TY - JOUR
T1 - Impact of Failure of Noninvasive Ventilation on the Safety of Pediatric Tracheal Intubation
AU - Emeriaud, Guillaume
AU - Napolitano, Natalie
AU - Polikoff, Lee
AU - Giuliano, John
AU - Toedt-Pingel, Iris
AU - Miksa, Michael
AU - Li, Simon
AU - Bysani, Kris
AU - Hsing, Deyin D.
AU - Nett, Sholeen
AU - Turner, David A.
AU - Sanders, Ronald C.
AU - Lee, Jan Hau
AU - Adu-Darko, Michelle
AU - Owen, Erin B.
AU - Gangadharan, Sandeep
AU - Parker, Margaret
AU - Montgomery, Vicki
AU - Craig, Nancy
AU - Crulli, Benjamin
AU - Edwards, Lauren
AU - Pinto, Matt
AU - Brunet, Fabrice
AU - Shults, Justine
AU - Nadkarni, Vinay
AU - Nishisaki, Akira
N1 - Publisher Copyright:
© 2020 Lippincott Williams and Wilkins. All rights reserved.
PY - 2020/10/1
Y1 - 2020/10/1
N2 - Objectives: Noninvasive ventilation is widely used to avoid tracheal intubation in critically ill children. The objective of this study was to assess whether noninvasive ventilation failure was associated with severe tracheal intubation-associated events and severe oxygen desaturation during tracheal intubation. Design: Prospective multicenter cohort study of consecutive intubated patients using the National Emergency Airway Registry for Children registry. Setting: Thirteen PICUs (in 12 institutions) in the United States and Canada. Patients: All patients undergoing tracheal intubation in participating sites were included. Noninvasive ventilation failure group included children with any use of high-flow nasal cannula, continuous positive airway pressure, or bilevel noninvasive ventilation in the 6 hours prior to tracheal intubation. Primary tracheal intubation group included children without exposure to noninvasive ventilation within 6 hours before tracheal intubation. Interventions: None. Measurements and Main Results: Severe tracheal intubation-associated events (cardiac arrest, esophageal intubation with delayed recognition, emesis with aspiration, hypotension requiring intervention, laryngospasm, pneumothorax, pneumomediastinum) and severe oxygen desaturation (< 70%) were recorded prospectively. The study included 956 tracheal intubation encounters; 424 tracheal intubations (44%) occurred after noninvasive ventilation failure, with a median of 13 hours (interquartile range, 4-38 hr) of noninvasive ventilation. Noninvasive ventilation failure group included more infants (47% vs 33%; p < 0.001) and patients with a respiratory diagnosis (56% vs 30%; p < 0.001). Noninvasive ventilation failure was not associated with severe tracheal intubation-associated events (5% vs 5% without noninvasive ventilation; p = 0.96) but was associated with severe desaturation (15% vs 9% without noninvasive ventilation; p = 0.005). After controlling for baseline differences, noninvasive ventilation failure was not independently associated with severe tracheal intubation-associated events (p = 0.35) or severe desaturation (p = 0.08). In the noninvasive ventilation failure group, higher Fio2before tracheal intubation (≥ 70%) was associated with severe tracheal intubation-associated events. Conclusions: Critically ill children are frequently exposed to noninvasive ventilation before intubation. Noninvasive ventilation failure was not independently associated with severe tracheal intubation-associated events or severe oxygen desaturation compared to primary tracheal intubation.
AB - Objectives: Noninvasive ventilation is widely used to avoid tracheal intubation in critically ill children. The objective of this study was to assess whether noninvasive ventilation failure was associated with severe tracheal intubation-associated events and severe oxygen desaturation during tracheal intubation. Design: Prospective multicenter cohort study of consecutive intubated patients using the National Emergency Airway Registry for Children registry. Setting: Thirteen PICUs (in 12 institutions) in the United States and Canada. Patients: All patients undergoing tracheal intubation in participating sites were included. Noninvasive ventilation failure group included children with any use of high-flow nasal cannula, continuous positive airway pressure, or bilevel noninvasive ventilation in the 6 hours prior to tracheal intubation. Primary tracheal intubation group included children without exposure to noninvasive ventilation within 6 hours before tracheal intubation. Interventions: None. Measurements and Main Results: Severe tracheal intubation-associated events (cardiac arrest, esophageal intubation with delayed recognition, emesis with aspiration, hypotension requiring intervention, laryngospasm, pneumothorax, pneumomediastinum) and severe oxygen desaturation (< 70%) were recorded prospectively. The study included 956 tracheal intubation encounters; 424 tracheal intubations (44%) occurred after noninvasive ventilation failure, with a median of 13 hours (interquartile range, 4-38 hr) of noninvasive ventilation. Noninvasive ventilation failure group included more infants (47% vs 33%; p < 0.001) and patients with a respiratory diagnosis (56% vs 30%; p < 0.001). Noninvasive ventilation failure was not associated with severe tracheal intubation-associated events (5% vs 5% without noninvasive ventilation; p = 0.96) but was associated with severe desaturation (15% vs 9% without noninvasive ventilation; p = 0.005). After controlling for baseline differences, noninvasive ventilation failure was not independently associated with severe tracheal intubation-associated events (p = 0.35) or severe desaturation (p = 0.08). In the noninvasive ventilation failure group, higher Fio2before tracheal intubation (≥ 70%) was associated with severe tracheal intubation-associated events. Conclusions: Critically ill children are frequently exposed to noninvasive ventilation before intubation. Noninvasive ventilation failure was not independently associated with severe tracheal intubation-associated events or severe oxygen desaturation compared to primary tracheal intubation.
KW - adverse events
KW - high-flow nasal cannula
KW - noninvasive ventilation
KW - patient safety
KW - pediatric critical care
KW - tracheal intubation
UR - http://www.scopus.com/inward/record.url?scp=85091125940&partnerID=8YFLogxK
U2 - 10.1097/CCM.0000000000004500
DO - 10.1097/CCM.0000000000004500
M3 - Article
C2 - 32701551
AN - SCOPUS:85091125940
SN - 0090-3493
VL - 48
SP - 1503
EP - 1512
JO - Critical Care Medicine
JF - Critical Care Medicine
IS - 10
ER -