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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2021
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.
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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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