Evidence map›Paper›PMID 39736088›Full record

ArticleActa paediatrica (Oslo, Norway : 1992)2025

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

Sakari Wahrmann, Leena Kainulainen, Johanna Lempainen, Ville Kytö

Abstract read
In one paragraph

Article in Acta paediatrica (Oslo, Norway : 1992), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Sakari WahrmannDepartment of Paediatrics and Adolescent Medicine, Turku University Hospital and University of Turku, Turku, Finland.ORCID 0000-0001-8692-6610
Leena KainulainenDepartment of Paediatrics and Adolescent Medicine, Turku University Hospital and University of Turku, Turku, Finland.
Johanna LempainenDepartment of Paediatrics and Adolescent Medicine, Turku University Hospital and University of Turku, Turku, Finland.
Ville KytöHeart Centre, Turku University Hospital and University of Turku, Turku, Finland.

Funding

Governor Wilho Kyttä FoundationPaavo Nurmen SäätiöSydäntutkimussäätiö
6 · The paper itself

Abstract

aimStudies 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.

Indexed as

DiGeorge SyndromeHospitalizationInfectionsAdolescentAnti-Bacterial AgentsCase-Control StudiesChildChild, PreschoolFemaleFinlandHumansInfantInfant, NewbornMaleRegistriesRetrospective StudiesAnti-Bacterial AgentsantibioticsDiGeorge syndromeinfection ratesmorbidityvelocardiofacial syndrome

Identifiers

PMID39736088
PMCPMC12066910

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.