Harris Birthright Research Centre for Fetal Medicine, King's College Hospital, London, UK.
Department of Fetal Medicine, Medway Maritime Hospital, Gillingham, UK.
Ultrasound Obstet Gynecol. 2016 Nov;48(5):607-612. doi: 10.1002/uog.17290. Epub 2016 Oct 5.
To develop a model for prediction of stillbirth based on maternal characteristics and components of medical history and to evaluate the performance of screening with this model for all stillbirths and those due to impaired placentation and to unexplained causes.
This was a prospective screening study of 113 415 singleton pregnancies at 11 + 0 to 13 + 6 weeks' gestation and at 19 + 0 to 24 + 6 weeks. The study population included 113 019 live births and 396 (0.35%) antepartum stillbirths; 230 (58%) were secondary to impaired placentation and 166 (42%) were due to other or unexplained causes. Multivariable logistic regression analysis was used to determine the factors from maternal characteristics and medical history which provided a significant contribution to the prediction of stillbirth.
The risk for stillbirth increased with maternal weight (odds ratio (OR), 1.01 per kg above 69 kg), was higher in women of Afro-Caribbean racial origin (OR, 2.01), those with assisted conception (OR, 1.79), cigarette smokers (OR, 1.71), and in those with a history of chronic hypertension (OR, 2.62), systemic lupus erythematosus/antiphospholipid syndrome (OR, 3.61) or diabetes mellitus (OR, 2.55) and was increased in women with a history of previous stillbirth (OR, 4.81). Screening with the model predicted 26% of unexplained stillbirths and 31% of those due to impaired placentation, at a false-positive rate of 10%; within the impaired-placentation group the detection rate of stillbirth < 32 weeks' gestation was higher than that of stillbirth ≥ 37 weeks (38% vs 28%).
A model based on maternal characteristics and medical history recorded in early pregnancy can potentially predict one-third of subsequent stillbirths. The extent to which such stillbirths could be prevented remains to be determined. Copyright © 2016 ISUOG. Published by John Wiley & Sons Ltd.
基于产妇特征和病史构成,建立预测死产的模型,并评估该模型筛查所有死产及因胎盘功能不良和不明原因导致的死产的效能。
这是一项前瞻性筛查研究,纳入 113 415 例孕 11+0 周至 13+6 周及 19+0 周至 24+6 周的单胎妊娠。研究人群包括 113 019 例活产儿和 396 例(0.35%)产前死产儿;其中 230 例(58%)由胎盘功能不良导致,166 例(42%)由其他或不明原因导致。多变量逻辑回归分析用于确定产妇特征和病史中对死产预测有显著贡献的因素。
死产风险随产妇体重增加而升高(每增加 69kg 以上,比值比(OR)为 1.01),非裔加勒比海种族产妇(OR 为 2.01)、辅助受孕产妇(OR 为 1.79)、吸烟产妇(OR 为 1.71)、慢性高血压产妇(OR 为 2.62)、系统性红斑狼疮/抗磷脂综合征产妇(OR 为 3.61)或糖尿病产妇(OR 为 2.55)的死产风险更高,且有既往死产史的产妇(OR 为 4.81)的死产风险也增加。该模型筛查预测了 26%的不明原因死产和 31%的因胎盘功能不良导致的死产,假阳性率为 10%;在胎盘功能不良组中,<32 周胎龄死产的检出率高于≥37 周胎龄死产(38% vs 28%)。
基于孕早期产妇特征和病史建立的模型,可能可以预测三分之一的后续死产。但尚不清楚通过这种模型筛查可以预防多少此类死产。版权所有©2016 ISUOG。由 John Wiley & Sons Ltd 出版。