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Corticosteroid exposure in pediatric acute respiratory distress syndrome
Nadir Yehya1, Sabah Servaes, Neal J Thomas
1Department of Anesthesiology and Critical Care Medicine, Children's Hospital of Philadelphia and University of Pennsylvania, Suite 7C-26, 34th Street and Civic Center Boulevard, Philadelphia, PA, 19104, USA, yehyan@email.chop.edu.
Insights
Systemic corticosteroids in pediatric acute respiratory distress syndrome (PARDS) may not improve survival. Prolonged corticosteroid use (>24 hours) was linked to longer ventilation duration in survivors, not increased mortality.
Area of Science:
- Pediatric Critical Care Medicine
- Pulmonology
- Pharmacology
Background:
- Systemic corticosteroid use in acute respiratory distress syndrome (ARDS) is debated.
- Limited research exists on corticosteroid efficacy in pediatric ARDS (PARDS).
Purpose of the Study:
- To investigate the association between prolonged corticosteroid exposure (>24 hours) and outcomes in children with PARDS.
Main Methods:
- Observational, single-center study of prospectively enrolled children with PARDS.
- Detailed data collected on corticosteroid type, timing, duration, and cumulative dose.
- Statistical analyses, including multivariate and propensity score adjustments, assessed outcomes.
Main Results:
- 60% of 283 children with PARDS received corticosteroids >24 hours.
- Prolonged corticosteroid use was associated with increased mortality, fewer ventilator-free days (VFD), and longer ventilation duration in unadjusted analyses.
- Adjusted analyses confirmed association with fewer VFD and longer ventilation in survivors, but not mortality.
Conclusions:
- Prolonged corticosteroid exposure (>24 hours) in pediatric ARDS is independently associated with fewer VFD and longer ventilation duration in survivors.
- No survival benefit was observed, and VFD were reduced in high-risk subgroups.
Purpose:
Use of systemic corticosteroids in acute respiratory distress syndrome (ARDS) remains controversial, and studies in children are lacking.
Methods:
We performed an observational, single-center study in a prospectively enrolled cohort of children meeting criteria for ARDS (both Berlin 2012 and AECC 1994 acute lung injury) and pediatric ARDS (PARDS, as defined by PALICC 2015). Comprehensive analysis of corticosteroid utilization was planned, and detailed information collected on corticosteroid use, timing, treatment duration, and cumulative dose while mechanically ventilated. We assessed the association between corticosteroid exposure >24 h and outcomes.
Results:
Of the 283 children with PARDS (37 deaths, 13%), 169 (60%) received corticosteroids for >24 h while ventilated: 51% hydrocortisone, 41% methylprednisolone, 5% dexamethasone, 3% combination of corticosteroids. Corticosteroid exposure >24 h was associated with increased mortality, fewer ventilator-free days at 28 days (VFD), and longer duration of ventilation in survivors in unadjusted analyses (all p < 0.05). Multivariate and propensity score adjusted analyses confirmed independent association of corticosteroid exposure with fewer VFD and longer duration of ventilation in survivors, but not with mortality. In planned analyses of high-risk subgroups, no benefit was seen with corticosteroids exposure, with fewer VFD associated with corticosteroid exposure >24 h in patients with ≥3 organ failures and immunocompromised patients.
Conclusions:
Corticosteroid exposure >24 h was independently associated with fewer VFD and longer duration of ventilation in survivors, even after adjustment for key potential confounders, including severity of illness, oxygenation index, immunocompromised status, and number of organ failures.
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