Am J Perinatol
DOI: 10.1055/s-0044-1782676
Original Article

Comparison of National Factor-based Models for Preeclampsia Screening

Louise Ghesquière
1   Reproduction, Mother and Child Health Unit, Research Center of the CHU de Québec, Université Laval, Québec City, QC, Canada
2   Department of Obstetrics, Université de Lille, CHU de Lille, Lille, France
,
1   Reproduction, Mother and Child Health Unit, Research Center of the CHU de Québec, Université Laval, Québec City, QC, Canada
3   Department of Obstetrics, Gynecology and Reproduction, CHU de Québec-Université Laval, Québec City, QC, Canada
,
Eric Dubé
1   Reproduction, Mother and Child Health Unit, Research Center of the CHU de Québec, Université Laval, Québec City, QC, Canada
,
Nils Chaillet
1   Reproduction, Mother and Child Health Unit, Research Center of the CHU de Québec, Université Laval, Québec City, QC, Canada
3   Department of Obstetrics, Gynecology and Reproduction, CHU de Québec-Université Laval, Québec City, QC, Canada
› Author Affiliations
Funding QUARISMA study was supported by grants (200702MCT-171307-RFA-CFCF-153236 and MOP 81275) from the Canadian Institutes of Health Research. The current secondary analysis was funded by the Jeanne et Jean-Louis Lévesque Perinatal Research Chair at Université Laval. E.B. holds a Researcher's Salary Award from the Fonds de la Recherche du Québec Santé.

Abstract

Objective This study aimed to compare the predictive values of the American College of Obstetricians and Gynecologists (ACOG), the National Institute for Health and Care Excellence (NICE), and the Society of Obstetricians and Gynecologists of Canada (SOGC) factor-based models for preeclampsia (PE) screening.

Study Design We conducted a secondary analysis of maternal and birth data from 32 hospitals. For each delivery, we calculated the risk of PE according to the ACOG, the NICE, and the SOGC models. Our primary outcomes were PE and preterm PE (PE combined with preterm birth) using the ACOG criteria. We calculated the detection rate (DR or sensitivity), the false positive rate (FPR or 1 − specificity), the positive (PPV) and negative (NPV) predictive values of each model for PE and for preterm PE using receiver operator characteristic (ROC) curves.

Results We used 130,939 deliveries including 4,635 (3.5%) cases of PE and 823 (0.6%) cases of preterm PE. The ACOG model had a DR of 43.6% for PE and 50.3% for preterm PE with FPR of 15.6%; the NICE model had a DR of 36.2% for PE and 41.3% for preterm PE with FPR of 12.8%; and the SOGC model had a DR of 49.1% for PE and 51.6% for preterm PE with FPR of 22.2%. The PPV for PE of the ACOG (9.3%) and NICE (9.4%) models were both superior than the SOGC model (7.6%; p < 0.001), with a similar trend for the PPV for preterm PE (1.9 vs. 1.9 vs. 1.4%, respectively; p < 0.01). The area under the ROC curves suggested that the ACOG model is superior to the NICE for the prediction of PE and preterm PE and superior to the SOGC models for the prediction of preterm PE (all with p < 0.001).

Conclusion The current ACOG factor-based model for the prediction of PE and preterm PE, without considering race, is superior to the NICE and SOGC models.

Key Points

  • Clinical factor-based model can predict PE in approximately 44% of the cases for a 16% false positive.

  • The ACOG model is superior to the NICE and SOGC models to predict PE.

  • Clinical factor-based models are better to predict PE in parous than in nulliparous.



Publication History

Received: 25 September 2023

Accepted: 26 February 2024

Article published online:
15 March 2024

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