Abstract
OBJECTIVES: Multicenter studies reporting outcomes following tracheostomy in children with congenital heart disease are limited, particularly in patients with single ventricle physiology. We aimed to describe clinical characteristics and outcomes in a multicenter cohort of patients with single ventricle physiology who underwent tracheostomy before Fontan operation. DESIGN: Multicenter retrospective cohort study. SETTING: Twenty-one tertiary care pediatric institutions participating in the Collaborative Research from the Pediatric Cardiac Intensive Care Society. PATIENTS: We reviewed 99 children with single ventricle physiology who underwent tracheostomy before the Fontan operation at 21 institutions participating in Collaborative Research from the Pediatric Cardiac Intensive Care Society between January 2010 and December 2020, with follow-up through December 31, 2021. INTERVENTIONS: None. MEASUREMENTS AND MAIN RESULTS: Death occurred in 51 of 99 patients (52%). Cox proportional hazard analysis was performed to determine factors associated with death after tracheostomy. Results are presented as hazard ratio (HR) with 95% CIs. Nonrespiratory indication(s) for tracheostomy (HR, 2.21; 95% CI, 1.14–4.32) and number of weeks receiving mechanical ventilation before tracheostomy (HR, 1.06; 95% CI, 1.02–1.11) were independently associated with greater hazard of death. In contrast, diagnosis of tricuspid atresia or Ebstein’s anomaly was associated with less hazard of death (HR, 0.16; 95% CI, 0.04–0.69). Favorable outcome, defined as survival to Fontan operation or decannulation while awaiting Fontan operation with viable cardiopulmonary physiology, occurred in 29 of 99 patients (29%). Median duration of mechanical ventilation before tracheostomy was shorter in patients who survived to favorable outcome (6.1 vs. 12.1wk; p < 0.001), and only one of 16 patients with neurologic indications for tracheostomy and 0 of ten patients with cardiac indications for tracheostomy survived to favorable outcome. CONCLUSIONS: For children with single ventricle physiology who undergo tracheostomy, mortality risk is high and should be carefully considered when discussing tracheostomy as an option for these children. Favorable outcomes are possible, although thoughtful attention to patient selection and tracheostomy timing are likely necessary to achieve this goal.
Original language | English (US) |
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Pages (from-to) | 728-739 |
Number of pages | 12 |
Journal | Pediatric Critical Care Medicine |
Volume | 25 |
Issue number | 8 |
DOIs | |
State | Published - Aug 1 2024 |
Funding
Dr. Mastropietro received funding from Telan, Meltz, Wallace, and Eide Law Firm, and Bioporto. Dr. Werho received funding from University of California San Diego; his institution received funding from the American Heart Association; and he disclosed that he is a board member of the Pediatric Cardiac Intensive Care Society and the Pediatric Cardiac Critical Care Consortium. Dr. Yates received funding from Alexion Pharmaceuticals. The remaining authors have disclosed that they do not have any potential conflicts of interest.
Keywords
- Fontan procedure
- artificial respiration
- congenital heart defects
- hypoplastic left heart syndrome
- risk factors
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health
- Critical Care and Intensive Care Medicine