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Prediction of perinatal survival in early‐onset fetal growth restriction: role of placental growth factor

OBJECTIVE: To analyze the ability to predict perinatal survival and severe neonatal morbidity of cases with early‐onset fetal growth restriction (eoFGR) using maternal variables, ultrasound parameters and angiogenic markers at the time of diagnosis. METHODS: This was a prospective observational stud...

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Autores principales: Rodríguez‐Calvo, J., Villalaín, C., Gómez‐Arriaga, P. I., Quezada, M. S., Herraiz, I., Galindo, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107431/
https://www.ncbi.nlm.nih.gov/pubmed/36370447
http://dx.doi.org/10.1002/uog.26116
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author Rodríguez‐Calvo, J.
Villalaín, C.
Gómez‐Arriaga, P. I.
Quezada, M. S.
Herraiz, I.
Galindo, A.
author_facet Rodríguez‐Calvo, J.
Villalaín, C.
Gómez‐Arriaga, P. I.
Quezada, M. S.
Herraiz, I.
Galindo, A.
author_sort Rodríguez‐Calvo, J.
collection PubMed
description OBJECTIVE: To analyze the ability to predict perinatal survival and severe neonatal morbidity of cases with early‐onset fetal growth restriction (eoFGR) using maternal variables, ultrasound parameters and angiogenic markers at the time of diagnosis. METHODS: This was a prospective observational study in a cohort of singleton pregnancies with a diagnosis of eoFGR (< 32 weeks of gestation). At diagnosis of eoFGR, complete assessment was performed, including ultrasound examination (anatomy, biometry and Doppler assessment) and maternal serum measurement of the angiogenic biomarkers, soluble fms‐like tyrosine kinase‐1 (sFlt‐1) and placental growth factor (PlGF). Logistic regression models for the prediction of perinatal survival (in cases diagnosed at < 28 weeks) and severe neonatal morbidity (in all liveborn cases) were calculated. RESULTS: In total, 210 eoFGR cases were included, of which 185 (88.1%) survived perinatally. The median gestational age at diagnosis was 27 + 0 weeks. All cases diagnosed at ≥ 28 weeks survived. In cases diagnosed < 28 weeks, survivors (vs non‐survivors) had a higher gestational age (26.1 vs 24.4 weeks), estimated fetal weight (EFW; 626 vs 384 g), cerebroplacental ratio (1.1 vs 0.9), PlGF (41 vs 18 pg/mL) and PlGF multiples of the median (MoM; 0.10 vs 0.06) and lower sFlt‐1/PlGF ratio (129 vs 479) at the time of diagnosis (all P < 0.001). The best combination of two variables for predicting perinatal survival was provided by EFW and PlGF MoM (area under the receiver‐operating‐characteristics curve (AUC), 0.84 (95% CI, 0.75–0.92)). These were also the best variables for predicting severe neonatal morbidity (AUC, 0.73 (95% CI, 0.66–0.80)). CONCLUSIONS: A model combining EFW and maternal serum PlGF predicts accurately perinatal survival in eoFGR cases diagnosed before 28 weeks of gestation. Prenatal prediction of severe neonatal morbidity in eoFGR cases is modest regardless of the model used. © 2022 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology.
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spelling pubmed-101074312023-04-18 Prediction of perinatal survival in early‐onset fetal growth restriction: role of placental growth factor Rodríguez‐Calvo, J. Villalaín, C. Gómez‐Arriaga, P. I. Quezada, M. S. Herraiz, I. Galindo, A. Ultrasound Obstet Gynecol Original Papers OBJECTIVE: To analyze the ability to predict perinatal survival and severe neonatal morbidity of cases with early‐onset fetal growth restriction (eoFGR) using maternal variables, ultrasound parameters and angiogenic markers at the time of diagnosis. METHODS: This was a prospective observational study in a cohort of singleton pregnancies with a diagnosis of eoFGR (< 32 weeks of gestation). At diagnosis of eoFGR, complete assessment was performed, including ultrasound examination (anatomy, biometry and Doppler assessment) and maternal serum measurement of the angiogenic biomarkers, soluble fms‐like tyrosine kinase‐1 (sFlt‐1) and placental growth factor (PlGF). Logistic regression models for the prediction of perinatal survival (in cases diagnosed at < 28 weeks) and severe neonatal morbidity (in all liveborn cases) were calculated. RESULTS: In total, 210 eoFGR cases were included, of which 185 (88.1%) survived perinatally. The median gestational age at diagnosis was 27 + 0 weeks. All cases diagnosed at ≥ 28 weeks survived. In cases diagnosed < 28 weeks, survivors (vs non‐survivors) had a higher gestational age (26.1 vs 24.4 weeks), estimated fetal weight (EFW; 626 vs 384 g), cerebroplacental ratio (1.1 vs 0.9), PlGF (41 vs 18 pg/mL) and PlGF multiples of the median (MoM; 0.10 vs 0.06) and lower sFlt‐1/PlGF ratio (129 vs 479) at the time of diagnosis (all P < 0.001). The best combination of two variables for predicting perinatal survival was provided by EFW and PlGF MoM (area under the receiver‐operating‐characteristics curve (AUC), 0.84 (95% CI, 0.75–0.92)). These were also the best variables for predicting severe neonatal morbidity (AUC, 0.73 (95% CI, 0.66–0.80)). CONCLUSIONS: A model combining EFW and maternal serum PlGF predicts accurately perinatal survival in eoFGR cases diagnosed before 28 weeks of gestation. Prenatal prediction of severe neonatal morbidity in eoFGR cases is modest regardless of the model used. © 2022 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology. John Wiley & Sons, Ltd. 2023-02-01 2023-02 /pmc/articles/PMC10107431/ /pubmed/36370447 http://dx.doi.org/10.1002/uog.26116 Text en © 2022 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Papers
Rodríguez‐Calvo, J.
Villalaín, C.
Gómez‐Arriaga, P. I.
Quezada, M. S.
Herraiz, I.
Galindo, A.
Prediction of perinatal survival in early‐onset fetal growth restriction: role of placental growth factor
title Prediction of perinatal survival in early‐onset fetal growth restriction: role of placental growth factor
title_full Prediction of perinatal survival in early‐onset fetal growth restriction: role of placental growth factor
title_fullStr Prediction of perinatal survival in early‐onset fetal growth restriction: role of placental growth factor
title_full_unstemmed Prediction of perinatal survival in early‐onset fetal growth restriction: role of placental growth factor
title_short Prediction of perinatal survival in early‐onset fetal growth restriction: role of placental growth factor
title_sort prediction of perinatal survival in early‐onset fetal growth restriction: role of placental growth factor
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107431/
https://www.ncbi.nlm.nih.gov/pubmed/36370447
http://dx.doi.org/10.1002/uog.26116
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