Oxygen Saturation Target Range for Extremely Preterm Infants A Systematic Review and Meta-analysis

被引:110
作者
Manja, Veena [1 ,2 ,3 ]
Lakshminrusimha, Satyan [4 ,5 ]
Cook, Deborah J. [3 ,6 ]
机构
[1] Vet Affairs Med Ctr, Dept Med, Div Cardiol, Buffalo, NY USA
[2] SUNY Buffalo, Dept Internal Med, Buffalo, NY 14260 USA
[3] McMaster Univ, Dept Clin Epidemiol & Biostat, Hamilton, ON, Canada
[4] Women & Childrens Hosp Buffalo, Dept Pediat, Div Neonatal Perinatal Med, Buffalo, NY 14222 USA
[5] SUNY Buffalo, Buffalo, NY 14260 USA
[6] McMaster Univ, Dept Med, Div Crit Care Med, Hamilton, ON, Canada
关键词
EUROPEAN CONSENSUS GUIDELINES; QUALITY; MANAGEMENT; OUTCOMES; LESSONS; SUPPORT;
D O I
10.1001/jamapediatrics.2014.3307
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
IMPORTANCE The optimal oxygen saturation (SpO(2)) target for extremely preterm infants is unknown. OBJECTIVE To systematically review evidence evaluating the effect of restricted vs liberal oxygen exposure on morbidity and mortality in extremely preterm infants. DATA SOURCES MEDLINE, PubMed, CENTRAL, and CINAHL databases from their inception to March 31, 2014, and abstracts submitted to Pediatric Academic Societies from 2000 to 2014. STUDY SELECTION All published randomized trials evaluating the effect of restricted (SpO(2), 85%-89%) vs liberal (SpO(2), 91%-95%) oxygen exposure in preterm infants (<28 weeks' gestation at birth). DATA EXTRACTION AND SYNTHESIS All meta-analyses were performed using Review Manager 5.2. The Cochrane risk-of-bias tool was used to assess study quality. The summary of the findings and the level of confidence in the estimate of effect were assessed using GRADEpro. Treatment effect was analyzed using a random-effects model. MAIN OUTCOMES AND MEASURES Death before hospital discharge, death or severe disability before 24 months, death before 24 months, neurodevelopmental outcomes, hearing loss, bronchopulmonary dysplasia, necrotizing enterocolitis, and severe retinopathy of prematurity. RESULTS Five trials were included in the final synthesis. These studies had a similar design with a prespecified composite outcome of death/disability at 18 to 24 months corrected for prematurity; however, this outcome has not been reported for 2 of the 5 trials. There was no difference in the outcome of death/disability before 24 months (risk ratio [RR], 1.02 [95% CI, 0.92-1.14]). Mortality before 24 months was not different (RR, 1.13 [95% CI, 0.97-1.33]); however, a significant increase in mortality before hospital discharge was found in the restricted oxygen group (RR, 1.18 [95% CI, 1.03-1.36]). The rates of bronchopulmonary dysplasia, neurodevelopmental outcomes, hearing loss, and retinopathy of prematurity were similar between the 2 groups. Necrotizing enterocolitis occurred more frequently in infants on restricted oxygen (RR, 1.24 [95% CI, 1.05-1.47]). Using the Grades of Recommendation, Assessment, Development, and Evaluation (GRADE) criteria, we found that the quality of evidence for these outcomes was moderate to low. CONCLUSIONS AND RELEVANCE Although infants cared for with a liberal oxygen target had significantly lower mortality before hospital discharge than infants cared for with a restricted oxygen target, the quality of evidence for this estimate of effect is low. Necrotizing enterocolitis occurred less frequently in the liberal oxygen group. We found no significant differences in death or disability at 24 months, bronchopulmonary dysplasia, retinopathy of prematurity, neurodevelopmental outcomes, or hearing loss at 24 months.
引用
收藏
页码:332 / 340
页数:9
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