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Intravenous sildenafil for treatment of early pulmonary hypertension in preterm infants
Data is lacking on the effect of continuous intravenous sildenafil treatment in preterm infants with early pulmonary hypertension (PH), especially in very low birth weight (VLBW) infants. Preterm infants (< 37 weeks of gestational age) with intravenous sildenafil treatment and diagnosis of PH bet...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10209068/ https://www.ncbi.nlm.nih.gov/pubmed/37225769 http://dx.doi.org/10.1038/s41598-023-35387-y |
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author | Schroeder, Lukas Monno, Paulina Strizek, Brigitte Dresbach, Till Mueller, Andreas Kipfmueller, Florian |
author_facet | Schroeder, Lukas Monno, Paulina Strizek, Brigitte Dresbach, Till Mueller, Andreas Kipfmueller, Florian |
author_sort | Schroeder, Lukas |
collection | PubMed |
description | Data is lacking on the effect of continuous intravenous sildenafil treatment in preterm infants with early pulmonary hypertension (PH), especially in very low birth weight (VLBW) infants. Preterm infants (< 37 weeks of gestational age) with intravenous sildenafil treatment and diagnosis of PH between 01/12 and 12/21 were retrospectively screened for analysis. The primary clinical endpoint was defined as response to sildenafil according to the improvement of the oxygenation index (OI), the saturation oxygenation pressure index (SOPI) and PaO(2)/FiO(2)-ratio. Early-PH was defined as diagnosis < 28 day of life (DOL). 58 infants were finally included, with 47% classified as very low birth weight (VLBW) infants. The primary endpoint was reached in 57%. The likelihood to die during in-hospital treatment was more than three times higher (72 vs 21%, p < 0.001) in infants without response to sildenafil. The echocardiographic severity of PH and right-ventricular dysfunction (RVD) decreased significantly from baseline to 24 h (p = 0.045, and p = 0.008, respectively). Sildenafil treatment leads to significant improvement of the oxygenation impairment in 57% of the preterm infants, with similar response rates in VLBW infants. Intravenous sildenafil treatment is associated with a significant decrease of the PH-severity and RVD. |
format | Online Article Text |
id | pubmed-10209068 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-102090682023-05-26 Intravenous sildenafil for treatment of early pulmonary hypertension in preterm infants Schroeder, Lukas Monno, Paulina Strizek, Brigitte Dresbach, Till Mueller, Andreas Kipfmueller, Florian Sci Rep Article Data is lacking on the effect of continuous intravenous sildenafil treatment in preterm infants with early pulmonary hypertension (PH), especially in very low birth weight (VLBW) infants. Preterm infants (< 37 weeks of gestational age) with intravenous sildenafil treatment and diagnosis of PH between 01/12 and 12/21 were retrospectively screened for analysis. The primary clinical endpoint was defined as response to sildenafil according to the improvement of the oxygenation index (OI), the saturation oxygenation pressure index (SOPI) and PaO(2)/FiO(2)-ratio. Early-PH was defined as diagnosis < 28 day of life (DOL). 58 infants were finally included, with 47% classified as very low birth weight (VLBW) infants. The primary endpoint was reached in 57%. The likelihood to die during in-hospital treatment was more than three times higher (72 vs 21%, p < 0.001) in infants without response to sildenafil. The echocardiographic severity of PH and right-ventricular dysfunction (RVD) decreased significantly from baseline to 24 h (p = 0.045, and p = 0.008, respectively). Sildenafil treatment leads to significant improvement of the oxygenation impairment in 57% of the preterm infants, with similar response rates in VLBW infants. Intravenous sildenafil treatment is associated with a significant decrease of the PH-severity and RVD. Nature Publishing Group UK 2023-05-24 /pmc/articles/PMC10209068/ /pubmed/37225769 http://dx.doi.org/10.1038/s41598-023-35387-y Text en © The Author(s) 2023 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Schroeder, Lukas Monno, Paulina Strizek, Brigitte Dresbach, Till Mueller, Andreas Kipfmueller, Florian Intravenous sildenafil for treatment of early pulmonary hypertension in preterm infants |
title | Intravenous sildenafil for treatment of early pulmonary hypertension in preterm infants |
title_full | Intravenous sildenafil for treatment of early pulmonary hypertension in preterm infants |
title_fullStr | Intravenous sildenafil for treatment of early pulmonary hypertension in preterm infants |
title_full_unstemmed | Intravenous sildenafil for treatment of early pulmonary hypertension in preterm infants |
title_short | Intravenous sildenafil for treatment of early pulmonary hypertension in preterm infants |
title_sort | intravenous sildenafil for treatment of early pulmonary hypertension in preterm infants |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10209068/ https://www.ncbi.nlm.nih.gov/pubmed/37225769 http://dx.doi.org/10.1038/s41598-023-35387-y |
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