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Respiratory severity score-guided postnatal systemic corticosteroid therapy for bronchopulmonary dysplasia in
Gyeong Eun Yeom1, Ju Sun Heo1,2, Baek Sup Shin1
1Department of Pediatrics, Seoul National University Children's Hospital, Seoul, Korea.
Insights
A new respiratory severity score (RSS)-guided protocol for extremely preterm (EP) infants reduced severe bronchopulmonary dysplasia (BPD) without impacting neurodevelopmental outcomes. This targeted approach refines steroid therapy for vulnerable newborns.
Area of Science:
- Neonatal Medicine
- Pediatric Pulmonology
- Clinical Trial Methodology
Background:
- Bronchopulmonary dysplasia (BPD) is a significant complication in extremely preterm (EP) infants.
- Postnatal systemic corticosteroids are used to manage BPD but raise concerns about neurodevelopmental outcomes.
- Optimal timing and criteria for initiating steroid therapy for BPD remain unclear.
Purpose of the Study:
- To evaluate a respiratory severity score (RSS)-guided postnatal systemic corticosteroid protocol.
- To assess the impact of this protocol on BPD severity and neurodevelopmental outcomes in mechanically ventilated EP infants.
Main Methods:
- A historical comparative study comparing pre- and post-protocol implementation (2010-2014 vs. 2016-2022).
- Inclusion criteria: infants born <28 weeks' gestation, ventilated on postnatal day 14.
- The protocol used RSS to guide corticosteroid initiation; BPD severity and neurodevelopmental impairment (NDI) were compared.
Main Results:
- The post-protocol group showed increased dexamethasone use and earlier initiation.
- Significant increase in Jensen grade 0 BPD in the post-protocol group, especially in non-steroid treated infants.
- Steroid-treated infants in the post-protocol group had decreased severe BPD (grade 3) and increased mild BPD (grade 1).
- No significant differences in mortality or severe neurodevelopmental impairment between groups.
Conclusions:
- The RSS-guided protocol facilitates targeted and earlier steroid administration.
- This strategy effectively reduces severe BPD without adverse neurodevelopmental effects.
- The RSS-guided approach offers a refined strategy for postnatal corticosteroid treatment in EP infants.
Background:
Bronchopulmonary dysplasia (BPD) is a major complication in extremely preterm (EP) infants. Postnatal systemic corticosteroids reduce inflammation and may help prevent or treat BPD. However, their use is limited because of concerns regarding neurodevelopmental outcomes. However, the optimal timing and criteria for steroid therapy initiation remain unclear.
Purpose:
This study aimed to evaluate the effect of a respiratory severity score (RSS)-guided postnatal systemic corticosteroid protocol on BPD and neurodevelopmental outcomes in mechanically ventilated infants with EP.
Methods:
A historical comparative study was conducted to compare the preprotocol (2010-2014; phase I) and postprotocol (2016-2022; phase II) periods. Infants born at <28 weeks' gestation and ventilated on postnatal day 14 were included in the study. The protocol implemented in 2015 used the RSS to guide corticosteroid initiation. Clinical outcomes including BPD severity and severe neurodevelopmental impairment (NDI) were compared.
Results:
Among the 208 infants, those in phase II had higher dexamethasone use (17.6% vs. 33.0%, P=0.017) and earlier initiation (postmenstrual age, 31.1 vs. 29.0 weeks; P=0.027). In phase II, Jensen grade 0 was significantly increased (15.2% vs. 30.2%; adjusted odds ratio [aOR], 2.31; P=0.024), particularly among patients who did not receive steroids. In steroid-treated infants, Jensen grade 3 BPD was decreased (47.4% vs. 21.2%; aOR, 0.26; P=0.050), whereas grade 1 BPD was increased (5.3% vs. 33.3%; aOR, 12.22; P=0.035) in phase II. There were no significant intergroup differences in mortality or NDI.
Conclusion:
The RSS-guided protocol enabled more targeted and earlier steroid administration, reducing severe BPD without worsening neurodevelopmental outcomes. This approach may refine postnatal corticosteroid treatment strategies for infants with EP.
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