Inhaled Nitric Oxide in Preterm Infants: A Systematic Review

被引:92
作者
Donohue, Pamela K. [1 ,4 ]
Gilmore, Maureen M. [1 ]
Cristofalo, Elizabeth [1 ]
Wilson, Renee F. [2 ]
Weiner, Jonathan Z. [2 ]
Lau, Brandyn D. [2 ]
Robinson, Karen A. [3 ]
Allen, Marilee C. [1 ]
机构
[1] Johns Hopkins Univ, Dept Pediat, Johns Hopkins Sch Med, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Johns Hopkins Sch Med, Evidence Based Practice Ctr, Baltimore, MD USA
[3] Johns Hopkins Univ, Dept Med, Johns Hopkins Sch Med, Baltimore, MD USA
[4] Johns Hopkins Univ, Johns Hopkins Bloomberg Sch Publ Hlth, Dept Populat Family & Reprod Hlth, Baltimore, MD USA
基金
美国医疗保健研究与质量局;
关键词
nitric oxide; premature infant; systematic reviews; RANDOMIZED CONTROLLED-TRIAL; SEVERE RESPIRATORY-FAILURE; PREMATURE-INFANTS; NEURODEVELOPMENTAL OUTCOMES; DISTRESS-SYNDROME; THERAPY; RISK; VENTILATION; NEWBORNS; STRENGTH;
D O I
10.1542/peds.2010-3428
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
CONTEXT: Studies of the efficacy of inhaled nitric oxide (iNO) to prevent or treat respiratory failure in preterm infants have had variable and contradictory findings. OBJECTIVES: To systematically review the evidence on the use of iNO in infants born at <= 34 weeks' gestation who receive respiratory support. METHODS: Medline, Embase, the Cochrane Central Register of Controlled Studies, PsycInfo, ClinicalTrials.gov, and proceedings of the 2009 and 2010 Pediatric Academic Societies meetings were searched in June 2010. Additional studies from reference lists of eligible articles, relevant reviews, and technical experts were considered. Two investigators independently screened search results and abstracted data from eligible articles. We focus here on mortality, bronchopulmonary dysplasia (BPD), the composite outcome of death or BPD, and neurodevelopmental impairment. RESULTS: Fourteen randomized controlled trials, 7 follow-up studies, and 1 observational study were eligible for inclusion. Mortality rates in the NICU did not differ for infants treated with iNO compared with controls (risk ratio [RR]: 0.97 [95% confidence interval (CI): 0.82-1.15]). BPD at 36 weeks for iNO and control groups also did not differ for survivors (RR: 0.93 [95% CI: 0.86-1.003]). A small difference was found in favor of iNO in the composite outcome of death or BPD (RR: 0.93 [95% CI: 0.87-0.99]). There was no evidence to suggest a difference in the incidence of cerebral palsy (RR: 1.36 [95% CI: 0.88-2.10]), neurodevelopmental impairment (RR: 0.91 [95% CI: 0.77-1.12]), or cognitive impairment (RR: 0.72 [95% CI: 0.35-1.45]). CONCLUSIONS: There was a 7% reduction in the risk of the composite outcome of death or BPD at 36 weeks for infants treated with iNO compared with controls but no reduction in death alone or BPD. There is currently no evidence to support the use of iNO in preterm infants with respiratory failure outside the context of rigorously conducted randomized clinical trials. Pediatrics 2011;127:e414-e422
引用
收藏
页码:E414 / E422
页数:9
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