Volume 127, Issue 7 pp. 1701-1706
Pediatrics

Characterizing mortality in pediatric tracheostomy patients

Jamie L. Funamura MD

Jamie L. Funamura MD

Department of Otolaryngology and Communication Enhancement, Boston Children's Hospital, Boston, Massachusetts, U.S.A.

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Sonia Yuen BA

Sonia Yuen BA

Department of Otolaryngology and Communication Enhancement, Boston Children's Hospital, Boston, Massachusetts, U.S.A.

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Kosuke Kawai ScD

Kosuke Kawai ScD

Department of Otolaryngology and Communication Enhancement, Boston Children's Hospital, Boston, Massachusetts, U.S.A.

Department of Otology and Laryngology, Harvard Medical School, Boston, Massachusetts, U.S.A.

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Ozgul Gergin MD

Ozgul Gergin MD

Department of Otolaryngology, Umraniye Education and Research Hospital, Istanbul, Turkey

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Eelam Adil MD, MBA

Eelam Adil MD, MBA

Department of Otolaryngology and Communication Enhancement, Boston Children's Hospital, Boston, Massachusetts, U.S.A.

Department of Otology and Laryngology, Harvard Medical School, Boston, Massachusetts, U.S.A.

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Reza Rahbar DMD, MD

Reza Rahbar DMD, MD

Department of Otolaryngology and Communication Enhancement, Boston Children's Hospital, Boston, Massachusetts, U.S.A.

Department of Otology and Laryngology, Harvard Medical School, Boston, Massachusetts, U.S.A.

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Karen Watters MB, BCh, MPH

Corresponding Author

Karen Watters MB, BCh, MPH

Department of Otolaryngology and Communication Enhancement, Boston Children's Hospital, Boston, Massachusetts, U.S.A.

Department of Otology and Laryngology, Harvard Medical School, Boston, Massachusetts, U.S.A.

Send correspondence to Karen F. Watters, MB, BCh, MPH, 300 Longwood Avenue, LO-367, Boston, MA 02115. E-mail: [email protected]Search for more papers by this author
First published: 03 November 2016
Citations: 78

Presented at the 2016 American Society of Pediatric Otolaryngology Spring Meeting, Chicago, Illinois, U.S.A., May 20–22, 2016.

The authors have no funding, financial relationships, or conflicts of interest to disclose.

Abstract

Objectives/Hypothesis

To assess the longitudinal risk of death following tracheostomy in the pediatric age group.

Study Design

Retrospective cohort study.

Methods

Hospital records of 513 children (≤18 years) at a tertiary care children's hospital who underwent tracheostomy between 1984 and 2015 were reviewed. The primary outcome measure was time from tracheostomy to death. Secondary patient demographic and clinical characteristics were assessed, with likelihood of death using χ2 tests and the Cox proportional hazards model.

Results

Median age at time of tracheostomy was 0.8 years (interquartile range, 0.3–5.2 years).The highest mortality rate (27.8%) was observed in patients in the 13- to 18-year-old age category; their mortality rate was significantly higher when compared to the lowest mortality risk group patients (age 1–4 years, P = .031). Timing of death was evenly distributed: <90 days (37.6%), 90 days to 1 year (27.1%), and >1 year after tracheostomy (35.3%). Patients who underwent tracheostomy for cardiopulmonary disease had an increased risk of mortality compared with airway obstruction (adjusted hazard ratio: 3.53, 95% confidence interval: 1.72-7.24, P < .001) and other indications. Adjusted hazard ratios for bronchopulmonary dysplasia (BPD) and congenital heart disease (CHD) were 2.63 and a 2.61, respectively (P < .001).

Conclusions

Pediatric patients with tracheostomy have a high mortality rate, with an increased risk of death associated with a cardiopulmonary indication for undergoing tracheostomy. The majority of deaths occur after the index hospitalization during which the tracheostomy was performed. BPD and CHD are independent predictors of mortality in pediatric tracheostomy patients.

Level of Evidence

4 Laryngoscope, 127:1701–1706, 2017

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