A1 Refereed original research article in a scientific journal
Finnish nationwide controlled register study found increased inpatient infections in children with 22q11.2 deletion syndrome
Authors: Wahrmann, Sakari; Kainulainen, Leena; Lempainen, Johanna; Kytö, Ville
Publisher: WILEY
Publishing place: HOBOKEN
Publication year: 2024
Journal:: Acta Paediatrica
Journal name in source: ACTA PAEDIATRICA
Journal acronym: ACTA PAEDIATR
Number of pages: 7
ISSN: 0803-5253
eISSN: 1651-2227
DOI: https://doi.org/10.1111/apa.17569
Web address : https://doi.org/10.1111/apa.17569
Self-archived copy’s web address: https://research.utu.fi/converis/portal/detail/Publication/477736993
Aim
Studies on treating infections in children with 22q11.2 deletion syndrome (22q11.2DS) have been limited. We characterised inpatient infections and outpatient antibiotic treatment.
MethodsChildren born during 2005–2018 were eligible for this national Finnish retrospective register-based study. We recruited 98 children (54% male) with DiGeorge or velocardiofacial syndrome. The 980 matched controls had a benign murmur diagnosed before 1 year of age. The cumulative incidence of infections and antibiotic prescriptions and total prescriptions were measured.
ResultsThe median age for 22q11.2DS diagnoses was under 1 year of age (range 0–14 years), with a median follow-up time of 9 years for diagnoses and 11 years for prescriptions. Children with 22q11.2DS had significantly higher hospitalisation rates than the controls for any infection (68.1% vs. 30.5%), gastroenteritis (16.8% vs. 4.0%), pneumonia (23.4% vs. 4.3%), severe bacterial infections, excluding pneumonia or pyelonephritis (15.0% vs. 4.1%) and viral wheezing (23.2% vs. 9.1%). Outpatient antibiotic prescriptions were similar, but the children with 22q11.2DS received them earlier than the controls, with a hazard ratio of 3.29 for ages 0–5 years and 1.84 for the entire follow-up.
ConclusionChildren with 22q11.2DS had significantly more infections requiring hospitalisation than controls without the syndrome.
Downloadable publication This is an electronic reprint of the original article. |
Funding information in the publication:
This study was supported by grants from the Paavo Nurmi Foundation, the Finnish Foundation for Cardiovascular Research and Governor Wilho Kyttä Foundation. The funders played no role in any aspect of the study or paper.