A Novel Approach to Predicting Early Pregnancy Outcomes Dynamically in a Prospective Cohort Using Repeated Ultrasound and Serum Biomarkers

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

A Novel Approach to Predicting Early Pregnancy Outcomes Dynamically in a Prospective Cohort Using Repeated Ultrasound and Serum Biomarkers. / Petersen, Jesper Friis; Friis-Hansen, Lennart Jan; Bryndorf, Thue; Jensen, Andreas Kryger; Andersen, Anders Nyboe; Løkkegaard, Ellen.

I: Reproductive Sciences, Bind 30, 2023, s. 3597–3609.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Petersen, JF, Friis-Hansen, LJ, Bryndorf, T, Jensen, AK, Andersen, AN & Løkkegaard, E 2023, 'A Novel Approach to Predicting Early Pregnancy Outcomes Dynamically in a Prospective Cohort Using Repeated Ultrasound and Serum Biomarkers', Reproductive Sciences, bind 30, s. 3597–3609. https://doi.org/10.1007/s43032-023-01323-8

APA

Petersen, J. F., Friis-Hansen, L. J., Bryndorf, T., Jensen, A. K., Andersen, A. N., & Løkkegaard, E. (2023). A Novel Approach to Predicting Early Pregnancy Outcomes Dynamically in a Prospective Cohort Using Repeated Ultrasound and Serum Biomarkers. Reproductive Sciences, 30, 3597–3609. https://doi.org/10.1007/s43032-023-01323-8

Vancouver

Petersen JF, Friis-Hansen LJ, Bryndorf T, Jensen AK, Andersen AN, Løkkegaard E. A Novel Approach to Predicting Early Pregnancy Outcomes Dynamically in a Prospective Cohort Using Repeated Ultrasound and Serum Biomarkers. Reproductive Sciences. 2023;30:3597–3609. https://doi.org/10.1007/s43032-023-01323-8

Author

Petersen, Jesper Friis ; Friis-Hansen, Lennart Jan ; Bryndorf, Thue ; Jensen, Andreas Kryger ; Andersen, Anders Nyboe ; Løkkegaard, Ellen. / A Novel Approach to Predicting Early Pregnancy Outcomes Dynamically in a Prospective Cohort Using Repeated Ultrasound and Serum Biomarkers. I: Reproductive Sciences. 2023 ; Bind 30. s. 3597–3609.

Bibtex

@article{28791812a90a4f0a9f7600af58a8ddcf,
title = "A Novel Approach to Predicting Early Pregnancy Outcomes Dynamically in a Prospective Cohort Using Repeated Ultrasound and Serum Biomarkers",
abstract = "This study aimed to develop a dynamic model for predicting outcome during the first trimester of pregnancy using baseline demographic data and serially collected blood samples and transvaginal sonographies. A prospective cohort of 203 unselected women with an assumed healthy pregnancy of < 8 weeks{\textquoteright} gestation was followed fortnightly from 4–14 weeks{\textquoteright} gestation until either miscarriage or confirmed first trimester viability. The main outcome was development of a model to predict outcome from gestational age-dependent hazard ratios using both baseline and updated serial data from each visit. Secondary outcomes were descriptions of risk factors for miscarriage. The results showed that 18% of the women experienced miscarriages. A fetal heart rate detected before 8 weeks{\textquoteright} gestation indicated a 90% (95% CI 85–95%) chance of subsequent delivery. Maternal age (≥ 35 years), insufficient crown-rump-length (CRL) and mean gestational sac diameter (MSD) development, and presence of bleeding increased the risk of miscarriage. Serum biomarkers, including hCG, progesterone, and estradiol, were found to impact the risk of miscarriage with estradiol as the most important. The best model to predict miscarriage was a combination of maternal age, vaginal bleeding, CRL, and hCG. The second-best model was the sonography-absent model of maternal age, bleeding, hCG, and estradiol. This study suggests that combining maternal age, and evolving data from hCG, estradiol, CRL, and bleeding could be used to predict fetal outcome during the first trimester of pregnancy. Trial registration ClinicalTrials.gov identifier: NCT02761772.",
keywords = "Early pregnancy, Estradiol, Miscarriage, Prediction model, Vaginal microbiota, Viability",
author = "Petersen, {Jesper Friis} and Friis-Hansen, {Lennart Jan} and Thue Bryndorf and Jensen, {Andreas Kryger} and Andersen, {Anders Nyboe} and Ellen L{\o}kkegaard",
note = "Publisher Copyright: {\textcopyright} 2023, The Author(s).",
year = "2023",
doi = "10.1007/s43032-023-01323-8",
language = "English",
volume = "30",
pages = "3597–3609",
journal = "Reproductive Sciences",
issn = "1933-7191",
publisher = "SAGE Publications",

}

RIS

TY - JOUR

T1 - A Novel Approach to Predicting Early Pregnancy Outcomes Dynamically in a Prospective Cohort Using Repeated Ultrasound and Serum Biomarkers

AU - Petersen, Jesper Friis

AU - Friis-Hansen, Lennart Jan

AU - Bryndorf, Thue

AU - Jensen, Andreas Kryger

AU - Andersen, Anders Nyboe

AU - Løkkegaard, Ellen

N1 - Publisher Copyright: © 2023, The Author(s).

PY - 2023

Y1 - 2023

N2 - This study aimed to develop a dynamic model for predicting outcome during the first trimester of pregnancy using baseline demographic data and serially collected blood samples and transvaginal sonographies. A prospective cohort of 203 unselected women with an assumed healthy pregnancy of < 8 weeks’ gestation was followed fortnightly from 4–14 weeks’ gestation until either miscarriage or confirmed first trimester viability. The main outcome was development of a model to predict outcome from gestational age-dependent hazard ratios using both baseline and updated serial data from each visit. Secondary outcomes were descriptions of risk factors for miscarriage. The results showed that 18% of the women experienced miscarriages. A fetal heart rate detected before 8 weeks’ gestation indicated a 90% (95% CI 85–95%) chance of subsequent delivery. Maternal age (≥ 35 years), insufficient crown-rump-length (CRL) and mean gestational sac diameter (MSD) development, and presence of bleeding increased the risk of miscarriage. Serum biomarkers, including hCG, progesterone, and estradiol, were found to impact the risk of miscarriage with estradiol as the most important. The best model to predict miscarriage was a combination of maternal age, vaginal bleeding, CRL, and hCG. The second-best model was the sonography-absent model of maternal age, bleeding, hCG, and estradiol. This study suggests that combining maternal age, and evolving data from hCG, estradiol, CRL, and bleeding could be used to predict fetal outcome during the first trimester of pregnancy. Trial registration ClinicalTrials.gov identifier: NCT02761772.

AB - This study aimed to develop a dynamic model for predicting outcome during the first trimester of pregnancy using baseline demographic data and serially collected blood samples and transvaginal sonographies. A prospective cohort of 203 unselected women with an assumed healthy pregnancy of < 8 weeks’ gestation was followed fortnightly from 4–14 weeks’ gestation until either miscarriage or confirmed first trimester viability. The main outcome was development of a model to predict outcome from gestational age-dependent hazard ratios using both baseline and updated serial data from each visit. Secondary outcomes were descriptions of risk factors for miscarriage. The results showed that 18% of the women experienced miscarriages. A fetal heart rate detected before 8 weeks’ gestation indicated a 90% (95% CI 85–95%) chance of subsequent delivery. Maternal age (≥ 35 years), insufficient crown-rump-length (CRL) and mean gestational sac diameter (MSD) development, and presence of bleeding increased the risk of miscarriage. Serum biomarkers, including hCG, progesterone, and estradiol, were found to impact the risk of miscarriage with estradiol as the most important. The best model to predict miscarriage was a combination of maternal age, vaginal bleeding, CRL, and hCG. The second-best model was the sonography-absent model of maternal age, bleeding, hCG, and estradiol. This study suggests that combining maternal age, and evolving data from hCG, estradiol, CRL, and bleeding could be used to predict fetal outcome during the first trimester of pregnancy. Trial registration ClinicalTrials.gov identifier: NCT02761772.

KW - Early pregnancy

KW - Estradiol

KW - Miscarriage

KW - Prediction model

KW - Vaginal microbiota

KW - Viability

U2 - 10.1007/s43032-023-01323-8

DO - 10.1007/s43032-023-01323-8

M3 - Journal article

C2 - 37640889

AN - SCOPUS:85168867529

VL - 30

SP - 3597

EP - 3609

JO - Reproductive Sciences

JF - Reproductive Sciences

SN - 1933-7191

ER -

ID: 370269687