Evidence map›Paper›PMID 39002866›Full record

ArticleJournal of biomedical informatics2024

Deep survival analysis for interpretable time-varying prediction of preeclampsia risk.

Braden W Eberhard, Kathryn J Gray, David W Bates, Vesela P Kovacheva

Abstract read
In one paragraph

Article in Journal of biomedical informatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Phenotyping Preeclampsia Using Unsupervised Machine Learning: A Prospective Cohort Study.BJOG : an international journal of obstetrics and gynaecology · 2026
    Article
  2. Article
  3. Review
  4. Journal of clinical medicine · 2025
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Braden W EberhardDepartment of Anesthesiology, Perioperative and Pain Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Kathryn J GrayDepartment of Obstetrics and Gynecology, University of Washington, Seattle, WA, USA.
David W BatesDivision of General Internal Medicine and Primary Care, Brigham and Women's Hospital, Boston, USA; Department of Health Care Policy and Management, Harvard T. H. Chan School of Public Health, Boston, USA.
Vesela P KovachevaDepartment of Anesthesiology, Perioperative and Pain Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA. Electronic address: vkovacheva@bwh.harvard.edu.

Funding

Integrative omics of preeclampsia in TOPMED and maternal cardiovascular healthR01HL163234 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI SAXENA, RICHA · 2022 to 2025
$2.8M
Signatures of dysfunctional mitochondrial fatty acid oxidation that predispose to early-onset preeclampsiaK08HL146963 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI GRAY, KATHRYN JOHNSON · 2019 to 2023
$940k
Personalized Postpartum Hemorrhage Prediction Using Machine Learning And Polygenic Risk ScoresK08HL161326 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI Vesela Kovacheva · 2022 to 2026
$842k
Clinical and functional follow-up of maternal and fetal preeclampsia genetic risk lociR03HL162756 · NHLBI · UNIVERSITY OF WASHINGTON · PI GRAY, KATHRYN JOHNSON · 2022 to 2023
$168k
NHLBI NIH HHS K08 HL146963NHLBI NIH HHS K08 HL161326NHLBI NIH HHS R01 HL163234NHLBI NIH HHS R03 HL162756
6 · The paper itself

Abstract

objectiveSurvival analysis is widely utilized in healthcare to predict the timing of disease onset. Traditional methods of survival analysis are usually based on Cox Proportional Hazards model and assume proportional risk for all subjects. However, this assumption is rarely true for most diseases, as the underlying factors have complex, non-linear, and time-varying relationships. This concern is especially relevant for pregnancy, where the risk for pregnancy-related complications, such as preeclampsia, varies across gestation. Recently, deep learning survival models have shown promise in addressing the limitations of classical models, as the novel models allow for non-proportional risk handling, capturing nonlinear relationships, and navigating complex temporal dynamics.

methodsWe present a methodology to model the temporal risk of preeclampsia during pregnancy and investigate the associated clinical risk factors. We utilized a retrospective dataset including 66,425 pregnant individuals who delivered in two tertiary care centers from 2015 to 2023. We modeled the preeclampsia risk by modifying DeepHit, a deep survival model, which leverages neural network architecture to capture time-varying relationships between covariates in pregnancy. We applied time series k-means clustering to DeepHit's normalized output and investigated interpretability using Shapley values.

resultsWe demonstrate that DeepHit can effectively handle high-dimensional data and evolving risk hazards over time with performance similar to the Cox Proportional Hazards model, achieving an area under the curve (AUC) of 0.78 for both models. The deep survival model outperformed traditional methodology by identifying time-varied risk trajectories for preeclampsia, providing insights for early and individualized intervention. K-means clustering resulted in patients delineating into low-risk, early-onset, and late-onset preeclampsia groups-notably, each of those has distinct risk factors.

conclusionThis work demonstrates a novel application of deep survival analysis in time-varying prediction of preeclampsia risk. Our results highlight the advantage of deep survival models compared to Cox Proportional Hazards models in providing personalized risk trajectory and demonstrating the potential of deep survival models to generate interpretable and meaningful clinical applications in medicine.

Indexed as

Pre-EclampsiaAdultDeep LearningFemaleHumansNeural Networks, ComputerPregnancyProportional Hazards ModelsRetrospective StudiesRisk AssessmentRisk FactorsSurvival AnalysisCox Proportional hazards modelDeep learningK-means clusteringNeural networksPreeclampsiaSurvival analysis

Identifiers

PMID39002866
PMCPMC11349290

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.