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. 2023 May 1;6(5):e2312277.
doi: 10.1001/jamanetworkopen.2023.12277.

Assessment of Corticosteroid Therapy and Death or Disability According to Pretreatment Risk of Death or Bronchopulmonary Dysplasia in Extremely Preterm Infants

Collaborators, Affiliations

Assessment of Corticosteroid Therapy and Death or Disability According to Pretreatment Risk of Death or Bronchopulmonary Dysplasia in Extremely Preterm Infants

Erik A Jensen et al. JAMA Netw Open. .

Abstract

Importance: Meta-analyses suggest that corticosteroids may be associated with increased survival without cerebral palsy in infants at high risk of bronchopulmonary dysplasia (BPD) but are associated with adverse neurologic outcomes in low-risk infants. Whether this association exists in contemporary practice is uncertain because most randomized clinical trials administered corticosteroids earlier and at higher doses than currently recommended.

Objective: To evaluate whether the pretreatment risk of death or grade 2 or 3 BPD at 36 weeks' postmenstrual age modified the association between postnatal corticosteroid therapy and death or disability at 2 years' corrected age in extremely preterm infants.

Design, setting, and participants: This cohort study analyzed data on 482 matched pairs of infants from 45 participating US hospitals in the National Institute of Child Health and Human Development Neonatal Research Network Generic Database (GDB). Infants were included in the cohort if they were born at less than 27 weeks' gestation between April 1, 2011, and March 31, 2017; survived the first 7 postnatal days; and had 2-year death or developmental follow-up data collected between January 2013 and December 2019. Corticosteroid-treated infants were propensity score matched with untreated controls. Data were analyzed from September 1, 2019, to November 30, 2022.

Exposure: Systemic corticosteroid therapy to prevent BPD that was initiated between day 8 and day 42 after birth.

Main outcomes and measures: The primary outcome was death or moderate to severe neurodevelopmental impairment at 2 years' corrected age. The secondary outcome was death or moderate to severe cerebral palsy at 2 years' corrected age.

Results: A total of 482 matched pairs of infants (mean [SD] gestational age, 24.1 [1.1] weeks]; 270 males [56.0%]) were included from 656 corticosteroid-treated infants and 2796 potential controls. Most treated infants (363 [75.3%]) received dexamethasone. The risk of death or disability associated with corticosteroid therapy was inversely associated with the estimated pretreatment probability of death or grade 2 or 3 BPD. The risk difference for death or neurodevelopmental impairment associated with corticosteroids decreased by 2.7% (95% CI, 1.9%-3.5%) for each 10% increase in the pretreatment risk of death or grade 2 or 3 BPD. This risk transitioned from estimated net harm to benefit when the pretreatment risk of death or grade 2 or 3 BPD exceeded 53% (95% CI, 44%-61%). For death or cerebral palsy, the risk difference decreased by 3.6% (95% CI, 2.9%-4.4%) for each 10% increase in the risk of death or grade 2 or 3 BPD and transitioned from estimated net harm to benefit at a pretreatment risk of 40% (95% CI, 33%-46%).

Conclusions and relevance: Results of this study suggested that corticosteroids were associated with a reduced risk of death or disability in infants at moderate to high pretreatment risk of death or grade 2 or 3 BPD but with possible harm in infants at lower risk.

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Conflict of interest statement

Conflict of Interest Disclosures: Dr Greenberg reported receiving personal fees from Provepharm Inc and Tellus Therapeutics outside the submitted work. Dr DeMauro reported receiving grants from the National Heart Lung and Blood Institute (NHLBI) of the National Institutes of Health (NIH), National Institute on Drug Abuse, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD/NIH), and Thrasher Research Fund outside the submitted work. No other disclosures were reported.

Figures

Figure 1.
Figure 1.. Study Flow Diagram
Figure 2.
Figure 2.. Risk Differences for Death or Disability vs the Pretreatment Probability of Death or Grade 2 or 3 Bronchopulmonary Dysplasia (BPD) at 36 Weeks’ Postmenstrual Age (PMA)
Circles represent values for individual matched pairs; shaded areas represent regression lines and 95% CIs. For death or neurodevelopmental impairment (NDI), the regression line equation is y = 0.144 – 0.272x and crosses the x-axis at an estimated probability of death or grade 2 or 3 BPD of 53% (95% CI, 44%-61%). For death or cerebral palsy (CP), the regression line equation is y = 0.144 − 0.361x and crosses the x-axis at 40% (95% CI, 33%-46%). Logistic regression model c-statistic values in the matched cohort are 0.753 for death or grade 2 or 3 BPD at 36 weeks’ PMA, 0.766 for death or NDI at 2 years, and 0.812 for death or CP at 2 years.
Figure 3.
Figure 3.. Risk Differences for Death or Disability Stratified by Treatment With Dexamethasone or Hydrocortisone
Circles and Xs represent values computed for individual matched pairs with dexamethasone and hydrocortisone treatment, respectively; shaded areas represent regression lines and 95% CIs. The regression line for death or neurodevelopmental impairment (NDI) is y = 0.131 – 0.221x for dexamethasone and y = 0.167 – 0.384x for hydrocortisone. For dexamethasone, the regression line crosses the x-axis at a pretreatment probability of death or grade 2 or 3 bronchopulmonary dysplasia (BPD) of 59% (95% CI, 48%-74%) for dexamethasone and 44% (95% CI, 21%-56%) for hydrocortisone. The regression line for death or cerebral palsy crosses the x-axis at 42% (95% CI, 31%-50%) for dexamethasone and 40% (95% CI, 28%-48%) for hydrocortisone. PMA indicates postmenstrual age.

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