首页> 外文期刊>JAMA: the Journal of the American Medical Association >Effect of maintenance tocolysis with nifedipine in threatened preterm labor on perinatal outcomes: A randomized controlled trial
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Effect of maintenance tocolysis with nifedipine in threatened preterm labor on perinatal outcomes: A randomized controlled trial

机译:硝苯地平维持早产在早产中对围产期结局的影响:一项随机对照试验

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Importance: In threatened preterm labor, maintenance tocolysis with nifedipine, after an initial course of tocolysis and corticosteroids for 48 hours, may improve perinatal outcome. Objective: To determine whether maintenance tocolysis with nifedipine will reduce adverse perinatal outcomes due to premature birth. Design, Setting, and Participants: APOSTEL-II (Assessment of Perinatal Outcome with Sustained Tocolysis in Early Labor) is a double-blind, placebo-controlled trial performed in 11 perinatal units including all tertiary centers in the Netherlands. From June 2008 to February 2010, women with threatened preterm labor between 26 weeks (plus 0 days) and 32 weeks (plus 2 days) gestation, who had not delivered after 48 hours of tocolysis and a completed course of corticosteroids, were enrolled. Surviving infants were followed up until 6 months after birth (ended August 2010). Intervention: Randomization assigned 406 women to maintenance tocolysis with nifedipine orally (80 mg/d; n=201) or placebo (n=205) for 12 days. Assigned treatment was masked from investigators, participants, clinicians, and research nurses. Main Outcome Measures: Primary outcome was a composite of adverse perinatal outcomes (perinatal death, chronic lung disease, neonatal sepsis, intraventricular hemorrhage >grade 2, periventricular leukomalacia >grade 1, or necrotizing enterocolitis). Analyses were completed on an intention-to-treat basis. Results: Mean (SD) gestational age at randomization was 29.2 (1.7) weeks for both groups. Adverse perinatal outcome was not significantly different between groups: 11.9% (24/201; 95% CI, 7.5%-16.4%) for nifedipine vs 13.7% (28/205; 95% CI, 9.0%-18.4%) for placebo (relative risk, 0.87; 95% CI, 0.53-1.45). Conclusions and Relevance: In patients with threatened preterm labor, nifedipine-maintained tocolysis did not result in a statistically significant reduction in adverse perinatal outcomes when compared with placebo. Although the lower than anticipated rate of adverse perinatal outcomes in the control group indicates that a benefit of nifedipine cannot completely be excluded, its use for maintenance tocolysis does not appear beneficial at this time. Trial Registration: trialregister.nl Identifier: NTR1336.
机译:重要性:在早产先兆中,在最初的宫缩和皮质类固醇治疗48小时后,用硝苯地平维持宫缩可能会改善围产期结局。目的:确定用硝苯地平维持母体溶解是否能减少早产引起的不良围产儿预后。设计,背景和参与者:APOSTEL-II(评估早期分娩中持续生育的围产期结果)是一项双盲,安慰剂对照试验,在11个围产期单位中进行,包括荷兰的所有第三级中心。从2008年6月到2010年2月,招募了处于早孕期在26周(加0天)至32周(加2天)之间的孕妇,这些妇女在进行了48小时的宫缩术和完整的皮质类固醇激素治疗后仍未分娩。对存活的婴儿进行随访,直到出生后6个月(截至2010年8月)。干预:随机分配406名妇女,口服硝苯地平(80 mg / d; n = 201)或安慰剂(n = 205)维持溶栓12天。研究人员,参与者,临床医生和研究护士掩盖了指定的治疗方法。主要结局指标:主要结局指标是围产期不良结局的综合指标(围产期死亡,慢性肺病,新生儿败血症,脑室内出血> 2级,脑室白细胞增多> 1级或坏死性小肠结肠炎)。分析是在意向性治疗的基础上完成的。结果:两组的平均(SD)胎龄为29.2(1.7)周。两组的围生期不良预后无显着差异:硝苯地平为11.9%(24/201; 95%CI,7.5%-16.4%),而安慰剂为13.7%(28/205; 95%CI,9.0%-18.4%)(相对风险0.87; 95%CI 0.53-1.45)。结论与相关性:与安慰剂相比,在早产先兆的患者中,硝苯地平维持的宫缩溶解术并未导致围生期不良结局的统计学显着降低。尽管对照组的围产期不良结局不良率低于预期,这表明硝苯地平的益处无法完全排除,但目前用于维持子宫溶解的益处似乎并不明显。试用注册:trialregister.nl标识符:NTR1336。

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