You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


ABOUT ARCHIVES
Advanced Search

Welcome   | My Account | E-mail Alerts | Access Rights | Sign In


  Vol. 125 No. 5, May 1999 TABLE OF CONTENTS
  Archives
  •  Online Features
  Original Article
 This Article
 •Full text
 •PDF
 • Reply to article
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on HighWire
 •Citing articles on Web of Science (21)
 •Contact me when this article is cited
 Related Content
 •Similar articles in this journal
 Topic Collections
 •Airway Obstruction
 •Congenital Anomalies of Head & Neck
 •Pediatric Otolaryngology
 •Pediatrics
 •Congenital Malformations
 •Alert me on articles by topic
 Social Bookmarking
  Add to CiteULike Add to Connotea Add to Del.icio.us Add to Digg Add to Reddit Add to Technorati Add to Twitter What's this?

Congenital Airway Abnormalities in Patients Requiring Hospitalization

Ken W. Altman, MD, PhD; Ralph F. Wetmore, MD; Roger R. Marsh, PhD

Arch Otolaryngol Head Neck Surg. 1999;125:525-528.

Objective  To determine the cause of congenital airway abnormalities in pediatric patients requiring hospitalization for their respiratory status.

Design and Setting  Case series in a tertiary care center.

Patients  A 5-year retrospective chart review was conducted at our institution. A total of 174 patients were identified who required hospitalization for their respiratory status as a result of a congenital airway abnormality.

Results  Of the 174 patients, 114 (65.5%) were male and 60 (34.5%) were female. Eighty patients (47%) presented within the first 3 months of life. Forty-six patients (26%) were born prematurely, and 49 patients (28%) were diagnosed as having gastroesophageal reflux. The majority of patients (139 [80%]) had multiple presenting symptoms or signs. Stridor was the most common (129 [74%]), followed by accessory respiratory effort, cyanosis, apnea, and failure to thrive. Diagnosis was made at the time of surgical evaluation in 91% of the patients, with the remaining diagnoses made using radiological findings and/or clinical evaluation. Sixty-five patients (37%) had multiple sites of airway abnormalities; laryngeal abnormalities were noted almost 3 times as often as tracheal abnormalities (161 vs 62, respectively). Of the laryngeal abnormalities, laryngomalacia was the most common, followed by glottic web, subglottic stenosis, vocal-cord paralysis, and subglottic hemangioma. Tracheomalacia was the most common tracheal abnormality, followed by external compression and tracheal stenosis. Thirty-three patients (19%) required tracheotomy for management of recurrent respiratory decompensation.

Conclusions  While congenital airway abnormalities are usually self-limited, those patients requiring hospitalization represent a group with a more severe respiratory status who have a greater chance of requiring tracheotomy. The recognizable percentage of patients with gastroesophageal reflux and prematurity accounts for comorbid factors in the need for hospitalization for respiratory issues related to congenital airway abnormalities.


From the Department of Otolaryngology, Children's Hospital of Philadelphia and the University of Pennsylvania School of Medicine, Philadelphia.



Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter     What's this?

THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Developmental Aspects of the Upper Airway: Report from an NHLBI Workshop, March 5-6, 2009
Marcus et al.
Proc Am Thorac Soc 2009;6:513-520.
ABSTRACT | FULL TEXT  

Tracheobronchomalacia in Infants and Children: Multidetector CT Evaluation
Lee and Boiselle
Radiology 2009;252:7-22.
ABSTRACT | FULL TEXT  

Case 7-2009 -- A Pregnant Woman with a Large Mass in the Fetal Oral Cavity
Hartnick et al.
NEJM 2009;360:913-921.
FULL TEXT  

Tracheomalacia and Tracheobronchomalacia in Children and Adults: An In-depth Review
Carden et al.
Chest 2005;127:984-1005.
ABSTRACT | FULL TEXT  

Potential Role of Sox9 in Patterning Tracheal Cartilage Ring Formation in an Embryonic Mouse Model
Elluru and Whitsett
Arch Otolaryngol Head Neck Surg 2004;130:732-736.
ABSTRACT | FULL TEXT  

Correlation of Findings at Direct Laryngoscopy and Bronchoscopy With Gastroesophageal Reflux Disease in Children: A Prospective Study
Carr et al.
Arch Otolaryngol Head Neck Surg 2001;127:369-374.
ABSTRACT | FULL TEXT  

Mapping of a Gene for Severe Pediatric Gastroesophageal Reflux to Chromosome 13q14
Hu et al.
JAMA 2000;284:325-334.
ABSTRACT | FULL TEXT  





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 1999 American Medical Association. All Rights Reserved.