因胎膜早破而并发临床重大心室内出血的风险因素。

W Giamberardino, V D Winn, J Armstrong
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引用次数: 0

摘要

目的:早产是围产期不良后果的主要原因,包括脑室内出血(IVH)。IVH已被证明会导致持久性神经系统残疾,但孕产妇特征和潜在的可改变风险因素对这些结果的影响尚未得到很好的界定。我们试图确定早期早产胎膜早破(PPROM)并发 IVH 的预测因素:我们对科罗拉多大学医院(UCH)自 2007 年 1 月 1 日至 2011 年 12 月 31 日期间发生的所有 22 周 GA 早期胎膜早破的单胎妊娠进行了回顾性队列研究。临床上明显的 IVH(III 级或 IV 级)是本研究的主要结果。为了确定 IVH 的独立预测因素,我们建立了一个多变量模型,其中包括所有 p 值小于 0.10 的单变量协变量:在我们的队列(n=229)中,如果对非白人种族进行调整,较年轻的孕产妇年龄和较高的体重指数(BMI)是具有临床意义的 IVH 的独立预测因素(OR=1.4 CI 1.04-1.79,p=0.03;OR 1.2 CI 1.04-1.33,p=0.01)。女性也是5分钟APGAR较差的独立预测因素(OR=2.3 CI 1.06-5.28,P=0.04):在我们的队列中,年龄较小的母亲或体重指数较高的母亲所生的婴儿发生临床重大 IVH 的风险似乎更高。有趣的是,在进一步分析中,我们发现女性新生儿的 5 分钟 APGAR 低于 7 的风险比男性高 2 倍。鉴于这些数据,有必要进行更大规模的研究,以探讨可改变和不可改变的妊娠风险,这些风险可能与早期 PPROM 并发妊娠中的 IVH 及随后的不良神经系统预后有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risk factors for clinically significant intra-ventricular hemorrhage in pregnancies complicated by preterm premature rupture of membranes.

Objectives: Preterm birth is a major cause of adverse perinatal outcomes, including intraventricular hemorrhage (IVH). IVH has been shown to contribute to lasting neurological disability, however the role of maternal characteristics and potentially modifiable risk factors that contribute to these outcomes have not been well defined. We sought to determine predictors of IVH in pregnancies complicated by early preterm premature rupture of membranes (PPROM).

Study design: We performed a retrospective cohort study of all singleton pregnancies with early PPROM <32 weeks GA and delivery >22 weeks GA at University of Colorado Hospital (UCH) from 1/1/2007-12/31/2011. Clinically significant IVH (Grade III or IV) was the primary outcome of this study. To determine independent predictors of IVH we created a multivariate model including all univariate covariates with p-value of ≤ 0.10.

Results: In our cohort (n=229), when adjusted for non-white race, younger maternal age and increased BMI were independent predictors of clinically significant IVH (OR=1.4 CI 1.04-1.79, p=0.03; OR 1.2 CI 1.04-1.33, p=0.01, respectively). Female gender was also found to be an independent predictor of poor 5 minute APGAR (OR=2.3 CI 1.06-5.28, p=0.04).

Conclusions: In our cohort, infants born to younger mothers or mothers with higher BMI appear to be at increased risk for clinically significant IVH. Interestingly, on further analysis, we found that female newborns had a 2-fold greater risk of poor 5 minute APGAR of less than 7. Given these data, larger studies are warranted to examine modifiable and non-modifiable risk pregnancy that may be associated with IVH and subsequent adverse neurological outcomes in pregnancies complicated by early PPROM.

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