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Factors associated with short-term response after systemic corticosteroid treatment in invasively ventilated preterm
Gyeong Eun Yeom1, Seung Han Shin2, Han-Suk Kim3
1Department of Pediatrics, Seoul National University Children's Hospital, Seoul National University College of Medicine, 103 Daehak-ro, Jongno-gu, Seoul, 110-799, Korea.
Insights
Pulmonary hypertension and patent ductus arteriosus predict poor response to corticosteroid therapy in preterm infants with bronchopulmonary dysplasia. Early respiratory severity score changes can help identify non-responders.
Area of Science:
- Neonatal medicine
- Pediatric pulmonology
- Critical care medicine
Background:
- Bronchopulmonary dysplasia (BPD) is a chronic lung disease in preterm infants.
- Systemic corticosteroid (CS) therapy is used to treat BPD, but its efficacy varies.
- Pulmonary hypertension (PH) and patent ductus arteriosus (PDA) are common complications in BPD.
Purpose of the Study:
- To evaluate factors influencing short-term efficacy of systemic CS therapy in preterm infants with BPD.
- To identify predictors of treatment response, focusing on PH and hemodynamically significant PDA (hsPDA).
Main Methods:
- Retrospective review of preterm infants (<32 weeks gestation or <1500g) receiving systemic CS for BPD.
- Responders defined by extubation within 14 days and/or ≥60% reduction in respiratory severity score (RSS).
- Multivariate analysis to identify predictors of non-response.
Main Results:
- Of 62 infants, 32 were responders and 30 non-responders.
- Non-responders had higher prevalence of PH (70.0% vs. 21.9%) and hsPDA (30.0% vs. 3.1%) at treatment initiation.
- PH and hsPDA were significant predictors of non-response (aOR 6.66 and 12.54, respectively).
Conclusions:
- Vascular phenotypes (PH, hsPDA) in BPD should be identified before CS therapy initiation.
- Early changes in RSS (day 1-4) can improve prediction of treatment failure.
- Optimizing patient selection and early identification of non-responders can improve treatment outcomes.
Purpose:
This study evaluated the factors affecting the short-term efficacy of systemic corticosteroid (CS) therapy, focusing on pulmonary hypertension (PH) and other clinical conditions in preterm infants with evolving or established bronchopulmonary dysplasia (BPD).
Methods:
A retrospective review was conducted on preterm infants (< 32 weeks of gestation and/or < 1,500 g birth weight) who received systemic CS therapy for BPD. Responders were defined as infants who were extubated within 14 days and/or achieved a ≥ 60% reduction in the respiratory severity score (RSS).
Results:
Of the 62 infants, 32 were classified as responders and 30 as non-responders. Non-responders had a significantly higher prevalence of PH requiring treatment (70.0% vs. 21.9%, p < 0.001) and hemodynamically significant patent ductus arteriosus (hsPDA) at treatment initiation (30.0% vs. 3.1%, p = 0.005). Responders showed a greater reduction in RSS from day 1 to day 4 (33.8% vs. 11.7%, p = 0.002). In multivariate analysis, PH requiring treatment (adjusted odds ratio [aOR]: 6.66, 95% confidence interval [CI]: 1.39-31.92, p = 0.018) and hsPDA (aOR: 12.54, 95% CI: 1.16-135.05, p = 0.037) at treatment initiation were significant predictors of non-response.
Conclusion:
Identifying the vascular phenotypes of BPD, including PH and hsPDA, before initiating systemic CS therapy may improve patient selection and optimize treatment outcomes. Incorporating early changes in RSS from treatment day 1 to day 4 enhanced the predictive accuracy for treatment failure and may facilitate the timely identification of non-responders.
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