Oxygen Saturation Targets in Preterm Infants and Outcomes at 18-24 Months: A Systematic Review

被引:48
|
作者
Manja, Veena [1 ,2 ]
Saugstad, Ola D. [3 ]
Lakshminrusimha, Satyan [4 ]
机构
[1] Vet Affairs Med Ctr, Dept Internal Med, Div Cardiol, Buffalo, NY USA
[2] McMasters Univ, Dept Clin Epidemiol & Biostat, Hamilton, ON, Canada
[3] Univ Oslo, Oslo Univ Hosp, Dept Pediat Res, Oslo, Norway
[4] SUNY Buffalo, Woman & Childrens Hosp Buffalo, Dept Pediat, Div Neonatal Perinatal Med, Buffalo, NY USA
基金
美国国家卫生研究院;
关键词
GENETIC SUSCEPTIBILITY; QUALITY; THERAPY; METAANALYSIS; RETINOPATHY; MORTALITY; CROSSOVER; TRIALS;
D O I
10.1542/peds.2016-1609
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
CONTEXT: The optimal oxygen saturation target for extremely preterm infants remains unclear. OBJECTIVE: To systematically review evidence evaluating the effect of lower (85%-89%) versus higher (91%-95%) pulse oxygen saturation (SpO(2)) target on mortality and neurodevelopmental impairment (NDI) at 18 to 24 months. DATA SOURCES: Electronic databases and all published randomized trials evaluating lower versus higher SpO(2) target in preterm infants. STUDY SELECTION: A total of 2896 relevant citations were identified; 5 trials were included in the final analysis. DATA EXTRACTION: Data from 5 trials were analyzed for quality of evidence and risk of bias. LIMITATIONS: Limitations include heterogeneity in age at enrollment and comorbidities between trials and change in oximeter algorithm midway through 3 trials. RESULTS: There was no difference in the incidence of primary outcome (death/NDI at 18-24 months) in the 2 groups; risk ratio, 1.05, 95% confidence interval 0.98-1.12, P = .18. Mortality before 18 to 24 months was higher in the lower-target group (risk ratio, 1.16, 95% confidence interval 1.03-1.31, P = .02). Rates of NDI and severe visual loss did not differ between the 2 groups. Proportion of time infants spent outside the target range while on supplemental oxygen ranged from 8.2% to 27.4% <85% and 8.1% to 22.4% >95% with significant overlap between the 2 groups. CONCLUSIONS: There was no difference in primary outcome between the 2 SpO(2) target groups. The collective data suggest that risks associated with restricting the upper SpO(2) target limit to 89% outweigh the benefits. The quality of evidence was moderate. We speculate that a wider target range (lower alarm limit, 89% and upper, 96%) may increase time spent within range, but the safety profile of this approach remains to be determined.
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页数:14
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