Department of Clinical Science, Intervention and Technology, Division of Pediatrics, Karolinska Institutet, Stockholm, Sweden.
Department of Obstetrics and Gynecology, Clinical Sciences, Lund University, Stockholm, Sweden.
BJOG. 2017 Sep;124(10):1567-1574. doi: 10.1111/1471-0528.14545. Epub 2017 Mar 15.
To explore the association between administration-to-birth interval of antenatal corticosteroids (ACS) and survival in extremely preterm infants.
Population-based prospective cohort study.
All obstetric and neonatal units in Sweden from 1 April 2004 to 31 March 2007.
All live-born infants (n = 707) born at 22-26 completed weeks of gestation.
The relationship between time from first administration of ACS to delivery and survival was investigated using Cox proportional hazards regression analysis.
Neonatal (0-27 days) and infant (0-365 days) survival, and infant survival without major neonatal morbidity (intraventricular haemorrhage grade ≥ 3, retinopathy of prematurity stage ≥ 3, periventricular leukomalacia, necrotising enterocolitis, or severe bronchopulmonary dysplasia).
Five-hundred and ninety-one (84%) infants were exposed to ACS. In the final adjusted model, infant survival was lower in infants unexposed to ACS [hazard ratio (HR) = 0.26; 95% confidence interval 0.15-0.43], in infants born <24 h [HR = 0.53 (0.33-0.87)] and >7 days after ACS [HR = 0.56 (0.32-0.97)], but not in infants born 24-47 h after ACS [HR = 1.60 (0.73-3.50)], as compared with infants born 48 h to 7 days after administration. The findings were similar for neonatal survival. Survival without major neonatal morbidity among live-born infants was 14% in unexposed infants and 30-39% in steroid-exposed groups, indicating that any ACS exposure was valuable.
Administration of ACS 24 h to 7 days before extremely preterm birth was associated with significantly higher survival than in unexposed infants and in infants exposed to ACS at shorter or longer administration-to-birth intervals.
Timing of antenatal corticosteroids is important for extremely preterm infants' survival.
探讨产前皮质类固醇(ACS)给药至分娩间隔与极早产儿生存之间的关系。
基于人群的前瞻性队列研究。
2004 年 4 月 1 日至 2007 年 3 月 31 日期间瑞典所有产科和新生儿单位。
所有在 22-26 孕周时出生的活产婴儿(n=707)。
采用 Cox 比例风险回归分析探讨 ACS 首次给药至分娩的时间与生存之间的关系。
新生儿(0-27 天)和婴儿(0-365 天)生存,以及无严重新生儿并发症(脑室内出血 3 级以上、早产儿视网膜病变 3 期以上、脑室周围白质软化、坏死性小肠结肠炎或严重支气管肺发育不良)的婴儿生存。
591 名(84%)婴儿接受了 ACS 治疗。在最终调整后的模型中,未接受 ACS 治疗的婴儿 [风险比(HR)=0.26;95%置信区间 0.15-0.43]、ACS 后 <24 小时出生的婴儿 [HR=0.53(0.33-0.87)] 和 >7 天出生的婴儿 [HR=0.56(0.32-0.97)],但 ACS 后 24-47 小时出生的婴儿 [HR=1.60(0.73-3.50)] 与 ACS 后 48 小时至 7 天出生的婴儿相比,其婴儿生存率较低。新生儿生存率的结果类似。未暴露于 ACS 的活产婴儿无严重新生儿并发症的生存率为 14%,而接受 ACS 治疗的婴儿在暴露于 ACS 的各组中的生存率为 30-39%,这表明任何 ACS 暴露都是有价值的。
极早产儿出生前 24 小时至 7 天给予 ACS 与未暴露于 ACS 的婴儿和 ACS 给药至分娩间隔较短或较长的婴儿相比,生存率显著提高。
产前皮质类固醇的给药时间对极早产儿的生存至关重要。