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External validation of preexisting first trimester preeclampsia prediction models
Rebecca E Allen1, Javier Zamora2, David Arroyo-Manzano2
1Barts Health NHS Trust, Royal London Hospital, Whitechapel, London, E1 1BB, United Kingdom.
European Journal of Obstetrics, Gynecology, and Reproductive Biology
|September 10, 2017
Summary
No single prediction model accurately identifies preeclampsia risk across different populations. Future research should focus on validating existing models and assessing their clinical impact.
Area of Science:
- Obstetrics and Gynecology
- Reproductive Medicine
- Clinical Prediction Modeling
Background:
- Preeclampsia is a significant cause of maternal and fetal morbidity worldwide.
- Numerous prognostic models have been developed for early prediction of preeclampsia.
- External validation of these models is crucial for reliable clinical application.
Purpose of the Study:
- To externally validate existing prognostic models for preeclampsia prediction.
- To assess the performance of selected models in a new prospective cohort.
- To determine the generalizability of current preeclampsia prediction models.
Main Methods:
- Systematic literature review to identify first-trimester preeclampsia prediction models.
- Selection of models based on predefined criteria including biomarkers, uterine artery Doppler, and maternal characteristics.
- Validation using regression coefficients applied to a prospective cohort, assessing discrimination (Area Under the Curve) and calibration.
Main Results:
- Twenty preeclampsia prediction models were identified and validated.
- Observed discrimination (AUC) varied significantly when models were applied to the validation cohort (0.504–0.833) compared to derivation studies (0.70–0.96).
- Statistically significant differences were found between derivation and validation AUCs for several models.
Conclusions:
- No current preeclampsia prediction model demonstrates adequate discrimination and calibration across different populations.
- The large number of existing models may limit the value of developing new ones.
- Future research should prioritize validating existing models and evaluating their impact on patient care and outcomes.
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