Second‐trimester contingent screening for small‐for‐gestational‐age neonate

Journal article


Nowacka, U., Papastefanou, I., Bouariu, A., Syngelaki, A., Akolekar, R. and Nicolaides, K. H. 2022. Second‐trimester contingent screening for small‐for‐gestational‐age neonate. Ultrasound in Obstetrics & Gynecology. 59 (2), pp. 177-184. https://doi.org/10.1002/uog.23730
AuthorsNowacka, U., Papastefanou, I., Bouariu, A., Syngelaki, A., Akolekar, R. and Nicolaides, K. H.
AbstractFirst, to investigate the additive value of second trimester placental growth factor (PlGF) for the prediction of small for gestational age (SGA) neonates. Second, to examine second trimester contingency screening strategies. This is a prospective observational study in 40,241 women with singleton pregnancies undergoing routine ultrasound examination at 19 - 24 weeks' gestation. We used the competing risks model for prediction of SGA. The parameters for the prior model and the likelihoods for estimated fetal weight (EFW) and uterine artery pulsatility index (UtA-PI) were those presented in previous studies. A folded plane regression model was fitted in the dataset of this study to describe the likelihood of PlGF. We compared the prediction of screening by maternal risk factors and EFW against the prediction provided by a combination of maternal risk factors EFW, UtA-PI and PlGF. We also examined the additive value of PlGF in a policy that uses maternal risk factors, EFW and UtA-PI. Overall, the prediction of SGA improved for increasing degree of prematurity, for higher severity of smallness and for coexistence of preeclampsia. The combination of maternal risk factors EFW, UtA-PI and PlGF improved significantly the prediction provided by maternal risk factors and EFW for all the examined cut-offs. Screening by a combination of maternal risk factors plus serum PIGF improved the prediction of SGA when compared to screening by maternal risk factors alone. However, the incremental improvement in prediction was decreased when PIGF was added to screening by a combination of maternal risk factors, EFW, and UtA-PI. If first line screening for SGA neonates with birth weight <10 percentile delivered at <37 weeks' gestation was by maternal risk factors and EFW, the same detection rate of 90% at overall FPR of 50% achieved by screening with maternal risk factors EFW, UtA-PI and PlGF of the whole population can be achieved by reserving the measurements of UtA-PI and PlGF to only 80% of the population. Similarly, in screening for SGA with birth weight <10 percentile delivered at <30 weeks the same detection rate of 90% at overall FPR of 14% achieved by screening with maternal risk factors EFW, UtA-PI and PlGF of the whole population can be achieved by reserving the measurements of UtA-PI and PlGF to only 70% of the population. The additive value of PlGF in reducing FPR to about 10% with a simultaneous detection rate of 90% for SGA <3 percentile born <30 weeks, is gained by measuring PlGF in only 50% of the population. The combination of maternal risk factors, EFW, UtA-PI and PlGF provide effective second trimester prediction of SGA. Serum PlGF is useful for predicting SGA <3 percentile born <30 weeks after an inclusive assessment by maternal risk factors and biophysical markers. Similar detection rates and FPRs can be achieved by the application of contingency screening strategies. This article is protected by copyright. All rights reserved. [Abstract copyright: This article is protected by copyright. All rights reserved.]
KeywordsObstetrics and Gynecology; Radiology, Nuclear Medicine and imaging; Reproductive Medicine; General Medicine; Radiological and Ultrasound Technology
Year2022
JournalUltrasound in Obstetrics & Gynecology
Journal citation59 (2), pp. 177-184
PublisherWiley
ISSN0960-7692
1469-0705
Digital Object Identifier (DOI)https://doi.org/10.1002/uog.23730
Official URLhttps://obgyn.onlinelibrary.wiley.com/doi/abs/10.1002/uog.23730
FunderFetal Medicine Foundation
Publication dates
Online12 Jan 2022
Publication process dates
Accepted28 Jun 2021
Deposited16 Aug 2021
Output statusPublished
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Yerlikaya, G., Akolekar, R., McPherson, K., Syngelaki, A. and Nicolaides, K. H. 2016. Prediction of stillbirth from maternal demographic and pregnancy characteristics. Ultrasound in Obstetrics and Gynecology. 48 (5), pp. 607-612. https://doi.org/10.1002/uog.17290
Endoscopic placental laser coagulation in dichorionic and monochorionic triplet pregnancies
Peeva, G., Chaveeva, P., Gil Guevara, E., Akolekar, R. and Nicolaides, K. H. 2016. Endoscopic placental laser coagulation in dichorionic and monochorionic triplet pregnancies. Fetal Diagnosis and Therapy. 40 (3), pp. 174-180. https://doi.org/10.1159/000443792
Prediction of stillbirth from maternal factors, fetal biometry and uterine artery Doppler at 19-24 weeks
Akolekar, R., Tokunaka, M., Ortega, N., Syngelaki, A. and Nicolaides, K. H. 2016. Prediction of stillbirth from maternal factors, fetal biometry and uterine artery Doppler at 19-24 weeks. Ultrasound in Obstetrics and Gynecology. 48 (5), pp. 624-630. https://doi.org/10.1002/uog.17295
Prediction of stillbirth from placental growth factor at 11-13 weeks
Akolekar, R., Machuca, M., Mendes, M., Paschos, V. and Nicolaides, K. H. 2016. Prediction of stillbirth from placental growth factor at 11-13 weeks. Ultrasound in Obstetrics and Gynecology. 48 (5), pp. 618-623. https://doi.org/10.1002/uog.17288
Prediction of stillbirth from placental growth factor at 19-24 weeks
Aupont J. E., Akolekar, R., Illian, A., Neonakis, S. and Nicolaides, K. H. 2016. Prediction of stillbirth from placental growth factor at 19-24 weeks. Ultrasound in Obstetrics and Gynecology. 48 (5), pp. 631-635. https://doi.org/10.1002/uog.17229
Biophysical and biochemical markers at 35-37 weeks' gestation in the prediction of adverse perinatal outcome
Valiño, N., Giunta, G., Gallo, D. M., Akolekar, R. and Nicolaides, K. H. 2015. Biophysical and biochemical markers at 35-37 weeks' gestation in the prediction of adverse perinatal outcome. Ultrasound in Obstetrics and Gynecology. 47 (2), pp. 203-209. https://doi.org/10.1002/uog.15663