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ASPRE trial: incidence of preterm pre-eclampsia in patients fulfilling ACOG and NICE criteria according to risk by FMF algorithm.

dc.contributor.authorPoon, L C
dc.contributor.authorRolnik, D L
dc.contributor.authorTan, M Y
dc.contributor.authorDelgado, J L
dc.contributor.authorTsokaki, T
dc.contributor.authorAkolekar, R
dc.contributor.authorSingh, M
dc.contributor.authorAndrade, W
dc.contributor.authorEfeturk, T
dc.contributor.authorJani, J C
dc.contributor.authorPlasencia, W
dc.contributor.authorPapaioannou, G
dc.contributor.authorBlazquez, A R
dc.contributor.authorCarbone, I F
dc.contributor.authorWright, D
dc.contributor.authorNicolaides, K H
dc.date.accessioned2023-01-25T10:03:10Z
dc.date.available2023-01-25T10:03:10Z
dc.date.issued2018-05-03
dc.description.abstractTo report the incidence of preterm pre-eclampsia (PE) in women who are screen positive according to the criteria of the National Institute for Health and Care Excellence (NICE) and the American College of Obstetricians and Gynecologists (ACOG), and compare the incidence with that in those who are screen positive or screen negative by The Fetal Medicine Foundation (FMF) algorithm. This was a secondary analysis of data from the ASPRE study. The study population consisted of women with singleton pregnancy who underwent prospective screening for preterm PE by means of the FMF algorithm, which combines maternal factors and biomarkers at 11-13 weeks' gestation. The incidence of preterm PE in women fulfilling the NICE and ACOG criteria was estimated; in these patients the incidence of preterm PE was then calculated in those who were screen negative relative to those who were screen positive by the FMF algorithm. A total of 34 573 women with singleton pregnancy delivering at ≥ 24 weeks' gestation underwent prospective screening for preterm PE, of which 239 (0.7%) cases developed preterm PE. At least one of the ACOG criteria was fulfilled in 22 287 (64.5%) pregnancies and the incidence of preterm PE was 0.97% (95% CI, 0.85-1.11%); in the subgroup that was screen positive by the FMF algorithm the incidence of preterm PE was 4.80% (95% CI, 4.14-5.55%), and in those that were screen negative it was 0.25% (95% CI, 0.18-0.33%), with a relative incidence in FMF screen negative to FMF screen positive of 0.051 (95% CI, 0.037-0.071). In 1392 (4.0%) pregnancies, at least one of the NICE high-risk criteria was fulfilled, and in this group the incidence of preterm PE was 5.17% (95% CI, 4.13-6.46%); in the subgroups of screen positive and screen negative by the FMF algorithm, the incidence of preterm PE was 8.71% (95% CI, 6.93-10.89%) and 0.65% (95% CI, 0.25-1.67%), respectively, and the relative incidence was 0.075 (95% CI, 0.028-0.205). In 2360 (6.8%) pregnancies fulfilling at least two of the NICE moderate-risk criteria, the incidence of preterm PE was 1.74% (95% CI, 1.28-2.35%); in the subgroups of screen positive and screen negative by the FMF algorithm the incidence was 4.91% (95% CI, 3.54-6.79%) and 0.42% (95% CI, 0.20-0.86%), respectively, and the relative incidence was 0.085 (95% CI, 0.038-0.192). In women who are screen positive for preterm PE by the ACOG or NICE criteria but screen negative by the FMF algorithm, the risk of preterm PE is reduced to within or below background levels. The results provide further evidence to support the personalized risk-based screening method that combines maternal factors and biomarkers. Copyright © 2018 ISUOG. Published by John Wiley & Sons Ltd.
dc.identifier.doi10.1002/uog.19019
dc.identifier.essn1469-0705
dc.identifier.pmid29380918
dc.identifier.urihttp://hdl.handle.net/10668/12062
dc.issue.number6
dc.journal.titleUltrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
dc.journal.titleabbreviationUltrasound Obstet Gynecol
dc.language.isoen
dc.organizationHospital Universitario San Cecilio
dc.organizationHospital Universitario San Cecilio
dc.page.number738-742
dc.pubmedtypeEvaluation Study
dc.pubmedtypeJournal Article
dc.pubmedtypeMulticenter Study
dc.subjectACOG guidelines
dc.subjectBayes' theorem
dc.subjectNICE guidelines
dc.subjectfirst-trimester screening
dc.subjectmean arterial pressure
dc.subjectplacental growth factor
dc.subjectpre-eclampsia
dc.subjectpregnancy-associated plasma protein-A
dc.subjectuterine artery Doppler
dc.subject.meshAdult
dc.subject.meshAlgorithms
dc.subject.meshClinical Trials as Topic
dc.subject.meshEurope
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshIncidence
dc.subject.meshPractice Guidelines as Topic
dc.subject.meshPre-Eclampsia
dc.subject.meshPregnancy
dc.subject.meshPregnancy Trimester, First
dc.subject.meshPrenatal Diagnosis
dc.subject.meshProspective Studies
dc.subject.meshRisk Factors
dc.titleASPRE trial: incidence of preterm pre-eclampsia in patients fulfilling ACOG and NICE criteria according to risk by FMF algorithm.
dc.typeresearch article
dc.volume.number51
dspace.entity.typePublication

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