Prospective, randomized clinical trial of laryngeal mask airway Supreme® used in patients undergoing general anesthesia
Background and objectives: Supraglottic airway devices are increasingly used as an option to tracheal intubation for elective procedures of varying complexity. The aim of this study was to prospectively evaluate the clinical use of the laryngeal mask airway Supreme® (LMAS) in patients undergoing ele...
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doaj-1ed7ca8e23b54303a1daff37333c967d2020-11-25T01:14:13ZengElsevierBrazilian Journal of Anesthesiology0104-00142013-11-01636456460Prospective, randomized clinical trial of laryngeal mask airway Supreme® used in patients undergoing general anesthesiaSara R. Barreira0Camila Machado Souza1Fernanda Fabrizia2Ana Bárbara G. Azevedo3Talitha G. Lelis4Claudia Lutke5Department of Anesthesiology, Pain, and Intensive Care, Universidade Federal de São Paulo, São Paulo, SP, BrazilCorresponding author.; Department of Anesthesiology, Pain, and Intensive Care, Universidade Federal de São Paulo, São Paulo, SP, BrazilDepartment of Anesthesiology, Pain, and Intensive Care, Universidade Federal de São Paulo, São Paulo, SP, BrazilDepartment of Anesthesiology, Pain, and Intensive Care, Universidade Federal de São Paulo, São Paulo, SP, BrazilDepartment of Anesthesiology, Pain, and Intensive Care, Universidade Federal de São Paulo, São Paulo, SP, BrazilDepartment of Anesthesiology, Pain, and Intensive Care, Universidade Federal de São Paulo, São Paulo, SP, BrazilBackground and objectives: Supraglottic airway devices are increasingly used as an option to tracheal intubation for elective procedures of varying complexity. The aim of this study was to prospectively evaluate the clinical use of the laryngeal mask airway Supreme® (LMAS) in patients undergoing elective breast surgery and compare it with endotracheal tube (ETT). Methods: Sixty patients undergoing breast procedures under general anesthesia were randomly divided into two groups according to the device used (LMAS or ETT). Time of insertion, number of insertion attempts, hemodynamic response to insertion, presence of blood on the device used; and incidence of sore throat, dysphagia, nausea and vomiting were assessed postoperatively. Results: There was no difference between groups regarding time of insertion, number of attempts for successful insertion, and presence of blood on the device. Heart rate and blood pressure after insertion were higher in ETT group. Incidence of sore throat and dysphagia was also higher in ETT group after two hours in the postoperative period. There was no difference regarding incidence and severity of complications evaluated after six hours postoperatively. Conclusions: The use of the LMAS technique to access airway during general anesthesia for elective breast surgery is as safe and effective as tracheal intubation, with the advantage of promoting smaller hemodynamic response during its management and lower incidence of sore throat and dysphagia in the first hours after surgery. Keywords: Equipment, Laryngeal mask airway, Complications, General anesthesiahttp://www.sciencedirect.com/science/article/pii/S0104001413001152 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Sara R. Barreira Camila Machado Souza Fernanda Fabrizia Ana Bárbara G. Azevedo Talitha G. Lelis Claudia Lutke |
spellingShingle |
Sara R. Barreira Camila Machado Souza Fernanda Fabrizia Ana Bárbara G. Azevedo Talitha G. Lelis Claudia Lutke Prospective, randomized clinical trial of laryngeal mask airway Supreme® used in patients undergoing general anesthesia Brazilian Journal of Anesthesiology |
author_facet |
Sara R. Barreira Camila Machado Souza Fernanda Fabrizia Ana Bárbara G. Azevedo Talitha G. Lelis Claudia Lutke |
author_sort |
Sara R. Barreira |
title |
Prospective, randomized clinical trial of laryngeal mask airway Supreme® used in patients undergoing general anesthesia |
title_short |
Prospective, randomized clinical trial of laryngeal mask airway Supreme® used in patients undergoing general anesthesia |
title_full |
Prospective, randomized clinical trial of laryngeal mask airway Supreme® used in patients undergoing general anesthesia |
title_fullStr |
Prospective, randomized clinical trial of laryngeal mask airway Supreme® used in patients undergoing general anesthesia |
title_full_unstemmed |
Prospective, randomized clinical trial of laryngeal mask airway Supreme® used in patients undergoing general anesthesia |
title_sort |
prospective, randomized clinical trial of laryngeal mask airway supreme® used in patients undergoing general anesthesia |
publisher |
Elsevier |
series |
Brazilian Journal of Anesthesiology |
issn |
0104-0014 |
publishDate |
2013-11-01 |
description |
Background and objectives: Supraglottic airway devices are increasingly used as an option to tracheal intubation for elective procedures of varying complexity. The aim of this study was to prospectively evaluate the clinical use of the laryngeal mask airway Supreme® (LMAS) in patients undergoing elective breast surgery and compare it with endotracheal tube (ETT). Methods: Sixty patients undergoing breast procedures under general anesthesia were randomly divided into two groups according to the device used (LMAS or ETT). Time of insertion, number of insertion attempts, hemodynamic response to insertion, presence of blood on the device used; and incidence of sore throat, dysphagia, nausea and vomiting were assessed postoperatively. Results: There was no difference between groups regarding time of insertion, number of attempts for successful insertion, and presence of blood on the device. Heart rate and blood pressure after insertion were higher in ETT group. Incidence of sore throat and dysphagia was also higher in ETT group after two hours in the postoperative period. There was no difference regarding incidence and severity of complications evaluated after six hours postoperatively. Conclusions: The use of the LMAS technique to access airway during general anesthesia for elective breast surgery is as safe and effective as tracheal intubation, with the advantage of promoting smaller hemodynamic response during its management and lower incidence of sore throat and dysphagia in the first hours after surgery. Keywords: Equipment, Laryngeal mask airway, Complications, General anesthesia |
url |
http://www.sciencedirect.com/science/article/pii/S0104001413001152 |
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