Safety and efficacy of inhaled nitric oxide treatment for premature infants with respiratory distress syndrome: follow-up evaluation at early school age.

Safety and efficacy of inhaled nitric oxide treatment for premature infants with respiratory distress syndrome: follow-up evaluation at early school age.
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DOI:
10.1111/j.1651-2227.2010.02077.x
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发表时间:
2011-04
期刊:
Acta paediatrica (Oslo, Norway : 1992)
影响因子:
--
通讯作者:
Schreiber MD
Schreiber MD
中科院分区:
其他
文献类型:
--
作者:
Patrianakos-Hoobler AI;Marks JD;Msall ME;Huo D;Schreiber MD

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To assess long-term safety and compare neurodevelopmental outcomes in school age children born prematurely who received inhaled nitric oxide or placebo during the first week of life in a randomized, double blind study. Children treated with inhaled nitric oxide had previously been shown to have decreased intraventricular hemorrhage and periventricular leukomalacia as newborns, and decreased cognitive impairment at 2 years. Follow-up study of medical outcomes, neurodevelopmental assessment and school readiness in 135 of 167 (81%) surviving premature infants seen at 5.7 ± 1.0 years. Compared to placebo (n=65), iNO-treated children (n=70) demonstrated no difference in growth parameters, school readiness, or need for subsequent hospitalization. However, iNO-treated children were less likely to have multiple chronic morbidities or technology-dependence (p=0.05). iNO-treated children also had less functional disability (p=0.05). These results demonstrate the long-term safety of iNO in premature infants. Furthermore, iNO treatment may improve health status by decreasing the incidence of severe ongoing morbidities and technology-dependence, and may also decrease the incidence of educational and community functional disability of premature infants at early school age. clinicaltrials.gov Identifier: NCT00152542
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