Publication:
ASPRE trial: performance of screening for preterm pre-eclampsia.

dc.contributor.authorRolnik, D L
dc.contributor.authorWright, D
dc.contributor.authorPoon, L C Y
dc.contributor.authorSyngelaki, A
dc.contributor.authorO'Gorman, N
dc.contributor.authorde Paco Matallana, C
dc.contributor.authorAkolekar, R
dc.contributor.authorCicero, S
dc.contributor.authorJanga, D
dc.contributor.authorSingh, M
dc.contributor.authorMolina, F S
dc.contributor.authorPersico, N
dc.contributor.authorJani, J C
dc.contributor.authorPlasencia, W
dc.contributor.authorPapaioannou, G
dc.contributor.authorTenenbaum-Gavish, K
dc.contributor.authorNicolaides, K H
dc.date.accessioned2023-01-25T09:49:31Z
dc.date.available2023-01-25T09:49:31Z
dc.date.issued2017-08-24
dc.description.abstractTo examine the performance of screening for preterm and term pre-eclampsia (PE) in the study population participating in the ASPRE (Combined Multimarker Screening and Randomized Patient Treatment with Aspirin for Evidence-Based Preeclampsia Prevention) trial. This was a prospective first-trimester multicenter study on screening for preterm PE in 26 941 singleton pregnancies by means of an algorithm that combines maternal factors, mean arterial pressure, uterine artery pulsatility index and maternal serum pregnancy-associated plasma protein-A and placental growth factor at 11-13 weeks' gestation. Eligible women with an estimated risk for preterm PE of > 1 in 100 were invited to participate in a double-blind trial of aspirin (150 mg per day) vs placebo from 11-14 until 36 weeks' gestation, which showed that, in the aspirin group, the incidence of preterm PE was reduced by 62%. In the screened population, the detection rates (DRs) and false-positive rates (FPRs) for delivery with PE  1 in 100 were invited to participate in a double-blind trial of aspirin (150 mg per day) vs placebo from 11-14 until 36 weeks' gestation, which showed that, in the aspirin group, the incidence of preterm PE was reduced by 62%. In the screened population, the detection rates (DRs) and false-positive rates (FPRs) for delivery with PE  The study population of 25 797 pregnancies included 180 (0.7%) cases of preterm PE, 450 (1.7%) of term PE and 25 167 (97.6%) without PE. In combined first-trimester screening for preterm PE with a risk cut-off of 1 in 100, the DR was 76.7% (138/180) for preterm PE and 43.1% (194/450) for term PE, at screen-positive rate of 10.5% (2707/25 797) and FPR of 9.2% (2375/25 797). The performance of screening in the ASPRE study was comparable with that of a study of approximately 60 000 singleton pregnancies used for development of the algorithm; in that study, combined screening detected 76.6% of cases of preterm PE and 38.3% of term PE at a FPR of 10%. Copyright © 2017 ISUOG. Published by John Wiley & Sons Ltd.
dc.identifier.doi10.1002/uog.18816
dc.identifier.essn1469-0705
dc.identifier.pmid28741785
dc.identifier.unpaywallURLhttps://obgyn.onlinelibrary.wiley.com/doi/pdfdirect/10.1002/uog.18816
dc.identifier.urihttp://hdl.handle.net/10668/11439
dc.issue.number4
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.page.number492-495
dc.pubmedtypeComparative Study
dc.pubmedtypeJournal Article
dc.pubmedtypeMulticenter Study
dc.pubmedtypeRandomized Controlled Trial
dc.rights.accessRightsopen access
dc.subjectASPRE trial
dc.subjectfirst-trimester screening
dc.subjectmean arterial pressure
dc.subjectplacental growth factor
dc.subjectpre-eclampsia
dc.subjectpregnancy-associated plasma protein-A
dc.subjectpyramid of pregnancy care
dc.subjectuterine artery Doppler
dc.subject.meshAdult
dc.subject.meshAlgorithms
dc.subject.meshAspirin
dc.subject.meshBiomarkers
dc.subject.meshDouble-Blind Method
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshMass Screening
dc.subject.meshPlacenta Growth Factor
dc.subject.meshPlatelet Aggregation Inhibitors
dc.subject.meshPre-Eclampsia
dc.subject.meshPregnancy
dc.subject.meshPregnancy Trimester, First
dc.subject.meshPregnancy-Associated Plasma Protein-A
dc.subject.meshProspective Studies
dc.subject.meshResearch Design
dc.subject.meshUterine Artery
dc.subject.meshYoung Adult
dc.titleASPRE trial: performance of screening for preterm pre-eclampsia.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number50
dspace.entity.typePublication

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