Anastasija Arechvo PhD , Argyro Syngelaki PhD , Ranjit Akolekar PhD , Peter von Dadelszen DPhil , Kypros H. Nicolaides MD , Laura A. Magee MD
{"title":"考虑种族和社会经济地位的子痫前期筛查-竞争风险模型和风险因素评分的比较。","authors":"Anastasija Arechvo PhD , Argyro Syngelaki PhD , Ranjit Akolekar PhD , Peter von Dadelszen DPhil , Kypros H. Nicolaides MD , Laura A. Magee MD","doi":"10.1016/j.jogc.2025.103087","DOIUrl":null,"url":null,"abstract":"<div><h3>Objectives</h3><div>This study aimed to compare preeclampsia (PE) risk screening by risk factors and the multivariable competing risks model.</div></div><div><h3>Methods</h3><div>This prospective cohort study enrolled singleton pregnancies, without major anomalies, and delivering at ≥24 weeks. PE risk was compared between the Fetal Medicine Foundation (FMF) model and clinical risk factors by National Institute for Health and Care Excellence (NICE) guidance, U.K. and “NICE-modified” by adding Black ethnicity and social deprivation (index of multiple deprivation deciles 1–4) as moderate risk factors. To compare screening strategies, we matched the FMF screen-positive rate (SPR) to NICE.</div></div><div><h3>Results</h3><div>At 11–13 weeks, preterm PE risk was assessed in 44 813 pregnancies; 368 (0.8%) developed preterm PE. At SPR = 7.4%, FMF (vs. NICE) almost tripled preterm PE detection rate (DR) but by more (by 19.8%) among Black women. The FMF model at SPR = 7.4% had DR = 67.7% for preterm PE, similar to NICE-modified screening (67.4%, which had SPR = 40.1%). At 35–36 weeks, subsequent PE risk was assessed in 29 035 pregnancies; 654 (2.3%) developed PE. At SPR = 10.9%, FMF (vs. NICE) more than doubled subsequent PE DR, regardless of index of multiple deprivation or Black ethnicity. FMF at SPR = 10.9% had DR for subsequent PE at least as high (70.5%) as NICE-modified screening (61.5%), which had SPR = 37.4%.</div></div><div><h3>Conclusions</h3><div>The FMF model detects PE risk similar to risk factor–based screening, with addition of Black ethnicity and social deprivation as moderate risk factors but at substantially lower SPR at 11–13 weeks when aspirin is offered to prevent preterm PE and at 35–36 weeks when timed birth at term may prevent term PE.</div></div>","PeriodicalId":16688,"journal":{"name":"Journal of obstetrics and gynaecology Canada","volume":"47 11","pages":"Article 103087"},"PeriodicalIF":2.2000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Preeclampsia Screening Taking Into Account Ethnicity and Socioeconomic Status—A Comparison of the Competing Risks Model and Risk Factor Scoring\",\"authors\":\"Anastasija Arechvo PhD , Argyro Syngelaki PhD , Ranjit Akolekar PhD , Peter von Dadelszen DPhil , Kypros H. Nicolaides MD , Laura A. Magee MD\",\"doi\":\"10.1016/j.jogc.2025.103087\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objectives</h3><div>This study aimed to compare preeclampsia (PE) risk screening by risk factors and the multivariable competing risks model.</div></div><div><h3>Methods</h3><div>This prospective cohort study enrolled singleton pregnancies, without major anomalies, and delivering at ≥24 weeks. PE risk was compared between the Fetal Medicine Foundation (FMF) model and clinical risk factors by National Institute for Health and Care Excellence (NICE) guidance, U.K. and “NICE-modified” by adding Black ethnicity and social deprivation (index of multiple deprivation deciles 1–4) as moderate risk factors. To compare screening strategies, we matched the FMF screen-positive rate (SPR) to NICE.</div></div><div><h3>Results</h3><div>At 11–13 weeks, preterm PE risk was assessed in 44 813 pregnancies; 368 (0.8%) developed preterm PE. At SPR = 7.4%, FMF (vs. NICE) almost tripled preterm PE detection rate (DR) but by more (by 19.8%) among Black women. The FMF model at SPR = 7.4% had DR = 67.7% for preterm PE, similar to NICE-modified screening (67.4%, which had SPR = 40.1%). At 35–36 weeks, subsequent PE risk was assessed in 29 035 pregnancies; 654 (2.3%) developed PE. At SPR = 10.9%, FMF (vs. NICE) more than doubled subsequent PE DR, regardless of index of multiple deprivation or Black ethnicity. FMF at SPR = 10.9% had DR for subsequent PE at least as high (70.5%) as NICE-modified screening (61.5%), which had SPR = 37.4%.</div></div><div><h3>Conclusions</h3><div>The FMF model detects PE risk similar to risk factor–based screening, with addition of Black ethnicity and social deprivation as moderate risk factors but at substantially lower SPR at 11–13 weeks when aspirin is offered to prevent preterm PE and at 35–36 weeks when timed birth at term may prevent term PE.</div></div>\",\"PeriodicalId\":16688,\"journal\":{\"name\":\"Journal of obstetrics and gynaecology Canada\",\"volume\":\"47 11\",\"pages\":\"Article 103087\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2025-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of obstetrics and gynaecology Canada\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1701216325003330\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"OBSTETRICS & GYNECOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of obstetrics and gynaecology Canada","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1701216325003330","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"OBSTETRICS & GYNECOLOGY","Score":null,"Total":0}
Preeclampsia Screening Taking Into Account Ethnicity and Socioeconomic Status—A Comparison of the Competing Risks Model and Risk Factor Scoring
Objectives
This study aimed to compare preeclampsia (PE) risk screening by risk factors and the multivariable competing risks model.
Methods
This prospective cohort study enrolled singleton pregnancies, without major anomalies, and delivering at ≥24 weeks. PE risk was compared between the Fetal Medicine Foundation (FMF) model and clinical risk factors by National Institute for Health and Care Excellence (NICE) guidance, U.K. and “NICE-modified” by adding Black ethnicity and social deprivation (index of multiple deprivation deciles 1–4) as moderate risk factors. To compare screening strategies, we matched the FMF screen-positive rate (SPR) to NICE.
Results
At 11–13 weeks, preterm PE risk was assessed in 44 813 pregnancies; 368 (0.8%) developed preterm PE. At SPR = 7.4%, FMF (vs. NICE) almost tripled preterm PE detection rate (DR) but by more (by 19.8%) among Black women. The FMF model at SPR = 7.4% had DR = 67.7% for preterm PE, similar to NICE-modified screening (67.4%, which had SPR = 40.1%). At 35–36 weeks, subsequent PE risk was assessed in 29 035 pregnancies; 654 (2.3%) developed PE. At SPR = 10.9%, FMF (vs. NICE) more than doubled subsequent PE DR, regardless of index of multiple deprivation or Black ethnicity. FMF at SPR = 10.9% had DR for subsequent PE at least as high (70.5%) as NICE-modified screening (61.5%), which had SPR = 37.4%.
Conclusions
The FMF model detects PE risk similar to risk factor–based screening, with addition of Black ethnicity and social deprivation as moderate risk factors but at substantially lower SPR at 11–13 weeks when aspirin is offered to prevent preterm PE and at 35–36 weeks when timed birth at term may prevent term PE.
期刊介绍:
Journal of Obstetrics and Gynaecology Canada (JOGC) is Canada"s peer-reviewed journal of obstetrics, gynaecology, and women"s health. Each monthly issue contains original research articles, reviews, case reports, commentaries, and editorials on all aspects of reproductive health. JOGC is the original publication source of evidence-based clinical guidelines, committee opinions, and policy statements that derive from standing or ad hoc committees of the Society of Obstetricians and Gynaecologists of Canada. JOGC is included in the National Library of Medicine"s MEDLINE database, and abstracts from JOGC are accessible on PubMed.