RSS-Feed abonnieren
DOI: 10.1055/a-2511-8702
Pathohistological Changes in the Lungs of Very Preterm Infants with Bronchopulmonary Dysplasia Depending on the Clinical Features
Funding None.

Abstract
Objective
Establishing clinical factors associated with histological changes in the lungs of very preterm infants with evolving or established bronchopulmonary dysplasia (BPD) is essential for the development of more effective preventive interventions.
Study Design
Thirty-two infants with a gestational age (GA) of <32 weeks who died of BPD or had BPD but died due to other causes were included in the study. The associations of clinical data with histopathological changes in the lungs were assessed.
Results
The mean (standard deviation) GA of infants was 26.7 (1.9) weeks, and the mean birth weight was 919.7 (242.9) g. We revealed significant associations of maternal smoking with vascular hypertension lesions (r s = 0.5, p < 0.05) in infants' lungs. Intrauterine growth retardation increased the risk of extensive fibroproliferation (r s = 0.4, p < 0.05). In infants with patent ductus arteriosus (PDA) requiring treatment, muscle hyperplasia (r s = 0.5, p < 0.05) was detected more often. The longer duration of mechanical ventilation (MV) correlated with diffuse interstitial fibroproliferation (r s = 0.5, p < 0.05), airway epithelial lesions (r s = 0.3, p < 0.05), and airway muscle hyperplasia (r s = 0.4, p < 0.05). In infants who needed the longer MV and/or oxygen supplementation, an increased incidence of extensive fibroproliferation was found (r s = 0.4 and r s = 0.4 respectively, p < 0.05). Antenatal steroids decreased the incidence of diffuse interstitial fibrosis (r s = − 0.4, p < 0.05).
Conclusion
In very preterm infants with a GA of less than 32 weeks, lack of antenatal steroid prophylaxis, intrauterine growth restriction, presence of hemodynamically significant PDA, and prolonged MV or oxygen supplementation are associated with the pathomorphological lung changes that are more typical for “old” BPD. Traditional preventive measures against BPD remain essential in a modern population of very preterm infants.
Key Points
-
Pathomorphological lung changes correlate with clinical data in very preterm infants who died of BPD.
-
Lack of antenatal steroids prophylaxis, growth retardation, PDA, and prolonged mechanical ventilation affect lungs.
-
Traditional BPD preventive measures remain essential in the modern population of preterm infants.
Keywords
bronchopulmonary dysplasia - pathomorphological lung changes - risk factors - very preterm infantsPublikationsverlauf
Eingereicht: 31. Juli 2024
Angenommen: 08. Januar 2025
Artikel online veröffentlicht:
31. Januar 2025
© 2025. Thieme. All rights reserved.
Thieme Medical Publishers, Inc.
333 Seventh Avenue, 18th Floor, New York, NY 10001, USA
-
References
- 1 van Kaam AH, De Luca D, Hentschel R. et al. Modes and strategies for providing conventional mechanical ventilation in neonates. Pediatr Res 2021; 90 (05) 957-962
- 2 Principi N, Di Pietro GM, Esposito S. Bronchopulmonary dysplasia: clinical aspects and preventive and therapeutic strategies. J Transl Med 2018; 16 (01) 36
- 3 Siffel C, Kistler KD, Lewis JFM, Sarda SP. Global incidence of bronchopulmonary dysplasia among extremely preterm infants: a systematic literature review. J Matern Fetal Neonatal Med 2021; 34 (11) 1721-1731
- 4 Jensen EA, Dysart K, Gantz MG. et al. The diagnosis of bronchopulmonary dysplasia in very preterm infants an evidence-based approach. Am J Respir Crit Care Med 2019; 200 (06) 751-759
- 5 Abman SH, Collaco JM, Shepherd EG. et al; Bronchopulmonary Dysplasia Collaborative. Interdisciplinary care of children with severe bronchopulmonary dysplasia. J Pediatr 2017; 181: 12-28.e1
- 6 Jobe AJ. The new BPD: an arrest of lung development. Pediatr Res 1999; 46 (06) 641-643
- 7 Moschino L, Bonadies L, Baraldi E. Lung growth and pulmonary function after prematurity and bronchopulmonary dysplasia. Pediatr Pulmonol 2021; 56 (11) 3499-3508
- 8 Day CL, Ryan RM. Bronchopulmonary dysplasia: new becomes old again!. Pediatr Res 2017; 81 (1-2): 210-213
- 9 Jobe AH, Bancalari E. Bronchopulmonary dysplasia. Am J Respir Crit Care Med 2001; 163 (07) 1723-1729
- 10 Higgins RD, Jobe AH, Koso-Thomas M. et al. Bronchopulmonary dysplasia: executive summary of a workshop. J Pediatr 2018; 197: 300-308
- 11 Papile LA, Burstein J, Burstein R, Koffler H. Incidence and evolution of subependymal and intraventricular hemorrhage: a study of infants with birth weights less than 1,500 gm. J Pediatr 1978; 92 (04) 529-534
- 12 Jain A, Shah PS. Diagnosis, evaluation, and management of patent ductus arteriosus in preterm neonates. JAMA Pediatr 2015; 169 (09) 863-872
- 13 Kliegman RM, Walsh MC. Neonatal necrotizing enterocolitis: pathogenesis, classification, and spectrum of illness. Curr Probl Pediatr 1987; 17 (04) 213-288
- 14 Oeser C, Lutsar I, Metsvaht T, Turner MA, Heath PT, Sharland M. Clinical trials in neonatal sepsis. J Antimicrob Chemother 2013; 68 (12) 2733-2745
- 15 Coalson JJ. Pathology of bronchopulmonary dysplasia. Semin Perinatol 2006; 30 (04) 179-184
- 16 Pérez-Tarazona S, Marset G, Part M, López C, Pérez-Lara L. Definitions of bronchopulmonary dysplasia: which one should we use?. J Pediatr 2022; 251: 67-73.e2
- 17 Jensen EA, DeMauro SB, Kornhauser M, Aghai ZH, Greenspan JS, Dysart KC. Effects of multiple ventilation courses and duration of mechanical ventilation on respiratory outcomes in extremely low-birth-weight infants. JAMA Pediatr 2015; 169 (11) 1011-1017
- 18 Laughon MM, Langer JC, Bose CL. et al; Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network. Prediction of bronchopulmonary dysplasia by postnatal age in extremely premature infants. Am J Respir Crit Care Med 2011; 183 (12) 1715-1722
- 19 Nascimento CP, Maia LP, Alves PT. et al. Invasive mechanical ventilation and biomarkers as predictors of bronchopulmonary dysplasia in preterm infants. J Pediatr (Rio J) 2021; 97 (03) 280-286
- 20 Escobar V, Soares DS, Kreling J. et al. Influence of time under mechanical ventilation on bronchopulmonary dysplasia severity in extremely preterm infants: a pilot study. BMC Pediatr 2020; 20 (01) 241
- 21 Choi YB, Lee J, Park J, Jun YH. Impact of prolonged mechanical ventilation in very low birth weight infants: results from a National Cohort Study. J Pediatr 2018; 194: 34-39.e3
- 22 Villamor-Martinez E, Álvarez-Fuente M, Ghazi AMT. et al. Association of chorioamnionitis with bronchopulmonary dysplasia among preterm infants. JAMA Netw Open 2019; 2 (11) e1914611
- 23 Liu W-L, Zhou Y, Zhang C. et al. Relationship between chorioamnionitis or funisitis and lung injury among preterm infants: meta-analysis involved 16 observational studies with 68,397 participants. BMC Pediatr 2024; 24 (01) 157
- 24 Kim CJ, Romero R, Chaemsaithong P, Chaiyasit N, Yoon BH, Kim YM. Acute chorioamnionitis and funisitis: definition, pathologic features, and clinical significance. Am J Obstet Gynecol 2015; 213 (04) S29-S52
- 25 Dankhara N, Holla I, Ramarao S, Kalikkot Thekkeveedu R. Bronchopulmonary dysplasia: pathogenesis and pathophysiology. J Clin Med 2023; 12 (13) 4207
- 26 Clyman RI. Patent ductus arteriosus, its treatments, and the risks of pulmonary morbidity. Semin Perinatol 2018; 42 (04) 235-242
- 27 Clyman RI, Liebowitz M, Kaempf J. et al; PDA-TOLERATE (PDA: TO LEave it alone or Respond And Treat Early) Trial Investigators. PDA-TOLERATE trial: an exploratory randomized controlled trial of treatment of moderate-to-large patent ductus arteriosus at 1 week of age. J Pediatr 2019; 205: 41-48.e6
- 28 Hundscheid T, Onland W, Kooi EMW. et al. Patent ductus arteriosus, its treatments, and the risks of pulmonary morbidity. N Engl J Med 2023; 388 (11) 980-990
- 29 McGoldrick E, Stewart F, Parker R, Dalziel SR. Antenatal corticosteroids for accelerating fetal lung maturation for women at risk of preterm birth. Cochrane Database Syst Rev 2020; 12 (12) CD004454