Evidence map›Paper›PMID 42755709›Full record

ArticleHypertension (Dallas, Tex. : 1979)2026

Development and External Validation of Mini PIERSdynamic Model for Predicting the Adverse Maternal Outcome of Preeclampsia in Low-Resource Settings.

Guiyou Yang, Tünde Montgomery-Csobán, Gerton Lunter, Wessel Ganzevoort, Sanne J Gordijn, Paul Murray, Kimberley Kavanagh, Laura A Magee, Henk Groen, Peter von Dadelszen

Abstract readValidation Study
In one paragraph

Article in Hypertension (Dallas, Tex. : 1979), 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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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Guiyou Yang *Department of Epidemiology (G.Y., G.L., H.G.), University Medical Center Groningen, University of Groningen, the Netherlands.ORCID 0000-0002-1976-9683
Tünde Montgomery-Csobán *Department of Mathematics and Statistics (T.M.-C., K.K.), University of Strathclyde, Glasgow, United Kingdom.ORCID 0000-0002-0498-3732
Gerton LunterDepartment of Epidemiology (G.Y., G.L., H.G.), University Medical Center Groningen, University of Groningen, the Netherlands.ORCID 0000-0002-3798-2058
Wessel GanzevoortDepartment of Obstetrics and Gynecology, Amsterdam University Medical Centers, the Netherlands (W.G.).ORCID 0000-0002-7243-2115
Sanne J GordijnDepartment of Obstetrics and Gynecology (S.J.G.), University Medical Center Groningen, University of Groningen, the Netherlands.ORCID 0000-0003-3915-8609
Paul MurrayDepartment of Electronic and Electrical Engineering (P.M.), University of Strathclyde, Glasgow, United Kingdom.ORCID 0000-0002-6980-9276
Kimberley KavanaghDepartment of Mathematics and Statistics (T.M.-C., K.K.), University of Strathclyde, Glasgow, United Kingdom.ORCID 0000-0002-2679-5409
Laura A MageeInstitute of Women and Children's Health, School of Life Course and Population Sciences, King's College London, United Kingdom (L.A.M., P.v.D.).ORCID 0000-0002-1355-610X
Henk Groen *Department of Epidemiology (G.Y., G.L., H.G.), University Medical Center Groningen, University of Groningen, the Netherlands.ORCID 0000-0002-6629-318X
Peter von Dadelszen *Institute of Women and Children's Health, School of Life Course and Population Sciences, King's College London, United Kingdom (L.A.M., P.v.D.).ORCID 0000-0003-4136-3070

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPreeclampsia remains a leading cause of maternal mortality, particularly in low-resource settings. We aimed to develop a dynamic prediction model accommodating repeated measurements for predicting adverse maternal outcomes in preeclampsia.

methodsWe utilized data from 7283 women with preeclampsia from the PIERS studies (Preeclampsia Integrated Estimate of Risk). Data from 6548 women were randomly split into a training set (80%) and an internal validation set (20%), while an independent cohort of 735 women was used for external validation. The outcome was a composite of maternal mortality and severe maternal morbidity. The mini PIERSdynamic model was fitted with the binary mixed model random forest algorithm. Threshold probabilities were calculated for 5 risk strata, ranging from very low to very high risk. Model performance was externally validated.

resultsIn the development cohort, 785 (12.0%) women experienced an adverse maternal outcome, compared with 91 (12.4%) women in the external validation cohort. The final model retained all candidate predictors. Model performance was similar in internal and external validation. The daily area under the receiver-operating-characteristics curve remained around 0.75 on days 0 to 9 in internal validation and 0.70 in external validation, with peak values of 0.92 and 0.94, respectively. The area under the precision-recall curve declined over time as outcome incidence decreased. Observed daily event rates corresponded closely with the assigned risk strata.

conclusionsWe developed the mini PIERSdynamic model and performed external validation, demonstrating its potential for dynamic prediction of adverse maternal outcomes in preeclampsia for up to 10 days after initial presentation. Further evaluation is required to verify its generalizability and clinical utility.

Indexed as

Pre-EclampsiaAdultFemaleHumansMaternal MortalityPrediction AlgorithmsPregnancyPregnancy OutcomeResource-Limited SettingsRisk Assessmentclinical decision-makingdeveloping countriesforecastinghypertension, pregnancy-inducedpre-eclampsiapregnancy complications

Identifiers

PMID42755709
PMCPMC13680779

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