Antenatal corticosteroid treatment and infectious diseases in children: a nationwide observational study
Räikkönen, Katri; Gissler, Mika; Kajantie, Eero; Tapiainen, Terhi (2023-10-12)
Räikkönen, Katri
Gissler, Mika
Kajantie, Eero
Tapiainen, Terhi
Elsevier
12.10.2023
Räikkönen, K., Gissler, M., Kajantie, E., & Tapiainen, T. (2023). Antenatal corticosteroid treatment and infectious diseases in children: a nationwide observational study. In The Lancet Regional Health - Europe (Vol. 35, p. 100750). Elsevier BV. https://doi.org/10.1016/j.lanepe.2023.100750.
https://creativecommons.org/licenses/by-nc-nd/4.0/
© 2023 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
https://creativecommons.org/licenses/by-nc-nd/4.0/
© 2023 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
https://creativecommons.org/licenses/by-nc-nd/4.0/
Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:oulu-202312153842
https://urn.fi/URN:NBN:fi:oulu-202312153842
Tiivistelmä
Summary
Background:
Antenatal Corticosteroid Treatment (ACT) improves the outcome of preterm infants, but may influence immune system development and risk of immune-related diseases. We investigated whether ACT is associated with infectious diseases in children born at term (≥37 gestational weeks), and very-to-moderate (<34 gestational weeks), and late (34–36 completed gestational weeks) preterm.
Methods:
All singleton live births in Finland between 01/01/2006 and 31/12/2021, were followed-up until 31/12/2021. Exposure was maternal ACT. Primary outcomes were numbers of inpatient treatment days, episodes, and specialized care outpatient visits with any infectious disease diagnoses between ages 0 and 4 years. We considered mother- and child-related covariates, and conducted term-born co-sibling comparisons.
Findings:
Data comprised 855,234 children. Of the 20,858 (2.4%) treatment-exposed children, 5981 (28.2%) were very-to-moderate preterm-born, 5809 (27.9%) late preterm-born, and 9069 (43.5%) term-born. Of the 271,767 term-born co-sibling pairs, 5010 (1.8%) were treatment-exposure-discordant, and 266,522 (98.1%) nonexposure-concordant. Among the term- and late preterm-born, treatment-exposed children had more inpatient treatment days than nonexposed children (term: 0.87 vs. 0.56 day/y, adjusted mean difference [aMD] 0.19, 95% CI 0.17–0.28; late preterm: 1.35 vs. 1.00 days/y, aMD 0.31,0.13–0.31), more inpatient treatment episodes (term: 0.43 vs. 0.33 episodes/y, aMD 0.06, 0.06–0.11; late preterm: 0.55 vs. 0.48 episodes/y, aMD 0.12, 0.06–0.18), and specialized care treatment visits (term: 1.46 vs. 0.95 visits/y, aMD 0.38; 0.34–0.43; late preterm: 1.63 vs. 1.28 visits/y, aMD 0.22, 0.12–0.32). Treatment-exposed and nonexposed very-to-moderate preterm-born children were similar in these outcomes, though they had less inpatient treatment days and episodes at 3–4 years. Differences remained in term-born co-sibling comparisons.
Interpretation:
These findings reinforce previous suggestions for careful consideration of risks and benefits of ACT.
Background:
Antenatal Corticosteroid Treatment (ACT) improves the outcome of preterm infants, but may influence immune system development and risk of immune-related diseases. We investigated whether ACT is associated with infectious diseases in children born at term (≥37 gestational weeks), and very-to-moderate (<34 gestational weeks), and late (34–36 completed gestational weeks) preterm.
Methods:
All singleton live births in Finland between 01/01/2006 and 31/12/2021, were followed-up until 31/12/2021. Exposure was maternal ACT. Primary outcomes were numbers of inpatient treatment days, episodes, and specialized care outpatient visits with any infectious disease diagnoses between ages 0 and 4 years. We considered mother- and child-related covariates, and conducted term-born co-sibling comparisons.
Findings:
Data comprised 855,234 children. Of the 20,858 (2.4%) treatment-exposed children, 5981 (28.2%) were very-to-moderate preterm-born, 5809 (27.9%) late preterm-born, and 9069 (43.5%) term-born. Of the 271,767 term-born co-sibling pairs, 5010 (1.8%) were treatment-exposure-discordant, and 266,522 (98.1%) nonexposure-concordant. Among the term- and late preterm-born, treatment-exposed children had more inpatient treatment days than nonexposed children (term: 0.87 vs. 0.56 day/y, adjusted mean difference [aMD] 0.19, 95% CI 0.17–0.28; late preterm: 1.35 vs. 1.00 days/y, aMD 0.31,0.13–0.31), more inpatient treatment episodes (term: 0.43 vs. 0.33 episodes/y, aMD 0.06, 0.06–0.11; late preterm: 0.55 vs. 0.48 episodes/y, aMD 0.12, 0.06–0.18), and specialized care treatment visits (term: 1.46 vs. 0.95 visits/y, aMD 0.38; 0.34–0.43; late preterm: 1.63 vs. 1.28 visits/y, aMD 0.22, 0.12–0.32). Treatment-exposed and nonexposed very-to-moderate preterm-born children were similar in these outcomes, though they had less inpatient treatment days and episodes at 3–4 years. Differences remained in term-born co-sibling comparisons.
Interpretation:
These findings reinforce previous suggestions for careful consideration of risks and benefits of ACT.
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