Respiratory tract infection-related healthcare utilisation in children with Down's syndrome

Logan Manikam1,2, Anne G M Schilder3,4, Monica Lakhanpaul5,6

  • 1UCL Institute of Epidemiology and Healthcare, University College London, 1-19 Torrington Place, London, WC1E 6BT, UK. logan.manikam.10@alumni.ucl.ac.uk.

Infection
|March 16, 2020
PubMed

Insights

Children with Down's syndrome (DS) experience significantly more respiratory tract infections (RTIs) and healthcare visits than other children. This highlights a substantial burden on families and necessitates further research for optimized care.

Area of Science:

  • Pediatric Health
  • Genetics and Disease
  • Healthcare Utilization Research

Background:

  • Children with Down's syndrome (DS) are susceptible to respiratory tract infections (RTIs) due to unique physiological and immunological factors.
  • Existing data on healthcare utilization for RTIs in children with DS, particularly in primary care, remains limited.

Purpose of the Study:

  • To quantify and compare RTI-related healthcare utilization between children with DS and matched controls without DS.
  • To analyze differences in primary and secondary care usage for RTIs in these groups.

Main Methods:

  • A retrospective cohort study utilizing linked electronic health records (CALIBER) from 1997-2010 in England.
  • Inclusion of 992 children with DS and 4874 matched controls.
  • Poisson regression and Wald tests were employed to compare consultation, hospitalization, and prescription rates, alongside admission risks and length of stay.

Main Results:

  • Children with DS showed significantly higher rates of GP consultations (aRR 1.73), hospitalizations (aRR 5.70), and antibiotic prescriptions (aRR 2.34) for RTIs compared to controls.
  • The risk of hospital admission following a GP consultation for an RTI was higher in children with DS (2%) versus controls (0.7%).

Conclusions:

  • Children with DS exhibit substantially elevated healthcare utilization for RTIs across primary and secondary care settings.
  • The findings underscore a significant healthcare burden on families of children with DS, indicating a need for targeted research into care optimization.
Abstract

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