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出生时早产儿的无创与有创呼吸支持:系统评价和荟萃分析。

Non-invasive versus invasive respiratory support in preterm infants at birth: systematic review and meta-analysis.

机构信息

Department of Pediatrics, University of Alberta, Edmonton, Canada.

出版信息

BMJ. 2013 Oct 17;347:f5980. doi: 10.1136/bmj.f5980.

Abstract

OBJECTIVE

To assess the role of nasal continuous positive airway pressure (CPAP) initiated at birth for prevention of death and bronchopulmonary dysplasia in very preterm infants.

DESIGN

Systematic review.

DATA SOURCES

PubMed, Embase, the Cochrane Central Register of Controlled Trials, and online Pediatric Academic Society abstracts from the year of inception to June 2013.

ELIGIBILITY CRITERIA FOR SELECTING STUDIES

Randomised controlled trials evaluating the effect of nasal CPAP compared with intubation in preterm infants born at less than 32 weeks' gestation and presenting the outcomes of either death or bronchopulmonary dysplasia, or both (defined as the need for oxygen support or mechanical ventilation at 36 weeks corrected gestation), during hospital stay.

RESULTS

Four randomised controlled trials (2782 participants) met the inclusion criteria, with 1296 infants in the nasal CPAP group and 1486 in the intubation group. All the trials reported bronchopulmonary dysplasia independently at 36 weeks corrected gestation, with borderline significance in favour of the nasal CPAP group (relative risk 0.84, 95% confidence interval 0.68 to 1.04, risk difference -0.02, 95% confidence interval -0.04 to 0.01). [corrected] No difference in death was observed (relative risk 0.88, 0.68 to 1.14, risk difference -0.02, -0.04 to 0.01, respectively). Pooled analysis showed a significant benefit for the combined outcome of death or bronchopulmonary dysplasia, or both, at 36 weeks corrected gestation for babies treated with nasal CPAP (relative risk 0.90 (95% confidence interval 0.83 to 0.98, risk difference -0.04 (95% confidence interval -0.08 to -0.00), NNT [corrected] of 25).

CONCLUSION

One additional infant could survive to 36 weeks without bronchopulmonary dysplasia for every 25 babies treated with nasal CPAP in the delivery room rather than being intubated.

摘要

目的

评估出生时即开始使用经鼻持续气道正压通气(CPAP)对预防极早产儿死亡和支气管肺发育不良的作用。

设计

系统评价。

资料来源

PubMed、Embase、Cochrane 对照试验中心注册库和 2013 年 6 月前在线儿科学会摘要。

入选研究的标准

评价与气管插管比较,对出生胎龄小于 32 周、需要经鼻 CPAP 或气管插管治疗的极早产儿,出生时使用经鼻 CPAP 对其在院内的死亡或支气管肺发育不良(定义为校正胎龄 36 周时需要吸氧或机械通气)结局影响的随机对照试验。

结果

纳入 4 项随机对照试验(2782 例患儿),经鼻 CPAP 组 1296 例,气管插管组 1486 例。所有试验均独立报道校正胎龄 36 周时支气管肺发育不良情况,经鼻 CPAP 组有边缘性优势(相对危险度 0.84,95%置信区间 0.68 至 1.04,差异风险 -0.02,95%置信区间 -0.04 至 0.01)。未观察到死亡率差异(相对危险度 0.88,95%置信区间 0.68 至 1.14,差异风险 -0.02,-0.04 至 0.01)。汇总分析显示,经鼻 CPAP 治疗的患儿在校正胎龄 36 周时死亡或发生支气管肺发育不良,或两者均发生的复合结局有显著获益(相对危险度 0.90,95%置信区间 0.83 至 0.98,差异风险 -0.04,95%置信区间 -0.08 至 -0.00),NNT 为 25。

结论

与气管插管相比,每 25 例出生时经鼻 CPAP 治疗的患儿中,就有 1 例患儿可在无支气管肺发育不良的情况下存活至校正胎龄 36 周。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7684/4793476/c3006ea3ad13/schg012218.f1_default.jpg

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