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Patent ductus arteriosus, tracheal ventilation, and the risk of bronchopulmonary dysplasia
BACKGROUND: An increased risk for bronchopulmonary dysplasia (BPD) exists when moderate-to-large patent ductus arteriosus shunts (hsPDA) persist beyond 14 days. GOAL: To examine the interaction between prolonged exposures to tracheal ventilation (≥10 days) and hsPDA on the incidence of BPD in infant...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group US
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8904244/ https://www.ncbi.nlm.nih.gov/pubmed/33790415 http://dx.doi.org/10.1038/s41390-021-01475-w |
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author | Clyman, Ronald I. Hills, Nancy K. Cambonie, Gilles Debillon, Thierry Ligi, Isabelle Gascoin, Geraldine Patkai, Juliana Beuchee, Alain Favrais, Geraldine Durrmeyer, Xavier Flamant, Cyril Rozé, Jean Christophe |
author_facet | Clyman, Ronald I. Hills, Nancy K. Cambonie, Gilles Debillon, Thierry Ligi, Isabelle Gascoin, Geraldine Patkai, Juliana Beuchee, Alain Favrais, Geraldine Durrmeyer, Xavier Flamant, Cyril Rozé, Jean Christophe |
author_sort | Clyman, Ronald I. |
collection | PubMed |
description | BACKGROUND: An increased risk for bronchopulmonary dysplasia (BPD) exists when moderate-to-large patent ductus arteriosus shunts (hsPDA) persist beyond 14 days. GOAL: To examine the interaction between prolonged exposures to tracheal ventilation (≥10 days) and hsPDA on the incidence of BPD in infants <28 weeks gestation. STUDY DESIGN: Predefined definitions of prolonged ventilation (≥10 days), hsPDA (≥14 days), and BPD (room air challenge test at 36 weeks) were used to analyze deidentified data from the multicenter TRIOCAPI RCT in a secondary analysis of the trial. RESULTS: Among 307 infants who survived >14 days, 41 died before 36 weeks. Among survivors, 93/266 had BPD. The association between BPD and hsPDA depended on the length of intubation. In multivariable analyses, prolonged hsPDA shunts were associated with increased BPD (odds ratio (OR) (95% confidence interval (CI)) = 3.00 (1.58–5.71)) when infants required intubation for ≥10 days. In contrast, there was no significant association between hsPDA exposure and BPD when infants were intubated <10 days (OR (95% CI) = 1.49 (0.98–2.26)). A similar relationship between prolonged hsPDA and length of intubation was found for BPD/death (n = 307): infants intubated ≥10 days: OR (95% CI) = 2.41 (1.47–3.95)); infants intubated <10 days: OR (95% CI) = 1.37 (0.86–2.19)). CONCLUSIONS: Moderate-to-large PDAs were associated with increased risks of BPD and BPD/death—but only when infants required intubation ≥10 days. IMPACT: Infants with a moderate-to-large hsPDA that persist beyond 14 days are only at risk for developing BPD if they also receive prolonged tracheal ventilation for ≥10 days. Infants who receive less ventilatory support (intubation for <10 days) have the same incidence of BPD whether the ductus closes shortly after birth or whether it persists as a moderate-to-large shunt for several weeks. Early PDA closure may be unnecessary in infants who require short durations of intubation since the PDA does not seem to alter the incidence of BPD in infants who require intubation for <10 days. |
format | Online Article Text |
id | pubmed-8904244 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group US |
record_format | MEDLINE/PubMed |
spelling | pubmed-89042442022-03-23 Patent ductus arteriosus, tracheal ventilation, and the risk of bronchopulmonary dysplasia Clyman, Ronald I. Hills, Nancy K. Cambonie, Gilles Debillon, Thierry Ligi, Isabelle Gascoin, Geraldine Patkai, Juliana Beuchee, Alain Favrais, Geraldine Durrmeyer, Xavier Flamant, Cyril Rozé, Jean Christophe Pediatr Res Clinical Research Article BACKGROUND: An increased risk for bronchopulmonary dysplasia (BPD) exists when moderate-to-large patent ductus arteriosus shunts (hsPDA) persist beyond 14 days. GOAL: To examine the interaction between prolonged exposures to tracheal ventilation (≥10 days) and hsPDA on the incidence of BPD in infants <28 weeks gestation. STUDY DESIGN: Predefined definitions of prolonged ventilation (≥10 days), hsPDA (≥14 days), and BPD (room air challenge test at 36 weeks) were used to analyze deidentified data from the multicenter TRIOCAPI RCT in a secondary analysis of the trial. RESULTS: Among 307 infants who survived >14 days, 41 died before 36 weeks. Among survivors, 93/266 had BPD. The association between BPD and hsPDA depended on the length of intubation. In multivariable analyses, prolonged hsPDA shunts were associated with increased BPD (odds ratio (OR) (95% confidence interval (CI)) = 3.00 (1.58–5.71)) when infants required intubation for ≥10 days. In contrast, there was no significant association between hsPDA exposure and BPD when infants were intubated <10 days (OR (95% CI) = 1.49 (0.98–2.26)). A similar relationship between prolonged hsPDA and length of intubation was found for BPD/death (n = 307): infants intubated ≥10 days: OR (95% CI) = 2.41 (1.47–3.95)); infants intubated <10 days: OR (95% CI) = 1.37 (0.86–2.19)). CONCLUSIONS: Moderate-to-large PDAs were associated with increased risks of BPD and BPD/death—but only when infants required intubation ≥10 days. IMPACT: Infants with a moderate-to-large hsPDA that persist beyond 14 days are only at risk for developing BPD if they also receive prolonged tracheal ventilation for ≥10 days. Infants who receive less ventilatory support (intubation for <10 days) have the same incidence of BPD whether the ductus closes shortly after birth or whether it persists as a moderate-to-large shunt for several weeks. Early PDA closure may be unnecessary in infants who require short durations of intubation since the PDA does not seem to alter the incidence of BPD in infants who require intubation for <10 days. Nature Publishing Group US 2021-03-31 2022 /pmc/articles/PMC8904244/ /pubmed/33790415 http://dx.doi.org/10.1038/s41390-021-01475-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Clinical Research Article Clyman, Ronald I. Hills, Nancy K. Cambonie, Gilles Debillon, Thierry Ligi, Isabelle Gascoin, Geraldine Patkai, Juliana Beuchee, Alain Favrais, Geraldine Durrmeyer, Xavier Flamant, Cyril Rozé, Jean Christophe Patent ductus arteriosus, tracheal ventilation, and the risk of bronchopulmonary dysplasia |
title | Patent ductus arteriosus, tracheal ventilation, and the risk of bronchopulmonary dysplasia |
title_full | Patent ductus arteriosus, tracheal ventilation, and the risk of bronchopulmonary dysplasia |
title_fullStr | Patent ductus arteriosus, tracheal ventilation, and the risk of bronchopulmonary dysplasia |
title_full_unstemmed | Patent ductus arteriosus, tracheal ventilation, and the risk of bronchopulmonary dysplasia |
title_short | Patent ductus arteriosus, tracheal ventilation, and the risk of bronchopulmonary dysplasia |
title_sort | patent ductus arteriosus, tracheal ventilation, and the risk of bronchopulmonary dysplasia |
topic | Clinical Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8904244/ https://www.ncbi.nlm.nih.gov/pubmed/33790415 http://dx.doi.org/10.1038/s41390-021-01475-w |
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