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Placental growth factor for the prognosis of women with preeclampsia (fullPIERS model extension): context matters
BACKGROUND: The fullPIERS risk prediction model was developed to identify which women admitted with confirmed diagnosis of preeclampsia are at highest risk of developing serious maternal complications. The model discriminates well between women who develop (vs. those who do not) adverse maternal out...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7643272/ https://www.ncbi.nlm.nih.gov/pubmed/33153436 http://dx.doi.org/10.1186/s12884-020-03332-w |
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author | Ukah, U. Vivian Payne, Beth A. Hutcheon, Jennifer A. Chappell, Lucy C. Seed, Paul T. Conti-Ramsden, Frances Inez Ansermino, J. Mark Magee, Laura A. von Dadelszen, Peter |
author_facet | Ukah, U. Vivian Payne, Beth A. Hutcheon, Jennifer A. Chappell, Lucy C. Seed, Paul T. Conti-Ramsden, Frances Inez Ansermino, J. Mark Magee, Laura A. von Dadelszen, Peter |
author_sort | Ukah, U. Vivian |
collection | PubMed |
description | BACKGROUND: The fullPIERS risk prediction model was developed to identify which women admitted with confirmed diagnosis of preeclampsia are at highest risk of developing serious maternal complications. The model discriminates well between women who develop (vs. those who do not) adverse maternal outcomes. It has been externally validated in several populations. We assessed whether placental growth factor (PlGF), a biomarker associated with preeclampsia risk, adds incremental value to the fullPIERS model. METHODS: Using a cohort of women admitted into tertiary hospitals in well-resourced settings (the USA and Canada), between May 2010 to February 2012, we evaluated the incremental value of PlGF added to fullPIERS for prediction of adverse maternal outcomes within 48 h after admission with confirmed preeclampsia. The discriminatory performance of PlGF and the fullPIERS model were assessed in this cohort using the area under the receiver’s operating characteristic curve (AUROC) while the extended model (fullPIERS +PlGF) was assessed based on net reclassification index (NRI) and integrated discrimination improvement (IDI) performances. RESULTS: In a cohort of 541 women delivered shortly (< 1 week) after presentation, 8.1% experienced an adverse maternal outcome within 48 h of admission. Prediction of adverse maternal outcomes was not improved by addition of PlGF to fullPIERS (NRI: -8.7, IDI − 0.06). Discriminatory performance (AUROC) was 0.67 [95%CI: 0.59–0.75] for fullPIERS only and 0.67 [95%CI: 0.58–0.76]) for fullPIERS extended with PlGF, a performance worse than previously documented in fullPIERS external validation studies (AUROC > 0.75). CONCLUSIONS: While fullPIERS model performance may have been affected by differences in healthcare context between this study cohort and the model development and validation cohorts, future studies are required to confirm whether PlGF adds incremental benefit to the fullPIERS model for prediction of adverse maternal outcomes in preeclampsia in settings where expectant management is practiced. |
format | Online Article Text |
id | pubmed-7643272 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-76432722020-11-05 Placental growth factor for the prognosis of women with preeclampsia (fullPIERS model extension): context matters Ukah, U. Vivian Payne, Beth A. Hutcheon, Jennifer A. Chappell, Lucy C. Seed, Paul T. Conti-Ramsden, Frances Inez Ansermino, J. Mark Magee, Laura A. von Dadelszen, Peter BMC Pregnancy Childbirth Research Article BACKGROUND: The fullPIERS risk prediction model was developed to identify which women admitted with confirmed diagnosis of preeclampsia are at highest risk of developing serious maternal complications. The model discriminates well between women who develop (vs. those who do not) adverse maternal outcomes. It has been externally validated in several populations. We assessed whether placental growth factor (PlGF), a biomarker associated with preeclampsia risk, adds incremental value to the fullPIERS model. METHODS: Using a cohort of women admitted into tertiary hospitals in well-resourced settings (the USA and Canada), between May 2010 to February 2012, we evaluated the incremental value of PlGF added to fullPIERS for prediction of adverse maternal outcomes within 48 h after admission with confirmed preeclampsia. The discriminatory performance of PlGF and the fullPIERS model were assessed in this cohort using the area under the receiver’s operating characteristic curve (AUROC) while the extended model (fullPIERS +PlGF) was assessed based on net reclassification index (NRI) and integrated discrimination improvement (IDI) performances. RESULTS: In a cohort of 541 women delivered shortly (< 1 week) after presentation, 8.1% experienced an adverse maternal outcome within 48 h of admission. Prediction of adverse maternal outcomes was not improved by addition of PlGF to fullPIERS (NRI: -8.7, IDI − 0.06). Discriminatory performance (AUROC) was 0.67 [95%CI: 0.59–0.75] for fullPIERS only and 0.67 [95%CI: 0.58–0.76]) for fullPIERS extended with PlGF, a performance worse than previously documented in fullPIERS external validation studies (AUROC > 0.75). CONCLUSIONS: While fullPIERS model performance may have been affected by differences in healthcare context between this study cohort and the model development and validation cohorts, future studies are required to confirm whether PlGF adds incremental benefit to the fullPIERS model for prediction of adverse maternal outcomes in preeclampsia in settings where expectant management is practiced. BioMed Central 2020-11-05 /pmc/articles/PMC7643272/ /pubmed/33153436 http://dx.doi.org/10.1186/s12884-020-03332-w Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Ukah, U. Vivian Payne, Beth A. Hutcheon, Jennifer A. Chappell, Lucy C. Seed, Paul T. Conti-Ramsden, Frances Inez Ansermino, J. Mark Magee, Laura A. von Dadelszen, Peter Placental growth factor for the prognosis of women with preeclampsia (fullPIERS model extension): context matters |
title | Placental growth factor for the prognosis of women with preeclampsia (fullPIERS model extension): context matters |
title_full | Placental growth factor for the prognosis of women with preeclampsia (fullPIERS model extension): context matters |
title_fullStr | Placental growth factor for the prognosis of women with preeclampsia (fullPIERS model extension): context matters |
title_full_unstemmed | Placental growth factor for the prognosis of women with preeclampsia (fullPIERS model extension): context matters |
title_short | Placental growth factor for the prognosis of women with preeclampsia (fullPIERS model extension): context matters |
title_sort | placental growth factor for the prognosis of women with preeclampsia (fullpiers model extension): context matters |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7643272/ https://www.ncbi.nlm.nih.gov/pubmed/33153436 http://dx.doi.org/10.1186/s12884-020-03332-w |
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