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Identifying effect modifiers of systemic hydrocortisone treatment initiated 7–14 days after birth in ventilated very preterm infants on long-term outcome: secondary analysis of a randomised controlled trial

  • Nienke Marjolein Halbmeijer
  • , Michel Sonnaert
  • , Renate M. Swarte
  • , Corine Koopman-Esseboom
  • , Margriet van Stuijvenberg
  • , Susanne Mulder De Tollenaer
  • , Ratna N.G.B. Tan
  • , Thilo Mohns
  • , Els Bruneel
  • , Katerina Steiner
  • , Boris W. Kramer
  • , Anne Debeer
  • , Mirjam M. van Weissenbruch
  • , Yoann Marechal
  • , Henry Blom
  • , Katleen Plaskie
  • , Martin Offringa
  • , Maruschka P. Merkus
  • , Wes Onland
  • , Aleid G. Leemhuis
  • Anton H. van Kaam*,
*Corresponding author for this work

Research output: Contribution to journal › Article › Academic › peer-review

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Abstract

Objective To explore clinical effect modifiers of systemic hydrocortisone in ventilated very preterm infants for survival and neurodevelopmental outcome at 2 years’ corrected age (CA). Design Secondary analysis of a randomised placebo-controlled trial. Setting Dutch and Belgian neonatal intensive care units. Patients Infants born <30 weeks’ gestational age (GA), ventilator-dependent in the second week of postnatal life. Intervention Infants were randomly assigned to systemic hydrocortisone (cumulative dose 72.5 mg/kg; n=182) or placebo (n=190). Main outcome measures The composite of death or neurodevelopmental impairment (NDI) at 2 years’ CA and its components. Candidate effect modifiers (GA, small for GA, respiratory index, sex, multiple births, risk of moderate/severe bronchopulmonary dysplasia or death) were analysed using regression models with interaction terms and subpopulation treatment effect pattern plots. Results The composite outcome was available in 356 (96.0%) of 371 patients (one consent withdrawn). For this outcome, treatment effect heterogeneity was seen across GA subgroups (<27 weeks: hydrocortisone (n=141) vs placebo (n=156), 54.6% vs 66.2%; OR 0.61 (95% CI 0.38 to 0.98); ≥27 weeks: hydrocortisone (n=30) vs placebo (n=31), 66.7% vs 45.2%; OR 2.43 (95% CI 0.86 to 6.85); p=0.02 for interaction). This effect was also found for the component death (<27 weeks: 20.1% vs 32.1%; OR 0.53 (95% CI 0.32 to 0.90); ≥27 weeks: 28.1% vs 16.1%; OR 2.04 (95% CI 0.60 to 6.95); p=0.049 for interaction) but not for the component NDI. No differential treatment effects were observed across other subgroups. Conclusion This secondary analysis suggests that in infants <27 weeks’ GA, systemic hydrocortisone may improve the outcome death or NDI, mainly driven by its component death. There was insufficient evidence for other selected candidate effect modifiers.

Original languageEnglish
Pages (from-to)159-165
Number of pages7
JournalArchives of Disease in Childhood: Fetal and Neonatal Edition
Volume109
Issue number2
DOIs
Publication statusPublished - 18 Sept 2023

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