Department of Women and Children's Health, School of Life Course Sciences, King's College London, London, UK.
Ultrasound Obstet Gynecol. 2020 Mar;55(3):348-356. doi: 10.1002/uog.20401.
Accurate mid-pregnancy prediction of spontaneous preterm birth (sPTB) is essential to ensure appropriate surveillance of high-risk women. Advancing the QUiPP App prototype, QUiPP App v.2 aimed to provide individualized risk of delivery based on cervical length (CL), quantitative fetal fibronectin (qfFN) or both tests combined, taking into account further risk factors, such as multiple pregnancy. Here we report development of the QUiPP App v.2 predictive models for use in asymptomatic high-risk women, and validation using a distinct dataset in order to confirm the accuracy and transportability of the QUiPP App, overall and within specific clinically relevant time frames.
This was a prospective secondary analysis of data of asymptomatic women at high risk of sPTB recruited in 13 UK preterm birth clinics. Women were offered longitudinal qfFN testing every 2-4 weeks and/or transvaginal ultrasound CL measurement between 18 + 0 and 36 + 6 weeks' gestation. A total of 1803 women (3878 visits) were included in the training set and 904 women (1400 visits) in the validation set. Prediction models were created based on the training set for use in three groups: patients with risk factors for sPTB and CL measurement alone, with risk factors for sPTB and qfFN measurement alone, and those with risk factors for sPTB and both CL and qfFN measurements. Survival analysis was used to identify the significant predictors of sPTB, and parametric structures for survival models were compared and the best selected. The estimated overall probability of delivery before six clinically important time points (< 30, < 34 and < 37 weeks' gestation and within 1, 2 and 4 weeks after testing) was calculated for each woman and analyzed as a predictive test for the actual occurrence of each event. This allowed receiver-operating-characteristics curves to be plotted, and areas under the curve (AUC) to be calculated. Calibration was performed to measure the agreement between expected and observed outcomes.
All three algorithms demonstrated high accuracy for the prediction of sPTB at < 30, < 34 and < 37 weeks' gestation and within 1, 2 and 4 weeks of testing, with AUCs between 0.75 and 0.90 for the use of qfFN and CL combined, between 0.68 and 0.90 for qfFN alone, and between 0.71 and 0.87 for CL alone. The differences between the three algorithms were not statistically significant. Calibration confirmed no significant differences between expected and observed rates of sPTB within 4 weeks and a slight overestimation of risk with the use of CL measurement between 22 + 0 and 25 + 6 weeks' gestation.
The QUiPP App v.2 is a highly accurate prediction tool for sPTB that is based on a unique combination of biomarkers, symptoms and statistical algorithms. It can be used reliably in the context of communicating to patients the risk of sPTB. Whilst further work is required to determine its role in identifying women requiring prophylactic interventions, it is a reliable and convenient screening tool for planning follow-up or hospitalization for high-risk women. Copyright © 2019 ISUOG. Published by John Wiley & Sons Ltd.
准确预测中期妊娠自发性早产(sPTB)对于确保高危女性的适当监测至关重要。推进 QUiPP App 原型,QUiPP App v.2 的目的是提供基于宫颈长度(CL)、定量胎儿纤维连接蛋白(qfFN)或两者联合检测的个体化分娩风险,同时考虑其他风险因素,如多胎妊娠。本研究旨在报告无症状高危女性使用 QUiPP App v.2 预测模型的开发情况,并使用独立数据集进行验证,以确认 QUiPP App 的准确性和可转移性,总体和特定临床相关时间框架内的准确性和可转移性。
这是一项针对在英国 13 家早产诊所招募的高危无症状 sPTB 女性的前瞻性二次分析。为高危无症状女性提供 qfFN 每 2-4 周或阴道超声 CL 测量,从 18+0 周到 36+6 周。共有 1803 名女性(3878 次就诊)被纳入训练集,904 名女性(1400 次就诊)被纳入验证集。基于训练集为 sPTB 风险因素和单独进行 CL 测量、sPTB 风险因素和单独进行 qfFN 测量以及 sPTB 风险因素和 CL 和 qfFN 测量的女性建立预测模型。生存分析用于识别 sPTB 的显著预测因子,并比较和选择参数结构生存模型。为每位女性计算了六个重要临床时间点(<30、<34 和<37 周妊娠以及检测后 1、2 和 4 周)之前发生 sPTB 的总概率,并将其分析为实际发生的预测性测试每个事件。这允许绘制接收者操作特征曲线,并计算曲线下面积(AUC)。进行校准以测量预期结果和观察结果之间的一致性。
所有三种算法在预测<30、<34 和<37 周妊娠以及检测后 1、2 和 4 周内的 sPTB 方面均表现出较高的准确性,qfFN 和 CL 联合使用的 AUC 在 0.75 至 0.90 之间,qfFN 单独使用的 AUC 在 0.68 至 0.90 之间,CL 单独使用的 AUC 在 0.71 至 0.87 之间。三种算法之间的差异无统计学意义。校准证实,在 4 周内,sPTB 的预期和观察发生率之间没有显著差异,在 22+0 至 25+6 周妊娠期间使用 CL 测量时存在轻微的风险高估。
QUiPP App v.2 是一种基于独特的生物标志物、症状和统计算法组合的 sPTB 高度准确的预测工具。它可以在向患者传达 sPTB 风险的背景下可靠地使用。虽然需要进一步研究来确定其在识别需要预防性干预的女性中的作用,但它是一种可靠且方便的筛查工具,可用于计划高危女性的随访或住院治疗。