Department of Obstetrics and Gynecology, Hospital Universitario de Torrejón, Torrejón de Ardoz, Madrid, Spain.
Faculty of Medicine, Universidad Francisco de Vitoria, Pozuelo de Alarcón, Madrid, Spain.
Ultrasound Obstet Gynecol. 2024 Jul;64(1):57-64. doi: 10.1002/uog.27622. Epub 2024 Jun 6.
To compare the predictive performance of three different mathematical models for first-trimester screening of pre-eclampsia (PE), which combine maternal risk factors with mean arterial pressure (MAP), uterine artery pulsatility index (UtA-PI) and serum placental growth factor (PlGF), and two risk-scoring systems.
This was a prospective cohort study performed in eight fetal medicine units in five different regions of Spain between September 2017 and December 2019. All pregnant women with singleton pregnancy and a non-malformed live fetus attending their routine ultrasound examination at 11 + 0 to 13 + 6 weeks' gestation were invited to participate in the study. Maternal characteristics and medical history were recorded and measurements of MAP, UtA-PI, serum PlGF and pregnancy-associated plasma protein-A (PAPP-A) were converted into multiples of the median (MoM). Risks for term PE, preterm PE (< 37 weeks' gestation) and early PE (< 34 weeks' gestation) were calculated according to the FMF competing-risks model, the Crovetto et al. logistic regression model and the Serra et al. Gaussian model. PE classification was also performed based on the recommendations of the National Institute for Health and Care Excellence (NICE) and the American College of Obstetricians and Gynecologists (ACOG). We estimated detection rates (DR) with their 95% CIs at a fixed 10% screen-positive rate (SPR), as well as the area under the receiver-operating-characteristics curve (AUC) for preterm PE, early PE and all PE for the three mathematical models. For the scoring systems, we calculated DR and SPR. Risk calibration was also assessed.
The study population comprised 10 110 singleton pregnancies, including 32 (0.3%) that developed early PE, 72 (0.7%) that developed preterm PE and 230 (2.3%) with any PE. At a fixed 10% SPR, the FMF, Crovetto et al. and Serra et al. models detected 82.7% (95% CI, 69.6-95.8%), 73.8% (95% CI, 58.7-88.9%) and 79.8% (95% CI, 66.1-93.5%) of early PE; 72.7% (95% CI, 62.9-82.6%), 69.2% (95% CI, 58.8-79.6%) and 74.1% (95% CI, 64.2-83.9%) of preterm PE; and 55.1% (95% CI, 48.8-61.4%), 47.1% (95% CI, 40.6-53.5%) and 53.9% (95% CI, 47.4-60.4%) of all PE, respectively. The best correlation between predicted and observed cases was achieved by the FMF model, with an AUC of 0.911 (95% CI, 0.879-0.943), a slope of 0.983 (95% CI, 0.846-1.120) and an intercept of 0.154 (95% CI, -0.091 to 0.397). The NICE criteria identified 46.7% (95% CI, 35.3-58.0%) of preterm PE at 11% SPR and ACOG criteria identified 65.9% (95% CI, 55.4-76.4%) of preterm PE at 33.8% SPR.
The best performance of screening for preterm PE is achieved by mathematical models that combine maternal factors with MAP, UtA-PI and PlGF, as compared to risk-scoring systems such as those of NICE and ACOG. While all three algorithms show similar results in terms of overall prediction, the FMF model showed the best performance at an individual level. © 2024 International Society of Ultrasound in Obstetrics and Gynecology.
比较三种不同的数学模型在子痫前期(PE)的早期筛查中的预测性能,这些模型将母体危险因素与平均动脉压(MAP)、子宫动脉搏动指数(UtA-PI)和血清胎盘生长因子(PlGF)相结合,并与两种风险评分系统相结合。
这是一项前瞻性队列研究,在西班牙五个不同地区的八个胎儿医学单位进行,时间为 2017 年 9 月至 2019 年 12 月。所有单胎妊娠和无畸形活胎的孕妇均受邀参加常规超声检查,检查时间为 11+0 周至 13+6 周。记录孕妇的特征和病史,并测量 MAP、UtA-PI、血清 PlGF 和妊娠相关血浆蛋白-A(PAPP-A),将其转换为中位数倍数(MoM)。根据 FMF 竞争风险模型、Crovetto 等人的逻辑回归模型和 Serra 等人的高斯模型计算足月 PE、早产 PE(<37 周)和早发性 PE(<34 周)的风险。根据英国国家卫生与保健卓越研究所(NICE)和美国妇产科医师学会(ACOG)的建议,还进行了 PE 分类。我们在固定的 10%筛查阳性率(SPR)下估计了检测率(DR)及其 95%CI,以及三种数学模型的早产 PE、早发性 PE 和所有 PE 的受试者工作特征曲线(ROC)下面积(AUC)。对于评分系统,我们计算了 DR 和 SPR。还评估了风险校准。
研究人群包括 10110 例单胎妊娠,其中 32 例(0.3%)发生早发性 PE,72 例(0.7%)发生早产 PE,230 例(2.3%)发生任何类型的 PE。在固定的 10%SPR 下,FMF、Crovetto 等人和 Serra 等人的模型分别检测到 82.7%(95%CI,69.6-95.8%)、73.8%(95%CI,58.7-88.9%)和 79.8%(95%CI,66.1-93.5%)的早发性 PE;72.7%(95%CI,62.9-82.6%)、69.2%(95%CI,58.8-79.6%)和 74.1%(95%CI,64.2-83.9%)的早产 PE;55.1%(95%CI,48.8-61.4%)、47.1%(95%CI,40.6-53.5%)和 53.9%(95%CI,47.4-60.4%)的所有 PE。FMF 模型与观察到的病例相关性最佳,AUC 为 0.911(95%CI,0.879-0.943),斜率为 0.983(95%CI,0.846-1.120),截距为 0.154(95%CI,-0.091 至 0.397)。NICE 标准在 11%SPR 时识别出 46.7%(95%CI,35.3-58.0%)的早产 PE,ACOG 标准在 33.8%SPR 时识别出 65.9%(95%CI,55.4-76.4%)的早产 PE。
与 NICE 和 ACOG 等风险评分系统相比,将母体因素与 MAP、UtA-PI 和 PlGF 相结合的数学模型在早产 PE 的筛查中具有最佳的性能。虽然所有三种算法在总体预测方面都显示出相似的结果,但 FMF 模型在个体水平上表现最佳。© 2024 年国际妇产科超声学会。