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Intubating extremely premature newborns: a randomised crossover simulation study

OBJECTIVE: Determine whether tracheal intubation of extremely low birthweight (ELBW) neonates is more successful with a size-0 or size-00 Miller laryngoscope blade. DESIGN: Randomised crossover simulation study SETTING: Simulated neonatal intensive care unit environment STUDY SUBJECTS: Neonatology p...

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Autores principales: O'Connell, Joseph, Weiner, Gary
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5862193/
https://www.ncbi.nlm.nih.gov/pubmed/29637161
http://dx.doi.org/10.1136/bmjpo-2017-000157
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author O'Connell, Joseph
Weiner, Gary
author_facet O'Connell, Joseph
Weiner, Gary
author_sort O'Connell, Joseph
collection PubMed
description OBJECTIVE: Determine whether tracheal intubation of extremely low birthweight (ELBW) neonates is more successful with a size-0 or size-00 Miller laryngoscope blade. DESIGN: Randomised crossover simulation study SETTING: Simulated neonatal intensive care unit environment STUDY SUBJECTS: Neonatology physicians and nurse practitioners (n=55) INTERVENTIONS: Subjects performed four intubations in succession on a high-fidelity ELBW manikin with size-0 Miller and size-00 Miller blades from two different manufacturers. The intubation sequence was randomised. Intubations were recorded and scored for time analysis. Subjects completed surveys about blade preferences before and after completing the series of intubations. MAIN OUTCOME MEASURES: Total laryngoscopy time and first attempt success in less than 30 s RESULTS: There was no difference in total laryngoscopy time (median 23.7 vs 20.6 s) or first attempt success in <30 s (67.3% vs 69.1%) between the size-0 and size-00 blades. Differences were noted between the same size blades made by different manufacturers. Among subjects expressing a prestudy blade size preference, there was no difference in laryngoscopy time or first attempt success between blades. Regardless of blade size, subjects were less successful with the first blade in the randomised sequence. CONCLUSIONS: Our findings support the Neonatal Resuscitation Program recommendation identifying the size-00 blade as optional equipment. Operators need to be aware of design variations between manufacturers and they may benefit from ‘just-in-time’ training with a manikin prior to intubating a live patient.
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spelling pubmed-58621932018-04-10 Intubating extremely premature newborns: a randomised crossover simulation study O'Connell, Joseph Weiner, Gary BMJ Paediatr Open Original Article OBJECTIVE: Determine whether tracheal intubation of extremely low birthweight (ELBW) neonates is more successful with a size-0 or size-00 Miller laryngoscope blade. DESIGN: Randomised crossover simulation study SETTING: Simulated neonatal intensive care unit environment STUDY SUBJECTS: Neonatology physicians and nurse practitioners (n=55) INTERVENTIONS: Subjects performed four intubations in succession on a high-fidelity ELBW manikin with size-0 Miller and size-00 Miller blades from two different manufacturers. The intubation sequence was randomised. Intubations were recorded and scored for time analysis. Subjects completed surveys about blade preferences before and after completing the series of intubations. MAIN OUTCOME MEASURES: Total laryngoscopy time and first attempt success in less than 30 s RESULTS: There was no difference in total laryngoscopy time (median 23.7 vs 20.6 s) or first attempt success in <30 s (67.3% vs 69.1%) between the size-0 and size-00 blades. Differences were noted between the same size blades made by different manufacturers. Among subjects expressing a prestudy blade size preference, there was no difference in laryngoscopy time or first attempt success between blades. Regardless of blade size, subjects were less successful with the first blade in the randomised sequence. CONCLUSIONS: Our findings support the Neonatal Resuscitation Program recommendation identifying the size-00 blade as optional equipment. Operators need to be aware of design variations between manufacturers and they may benefit from ‘just-in-time’ training with a manikin prior to intubating a live patient. BMJ Publishing Group 2017-09-05 /pmc/articles/PMC5862193/ /pubmed/29637161 http://dx.doi.org/10.1136/bmjpo-2017-000157 Text en © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted. This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Original Article
O'Connell, Joseph
Weiner, Gary
Intubating extremely premature newborns: a randomised crossover simulation study
title Intubating extremely premature newborns: a randomised crossover simulation study
title_full Intubating extremely premature newborns: a randomised crossover simulation study
title_fullStr Intubating extremely premature newborns: a randomised crossover simulation study
title_full_unstemmed Intubating extremely premature newborns: a randomised crossover simulation study
title_short Intubating extremely premature newborns: a randomised crossover simulation study
title_sort intubating extremely premature newborns: a randomised crossover simulation study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5862193/
https://www.ncbi.nlm.nih.gov/pubmed/29637161
http://dx.doi.org/10.1136/bmjpo-2017-000157
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