Pulmonary complications in children with Down syndrome: A scoping review

Mariska De Lausnay1, Kris Ides2, Mark Wojciechowski3

  • 1Department of Pediatrics, Antwerp University Hospital, Drie Eikenstraat 655, 2650 Edegem, Belgium; Laboratory of Experimental Medicine and Pediatrics (LEMP), Antwerp University, Belgium.

Insights

Children with Down syndrome (DS) frequently experience complex lower airway issues, including infections and anomalies. Early diagnosis and a multidisciplinary team approach are crucial for better outcomes in these pediatric patients.

Area of Science:

  • Pediatric Pulmonology
  • Genetics
  • Clinical Medicine

Background:

  • Down syndrome (DS) is a common genetic disorder.
  • DS is associated with numerous congenital anomalies and health concerns.
  • Lower airway problems represent a significant health burden in children with DS.

Purpose of the Study:

  • To provide a comprehensive scoping review of lower airway conditions in children with Down syndrome.
  • To identify both infectious and non-infectious respiratory issues encountered in this population.

Main Methods:

  • Systematic literature search of MEDLINE and PubMed databases.
  • Inclusion of original studies on pediatric airway problems in DS, adhering to PRISMA guidelines.
  • Critical review and thematic summarization of extracted data on patient characteristics, methods, and outcomes.

Main Results:

  • Sixty studies were reviewed, highlighting prevalent airway anomalies, dysphagia, aspiration, and severe respiratory infections.
  • Children with DS exhibit a higher incidence of airway anomalies and often experience silent aspiration.
  • Respiratory infections, including bronchiolitis, are more severe in DS, leading to increased hospitalization; pulmonary hypertension and wheeze are also more common.

Conclusions:

  • Lower airway problems are more frequent and complex in children with Down syndrome.
  • Airway anomalies and aspiration require specialized management strategies.
  • A multidisciplinary team approach is essential for timely diagnosis, effective management, and improved long-term outcomes for DS children with respiratory issues.
Abstract

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