First Trimester Preeclampsia Screening: Uterine Artery Doppler Using the FMF Algorithm — МЕДТРЕЙН Asia
Obstetrics and Gynecology

First Trimester Preeclampsia Screening: Uterine Artery Doppler Using the FMF Algorithm

Briefly. First trimester preeclampsia screening using the Fetal Medicine Foundation (FMF) algorithm is performed at 11–13 weeks and combines maternal factors, mean arterial pressure (MAP), uterine artery pulsatility index (UtA-PI), and PAPP-A. Assessment of UtA-PI and MAP is performed according to established protocols during routine ultrasound at 11–13 weeks. Early risk stratification allows for timely implementation of prophylaxis.

Timing of Screening

According to ISUOG recommendations for preeclampsia screening, Doppler assessment of uterine arteries in the first trimester is performed between 11 weeks 0 days and 13 weeks 6 days. A second screening window has also been described at approximately 20–24 weeks. ISUOG patient materials also indicate first trimester screening between 11 and 14 weeks with repeat assessment typically at 20–24 weeks.

The rationale for early screening is that uterine artery Doppler is most informative when used to identify increased risk early enough for preventive strategies or enhanced surveillance to be meaningful. By the late third trimester, the predictive contribution of UtA-PI decreases, and other markers come to the forefront.

Components of the FMF Algorithm

Screening for preterm preeclampsia (preterm PE) using the Fetal Medicine Foundation algorithm (competing risk model) includes:

ComponentDescription
Maternal factorsMaternal history and characteristics
MAPMean arterial pressure
UtA-PIUterine artery pulsatility index (Doppler)
PAPP-APregnancy-associated plasma protein-A

PAPP-A has been shown to demonstrate efficacy in preterm preeclampsia screening comparable to placental growth factor (PlGF) when applied in clinical practice.

Technical Aspects of Performance

During routine ultrasound examination at 11–13 weeks, gestational age is calculated using crown-rump length (CRL). MAP and UtA-PI are assessed according to established protocols. Specific threshold values of UtA-PI for risk stratification are not provided in the available fragments [to be clarified].

Algorithm Validation

The FMF competing risk model based on maternal factors and biomarkers at 11–13 weeks (O'Gorman N. et al., 2016) has undergone external validation in multiple cohorts, including studies by Mosimann B. et al. (2017) and Allen RE. et al. (2017).

Frequently asked questions

At what gestational age is uterine artery Doppler performed in the first trimester?

Between 11 weeks 0 days and 13 weeks 6 days (ISUOG); patient materials indicate a range of 11–14 weeks. A second screening window is approximately 20–24 weeks.

Which parameters are included in the FMF algorithm?

Maternal factors, mean arterial pressure (MAP), uterine artery pulsatility index (UtA-PI), and PAPP-A.

Can PAPP-A be replaced with PlGF?

PAPP-A has been shown to demonstrate efficacy in preterm preeclampsia screening comparable to placental growth factor (PlGF) in clinical practice.

Why is uterine artery Doppler more important at an earlier gestational age?

By the late third trimester, the predictive contribution of UtA-PI decreases, whereas early assessment allows timely initiation of prophylaxis or enhanced surveillance.

How is gestational age calculated during screening?

Using crown-rump length (CRL) at routine ultrasound at 11–13 weeks; MAP and UtA-PI are assessed according to established protocols.

The material is intended for specialists and does not replace clinical judgment. Threshold values are periodically reviewed — refer to the current edition of the applicable consensus.
Sources: Holland R. Clinical Ultrasound in Gynecology and Obstetrics, 2026; Ultrasound in Obstetrics & Gynecology (ISUOG), Vol. 63 (№1, 3, 5, 6), Vol. 64 (№1), 2024; O'Gorman N. et al. Am J Obstet Gynecol 2016;214:103.e1-12; Mosimann B. et al. Swiss Med Wkly 2017;147:w14498; Plasencia W. et al. UOG 2008;32(2):138-146; Poon LCY. et al. Hypertension 2009;53(5):812-818.
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