Otitis media prone children with cystic fibrosis: A new normal

Jennifer L McCoy1, Thomas M Kaffenberger2, Tiffany S Yang3

  • 1Division of Pediatric Otolaryngology, UPMC Children's Hospital of Pittsburgh, Pittsburgh, PA, United States of America.

Insights

Children with cystic fibrosis (CF) prone to otitis media requiring tympanostomy tube placement (TTP) show similar rates of tympanostomy tube otorrhea (TTO) as non-CF children. This study highlights TTO incidence in CF patients post-TTP.

Area of Science:

  • Pediatric Otolaryngology
  • Pediatric Pulmonology
  • Genetics and Rare Diseases

Background:

  • Recurrent acute otitis media (RAOM) is common in children.
  • Cystic Fibrosis (CF) is a genetic disorder affecting multiple organs, including the respiratory system.
  • Otitis media is a frequent complication in children with CF.

Purpose of the Study:

  • To investigate the incidence of tympanostomy tube otorrhea (TTO) in children with cystic fibrosis (CF) who have undergone tympanostomy tube placement (TTP).
  • To compare the natural course of TTO in CF patients with the established incidence in non-CF children (21-34%).

Main Methods:

  • Retrospective review of CF patients at a tertiary pediatric hospital from 2010-2019.
  • Inclusion criteria identified 17 CF patients who had undergone TTP.
  • Data collection included demographics, CF diagnosis, genotype, TTP history, and TTO occurrences up to 18 months post-TTP.

Main Results:

  • CF diagnosed at a median age of 13 days; 82.4% had one TTP, 11.8% had two, and 5.9% had five.
  • Median age at first TTP was 2 years.
  • TTO occurred in 29.4% at 3 months, 35.3% at 6-9 months, and 41.2% at 12-18 months post-TTP.

Conclusions:

  • CF children are more prone to severe RAOM, necessitating TTP.
  • The incidence of TTO in CF children following TTP aligns with the natural history observed in the non-CF population.
  • This is the first study to report TTO rates in CF patients post-TTP, confirming a similar trajectory to non-CF peers.
Abstract

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