Hemodynamic Impact of Oxygen Desaturation During Tracheal Intubation Among Critically Ill Children With Cyanotic and Noncyanotic Heart Disease.


Journal

Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies
ISSN: 1529-7535
Titre abrégé: Pediatr Crit Care Med
Pays: United States
ID NLM: 100954653

Informations de publication

Date de publication:
01 2019
Historique:
pubmed: 6 11 2018
medline: 17 3 2020
entrez: 6 11 2018
Statut: ppublish

Résumé

To determine a level of oxygen desaturation from baseline that is associated with increased risk of tracheal intubation associated events in children with cyanotic and noncyanotic heart disease. Retrospective analysis of prospectively collected data from the National Emergency Airway Registry for Children, an international multicenter quality improvement collaborative for airway management in critically ill children. Thirty-eight PICUs from July 2012 to December 2016. Children with cyanotic and noncyanotic heart disease who underwent tracheal intubation in a pediatric or cardiac ICU. None. Our exposure of interest was oxygen desaturation measured by a fall in pulse oximetry from baseline after preoxygenation. Primary outcome was the occurrence of hemodynamic tracheal intubation associated events defined as cardiac arrest, hypotension or dysrhythmia. One-thousand nine-hundred ten children (cyanotic, 999; noncyanotic, 911) were included. Patients with cyanotic heart disease who underwent tracheal intubations were younger (p < 0.001) with higher Pediatric Index of Mortality 2 scores (p < 0.001), more likely to have a cardiac surgical diagnosis (p < 0.001), and less likely to have hemodynamic instability (p = 0.009) or neurologic failure as an indication (p = 0.008). Oxygen desaturation was observed more often in children with cyanotic versus noncyanotic heart disease (desaturation of 15% to < 30%: 23% vs 16%, desaturation ≥ 30%: 23% vs 17%; p < 0.001), with no significant difference in occurrence of hemodynamic tracheal intubation associated events (7.5% vs 6.9%; p = 0.618). After adjusting for confounders, oxygen desaturation by 30% or more is associated with increased odds for adverse hemodynamic events (odds ratio, 4.03; 95% CI, 2.12-7.67) for children with cyanotic heart disease and (odds ratio, 3.80; 95% CI, 1.96-7.37) for children with noncyanotic heart disease. Oxygen desaturation was more commonly observed during tracheal intubation in children with cyanotic versus noncyanotic heart disease. However, hemodynamic tracheal intubation associated event rates were similar. In both groups, oxygen desaturation greater than or equal to 30% was significantly associated with increased occurrence of hemodynamic tracheal intubation associated events.

Identifiants

pubmed: 30395028
doi: 10.1097/PCC.0000000000001766
doi:

Substances chimiques

Oxygen S88TT14065

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

19-26

Subventions

Organisme : AHRQ HHS
ID : R03 HS021583
Pays : United States
Organisme : AHRQ HHS
ID : R18 HS022464
Pays : United States
Organisme : AHRQ HHS
ID : R18 HS024511
Pays : United States

Commentaires et corrections

Type : CommentIn

Auteurs

Tanya Mokhateb-Rafii (T)

Division of Pediatric Critical Care Medicine, Department of Pediatrics, Steven and Alexandra Cohen Children's Medical Center, New Hyde Park, NY.

Adnan Bakar (A)

Division of Pediatric Critical Care Medicine, Department of Pediatrics, Steven and Alexandra Cohen Children's Medical Center, New Hyde Park, NY.
Division of Pediatric Cardiology, Department of Pediatrics, Steven and Alexandra Cohen Children's Medical Center, New Hyde Park, NY.

Sandeep Gangadharan (S)

Division of Pediatric Critical Care Medicine, Department of Pediatrics, Steven and Alexandra Cohen Children's Medical Center, New Hyde Park, NY.

Eleanor A Gradidge (EA)

Department of Pediatrics, Ochsner Hospital for Children, New Orleans, LA.

David Tellez (D)

Department of Critical Care, Phoenix Children's Hospital, Phoenix, AZ.

Michael Ruppe (M)

Division of Critical Care Medicine, Department of Pediatrics, Norton Children's Hospital, University of Louisville School of Medicine, Louisville, KY.

Sarah Tallent (S)

Division of Pediatric and Congenital Heart Center, Department of Pediatric Critical Care Medicine, Duke University Hospital, Durham, NC.

Geoffrey Bird (G)

Division of Cardiac Critical Care, Department of Anesthesiology and Critical Care Medicine, Children's Hospital of Philadelphia, Philadelphia, PA.

Natasha Lavin (N)

Department of Respiratory Therapy, Children's Hospital of Philadelphia, Philadelphia, PA.

Anthony Lee (A)

Division of Pediatric Critical Care Medicine, Department of Pediatrics, Nationwide Children's Hospital, Columbus, OH.

Natalie Napolitano (N)

Department of Respiratory Therapy, Children's Hospital of Philadelphia, Philadelphia, PA.

Vinay Nadkarni (V)

Division of Critical Care Medicine, Department of Anesthesiology and Critical Care Medicine, Children's Hospital of Philadelphia, Philadelphia, PA.

Justine Shults (J)

Department of Biostatistics and Epidemiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.

Akira Nishisaki (A)

Division of Critical Care Medicine, Department of Anesthesiology and Critical Care Medicine, Children's Hospital of Philadelphia, Philadelphia, PA.

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Classifications MeSH