Harris Birthright Research Centre for Fetal Medicine, King's College Hospital, London, UK.
Institute of Health Research, University of Exeter, Exeter, UK.
Ultrasound Obstet Gynecol. 2017 Sep;50(3):367-372. doi: 10.1002/uog.17418. Epub 2017 Jul 31.
To estimate the patient-specific risk of pre-eclampsia (PE) at 19-24 weeks' gestation by a combination of maternal characteristics and medical history with multiples of the median (MoM) values of mean arterial pressure (MAP), uterine artery pulsatility index (UtA-PI), serum placental growth factor (PlGF) and serum soluble fms-like tyrosine kinase-1 (sFlt-1), and stratify women into high-, intermediate- and low-risk management groups.
This was a prospective observational study in women attending a second-trimester ultrasound scan at 19-24 weeks as part of routine pregnancy care. Patient-specific risks of delivery with PE < 32 weeks and < 36 weeks' gestation were calculated using the competing-risks model to combine the prior risk from maternal characteristics and medical history with MoM values of MAP, UtA-PI, PlGF and sFlt-1. On the basis of these risks, the population was stratified into high-, intermediate- and low-risk groups. Different risk cut-offs were used to vary the proportion of the population stratified into each risk category and the performance of screening for delivery with PE at < 32 weeks' gestation, at 32-35 weeks and at ≥ 36 weeks was estimated. In addition to empirical performance, we also derived model-based performance because the number of cases of PE delivering < 32 weeks was low.
The study population of 7748 singleton pregnancies included 268 (3.5%) that subsequently developed PE. Using a risk cut-off of 1 in 100 for PE delivering < 32 weeks' gestation and a risk cut-off of 1 in 300 for PE delivering < 36 weeks, the proportion of the population stratified into high-, intermediate- and low-risk was 0.9%, 17.2% and 81.9%, respectively. The high-risk group contained 97% of pregnancies with PE < 32 weeks and 45% of those with PE at 32-35 weeks. The intermediate-risk group contained a further 46% of women with PE at 32-35 weeks. The low-risk group contained only 0.03% of pregnancies with PE < 32 weeks and 9% of those with PE at 32-35 weeks.
Risk stratification of PE by the combined test at 19-24 weeks' gestation can identify, first, a group which constitutes < 1% of the total population and contains > 95% of those that will develop PE < 32 weeks and are in need of intensive monitoring at 24-31 weeks and, second, a group which constitutes < 20% of the total and contains > 90% of those that will develop PE at 32-35 weeks and are in need of reassessment at 32 weeks. Copyright © 2017 ISUOG. Published by John Wiley & Sons Ltd.
通过将母体特征和病史与平均动脉压(MAP)、子宫动脉搏动指数(UtA-PI)、血清胎盘生长因子(PlGF)和可溶性 fms 样酪氨酸激酶-1(sFlt-1)的中位数倍数(MoM)值相结合,来估计 19-24 周妊娠时子痫前期(PE)的患者特异性风险,并将女性分为高、中、低风险管理组。
这是一项前瞻性观察性研究,纳入在 19-24 周进行第二次超声检查的女性,这是常规妊娠护理的一部分。使用竞争风险模型计算<32 周和<36 周妊娠时发生 PE 的患者特异性风险,以结合母体特征和病史的先验风险与 MAP、UtA-PI、PlGF 和 sFlt-1 的 MoM 值。基于这些风险,人群被分为高、中、低风险组。使用不同的风险截止值来改变每个风险类别分层的人群比例,并估计<32 周、32-35 周和≥36 周时 PE 分娩的筛查性能。除了经验性能外,我们还推导出基于模型的性能,因为<32 周时发生 PE 的病例数较少。
在 7748 例单胎妊娠的研究人群中,有 268 例(3.5%)随后发生了 PE。使用<32 周时发生 PE 的风险截止值为 1/100 和<36 周时发生 PE 的风险截止值为 1/300,高、中、低风险人群的比例分别为 0.9%、17.2%和 81.9%。高危组包含 97%的<32 周 PE 病例和 45%的 32-35 周 PE 病例。中间风险组包含另外 46%的 32-35 周 PE 病例。低危组仅包含 0.03%的<32 周 PE 病例和 9%的 32-35 周 PE 病例。
在 19-24 周妊娠时通过联合检测对 PE 进行风险分层,可以首先确定一个构成总人群<1%的组,其中包含>95%将在 24-31 周发生<32 周 PE 且需要加强监测的患者,其次可以确定一个构成总人群<20%的组,其中包含>90%将在 32-35 周发生 PE 且需要在 32 周时重新评估的患者。版权所有©2017ISUOG。由 John Wiley & Sons Ltd 出版。