A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä

Finnish nationwide controlled register study found increased inpatient infections in children with 22q11.2 deletion syndrome




TekijätWahrmann, Sakari; Kainulainen, Leena; Lempainen, Johanna; Kytö, Ville

KustantajaWILEY

KustannuspaikkaHOBOKEN

Julkaisuvuosi2024

Lehti:Acta Paediatrica

Tietokannassa oleva lehden nimiACTA PAEDIATRICA

Lehden akronyymiACTA PAEDIATR

Sivujen määrä7

ISSN0803-5253

eISSN1651-2227

DOIhttps://doi.org/10.1111/apa.17569

Verkko-osoitehttps://doi.org/10.1111/apa.17569

Rinnakkaistallenteen osoitehttps://research.utu.fi/converis/portal/detail/Publication/477736993


Tiivistelmä
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.

Methods

Children 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.

Results

The 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.

Conclusion

Children with 22q11.2DS had significantly more infections requiring hospitalisation than controls without the syndrome.


Ladattava julkaisu

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Julkaisussa olevat rahoitustiedot
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.


Last updated on 2025-27-01 at 19:49