Evidence map›Paper›PMID 39600889›Full record

ReviewFrontiers in bioengineering and biotechnology2024

Computational modelling of valvular heart disease: haemodynamic insights and clinical implications.

Michael Šeman, Andrew F Stephens, David M Kaye, Shaun D Gregory, Dion Stub

Abstract readReview
In one paragraph

Review in Frontiers in bioengineering and biotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

5 authors.

Michael ŠemanSchool of Public Health and Preventative Medicine, Monash University, Melbourne, VIC, Australia.
Andrew F StephensCardio-Respiratory Engineering and Technology Laboratory, Department of Mechanical and Aerospace Engineering, Monash University, Melbourne, VIC, Australia.
David M KayeCardio-Respiratory Engineering and Technology Laboratory, Department of Mechanical and Aerospace Engineering, Monash University, Melbourne, VIC, Australia.
Shaun D Gregory *Cardio-Respiratory Engineering and Technology Laboratory, Department of Mechanical and Aerospace Engineering, Monash University, Melbourne, VIC, Australia.
Dion Stub *School of Public Health and Preventative Medicine, Monash University, Melbourne, VIC, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An aging population and an increasing incidence of cardiovascular risk factors form the basis for a global rising prevalence of valvular heart disease (VHD). Research to further our understanding of the pathophysiology of VHD is often confined to the clinical setting. However, in recent years, sophisticated computational models of the cardiovascular system have been increasingly used to investigate a variety of VHD states. Computational modelling provides new opportunities to gain insights into pathophysiological processes that may otherwise be difficult, or even impossible, to attain in human or animal studies. Simulations of co-existing cardiac pathologies, such as heart failure, atrial fibrillation, and mixed valvular disease, have unveiled new insights that can inform clinical research and practice. More recently, advancements have been made in using models for making patient-specific diagnostic predictions. This review showcases valuable insights gained from computational studies on VHD and their clinical implications.

Indexed as

aortic stenosiscardiovascular modellumped parametermathematical modelmitral regurgitation

Identifiers

PMID39600889
PMCPMC11588460

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.