Evidence map›Paper›PMID 33406155›Full record

ArticlePloS one2021

Recurrent disease progression networks for modelling risk trajectory of heart failure.

Xing Han Lu, Aihua Liu, Shih-Chieh Fuh, Yi Lian, Liming Guo, Yi Yang, Ariane Marelli, Yue Li

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.4field-weighted citation impact, top 7% of its field
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

9 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
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  5. The molecular mechanisms of cardiac development and related diseases.Signal transduction and targeted therapy · 2024
    Review
  6. Tetralogy of Fallot Across the Lifespan: A Focus on the Right Ventricle.CJC pediatric and congenital heart disease · 2023
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Xing Han LuSchool of Computer Science, McGill University, Montreal, Canada.
Aihua LiuMcGill Adult Unit for Congenital Heart Disease Excellence (MAUDE Unit), Montreal, Canada.
Shih-Chieh FuhSchool of Computer Science, McGill University, Montreal, Canada.
Yi LianDepartment of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, Canada.
Liming GuoMcGill Adult Unit for Congenital Heart Disease Excellence (MAUDE Unit), Montreal, Canada.
Yi YangDepartment of Mathematics and Statistics, McGill University, Montreal, Canada.
Ariane MarelliMcGill Adult Unit for Congenital Heart Disease Excellence (MAUDE Unit), Montreal, Canada.
Yue LiSchool of Computer Science, McGill University, Montreal, Canada.ORCID 0000-0003-3844-4865
McGill University · CA

Funding

CIHR 35223
6 · The paper itself

Abstract

motivationRecurrent neural networks (RNN) are powerful frameworks to model medical time series records. Recent studies showed improved accuracy of predicting future medical events (e.g., readmission, mortality) by leveraging large amount of high-dimensional data. However, very few studies have explored the ability of RNN in predicting long-term trajectories of recurrent events, which is more informative than predicting one single event in directing medical intervention.

methodsIn this study, we focus on heart failure (HF) which is the leading cause of death among cardiovascular diseases. We present a novel RNN framework named Deep Heart-failure Trajectory Model (DHTM) for modelling the long-term trajectories of recurrent HF. DHTM auto-regressively predicts the future HF onsets of each patient and uses the predicted HF as input to predict the HF event at the next time point. Furthermore, we propose an augmented DHTM named DHTM+C (where "C" stands for co-morbidities), which jointly predicts both the HF and a set of acute co-morbidities diagnoses. To efficiently train the DHTM+C model, we devised a novel RNN architecture to model disease progression implicated in the co-morbidities.

resultsOur deep learning models confers higher prediction accuracy for both the next-step HF prediction and the HF trajectory prediction compared to the baseline non-neural network models and the baseline RNN model. Compared to DHTM, DHTM+C is able to output higher probability of HF for high-risk patients, even in cases where it is only given less than 2 years of data to predict over 5 years of trajectory. We illustrated multiple non-trivial real patient examples of complex HF trajectories, indicating a promising path for creating highly accurate and scalable longitudinal deep learning models for modeling the chronic disease.

Indexed as

Neural Networks, ComputerDatabases, FactualDisease ProgressionHeart Defects, CongenitalHeart FailureHumansRecurrenceRisk Factors

Identifiers

PMID33406155
PMCPMC7787457
OpenAlexW3118404085

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

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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.