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Inhaled nitric oxide as an adjunct to neonatal resuscitation in premature infants: a pilot, double blind, randomized controlled trial

BACKGROUND: Nitric oxide (NO) plays an important role in normal postnatal transition. Our aims were to determine whether adding inhaled NO (iNO) decreases supplemental oxygen exposure in preterm infants requiring positive pressure ventilation (PPV) during resuscitation and to study iNO effects on he...

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Autores principales: Sekar, Krishnamurthy, Szyld, Edgardo, McCoy, Michael, Wlodaver, Anne, Dannaway, Douglas, Helmbrecht, Ashley, Riley, Julee, Manfredo, Amy, Anderson, Michael, Lakshminrusimha, Satyan, Noori, Shahab
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7223624/
https://www.ncbi.nlm.nih.gov/pubmed/31666688
http://dx.doi.org/10.1038/s41390-019-0643-x
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author Sekar, Krishnamurthy
Szyld, Edgardo
McCoy, Michael
Wlodaver, Anne
Dannaway, Douglas
Helmbrecht, Ashley
Riley, Julee
Manfredo, Amy
Anderson, Michael
Lakshminrusimha, Satyan
Noori, Shahab
author_facet Sekar, Krishnamurthy
Szyld, Edgardo
McCoy, Michael
Wlodaver, Anne
Dannaway, Douglas
Helmbrecht, Ashley
Riley, Julee
Manfredo, Amy
Anderson, Michael
Lakshminrusimha, Satyan
Noori, Shahab
author_sort Sekar, Krishnamurthy
collection PubMed
description BACKGROUND: Nitric oxide (NO) plays an important role in normal postnatal transition. Our aims were to determine whether adding inhaled NO (iNO) decreases supplemental oxygen exposure in preterm infants requiring positive pressure ventilation (PPV) during resuscitation and to study iNO effects on heart rate (HR), oxygen saturation (SpO(2)), and need for intubation during the first 20 min of life. METHODS: This was a pilot, double-blind, randomized, placebo-controlled trial. Infants 25 0/7–31 6/7 weeks’ gestational age requiring PPV with supplemental oxygen during resuscitation were enrolled. PPV was initiated with either oxygen (FiO(2)–0.30) + iNO at 20 ppm (iNO group) or oxygen (FiO(2)–0.30) + nitrogen (placebo group). Oxygen was titrated targeting defined SpO(2) per current guidelines. After 10 min, iNO/nitrogen was weaned stepwise per protocol and terminated at 17 min. RESULTS: Twenty-eight infants were studied (14 per group). The mean gestational age in both groups was similar. Cumulative FiO(2) and rate of exposure to high FiO(2) (>0.60) were significantly lower in the iNO group. There were no differences in HR, SpO(2), and need for intubation. CONCLUSIONS: Administration of iNO as an adjunct during neonatal resuscitation is feasible without side effects. It diminishes exposure to high levels of supplemental oxygen.
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spelling pubmed-72236242020-05-15 Inhaled nitric oxide as an adjunct to neonatal resuscitation in premature infants: a pilot, double blind, randomized controlled trial Sekar, Krishnamurthy Szyld, Edgardo McCoy, Michael Wlodaver, Anne Dannaway, Douglas Helmbrecht, Ashley Riley, Julee Manfredo, Amy Anderson, Michael Lakshminrusimha, Satyan Noori, Shahab Pediatr Res Clinical Research Article BACKGROUND: Nitric oxide (NO) plays an important role in normal postnatal transition. Our aims were to determine whether adding inhaled NO (iNO) decreases supplemental oxygen exposure in preterm infants requiring positive pressure ventilation (PPV) during resuscitation and to study iNO effects on heart rate (HR), oxygen saturation (SpO(2)), and need for intubation during the first 20 min of life. METHODS: This was a pilot, double-blind, randomized, placebo-controlled trial. Infants 25 0/7–31 6/7 weeks’ gestational age requiring PPV with supplemental oxygen during resuscitation were enrolled. PPV was initiated with either oxygen (FiO(2)–0.30) + iNO at 20 ppm (iNO group) or oxygen (FiO(2)–0.30) + nitrogen (placebo group). Oxygen was titrated targeting defined SpO(2) per current guidelines. After 10 min, iNO/nitrogen was weaned stepwise per protocol and terminated at 17 min. RESULTS: Twenty-eight infants were studied (14 per group). The mean gestational age in both groups was similar. Cumulative FiO(2) and rate of exposure to high FiO(2) (>0.60) were significantly lower in the iNO group. There were no differences in HR, SpO(2), and need for intubation. CONCLUSIONS: Administration of iNO as an adjunct during neonatal resuscitation is feasible without side effects. It diminishes exposure to high levels of supplemental oxygen. Nature Publishing Group US 2019-10-30 2020 /pmc/articles/PMC7223624/ /pubmed/31666688 http://dx.doi.org/10.1038/s41390-019-0643-x Text en © International Pediatric Research Foundation, Inc 2019 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Clinical Research Article
Sekar, Krishnamurthy
Szyld, Edgardo
McCoy, Michael
Wlodaver, Anne
Dannaway, Douglas
Helmbrecht, Ashley
Riley, Julee
Manfredo, Amy
Anderson, Michael
Lakshminrusimha, Satyan
Noori, Shahab
Inhaled nitric oxide as an adjunct to neonatal resuscitation in premature infants: a pilot, double blind, randomized controlled trial
title Inhaled nitric oxide as an adjunct to neonatal resuscitation in premature infants: a pilot, double blind, randomized controlled trial
title_full Inhaled nitric oxide as an adjunct to neonatal resuscitation in premature infants: a pilot, double blind, randomized controlled trial
title_fullStr Inhaled nitric oxide as an adjunct to neonatal resuscitation in premature infants: a pilot, double blind, randomized controlled trial
title_full_unstemmed Inhaled nitric oxide as an adjunct to neonatal resuscitation in premature infants: a pilot, double blind, randomized controlled trial
title_short Inhaled nitric oxide as an adjunct to neonatal resuscitation in premature infants: a pilot, double blind, randomized controlled trial
title_sort inhaled nitric oxide as an adjunct to neonatal resuscitation in premature infants: a pilot, double blind, randomized controlled trial
topic Clinical Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7223624/
https://www.ncbi.nlm.nih.gov/pubmed/31666688
http://dx.doi.org/10.1038/s41390-019-0643-x
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