ArticlePregnancy (Hoboken, N.J.)2026
Soluble fms-like tyrosine kinase-1 and placental growth factor as predictors of adverse maternal events in women with a confirmed diagnosis of preeclampsia.
Article in Pregnancy (Hoboken, N.J.), 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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Abstract
Objective: Soluble fms-like tyrosine kinase-1 (sFlt-1) and placental growth factor (PlGF) have been identified as predictors for preeclampsia and time to birth in women with suspected preeclampsia. This study aims to investigate these markers as predictors of adverse maternal events in women with confirmed preeclampsia. Study design: This was a prospective observational cohort study. Pregnant women admitted to hospitals due to preeclampsia were included from May 2019 to May 2024. Main outcome measures: The primary outcome was a composite of adverse maternal events (maternal mortality, eclampsia, stroke, cortical blindness, retinal detachment, pulmonary edema, acute kidney injury, liver capsule hematoma or rupture, placental abruption, postpartum hemorrhage, elevated liver enzymes, thrombocytopenia, admission to intensive care unit (ICU) required, and intubation and mechanical ventilation), with the individual components as secondary outcomes. Kaplan-Meier and receiver operating characteristic curves were constructed for sFlt-1, PlGF, and the sFlt-1/PlGF ratio. Area under the curve (AUC), sensitivity, specificity, positive and negative predicted value, and likelihood ratio were calculated. Results: A total of 307 women were enrolled, of which 36.5% gave birth preterm. In total, 129 women developed 166 adverse maternal events. The most common adverse maternal events were postpartum hemorrhage ( Conclusion: SFlt-1 and PlGF show limited value in predicting adverse maternal events in women with preeclampsia in a high-income country setting, irrespective of early or late disease. sFlt-1 may be useful for predicting the individual outcomes of thrombocytopenia, elevated liver enzymes, and acute kidney injury.
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