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Surgivet advisor

Manufactured by Smith & Nephew
Sourced in United States

The SurgiVet Advisor is a veterinary monitoring system designed to provide vital signs and patient data during surgical procedures. It offers continuous monitoring of parameters such as heart rate, respiratory rate, oxygen saturation, and temperature. The device is intended to assist veterinary professionals in managing patient health and safety during operations.

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5 protocols using surgivet advisor

1

Cardiopulmonary Function Measurement Protocol

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Expired gases were passed through heated tubing to a mixing chamber set to maintain temperature >37° C in order to avoid condensation of water vapor. Expired O2 and CO2 were measured (Analyzers 17625/17630; Vacumed, Ventura, CA USA), ventilation was determined by pneumotachometer (Series 3700A, Hans Rudolph Inc., Shawnee, KS USA) and O2 consumption and CO2 production were calculated (Powerlab, AD Instruments, Colorado Springs, CO USA). The pressure transducers (Surgivet Advisor, Smiths Medical, Dublin OH USA) were zeroed to the level of the right atrium. Mean arterial, pulmonary arterial, and pulmonary arterial wedge pressures were recorded immediately before each set of inert-gas measurements. Cardiac output was calculated from the systemic arterial - pulmonary arterial O2 concentration difference, and oxygen consumption using the Fick equation.
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2

Cardiopulmonary Metabolic Measurements

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Expired gases were passed through heated tubing to a mixing chamber set to maintain temperature > 37° C in order to avoid condensation of water vapor. Expired O2 and CO2 were measured (Analyzers 17625/17630; Vacumed, Ventura, CA USA), ventilation was determined by pneumotachometer (Series 3700A, Hans Rudolph Inc., Shawnee, KS USA) and oxygen consumption and carbon dioxide production were calculated (Powerlab, AD Instruments, Colorado Springs, CO USA). Pressure transducers (Surgivet Advisor, Smiths Medical, Dublin OH USA) were zeroed to the level of the right atrium. Mean arterial, pulmonary arterial, and pulmonary arterial wedge pressures were recorded immediately before each set of inert-gas measurements. Cardiac output was calculated from the systemic arterial - pulmonary arterial O2 concentration difference and O2 consumption using the Fick equation.
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3

Gene Delivery to the Brain via Stereotactic Injection

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Anesthesia was initiated with an intramuscular injection of 20 mg/kg ketamine (Fort Dodge Animal Health, Overland Park, KS, Cat# NDC 59390-198-50). An endotracheal tube with 0.5–3% isoflurane (MWI Supply, Boise, ID, Cat# 502017) was used to maintain the animal under anesthesia. The animal was placed on a heating pad and secured into a stereotactic frame (Stoelting, Wood Dale, IL, Cat# 51600). Heart rate, respiration, and temperature were monitored throughout the procedure using a SurgiVet Advisor (Smiths Medical, Dublin, OH). Under sterile conditions, a midline incision over the skull was made, and two burr holes were drilled through the cranium at the two injection sites. 2.5 × 108 vp of HC-Ad-TetOn-Ftl3L were injected by Hamilton syringe (Hamilton, Reno, NV, Cat# 7635-01) at four sites in the brain, for a total of 1 × 109 vp. The four stereotactic injection sites, with respect to the bregma, were 5.0 mm anterior, 6.0 mm lateral, 8.0 ventral; 5.0 mm anterior, 6.0 mm lateral, 6.0 mm ventral; 5.0 mm anterior, 8.0 mm lateral, 8.0 mm ventral; and 5.0 mm anterior, 8.0 mm lateral, 6.0 mm ventral. At each site, the vector was slowly injected over a period of 2 minutes, with a 3-minute waiting period between each injection.
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4

Canine Periodontal Disease Treatment Protocol

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The experimental group (E) comprised 87 dogs which were diagnosed with periodontal disease. They were examined for dental disorders because of the following symptoms: food intake disorders, foetor ex ore, gum redness, swelling and bleeding, purulent exudate, erosions and ulceration on the mucosa, and the presence of dental calculus.
Physical dental examination, periodontal examination and swabbing for microbiological tests were performed on the dogs under general anaesthesia before performing cavity cleaning, as part of the treatment of the periodontal disease. The anaesthesia regimen presented below was used for each patient. The premedication was xylazine (Sedazin; Biowet Puławy, Poland) at a dose of 2 mg/kg body weight (b.w.). After 15 min, the patient had an intravenous line inserted and received ketamine (Vetaketam; VetAgro, Lublin, Poland) at a dose of 8 mg/kg b.w., combined at a 1:1 ratio with diazepam (Relanium; Polfa, Warsaw, Poland) at a dose of 0.5 mg/kg b.w. (administered proportionately to the effect seen). Next, the patient was intubated, and a device monitoring vital signs (SurgiVet Advisor, Smiths Medical, Dublin, OH, USA) was connected. In order to maintain anaesthesia, inhalation (Matrx VMS Plus; Midmark Animal Health, Versailles, OH, USA) was used of a mixture of oxygen and isoflurane at a concentration of 2% (Aerrane; Baxter, Deerfield, IL, USA).
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5

Intracerebral Adenoviral Vector Delivery in Mice

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Anesthesia was initiated with an intramuscular injection of 20 mg/kg ketamine (Fort Dodge Animal Health, Overland Park, KS, Cat# NDC 59390-198-50). An endotracheal tube with 0.5–3% isoflurane (MWI Supply, Boise, ID, Cat# 502017) was used to maintain the animal under anesthesia. The animal was placed on a heating pad and secured into a stereotactic frame (Stoelting, Wood Dale, IL, Cat# 51600). Heart rate, respiration, and temperature were monitored throughout the procedure using a SurgiVet Advisor (Smiths Medical, Dublin, OH). Under sterile conditions, a midline incision over the skull was made, and two burr holes were drilled through the cranium at the two injection sites. 2.5 × 108 vp of HC-Ad-TetOn-Ftl3L were injected by Hamilton syringe (Hamilton, Reno, NV, Cat# 7635-01) at four sites in the brain, for a total of 1 × 109 vp. The four stereotactic injection sites, with respect to the bregma, were 5.0 mm anterior, 6.0 mm lateral, 8.0 ventral; 5.0 mm anterior, 6.0 mm lateral, 6.0 mm ventral; 5.0 mm anterior, 8.0 mm lateral, 8.0 mm ventral; and 5.0 mm anterior, 8.0 mm lateral, 6.0 mm ventral. At each site, the vector was slowly injected over a period of 2 minutes, with a 3-minute waiting period between each injection.
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