Childhood interstitial lung disease in Turkey: first data from the national registry

Halime Nayır-Büyükşahin1,2, Nagehan Emiralioğlu3, Ayşe Ayzıt Kılınç4

  • 1Division of Pulmonology, Department of Pediatrics, Faculty of Medicine, Hacettepe University, Ankara, Turkey. hnayirbuyuksahin@gmail.com.

PubMed

Insights

The first results from the childhood interstitial lung diseases (chILD) registry in Turkey reveal key differences in presentation and treatment between infant-onset and all-age diffuse parenchymal lung diseases. Findings highlight the need to consider nutrition, especially in infants with chILD.

Area of Science:

  • Pediatric Pulmonology
  • Rare Diseases
  • Medical Registries

Background:

  • Childhood interstitial lung diseases (chILD) are a heterogeneous group of rare disorders that pose diagnostic and management challenges.
  • Establishing national registries is crucial for understanding the epidemiology and clinical characteristics of chILD.
  • The chILD Turkey registry (chILD-TR) was created to improve awareness, diagnosis, and treatment standards.

Purpose of the Study:

  • To present the initial findings from the chILD-TR, a prospective cohort study.
  • To analyze the demographic, clinical, radiologic, and treatment characteristics of registered chILD patients in Turkey.
  • To compare clinical features between infants with chILD and those diagnosed at all ages.

Main Methods:

  • Prospective cohort study utilizing a data-entry software system.
  • Inclusion of 416 patients from 19 centers, with 370 analyzed after exclusions.
  • Comparison of clinical characteristics between two groups: Group 1 (infancy-onset DPLD) and Group 2 (all-age DPLD).

Main Results:

  • The median age of diagnosis was 6.05 years. Group 1 comprised 21.8% and Group 2 comprised 78.1% of patients.
  • Group 1 showed significantly lower weight z-scores and more frequent ground-glass opacities on CT scans.
  • Group 2 had more frequent nodular opacities, bronchiectasis, mosaic perfusion, and mediastinal lymphadenopathy; oral steroid use was higher in Group 2.

Conclusions:

  • The chILD-TR provides valuable insights into the frequency, types, and treatment of chILD in Turkey, identifying diagnostic and management challenges.
  • Significant differences exist in clinical presentation and radiologic findings between infant-onset and later-onset chILD.
  • Nutritional status is a critical consideration for all chILD patients, particularly those with infancy-onset disease.

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