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Ophthalmic artery Doppler in combination with other biomarkers in prediction of pre‐eclampsia at 35–37 weeks' gestation

ABSTRACT Objective To examine the potential value of maternal ophthalmic artery Doppler at 35–37 weeks' gestation in combination with the established biomarkers of pre‐eclampsia (PE), including mean arterial pressure (MAP), uterine artery pulsatility index (UtA‐PI), serum placental growth facto...

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Published in:Ultrasound in obstetrics & gynecology 2021-04, Vol.57 (4), p.600-606
Main Authors: Sarno, M., Wright, A., Vieira, N., Sapantzoglou, I., Charakida, M., Nicolaides, K. H.
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Nicolaides, K. H.
description ABSTRACT Objective To examine the potential value of maternal ophthalmic artery Doppler at 35–37 weeks' gestation in combination with the established biomarkers of pre‐eclampsia (PE), including mean arterial pressure (MAP), uterine artery pulsatility index (UtA‐PI), serum placental growth factor (PlGF) and serum soluble fms‐like tyrosine kinase‐1 (sFlt‐1), in the prediction of subsequent development of PE. Methods This was a prospective observational study in women attending for a routine hospital visit at 35 + 0 to 36 + 6 weeks' gestation. This visit included recording of maternal demographic characteristics and medical history, ultrasound examination for fetal anatomy and growth, assessment of flow velocity waveforms from the maternal ophthalmic arteries, and measurement of MAP, UtA‐PI, serum PlGF and serum sFlt‐1. The competing‐risks model was used to estimate the individual patient‐specific risks of delivery with PE at any time and at
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H.</creator><creatorcontrib>Sarno, M. ; Wright, A. ; Vieira, N. ; Sapantzoglou, I. ; Charakida, M. ; Nicolaides, K. H.</creatorcontrib><description>ABSTRACT Objective To examine the potential value of maternal ophthalmic artery Doppler at 35–37 weeks' gestation in combination with the established biomarkers of pre‐eclampsia (PE), including mean arterial pressure (MAP), uterine artery pulsatility index (UtA‐PI), serum placental growth factor (PlGF) and serum soluble fms‐like tyrosine kinase‐1 (sFlt‐1), in the prediction of subsequent development of PE. Methods This was a prospective observational study in women attending for a routine hospital visit at 35 + 0 to 36 + 6 weeks' gestation. This visit included recording of maternal demographic characteristics and medical history, ultrasound examination for fetal anatomy and growth, assessment of flow velocity waveforms from the maternal ophthalmic arteries, and measurement of MAP, UtA‐PI, serum PlGF and serum sFlt‐1. The competing‐risks model was used to estimate the individual patient‐specific risks of delivery with PE at any time and at &lt; 3 weeks after assessment by a combination of maternal demographic characteristics and medical history with biomarkers. The area under the receiver‐operating‐characteristics curve and detection rate (DR) of delivery with PE, at a 10% false‐positive rate (FPR), in screening by combinations of maternal factors with ophthalmic artery second to first peak of systolic velocity ratio (PSV ratio), MAP, UtA‐PI, serum PlGF and serum sFlt‐1 were determined. The modeled performance of screening for PE was also estimated. Results The study population of 2287 pregnancies contained 60 (2.6%) that developed PE, including 19 (0.8%) that delivered with PE at &lt; 3 weeks after assessment. The PSV ratio improved the prediction of PE with delivery at any stage after assessment provided by maternal factors alone (from 25.4% to 50.6%), maternal factors and MAP (54.3% to 62.7%), maternal factors, MAP and PlGF (68.3% to 70.8%) and maternal factors, MAP, PlGF and sFlt‐1 (75.7% to 76.7%), at a FPR of 10%. The PSV ratio also improved the prediction of PE with delivery at &lt; 3 weeks after assessment provided by maternal factors alone (from 31.0% to 69.4%), maternal factors and MAP (74.1% to 83.4%), maternal factors, MAP and UtA‐PI (77.1% to 85.0%) and maternal factors, MAP and PlGF (84.8% to 88.6%). The empirical results for DR at a 10% FPR were consistent with the modeled results. Screening by a combination of maternal factors with MAP and PSV ratio also detected 59.4% (95% CI, 58.6–82.5%) of cases of gestational hypertension with delivery at any stage after assessment, and 86.7% (95% CI, 82.4–100%) of those with delivery at &lt; 3 weeks after assessment. Conclusion Ophthalmic artery Doppler could potentially improve the performance of screening for PE at 35–37 weeks, especially imminent PE with delivery within 3 weeks after assessment, but further studies are needed to validate this finding. © 2020 International Society of Ultrasound in Obstetrics and Gynecology</description><identifier>ISSN: 0960-7692</identifier><identifier>EISSN: 1469-0705</identifier><identifier>DOI: 10.1002/uog.23517</identifier><identifier>PMID: 33073902</identifier><language>eng</language><publisher>Chichester, UK: John Wiley &amp; Sons, Ltd</publisher><subject>Adult ; Arterial Pressure ; Biomarkers - blood ; Female ; Gestational Age ; Humans ; Maternal Serum Screening Tests - statistics &amp; numerical data ; Ophthalmic Artery - diagnostic imaging ; Ophthalmic Artery - physiopathology ; ophthalmic artery Doppler ; Placenta Growth Factor - blood ; Pre-Eclampsia - diagnosis ; prediction ; Predictive Value of Tests ; Pregnancy ; Pregnancy Trimester, Third - blood ; pre‐eclampsia ; Prospective Studies ; Pulsatile Flow ; third trimester ; Ultrasonography, Doppler - methods ; Ultrasonography, Doppler - statistics &amp; numerical data ; Ultrasonography, Prenatal - methods ; Ultrasonography, Prenatal - statistics &amp; numerical data ; Uterine Artery - diagnostic imaging ; Uterine Artery - physiopathology ; Vascular Endothelial Growth Factor Receptor-1 - blood</subject><ispartof>Ultrasound in obstetrics &amp; gynecology, 2021-04, Vol.57 (4), p.600-606</ispartof><rights>2020 International Society of Ultrasound in Obstetrics and Gynecology</rights><rights>2020 International Society of Ultrasound in Obstetrics and Gynecology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3607-7df804bd6129f5d152300a9f97c1c26ed92f82739d785ffae44938b9b3d64e633</citedby><cites>FETCH-LOGICAL-c3607-7df804bd6129f5d152300a9f97c1c26ed92f82739d785ffae44938b9b3d64e633</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33073902$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sarno, M.</creatorcontrib><creatorcontrib>Wright, A.</creatorcontrib><creatorcontrib>Vieira, N.</creatorcontrib><creatorcontrib>Sapantzoglou, I.</creatorcontrib><creatorcontrib>Charakida, M.</creatorcontrib><creatorcontrib>Nicolaides, K. H.</creatorcontrib><title>Ophthalmic artery Doppler in combination with other biomarkers in prediction of pre‐eclampsia at 35–37 weeks' gestation</title><title>Ultrasound in obstetrics &amp; gynecology</title><addtitle>Ultrasound Obstet Gynecol</addtitle><description>ABSTRACT Objective To examine the potential value of maternal ophthalmic artery Doppler at 35–37 weeks' gestation in combination with the established biomarkers of pre‐eclampsia (PE), including mean arterial pressure (MAP), uterine artery pulsatility index (UtA‐PI), serum placental growth factor (PlGF) and serum soluble fms‐like tyrosine kinase‐1 (sFlt‐1), in the prediction of subsequent development of PE. Methods This was a prospective observational study in women attending for a routine hospital visit at 35 + 0 to 36 + 6 weeks' gestation. This visit included recording of maternal demographic characteristics and medical history, ultrasound examination for fetal anatomy and growth, assessment of flow velocity waveforms from the maternal ophthalmic arteries, and measurement of MAP, UtA‐PI, serum PlGF and serum sFlt‐1. The competing‐risks model was used to estimate the individual patient‐specific risks of delivery with PE at any time and at &lt; 3 weeks after assessment by a combination of maternal demographic characteristics and medical history with biomarkers. The area under the receiver‐operating‐characteristics curve and detection rate (DR) of delivery with PE, at a 10% false‐positive rate (FPR), in screening by combinations of maternal factors with ophthalmic artery second to first peak of systolic velocity ratio (PSV ratio), MAP, UtA‐PI, serum PlGF and serum sFlt‐1 were determined. The modeled performance of screening for PE was also estimated. Results The study population of 2287 pregnancies contained 60 (2.6%) that developed PE, including 19 (0.8%) that delivered with PE at &lt; 3 weeks after assessment. The PSV ratio improved the prediction of PE with delivery at any stage after assessment provided by maternal factors alone (from 25.4% to 50.6%), maternal factors and MAP (54.3% to 62.7%), maternal factors, MAP and PlGF (68.3% to 70.8%) and maternal factors, MAP, PlGF and sFlt‐1 (75.7% to 76.7%), at a FPR of 10%. The PSV ratio also improved the prediction of PE with delivery at &lt; 3 weeks after assessment provided by maternal factors alone (from 31.0% to 69.4%), maternal factors and MAP (74.1% to 83.4%), maternal factors, MAP and UtA‐PI (77.1% to 85.0%) and maternal factors, MAP and PlGF (84.8% to 88.6%). The empirical results for DR at a 10% FPR were consistent with the modeled results. Screening by a combination of maternal factors with MAP and PSV ratio also detected 59.4% (95% CI, 58.6–82.5%) of cases of gestational hypertension with delivery at any stage after assessment, and 86.7% (95% CI, 82.4–100%) of those with delivery at &lt; 3 weeks after assessment. Conclusion Ophthalmic artery Doppler could potentially improve the performance of screening for PE at 35–37 weeks, especially imminent PE with delivery within 3 weeks after assessment, but further studies are needed to validate this finding. © 2020 International Society of Ultrasound in Obstetrics and Gynecology</description><subject>Adult</subject><subject>Arterial Pressure</subject><subject>Biomarkers - blood</subject><subject>Female</subject><subject>Gestational Age</subject><subject>Humans</subject><subject>Maternal Serum Screening Tests - statistics &amp; numerical data</subject><subject>Ophthalmic Artery - diagnostic imaging</subject><subject>Ophthalmic Artery - physiopathology</subject><subject>ophthalmic artery Doppler</subject><subject>Placenta Growth Factor - blood</subject><subject>Pre-Eclampsia - diagnosis</subject><subject>prediction</subject><subject>Predictive Value of Tests</subject><subject>Pregnancy</subject><subject>Pregnancy Trimester, Third - blood</subject><subject>pre‐eclampsia</subject><subject>Prospective Studies</subject><subject>Pulsatile Flow</subject><subject>third trimester</subject><subject>Ultrasonography, Doppler - methods</subject><subject>Ultrasonography, Doppler - statistics &amp; numerical data</subject><subject>Ultrasonography, Prenatal - methods</subject><subject>Ultrasonography, Prenatal - statistics &amp; numerical data</subject><subject>Uterine Artery - diagnostic imaging</subject><subject>Uterine Artery - physiopathology</subject><subject>Vascular Endothelial Growth Factor Receptor-1 - blood</subject><issn>0960-7692</issn><issn>1469-0705</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp1kE1PGzEQhq2qVQkfB_4A8q30sDC2d-34WAEFJKRcynnl9Y6JYTde7I2iHJBy5YbEP8wvYZPQ3noajebRM3pfQo4ZnDEAfj4PD2dcFEx9ISOWS52BguIrGYGWkCmp-R7ZT-kRAGQu5HeyJwQooYGPyMukm_ZT07TeUhN7jEt6GbquwUj9jNrQVn5meh9mdOH7KQ39dLhUPrQmPmFMG6iLWHu7ZYLbbOvVG9rGtF3yhpqeimK9ehdqvXpdID6lH_QBU7-VHpJvzjQJjz7nAbn_ffXn4ia7m1zfXvy6y6yQoDJVuzHkVS0Z166oWcEFgNFOK8ssl1hr7sZ8SFSrceGcwTzXYlzpStQyRynEATndebsYnufD97L1yWLTmBmGeSp5XnDQOTAY0J871MaQUkRXdtEPaZclg3LTdjm0XW7bHtiTT-28arH-R_6tdwDOd8DCN7j8v6m8n1zvlB8_7oz0</recordid><startdate>202104</startdate><enddate>202104</enddate><creator>Sarno, M.</creator><creator>Wright, A.</creator><creator>Vieira, N.</creator><creator>Sapantzoglou, I.</creator><creator>Charakida, M.</creator><creator>Nicolaides, K. H.</creator><general>John Wiley &amp; Sons, Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202104</creationdate><title>Ophthalmic artery Doppler in combination with other biomarkers in prediction of pre‐eclampsia at 35–37 weeks' gestation</title><author>Sarno, M. ; Wright, A. ; Vieira, N. ; Sapantzoglou, I. ; Charakida, M. ; Nicolaides, K. H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3607-7df804bd6129f5d152300a9f97c1c26ed92f82739d785ffae44938b9b3d64e633</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adult</topic><topic>Arterial Pressure</topic><topic>Biomarkers - blood</topic><topic>Female</topic><topic>Gestational Age</topic><topic>Humans</topic><topic>Maternal Serum Screening Tests - statistics &amp; numerical data</topic><topic>Ophthalmic Artery - diagnostic imaging</topic><topic>Ophthalmic Artery - physiopathology</topic><topic>ophthalmic artery Doppler</topic><topic>Placenta Growth Factor - blood</topic><topic>Pre-Eclampsia - diagnosis</topic><topic>prediction</topic><topic>Predictive Value of Tests</topic><topic>Pregnancy</topic><topic>Pregnancy Trimester, Third - blood</topic><topic>pre‐eclampsia</topic><topic>Prospective Studies</topic><topic>Pulsatile Flow</topic><topic>third trimester</topic><topic>Ultrasonography, Doppler - methods</topic><topic>Ultrasonography, Doppler - statistics &amp; numerical data</topic><topic>Ultrasonography, Prenatal - methods</topic><topic>Ultrasonography, Prenatal - statistics &amp; numerical data</topic><topic>Uterine Artery - diagnostic imaging</topic><topic>Uterine Artery - physiopathology</topic><topic>Vascular Endothelial Growth Factor Receptor-1 - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sarno, M.</creatorcontrib><creatorcontrib>Wright, A.</creatorcontrib><creatorcontrib>Vieira, N.</creatorcontrib><creatorcontrib>Sapantzoglou, I.</creatorcontrib><creatorcontrib>Charakida, M.</creatorcontrib><creatorcontrib>Nicolaides, K. H.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Ultrasound in obstetrics &amp; gynecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sarno, M.</au><au>Wright, A.</au><au>Vieira, N.</au><au>Sapantzoglou, I.</au><au>Charakida, M.</au><au>Nicolaides, K. H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ophthalmic artery Doppler in combination with other biomarkers in prediction of pre‐eclampsia at 35–37 weeks' gestation</atitle><jtitle>Ultrasound in obstetrics &amp; gynecology</jtitle><addtitle>Ultrasound Obstet Gynecol</addtitle><date>2021-04</date><risdate>2021</risdate><volume>57</volume><issue>4</issue><spage>600</spage><epage>606</epage><pages>600-606</pages><issn>0960-7692</issn><eissn>1469-0705</eissn><abstract>ABSTRACT Objective To examine the potential value of maternal ophthalmic artery Doppler at 35–37 weeks' gestation in combination with the established biomarkers of pre‐eclampsia (PE), including mean arterial pressure (MAP), uterine artery pulsatility index (UtA‐PI), serum placental growth factor (PlGF) and serum soluble fms‐like tyrosine kinase‐1 (sFlt‐1), in the prediction of subsequent development of PE. Methods This was a prospective observational study in women attending for a routine hospital visit at 35 + 0 to 36 + 6 weeks' gestation. This visit included recording of maternal demographic characteristics and medical history, ultrasound examination for fetal anatomy and growth, assessment of flow velocity waveforms from the maternal ophthalmic arteries, and measurement of MAP, UtA‐PI, serum PlGF and serum sFlt‐1. The competing‐risks model was used to estimate the individual patient‐specific risks of delivery with PE at any time and at &lt; 3 weeks after assessment by a combination of maternal demographic characteristics and medical history with biomarkers. The area under the receiver‐operating‐characteristics curve and detection rate (DR) of delivery with PE, at a 10% false‐positive rate (FPR), in screening by combinations of maternal factors with ophthalmic artery second to first peak of systolic velocity ratio (PSV ratio), MAP, UtA‐PI, serum PlGF and serum sFlt‐1 were determined. The modeled performance of screening for PE was also estimated. Results The study population of 2287 pregnancies contained 60 (2.6%) that developed PE, including 19 (0.8%) that delivered with PE at &lt; 3 weeks after assessment. The PSV ratio improved the prediction of PE with delivery at any stage after assessment provided by maternal factors alone (from 25.4% to 50.6%), maternal factors and MAP (54.3% to 62.7%), maternal factors, MAP and PlGF (68.3% to 70.8%) and maternal factors, MAP, PlGF and sFlt‐1 (75.7% to 76.7%), at a FPR of 10%. The PSV ratio also improved the prediction of PE with delivery at &lt; 3 weeks after assessment provided by maternal factors alone (from 31.0% to 69.4%), maternal factors and MAP (74.1% to 83.4%), maternal factors, MAP and UtA‐PI (77.1% to 85.0%) and maternal factors, MAP and PlGF (84.8% to 88.6%). The empirical results for DR at a 10% FPR were consistent with the modeled results. Screening by a combination of maternal factors with MAP and PSV ratio also detected 59.4% (95% CI, 58.6–82.5%) of cases of gestational hypertension with delivery at any stage after assessment, and 86.7% (95% CI, 82.4–100%) of those with delivery at &lt; 3 weeks after assessment. Conclusion Ophthalmic artery Doppler could potentially improve the performance of screening for PE at 35–37 weeks, especially imminent PE with delivery within 3 weeks after assessment, but further studies are needed to validate this finding. © 2020 International Society of Ultrasound in Obstetrics and Gynecology</abstract><cop>Chichester, UK</cop><pub>John Wiley &amp; Sons, Ltd</pub><pmid>33073902</pmid><doi>10.1002/uog.23517</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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source Wiley-Blackwell Read & Publish Collection
subjects Adult
Arterial Pressure
Biomarkers - blood
Female
Gestational Age
Humans
Maternal Serum Screening Tests - statistics & numerical data
Ophthalmic Artery - diagnostic imaging
Ophthalmic Artery - physiopathology
ophthalmic artery Doppler
Placenta Growth Factor - blood
Pre-Eclampsia - diagnosis
prediction
Predictive Value of Tests
Pregnancy
Pregnancy Trimester, Third - blood
pre‐eclampsia
Prospective Studies
Pulsatile Flow
third trimester
Ultrasonography, Doppler - methods
Ultrasonography, Doppler - statistics & numerical data
Ultrasonography, Prenatal - methods
Ultrasonography, Prenatal - statistics & numerical data
Uterine Artery - diagnostic imaging
Uterine Artery - physiopathology
Vascular Endothelial Growth Factor Receptor-1 - blood
title Ophthalmic artery Doppler in combination with other biomarkers in prediction of pre‐eclampsia at 35–37 weeks' gestation
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