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https://hdl.handle.net/2440/98677
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Type: | Journal article |
Title: | General anesthesia with an injectable 8% v/v sevoflurane lipid emulsion administered intravenously to dogs |
Author: | Natalini, C. Da Silva Serpa, P. Cavalcanti, R. Polydoro, A. Griffith, J. Santos, L. Nicholson, A. |
Citation: | Veterinary Anaesthesia and Analgesia, 2016; 43(3):271-280 |
Publisher: | Wiley |
Issue Date: | 2016 |
ISSN: | 1467-2987 1467-2995 |
Statement of Responsibility: | Claudio C Natalini, Priscila B Da Silva Serpa, Ruben L Cavalcanti, Alexandre S Polydoro, Joanna E Griffith, Luiz CP Santos, and Anthony Nicholson |
Abstract: | Objective: To evaluate the potential of an intravenous (IV) sevoflurane formulation for maintenance of general anesthesia in dogs. Study design: Prospective crossover design. Animals: Six healthy, mature, mixed-breed dogs, four males and two females, weighing 11.7 ± 3.4 kg. Methods: Anesthesia was induced and maintained with propofol IV for instrumentation. Baseline measurements were recorded before administration of either sevoflurane in oxygen (Sevo-Inh) or lipid-emulsified sevoflurane 8% v/v in 30% Intralipid IV (Sevo-E), 0.5 mL kg−1 over 5 minutes followed by an infusion at 0.1–0.3 mL kg−1 minute−1. Dogs were breathing spontaneously. The ‘up-and-down’ technique was used to determine the minimum alveolar concentration (MAC) of sevoflurane. Over 120 minutes, a tail clamp was applied every 15 minutes and sevoflurane administration was adjusted depending on the response. End-tidal sevoflurane concentration and variables were recorded at 30, 60, 90, and 120 minutes: heart rate (HR), systemic arterial pressure (sAP), respiratory rate (fR), end-tidal carbon dioxide tension, hemoglobin oxygen saturation (SaO2), arterial pH and blood gases, blood urea nitrogen, alanine aminotransferase, creatine kinase, gamma-glutamyl transferase, and aspartate aminotransferase. Results: There were no significant differences between treatments for HR, sAP, fR, SaO2, and biochemical variables (p > 0.05). pH and inline imagewere significantly decreased, and PaCO2 increased from baseline in Sevo-E (p < 0.05). MAC was significantly lower for Sevo-E than for Sevo-Inh, although the required dose of sevoflurane (g hour−1) to maintain general anesthesia was not significantly different between treatments. Conclusions and clinical relevance: Administration of 8% v/v sevoflurane lipid emulsion IV was effective in maintaining general anesthesia in dogs, but resulted in moderate cardiopulmonary depression, metabolic and respiratory acidosis. The amount of sevoflurane (g hour−1) required to maintain general anesthesia was significantly lower for inhaled than for IV sevoflurane. |
Keywords: | canine; hemodynamics; lipid emulsion; sevoflurane |
Rights: | © 2015 Association of Veterinary Anaesthetists and the American College of Veterinary Anesthesia and Analgesia |
DOI: | 10.1111/vaa.12317 |
Published version: | http://dx.doi.org/10.1111/vaa.12317 |
Appears in Collections: | Animal and Veterinary Sciences publications Aurora harvest 7 |
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