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Surfactant-Budesonide Combination to Prevent Death or Bronchopulmonary Dysplasia: A Systematic Review and
Ilari Kuitunen1,2, Giulia Res3,4, Kati Räsänen5
1Institute of Clinical Medicine, University of Eastern Finland, Kuopio, Finland, ilari.kuitunen@uef.fi.
Insights
Combining surfactant with budesonide may reduce mortality and bronchopulmonary dysplasia (BPD) in preterm infants. Further research is needed to identify which infants benefit most from this combination therapy.
Area of Science:
- Neonatal Medicine
- Pediatric Pulmonology
- Pharmacology
Background:
- Bronchopulmonary dysplasia (BPD) is a significant complication of prematurity.
- Current treatments for BPD have limitations.
- Investigating novel therapeutic strategies is crucial.
Purpose of the Study:
- To evaluate the efficacy of intratracheal budesonide combined with surfactant in reducing mortality and BPD in preterm infants.
- To synthesize evidence from existing randomized and observational studies.
Main Methods:
- Systematic review and meta-analysis of randomized and observational studies.
- Searched PubMed, Scopus, and Web of Science.
- Included studies comparing surfactant-budesonide vs. surfactant alone in preterm neonates.
- Random-effects meta-analyses and GRADE certainty assessment.
Main Results:
- Combination therapy significantly reduced mortality (RR 0.83) and BPD (RR 0.84).
- Benefits were consistent across study designs and surfactant types.
- Moderate certainty of evidence for both outcomes.
Conclusions:
- Surfactant-budesonide combination therapy shows potential for reducing mortality and BPD in preterm infants.
- Evidence is currently insufficient for widespread primary treatment recommendation.
- Future research should focus on identifying specific infant subgroups who may benefit most.
Introduction:
Bronchopulmonary dysplasia (BPD) remains a major complication of prematurity. We aimed to assess whether intratracheal administration of budesonide mixed with surfactant reduces mortality and BPD in preterm infants.
Methods:
We conducted a systematic review and meta-analysis of randomised and observational studies enrolling preterm neonates. PubMed, Scopus, and Web of Science were searched from inception to October 2025 without language or year restrictions. Studies comparing bolus administration of bovine or porcine surfactant mixed with budesonide versus surfactant alone were included. Random-effects meta-analyses using inverse variance weighting were performed to estimate risk ratios (RRs) with 95% confidence intervals (CIs). Certainty of evidence was assessed using GRADE.
Results:
Twenty randomised and five observational studies were included. Surfactant-budesonide combination therapy reduced mortality (RR: 0.83, 95% CI: 0.69-0.99; 18 studies, 5,117 infants) and BPD (RR: 0.84, 95% CI: 0.75-0.94; 25 studies, 5,732 infants). Mortality reduction was observed when all studies were pooled, with no significant difference between study designs. Prenatal steroid exposure was associated with greater mortality reduction. Reduction in BPD remained significant when restricted to randomised trials, irrespective of surfactant type. Sensitivity analyses excluding studies at high risk of bias yielded similar results. Certainty of evidence was moderate for both outcomes.
Conclusion:
Surfactant combined with budesonide may reduce mortality and BPD in preterm infants. However, the evidence remains insufficient to recommend the combination as generalised primary treatment for all preterm neonates. Future studies should incorporate pathophysiological phenotyping to identify infants most likely to benefit.
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