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Extremely premature infants born at 23–25 weeks gestation are at substantial risk for pulmonary hypertension

OBJECTIVE: Extremely low gestational age newborns (ELGANs) represent an especially vulnerable population. Herein, we aimed to determine incidence and severity of pulmonary hypertension associated with bronchopulmonary dysplasia (BPD-PH) in extremely immature ELGANs (gestational age: 23(0/6)–25(6/7)...

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Autores principales: Sallmon, Hannes, Koestenberger, Martin, Avian, Alexander, Reiterer, Friedrich, Schwaberger, Bernhard, Meinel, Katharina, Cvirn, Gerhard, Kurath-Koller, Stefan, Gamillscheg, Andreas, Hansmann, Georg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9184271/
https://www.ncbi.nlm.nih.gov/pubmed/35365772
http://dx.doi.org/10.1038/s41372-022-01374-w
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author Sallmon, Hannes
Koestenberger, Martin
Avian, Alexander
Reiterer, Friedrich
Schwaberger, Bernhard
Meinel, Katharina
Cvirn, Gerhard
Kurath-Koller, Stefan
Gamillscheg, Andreas
Hansmann, Georg
author_facet Sallmon, Hannes
Koestenberger, Martin
Avian, Alexander
Reiterer, Friedrich
Schwaberger, Bernhard
Meinel, Katharina
Cvirn, Gerhard
Kurath-Koller, Stefan
Gamillscheg, Andreas
Hansmann, Georg
author_sort Sallmon, Hannes
collection PubMed
description OBJECTIVE: Extremely low gestational age newborns (ELGANs) represent an especially vulnerable population. Herein, we aimed to determine incidence and severity of pulmonary hypertension associated with bronchopulmonary dysplasia (BPD-PH) in extremely immature ELGANs (gestational age: 23(0/6)–25(6/7) weeks). METHODS: In this prospective observational cohort study, we assessed BPD-PH by means of several echocardiography markers and serum N-terminal pro-B-type natriuretic peptide (NT-proBNP) levels at 3 and 12 months of chronological age. In addition, we analyzed incidence and efficacy of pharmacologic treatment for BPD-PH. RESULTS: At 3 months 15/34 ELGANs had echocardiographic evidence of BPD-PH, while at 12 months of age 6/34 still had PH. PH-targeted therapy consisted of sildenafil monotherapy in 11 and dual oral combination therapy (sildenafil and macitentan) in four ELGANs at 3 and 12 months. CONCLUSION: 44% (15/34) of ELGANs developed BPD-PH. All received PH-targeted pharmacotherapy at 3 months, leading to hemodynamic improvements at 12 months in most infants.
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spelling pubmed-91842712022-06-11 Extremely premature infants born at 23–25 weeks gestation are at substantial risk for pulmonary hypertension Sallmon, Hannes Koestenberger, Martin Avian, Alexander Reiterer, Friedrich Schwaberger, Bernhard Meinel, Katharina Cvirn, Gerhard Kurath-Koller, Stefan Gamillscheg, Andreas Hansmann, Georg J Perinatol Article OBJECTIVE: Extremely low gestational age newborns (ELGANs) represent an especially vulnerable population. Herein, we aimed to determine incidence and severity of pulmonary hypertension associated with bronchopulmonary dysplasia (BPD-PH) in extremely immature ELGANs (gestational age: 23(0/6)–25(6/7) weeks). METHODS: In this prospective observational cohort study, we assessed BPD-PH by means of several echocardiography markers and serum N-terminal pro-B-type natriuretic peptide (NT-proBNP) levels at 3 and 12 months of chronological age. In addition, we analyzed incidence and efficacy of pharmacologic treatment for BPD-PH. RESULTS: At 3 months 15/34 ELGANs had echocardiographic evidence of BPD-PH, while at 12 months of age 6/34 still had PH. PH-targeted therapy consisted of sildenafil monotherapy in 11 and dual oral combination therapy (sildenafil and macitentan) in four ELGANs at 3 and 12 months. CONCLUSION: 44% (15/34) of ELGANs developed BPD-PH. All received PH-targeted pharmacotherapy at 3 months, leading to hemodynamic improvements at 12 months in most infants. Nature Publishing Group US 2022-04-01 2022 /pmc/articles/PMC9184271/ /pubmed/35365772 http://dx.doi.org/10.1038/s41372-022-01374-w Text en © The Author(s) 2022 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 Article
Sallmon, Hannes
Koestenberger, Martin
Avian, Alexander
Reiterer, Friedrich
Schwaberger, Bernhard
Meinel, Katharina
Cvirn, Gerhard
Kurath-Koller, Stefan
Gamillscheg, Andreas
Hansmann, Georg
Extremely premature infants born at 23–25 weeks gestation are at substantial risk for pulmonary hypertension
title Extremely premature infants born at 23–25 weeks gestation are at substantial risk for pulmonary hypertension
title_full Extremely premature infants born at 23–25 weeks gestation are at substantial risk for pulmonary hypertension
title_fullStr Extremely premature infants born at 23–25 weeks gestation are at substantial risk for pulmonary hypertension
title_full_unstemmed Extremely premature infants born at 23–25 weeks gestation are at substantial risk for pulmonary hypertension
title_short Extremely premature infants born at 23–25 weeks gestation are at substantial risk for pulmonary hypertension
title_sort extremely premature infants born at 23–25 weeks gestation are at substantial risk for pulmonary hypertension
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9184271/
https://www.ncbi.nlm.nih.gov/pubmed/35365772
http://dx.doi.org/10.1038/s41372-022-01374-w
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