Evidence map›Paper›PMID 42383395›Full record

ArticleBJOG : an international journal of obstetrics and gynaecology2026

First Trimester Screening for Preterm Preeclampsia in the United Kingdom: A Cost-Effectiveness Analysis.

Mohammad A Ani, Liona C Poon, Laura A Magee, A Joy Allen, Kypros H Nicolaides

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Article in BJOG : an international journal of obstetrics and gynaecology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Mohammad A AniRoche Diagnostics UK and Ireland, Burgess Hill, UK.
Liona C PoonDepartment of Obstetrics and Gynaecology, The Chinese University of Hong Kong, Shatin, Hong Kong Special Administrative Region of China.ORCID https://orcid.org/0000-0002-3944-4130
Laura A MageeDepartment of Women and Children's Health, School of Life Course and Population Sciences, King's College London, London, UK.ORCID https://orcid.org/0000-0002-1355-610X
A Joy AllenRoche Diagnostics UK and Ireland, Burgess Hill, UK.
Kypros H NicolaidesHarris Birthright Research Centre for Fetal Medicine, King's College Hospital, London, UK.

Funding

Roche Diagnostics UK & Ireland
6 · The paper itself

Abstract

objectiveTo evaluate the cost-effectiveness of the Fetal Medicine Foundation (FMF) strategy, compared with the National Institute for Health and Care Excellence (NICE) strategy, for first-trimester screening for preterm preeclampsia (PE) in the United Kingdom (UK).

designCost-effectiveness analysis.

settingUK National Health Service and personal social services perspective. POPULATION: A total of 10 000 simulated patients with singleton pregnancies at 11-13 weeks' gestation, across a lifetime time horizon.

methodsA decision-tree model was developed to perform a cost-effectiveness analysis. In the base-case analysis, NICE-recommended screening was compared with FMF screening, using maternal factors, mean arterial pressure (MAP), uterine artery pulsatility index (UtA-PI) and placental growth factor (PlGF). The model assumed that patients identified as high-risk for PE were prescribed 150 mg aspirin daily until 36 weeks' gestation. Scenario analyses varied PE incidence, aspirin adherence and biomarker combinations of FMF strategy components.

main outcome measureIncremental cost-effectiveness ratios (ICERs) were calculated using incremental costs and quality-adjusted life years (QALYs). Dominant ICERs demonstrated lower costs and higher QALYs.

resultsCompared with NICE-recommended screening, the FMF strategy demonstrated a cost-saving of £3191 and QALY gain of 0.92 per 10 000 patients (dominant ICER), with a cost-saving of £199 per preterm PE case avoided. In scenario analyses, the FMF strategy was cost-effective across 3%, 5% and 7% PE incidence, and 75% and 100% aspirin adherence. The base-case FMF strategy (maternal factors + MAP + UtA-PI + PlGF) was the most clinically effective option.

conclusionsThe FMF strategy was more cost-effective versus the NICE strategy for first-trimester preterm PE screening in the UK.

Indexed as

Pre-EclampsiaPrenatal DiagnosisAspirinCost-Benefit AnalysisCost-Effectiveness AnalysisDecision TreesFemaleHumansMass ScreeningPregnancyPregnancy Trimester, FirstQuality-Adjusted Life YearsUnited KingdomAspirinalgorithmaspirincost‐effectivenessfirst‐trimesterpredictionpreeclampsiapreventionscreening

Identifiers

PMID42383395
PMCPMC13659417

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.