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Development of multivariable models to predict perinatal depression before and after delivery using patient reported survey responses at weeks 4–10 of pregnancy
BACKGROUND: Perinatal depression is estimated to affect ~ 12% of pregnancies and is linked to numerous negative outcomes. There is currently no model to predict perinatal depression at multiple time-points during and after pregnancy using variables ascertained early into pregnancy. METHODS: A prospe...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9137134/ https://www.ncbi.nlm.nih.gov/pubmed/35619056 http://dx.doi.org/10.1186/s12884-022-04741-9 |
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author | Reps, Jenna M. Wilcox, Marsha McGee, Beth Ann Leonte, Marie LaCross, Lauren Wildenhaus, Kevin |
author_facet | Reps, Jenna M. Wilcox, Marsha McGee, Beth Ann Leonte, Marie LaCross, Lauren Wildenhaus, Kevin |
author_sort | Reps, Jenna M. |
collection | PubMed |
description | BACKGROUND: Perinatal depression is estimated to affect ~ 12% of pregnancies and is linked to numerous negative outcomes. There is currently no model to predict perinatal depression at multiple time-points during and after pregnancy using variables ascertained early into pregnancy. METHODS: A prospective cohort design where 858 participants filled in a baseline self-reported survey at week 4–10 of pregnancy (that included social economics, health history, various psychiatric measures), with follow-up until 3 months after delivery. Our primary outcome was an Edinburgh Postnatal Depression Score (EPDS) score of 12 or more (a proxy for perinatal depression) assessed during each trimester and again at two time periods after delivery. Five gradient boosting machines were trained to predict the risk of having EPDS score > = 12 at each of the five follow-up periods. The predictors consisted of 21 variables from 3 validated psychometric scales. As a sensitivity analysis, we also investigated different predictor sets that contained: i) 17 of the 21 variables predictors by only including two of the psychometric scales and ii) including 143 additional social economics and health history predictors, resulting in 164 predictors. RESULTS: We developed five prognostic models: PND-T1 (trimester 1), PND-T2 (trimester 2), PND-T3 (trimester 3), PND-A1 (after delivery 1) and PND-A2 (delayed onset after delivery) that calculate personalised risks while only requiring that women be asked 21 questions from 3 validated psychometric scales at weeks 4–10 of pregnancy. C-statistics (also known as AUC) ranged between 0.69 (95% CI 0.65–0.73) and 0.77 (95% CI 0.74–0.80). At 50% sensitivity the positive predictive value ranged between 30%-50% across the models, generally identifying groups of patients with double the average risk. Models trained using the 17 predictors and 164 predictors did not improve model performance compared to the models trained using 21 predictors. CONCLUSIONS: The five models can predict risk of perinatal depression within each trimester and in two post-natal periods using survey responses as early as week 4 of pregnancy with modest performance. The models need to be externally validated and prospectively tested to ensure generalizability to any pregnant patient. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12884-022-04741-9. |
format | Online Article Text |
id | pubmed-9137134 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-91371342022-05-28 Development of multivariable models to predict perinatal depression before and after delivery using patient reported survey responses at weeks 4–10 of pregnancy Reps, Jenna M. Wilcox, Marsha McGee, Beth Ann Leonte, Marie LaCross, Lauren Wildenhaus, Kevin BMC Pregnancy Childbirth Research Article BACKGROUND: Perinatal depression is estimated to affect ~ 12% of pregnancies and is linked to numerous negative outcomes. There is currently no model to predict perinatal depression at multiple time-points during and after pregnancy using variables ascertained early into pregnancy. METHODS: A prospective cohort design where 858 participants filled in a baseline self-reported survey at week 4–10 of pregnancy (that included social economics, health history, various psychiatric measures), with follow-up until 3 months after delivery. Our primary outcome was an Edinburgh Postnatal Depression Score (EPDS) score of 12 or more (a proxy for perinatal depression) assessed during each trimester and again at two time periods after delivery. Five gradient boosting machines were trained to predict the risk of having EPDS score > = 12 at each of the five follow-up periods. The predictors consisted of 21 variables from 3 validated psychometric scales. As a sensitivity analysis, we also investigated different predictor sets that contained: i) 17 of the 21 variables predictors by only including two of the psychometric scales and ii) including 143 additional social economics and health history predictors, resulting in 164 predictors. RESULTS: We developed five prognostic models: PND-T1 (trimester 1), PND-T2 (trimester 2), PND-T3 (trimester 3), PND-A1 (after delivery 1) and PND-A2 (delayed onset after delivery) that calculate personalised risks while only requiring that women be asked 21 questions from 3 validated psychometric scales at weeks 4–10 of pregnancy. C-statistics (also known as AUC) ranged between 0.69 (95% CI 0.65–0.73) and 0.77 (95% CI 0.74–0.80). At 50% sensitivity the positive predictive value ranged between 30%-50% across the models, generally identifying groups of patients with double the average risk. Models trained using the 17 predictors and 164 predictors did not improve model performance compared to the models trained using 21 predictors. CONCLUSIONS: The five models can predict risk of perinatal depression within each trimester and in two post-natal periods using survey responses as early as week 4 of pregnancy with modest performance. The models need to be externally validated and prospectively tested to ensure generalizability to any pregnant patient. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12884-022-04741-9. BioMed Central 2022-05-26 /pmc/articles/PMC9137134/ /pubmed/35619056 http://dx.doi.org/10.1186/s12884-022-04741-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 Reps, Jenna M. Wilcox, Marsha McGee, Beth Ann Leonte, Marie LaCross, Lauren Wildenhaus, Kevin Development of multivariable models to predict perinatal depression before and after delivery using patient reported survey responses at weeks 4–10 of pregnancy |
title | Development of multivariable models to predict perinatal depression before and after delivery using patient reported survey responses at weeks 4–10 of pregnancy |
title_full | Development of multivariable models to predict perinatal depression before and after delivery using patient reported survey responses at weeks 4–10 of pregnancy |
title_fullStr | Development of multivariable models to predict perinatal depression before and after delivery using patient reported survey responses at weeks 4–10 of pregnancy |
title_full_unstemmed | Development of multivariable models to predict perinatal depression before and after delivery using patient reported survey responses at weeks 4–10 of pregnancy |
title_short | Development of multivariable models to predict perinatal depression before and after delivery using patient reported survey responses at weeks 4–10 of pregnancy |
title_sort | development of multivariable models to predict perinatal depression before and after delivery using patient reported survey responses at weeks 4–10 of pregnancy |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9137134/ https://www.ncbi.nlm.nih.gov/pubmed/35619056 http://dx.doi.org/10.1186/s12884-022-04741-9 |
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