Evaluation of the SaCoVLM, a novel third-generation video laryngeal mask: a prospective observational pilot study
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00064211%3A_____%2F26%3AW0000102" target="_blank" >RIV/00064211:_____/26:W0000102 - isvavai.cz</a>
Výsledek na webu
<a href="https://oadoi.org/10.1186/s12871-026-03653-x" target="_blank" >https://oadoi.org/10.1186/s12871-026-03653-x</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1186/s12871-026-03653-x" target="_blank" >10.1186/s12871-026-03653-x</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Evaluation of the SaCoVLM, a novel third-generation video laryngeal mask: a prospective observational pilot study
Popis výsledku v původním jazyce
Background: The laryngeal mask airway ( LMA ) is a well-established device for securing the airway, typically inserted using a blind technique. However, blind insertion may result in suboptimal alignment and the need for reinsertion, which can increase the risk of adverse events. Therefore, in this pilot study, we aimed to conduct a preliminary evaluation and gather initial clinical experience with the new video laryngeal mask, SaCoVLM (TM). Methods and materials: In this prospective observational study, the SaCoVLM (TM) was used for airway management in patients undergoing general anaesthesia. We assessed key quality parameters commonly used to compare the performance of different laryngeal masks. Primary outcome was first attempt success rate. Secondary outcomes were time to achieve adequate ventilation, oropharyngeal leak pressure (OLP), and the incidence of adverse events. Results: A total of 50 patients undergoing general anaesthesia were enrolled. The first-attempt insertion success rate was 96%. The mean time to achieve adequate ventilation was 13 +/- 2.4 s, and the mean OLP was 38 +/- 3.8 mbar. The overall incidence of adverse events related to video laryngeal mask usage was 6%, with no serious adverse events observed. Conclusion: The SaCoVLM (TM) appears to be a promising alternative for airway management in patients undergoing general anaesthesia, demonstrating favourable performance across key clinical parameters.
Název v anglickém jazyce
Evaluation of the SaCoVLM, a novel third-generation video laryngeal mask: a prospective observational pilot study
Popis výsledku anglicky
Background: The laryngeal mask airway ( LMA ) is a well-established device for securing the airway, typically inserted using a blind technique. However, blind insertion may result in suboptimal alignment and the need for reinsertion, which can increase the risk of adverse events. Therefore, in this pilot study, we aimed to conduct a preliminary evaluation and gather initial clinical experience with the new video laryngeal mask, SaCoVLM (TM). Methods and materials: In this prospective observational study, the SaCoVLM (TM) was used for airway management in patients undergoing general anaesthesia. We assessed key quality parameters commonly used to compare the performance of different laryngeal masks. Primary outcome was first attempt success rate. Secondary outcomes were time to achieve adequate ventilation, oropharyngeal leak pressure (OLP), and the incidence of adverse events. Results: A total of 50 patients undergoing general anaesthesia were enrolled. The first-attempt insertion success rate was 96%. The mean time to achieve adequate ventilation was 13 +/- 2.4 s, and the mean OLP was 38 +/- 3.8 mbar. The overall incidence of adverse events related to video laryngeal mask usage was 6%, with no serious adverse events observed. Conclusion: The SaCoVLM (TM) appears to be a promising alternative for airway management in patients undergoing general anaesthesia, demonstrating favourable performance across key clinical parameters.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
30223 - Anaesthesiology
Návaznosti výsledku
Projekt
—
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2026
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
BMC ANESTHESIOLOGY
ISSN
1471-2253
e-ISSN
—
Svazek periodika
26
Číslo periodika v rámci svazku
1
Stát vydavatele periodika
GB - Spojené království Velké Británie a Severního Irska
Počet stran výsledku
7
Strana od-do
-
Kód UT WoS článku
001696791900002
EID výsledku v databázi Scopus
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