NIH Consensus Development Conference statement: inhaled nitric-oxide therapy for premature infants
- PMID: 21220405
- DOI: 10.1542/peds.2010-3507
NIH Consensus Development Conference statement: inhaled nitric-oxide therapy for premature infants
Abstract
Premature birth is a major public health problem in the United States and internationally. Infants born at or before 32 weeks' gestation (2% of all births in the United States in 2007) are at extremely high risk for death in the neonatal period or for pulmonary, visual, and neurodevelopmental morbidities with lifelong consequences including bronchopulmonary dysplasia, retinopathy of prematurity, and brain injury. Risks for adverse outcomes increase with decreasing gestational age. The economic costs to care for these infants are also substantial (estimated at $26 billion in 2005 in the United States). It is clear that the need for strategies to improve outcomes for this high-risk population is great, and this need has prompted testing of new therapies with the potential to decrease pulmonary and other complications of prematurity. Inhaled nitric oxide (iNO) emerged as one such therapy. To provide health care professionals, families, and the general public with a responsible assessment of currently available data regarding the benefits and risks of iNO in premature infants, the Eunice Kennedy Shriver National Institute of Child Health and Human Development, the National Heart, Lung, and Blood Institute, and the Office of Medical Applications of Research of the National Institutes of Health convened a consensus-development conference. Findings from a substantial body of experimental work in developing animals and other model systems suggest that nitric oxide may enhance lung growth and reduce lung inflammation independently of its effects on blood vessel resistance. Although this work demonstrates biological plausibility and the results of randomized controlled trials in term and near-term infants were positive, combined evidence from the 14 randomized controlled trials of iNO treatment in premature infants of ≤ 34 weeks' gestation shows equivocal effects on pulmonary outcomes, survival, and neurodevelopmental outcomes.
Similar articles
-
NIH consensus development conference: Inhaled nitric oxide therapy for premature infants.NIH Consens State Sci Statements. 2010 Oct 29;27(5):1-34. NIH Consens State Sci Statements. 2010. PMID: 21042341 Review.
-
Validation of the National Institutes of Health consensus definition of bronchopulmonary dysplasia.Pediatrics. 2005 Dec;116(6):1353-60. doi: 10.1542/peds.2005-0249. Pediatrics. 2005. PMID: 16322158
-
Inhaled nitric oxide in premature infants--a meta-analysis.J Perinat Med. 2000;28(1):7-13. doi: 10.1515/JPM.2000.001. J Perinat Med. 2000. PMID: 10765508
-
Off-label use of inhaled nitric oxide after release of NIH consensus statement.Pediatrics. 2015 Apr;135(4):643-8. doi: 10.1542/peds.2014-3290. Epub 2015 Mar 9. Pediatrics. 2015. PMID: 25755237
-
Neonatal Ventilation With Inhaled Nitric Oxide Versus Ventilatory Support Without Inhaled Nitric Oxide for Preterm Infants With Severe Respiratory Failure: the INNOVO multicentre randomised controlled trial (ISRCTN 17821339).Pediatrics. 2005 Apr;115(4):926-36. doi: 10.1542/peds.2004-1209. Pediatrics. 2005. PMID: 15805366 Clinical Trial.
Cited by
-
First-year outcomes of very low birth weight preterm singleton infants with hypoxemic respiratory failure treated with milrinone and inhaled nitric oxide (iNO) compared to iNO alone: A nationwide retrospective study.PLoS One. 2024 May 9;19(5):e0297137. doi: 10.1371/journal.pone.0297137. eCollection 2024. PLoS One. 2024. PMID: 38722851 Free PMC article.
-
Efficacy of inhaled nitric oxide in preterm infants ≤ 34 weeks: a systematic review and meta-analysis of randomized controlled trials.Front Pharmacol. 2024 Jan 11;14:1268795. doi: 10.3389/fphar.2023.1268795. eCollection 2023. Front Pharmacol. 2024. PMID: 38273818 Free PMC article. Review.
-
The early use of inhaled nitric oxide in premature infants requiring respiratory support.Ann Med. 2023;55(2):2266633. doi: 10.1080/07853890.2023.2266633. Epub 2023 Dec 11. Ann Med. 2023. PMID: 38079494 Free PMC article. Review.
-
Exogenous hydrogen sulfide attenuates hyperoxia effects on neonatal mouse airways.Am J Physiol Lung Cell Mol Physiol. 2024 Jan 1;326(1):L52-L64. doi: 10.1152/ajplung.00196.2023. Epub 2023 Nov 21. Am J Physiol Lung Cell Mol Physiol. 2024. PMID: 37987780
-
[Recent research on inhaled nitric oxide in preterm infants with a gestational age of <34 weeks].Zhongguo Dang Dai Er Ke Za Zhi. 2023 Sept 15;25(9):982-988. doi: 10.7499/j.issn.1008-8830.2303146. Zhongguo Dang Dai Er Ke Za Zhi. 2023. PMID: 37718407 Free PMC article. Chinese.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
