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Outcomes in children after mild neonatal hypoxic ischaemic encephalopathy: A population‐based cohort study
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Women's and Children's Health, Clinical Obstetrics.ORCID iD: 0000-0001-6904-8115
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Women's and Children's Health, Clinical Obstetrics. Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Disciplinary Domain of Medicine and Pharmacy, research centers etc., Center for Clinical Research Dalarna.ORCID iD: 0000-0001-9173-2909
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Women's and Children's Health, Healthcare Sciences and e-Health.ORCID iD: 0000-0002-9212-8452
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Women's and Children's Health, Perinatal, Neonatal and Pediatric Cardiology Research.ORCID iD: 0000-0002-9510-048x
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2023 (English)In: British Journal of Obstetrics and Gynecology, ISSN 1470-0328, E-ISSN 1471-0528Article in journal (Refereed) Epub ahead of print
Abstract [en]

Objective

To investigate whether mild neonatal hypoxic ischaemic encephalopathy (HIE) in term born infants is associated with cerebral palsy, epilepsy, mental retardation and death up to 6 years of age.

Design

Population-based cohort study.

Setting

Sweden, 2009–2015.

Population

Live term born infants without congenital malformations or chromosomal abnormalities (n = 505 075).

Methods

Birth and health data were retrieved from Swedish national health and quality registers. Mild HIE was identified by diagnosis in either the Swedish Medical Birth Register or the Swedish Neonatal Quality Register. Cox proportional hazards regression was used to estimate hazard ratios (HRs) with 95% confidence intervals (CIs).

Main outcome measures

A composite of the outcomes cerebral palsy, epilepsy, mental retardation and death up to 6 years of age.

Results

Median follow-up time was 3.3 years after birth. Of 414 infants diagnosed with mild HIE, 17 were classified according to the composite outcome and incidence rates were 12.6 and 2.9 per 1000 child-years in infants with and without HIE respectively. Infants with mild HIE was four times as likely to be diagnosed with the composite outcome (HR 4.42, 95% CI 2.75–7.12) compared with infants without HIE. When analysed separately, associations were found with cerebral palsy (HR 21.50, 95% CI 9.59–48.19) and death (HR 19.10, 95% CI 7.90–46.21). HRs remained essentially unchanged after adjustment for covariates.

Conclusions

Mild neonatal HIE was associated with neurological morbidity and mortality in childhood. Challenges include identifying infants who may develop morbidity and how to prevent adverse outcomes.

Place, publisher, year, edition, pages
John Wiley & Sons, 2023.
National Category
Public Health, Global Health and Social Medicine
Identifiers
URN: urn:nbn:se:uu:diva-504414DOI: 10.1111/1471-0528.17533ISI: 000991569400001PubMedID: 37199188OAI: oai:DiVA.org:uu-504414DiVA, id: diva2:1766716
Funder
Gillbergska stiftelsenAvailable from: 2023-06-13 Created: 2023-06-13 Last updated: 2025-02-20

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Törn, Anna E.Hesselman, SusanneJohansen, KineÅgren, JohanWikström, Anna-KarinJonsson, Maria

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Clinical ObstetricsCenter for Clinical Research DalarnaHealthcare Sciences and e-HealthPerinatal, Neonatal and Pediatric Cardiology Research
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Public Health, Global Health and Social Medicine

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