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Single-center experience of outcomes of tracheostomy in children with congenital heart disease.
- Source :
-
Congenital heart disease [Congenit Heart Dis] 2013 Nov-Dec; Vol. 8 (6), pp. 556-60. Date of Electronic Publication: 2013 Mar 20. - Publication Year :
- 2013
-
Abstract
- Objective: A subset of children with repaired congenital heart disease (CHD) may require tracheostomy for ongoing ventilatory support. Data on outcomes of children with CHD and tracheostomy are scarce. Our objectives were to describe indications for tracheostomy and outcomes, including readmission data in this population.<br />Methods: This is a retrospective chart review of children (<18 years old) with CHD who underwent tracheostomy at a single center over a 12-year period. Exclusion criteria were prematurity with isolated patent ductus arteriosus ligation. Outcomes until discharge and data on all readmissions after the initial discharge were reviewed.<br />Results: A total of 21 subjects with CHD underwent tracheostomy at a median (range) age of 4 (1-84) months and mean (standard deviation) weight of 7.2 (5.9) kg. The most common indication for tracheostomy was tracheomalacia with ventilator-dependent respiratory failure (14/21 subjects), followed by subglottic stenosis (5) and vocal cord palsy (2). Genetic syndromes were present in 13 (62%) subjects. The mean (standard deviation) post-tracheostomy length of stay was 55 (35) days. All subjects survived to discharge; 17 (81%) required home ventilation. A total of 11 (52%) subjects died during follow-up, all of whom were mechanically ventilated while three (14%) children underwent successful decannulation. The mean number of nonelective readmissions decreased from 2.4/patient-year in the first year to 1.4/patient-year in the second year, respectively. The commonest reasons for readmission were respiratory deterioration, infections, and mechanical tracheostomy-related problems.<br />Conclusions: The majority of children with CHD who underwent tracheostomy did so for ventilator dependence and tracheomalacia and had coexisting genetic syndromes. About half the cohort died; among survivors, readmissions were common but decreased after the first year. These results underscore the ongoing mortality and morbidity risks faced by this vulnerable population.<br /> (© 2013 Wiley Periodicals, Inc.)
- Subjects :
- Child
Child, Preschool
Comorbidity
Female
Heart Defects, Congenital diagnosis
Heart Defects, Congenital genetics
Heart Defects, Congenital mortality
Home Care Services
Hospital Mortality
Humans
Infant
Laryngostenosis diagnosis
Laryngostenosis genetics
Laryngostenosis mortality
Male
Patient Discharge
Patient Readmission
Respiratory Insufficiency diagnosis
Respiratory Insufficiency mortality
Retrospective Studies
Risk Factors
Time Factors
Tracheomalacia diagnosis
Tracheomalacia genetics
Tracheomalacia mortality
Treatment Outcome
Vocal Cord Paralysis diagnosis
Vocal Cord Paralysis mortality
Heart Defects, Congenital therapy
Laryngostenosis therapy
Respiration, Artificial adverse effects
Respiration, Artificial mortality
Respiratory Insufficiency therapy
Tracheomalacia therapy
Tracheostomy adverse effects
Tracheostomy mortality
Vocal Cord Paralysis therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1747-0803
- Volume :
- 8
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Congenital heart disease
- Publication Type :
- Academic Journal
- Accession number :
- 23510243
- Full Text :
- https://doi.org/10.1111/chd.12048