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Verfasst von:Katzenschlager, Stephan [VerfasserIn]   i
 Mohr, Stefan [VerfasserIn]   i
 Kaltschmidt, Nikolai [VerfasserIn]   i
 Peterstorfer, Franziska [VerfasserIn]   i
 Weilbacher, Frank [VerfasserIn]   i
 Günther, Patrick [VerfasserIn]   i
 Ries, Markus [VerfasserIn]   i
 Weigand, Markus A. [VerfasserIn]   i
 Popp, Erik [VerfasserIn]   i
Titel:Laryngeal mask vs. laryngeal tube trial in paediatric patients (LaMaTuPe)
Titelzusatz:a single-blinded, open-label, randomised-controlled trial
Verf.angabe:Stephan Katzenschlager, Stefan Mohr, Nikolai Kaltschmidt, Franziska Peterstorfer, Frank Weilbacher, Patrick Günther, Markus Ries, Markus A. Weigand and Erik Popp
E-Jahr:2024
Jahr:September 12, 2024
Umfang:8 S.
Fussnoten:Gesehen am 16.09.2024
Titel Quelle:Enthalten in: European journal of emergency medicine
Ort Quelle:London : Lippincott, Williams & Wilkins, 1994
Jahr Quelle:2024
Band/Heft Quelle:(2024), Artikel-Nummer 1178, online ahead of print, Seite 1-8
ISSN Quelle:1473-5695
Abstract:Background: In hypoxemic children with difficult airway, or for minor elective procedures, the use of a supraglottic airway device may be preferred to endotracheal intubation, whether with a laryngeal mask or laryngeal tube. Second-generation laryngeal masks may offer a better safety profile. Whether they should be preferred to laryngeal tubes is unknown. This study aimed to compare the efficacy and safety of second-generation laryngeal masks and laryngeal tubes in children. - Methods: This randomised-controlled trial was conducted in a single university hospital in children <18 years undergoing elective anaesthesia in urology, minor paediatric surgery and gynaecology. Patients were 1 : 1 randomised to the laryngeal mask or laryngeal tube group. Children were allocated a second-generation laryngeal tube or a second-generation laryngeal mask as the primary airway device. The primary endpoint was insertion time. Secondary endpoints included first-attempt success, overall success and complications, which included hypoxia (SpO2 < 90%), laryngospasm, bronchospasm, aspiration and bleeding. - Results: In total, 135 patients were randomised, with 61 allocated to the laryngeal tube and 74 to the laryngeal mask group, with a median age of 5.4 and 4.9 years, respectively. Median insertion time was significantly longer in the laryngeal tube group (37 vs. 31 s; difference of medians: 6.0 s; 95% confidence interval: 0.0-13.0). The laryngeal tube had a significantly lower first-attempt (41.0%) and overall success rate (45.9%) than the laryngeal mask (90.5% and 97.3%, respectively). Those allocated to the laryngeal tube group had a higher ratio of complications (27.8%) compared to the laryngeal mask group (2.7%). - Conclusion: This randomised-controlled trial reported that in children undergoing elective anaesthesia, the use of a laryngeal tube was associated with a longer insertion time.
DOI:doi:10.1097/MEJ.0000000000001178
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

kostenfrei: Volltext: https://doi.org/10.1097/MEJ.0000000000001178
 kostenfrei: Volltext: https://journals.lww.com/euro-emergencymed/fulltext/9900/laryngeal_mask_vs__laryngeal_tube_trial_in.149.aspx
 DOI: https://doi.org/10.1097/MEJ.0000000000001178
Datenträger:Online-Ressource
Sprache:eng
Bibliogr. Hinweis:Forschungsdaten: Katzenschlager, Stephan, 1989 - : Laryngeal mask vs. laryngeal tube trial in pediatric patients (LaMaTuPe)
K10plus-PPN:1902561317
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