Evidence map›Paper›PMID 41383573›Full record

ArticleFrontiers in pediatrics2025

Efficacy of lung surfactant combined with budesonide in improving bronchopulmonary dysplasia and growth of very low birth weight infants.

Yu Zhang, Ming Liu, Yue Li, Di Chi, Jinpu Zhang, Yunfeng Zhang

Abstract read
In one paragraph

Article in Frontiers in pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Yu ZhangDepartment of Neonatology, The Second Hospital of Jilin University, Changchun, Jilin, China.
Ming LiuDepartment of Neonatology, The Second Hospital of Jilin University, Changchun, Jilin, China.
Yue LiDepartment of Neonatology, The Second Hospital of Jilin University, Changchun, Jilin, China.
Di ChiDepartment of Neonatology, The Second Hospital of Jilin University, Changchun, Jilin, China.
Jinpu ZhangDepartment of Neonatology, The Second Hospital of Jilin University, Changchun, Jilin, China.
Yunfeng ZhangDepartment of Neonatology, The Second Hospital of Jilin University, Changchun, Jilin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: There is few treatments for bronchopulmonary dysplasia (BPD), and systemic glucocorticoid therapy has serious side effects. Methods: Low birth weight infants were classified randomly into control group administered with pulmonary surfactant (200 mg/kg) and intervention group administered with pulmonary surfactant (200 mg/kg) and budesonide suspension (0.25 mg/kg) to explore the efficacy of combination of pulmonary surfactant and budesonide suspension is better than that of pulmonary surfactant alone. Results: The incidence of bronchopulmonary dysplasia was significantly lower in the intervention group (45%) compared to the control group (64%). Additionally, the duration of invasive ventilator use was significantly shorter in the intervention group (66.39 ± 37.09 h) than in the control group (82.05 ± 54.55 h); and the infants from the intervention group had a significantly shorter supplemental oxygen time, with the intervention group at 775.32 ± 396.06 h and the control group at 844.01 ± 414.18 h. Comparison of the basic conditions of the two groups of children showed no statistically significant differences in maternal medical history, gestational age, birth weight, sex, whether hormones were used prenatally, and delivery method ( Conclusion: Combination of pulmonary surfactant with budesonide suspension can significantly decrease the incidence of bronchopulmonary dysplasia in very low birth weight infants, reduce the duration of invasive mechanical ventilation, and promote earlier weaning from oxygen supplement. Clinical Trial Registration: Effect of budesonide combined with pulmonary surfactant on lung development in very low birth weight infants, ChiCTR2400086677, https://www.chictr.org.cn/showproj.html?proj=233373.

Indexed as

bronchopulmonary dysplasiabudesonide suspensionclinical triallocal applicationpulmonary surfactant

Identifiers

PMID41383573
PMCPMC12689501

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.