methyl acetate and diluted in NaCl 0.9% to a final concentration of 30 μg mL−1. PDNO was supplied in a solution of 27 mM (SP Process Development, Södertälje, Sweden). All solutions were administered through syringe pumps. iNO was supplied from a tank (1000 parts per million [ppm] of nitrogen) and introduced to the inspiratory limb of the non-rebreathing ventilator circuit to mix NO with inspired gas in a Servo 300 ventilator (Siemens-Elema, Stockholm, Sweden). A portion of inhaled NO and nitric dioxide continuously passed through a chemiluminescence analyzer to monitor concentrations.
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