Association between antenatal corticosteroids and risk of serious infection in children: nationwide cohort study.


Journal

BMJ (Clinical research ed.)
ISSN: 1756-1833
Titre abrégé: BMJ
Pays: England
ID NLM: 8900488

Informations de publication

Date de publication:
02 08 2023
Historique:
medline: 4 8 2023
pubmed: 3 8 2023
entrez: 2 8 2023
Statut: epublish

Résumé

To investigate the associations between exposure to antenatal corticosteroids and serious infection in children during the first three, six, and 12 months of life. Nationwide cohort study. National Health Insurance Research Database, Birth Reporting Database, and Maternal and Child Health Database, 1 January 2008 to 31 December 2019, to identify all pregnant individuals and their offspring in Taiwan. 1 960 545 pairs of pregnant individuals and their singleton offspring. 45 232 children were exposed and 1 915 313 were not exposed to antenatal corticosteroids. Incidence rates were estimated for overall serious infection, sepsis, pneumonia, acute gastroenteritis, pyelonephritis, meningitis or encephalitis, cellulitis or soft tissue infection, septic arthritis or osteomyelitis, and endocarditis during the first three, six, and 12 months of life in children exposed versus those not exposed to antenatal corticosteroids. Cox proportional hazards models were performed to quantify adjusted hazard ratios with 95% confidence intervals for each study outcome. The study cohort was 1 960 545 singleton children: 45 232 children were exposed to one course of antenatal corticosteroids and 1 915 313 children were not exposed to antenatal corticosteroids. The adjusted hazard ratios for overall serious infection, sepsis, pneumonia, and acute gastroenteritis among children exposed to antenatal corticosteroids were significantly higher than those not exposed to antenatal corticosteroids during the first six months of life (adjusted hazard ratio 1.32, 95% confidence interval 1.18 to 1.47, P<0.001, for overall serious infection; 1.74, 1.16 to 2.61, P=0.01, for sepsis; 1.39, 1.17 to 1.65, P<0.001, for pneumonia; and 1.35, 1.10 to 1.65, P<0.001, for acute gastroenteritis).Similarly, the adjusted hazard ratios for overall serious infection (P<0.001), sepsis (P=0.02), pneumonia (P<0.001), and acute gastroenteritis (P<0.001) were significantly higher from birth to 12 months of life. In the sibling matched cohort, the results were comparable with those observed in the whole cohort, with a significantly increased risk of sepsis in the first six (P=0.01) and 12 (P=0.04) months of life. This nationwide cohort study found that children exposed to one course of antenatal corticosteroids were significantly more likely to have an increased risk of serious infection during the first 12 months of life. These findings suggest that before starting treatment, the long term risks of rare but serious infection associated with antenatal corticosteroids should be carefully weighed against the benefits in the perinatal period.

Identifiants

pubmed: 37532264
doi: 10.1136/bmj-2023-075835
pmc: PMC10394679
doi:

Substances chimiques

Adrenal Cortex Hormones 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e075835

Commentaires et corrections

Type : CommentIn

Informations de copyright

© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

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Auteurs

Tsung-Chieh Yao (TC)

Division of Allergy, Asthma, and Rheumatology, Department of Paediatrics, Chang Gung Memorial Hospital, Taoyuan, Taiwan yao@adm.cgmh.org.tw.
School of Medicine, Chang Gung University College of Medicine, Taoyuan, Taiwan.

Sheng-Mao Chang (SM)

Department of Statistics, National Taipei University, Taipei, Taiwan.

Chi-Shin Wu (CS)

National Centre for Geriatrics and Welfare Research, National Health Research Institutes, Zhunan, Taiwan.
Department of Psychiatry, National Taiwan University Hospital, Yunlin Branch, Douliu, Taiwan.

Yi-Fen Tsai (YF)

Institute of Population Health Sciences, National Health Research Institutes, Zhunan, Taiwan.

Kun-Hua Sheen (KH)

Department of Medical Science, National Tsing-Hua University, Hsinchu, Taiwan.

Xiumei Hong (X)

Department of Population, Family, and Reproductive Health, Center on Early Life Origins of Disease, Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD, USA.

Hui-Yu Chen (HY)

Department of Pharmacy, Chang Gung Memorial Hospital, Taoyuan, Taiwan.

Ann Chen Wu (AC)

Harvard Medical School, Boston, MA, USA.

Hui-Ju Tsai (HJ)

Institute of Population Health Sciences, National Health Research Institutes, Zhunan, Taiwan.
Department of Medical Science, National Tsing-Hua University, Hsinchu, Taiwan.

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