Sensorineural hearing impairment among preterm children: a Norwegian population-based study.

Audiology Epidemiology Neonatology

Journal

Archives of disease in childhood. Fetal and neonatal edition
ISSN: 1468-2052
Titre abrégé: Arch Dis Child Fetal Neonatal Ed
Pays: England
ID NLM: 9501297

Informations de publication

Date de publication:
05 Jun 2024
Historique:
received: 14 01 2024
accepted: 22 05 2024
medline: 6 6 2024
pubmed: 6 6 2024
entrez: 5 6 2024
Statut: aheadofprint

Résumé

To investigate the risk for sensorineural hearing impairment (SNHI) in preterm infants, and to what extent the risk is attributed to perinatal morbidities and therapies. Population-based cohort study using data from several nationwide registries. Norwegian birth cohort 1999-2014, with data on SNHI until 2019. 60 023 live-born preterm infants, divided in moderate-late preterm (MLP) infants (32-36 weeks), very preterm (VP) infants (28-31 weeks) and extremely preterm (EP) infants (22-27 weeks), and a reference group with all 869 797 term-born infants from the study period. SNHI defined by selected ICD-10 codes, recorded during minimum 5-year observation period after birth. The overall SNHI prevalence in the preterm cohort was 1.4% compared with 0.7% in the reference group. The adjusted risk ratios (95% CIs) for SNHI were 1.7 (1.5-1.8) in MLP infants, 3.3 (2.8-3.9) in VP infants and 7.6 (6.3-9.1) in EP infants. Among EP infants, decreasing gestational age was associated with a steep increase in the risk ratio of SNHI reaching 14.8 (7.7-28.7) if born at 22-23 weeks gestation. Among the VP and MLP infants, mechanical ventilation and antibiotic therapy had strongest association with increased risk of SNHI, but infants not receiving these therapies remained at increased risk. Among EP infants intracranial haemorrhage increased the already high risk for SNHI. We found no signs of delayed or late-onset SNHI in preterm infants. Preterm birth is an independent risk factor for SNHI. Invasive therapies and comorbidities increase the risk, predominantly in infants born after 28 weeks gestation.

Identifiants

pubmed: 38839263
pii: archdischild-2024-326870
doi: 10.1136/archdischild-2024-326870
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2024. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Dagny Elise Hemmingsen (DE)

Department of Otorhinolaryngology and Head and Neck Surgery, University Hospital of North Norway, Tromso, Norway dagny.e.hemmingsen@uit.no.
Paediatric Research Group, UiT The Arctic University of Norway Faculty of Health Sciences, Tromso, Norway.

Dag Moster (D)

Institute of Global Public Health and Primary Care, UiB, Bergen, Norway.

Bo Lars Engdahl (BL)

Norwegian Institute of Public Health, Oslo, Norway.

Claus Klingenberg (C)

Paediatric Research Group, UiT The Arctic University of Norway Faculty of Health Sciences, Tromso, Norway.
Department of Paediatrics, University Hospital of North Norway, Tromsø, Norway.

Classifications MeSH