Evidence map›Paper›PMID 29166877›Full record

Trial reportBMC cardiovascular disorders2017

A prospective study examining the role of myocardial Fibrosis in outcome following mitral valve repair IN DEgenerative mitral Regurgitation: rationale and design of the mitral FINDER study.

Boyang Liu, Nicola C Edwards, Desley A H Neal, Christopher Weston, Gerard Nash, Nicolas Nikolaidis, Thomas Barker, Ramesh Patel, Moninder Bhabra, Richard P Steeds

Registry-linked trialOpen access · goldAbstract readClinical TrialComparative StudyMulticenter Study
In one paragraph

Trial report in BMC cardiovascular disorders, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02355418 (A Prospective Observational Study Examining the Role of Myocardial Fibrosis in Outcome Following Mitral Valve Repair in Degenerative Mitral Regurgitation.), which is not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 20% 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.

NCT02355418 completednot on this map

A Prospective Observational Study Examining the Role of Myocardial Fibrosis in Outcome Following Mitral Valve Repair in Degenerative Mitral Regurgitation.

TypeobservationalSponsorUniversity Hospital Birmingham NHS Foundation TrustRan2015 to 2019Enrolled147ConditionsMitral Valve Regurgitation, Mitral RegurgitationArmsMitral valve repair
3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Observational
  5. Review
  6. Mitral Valve Prolapse: A Disease of Valve and Ventricle.Journal of the American College of Cardiology · 2018
    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

10 authors at 4 institutions in 1 country.

Boyang LiuUniversity Hospital Birmingham NHS Foundation Trust, Birmingham, UK. Boyang.Liu@uhb.nhs.uk.ORCID http://orcid.org/0000-0002-3497-6867
Nicola C EdwardsUniversity Hospital Birmingham NHS Foundation Trust, Birmingham, UK.
Desley A H NealUniversity Hospital Birmingham NHS Foundation Trust, Birmingham, UK.
Christopher WestonInstitute of Cardiovascular Sciences, University of Birmingham, Birmingham, UK.
Gerard NashInstitute of Cardiovascular Sciences, University of Birmingham, Birmingham, UK.
Nicolas NikolaidisThe Royal Wolverhampton NHS Trust, Wolverhampton, UK.
Thomas BarkerUniversity Hospitals Coventry and Warwickshire NHS Trust, Coventry, UK.
Ramesh PatelUniversity Hospitals Coventry and Warwickshire NHS Trust, Coventry, UK.
Moninder BhabraUniversity Hospital Birmingham NHS Foundation Trust, Birmingham, UK.
Richard P SteedsUniversity Hospital Birmingham NHS Foundation Trust, Birmingham, UK.
University Hospitals Birmingham NHS Foundation Trust · GBUniversity Hospitals Coventry and Warwickshire NHS Trust · GBUniversity of Birmingham · GBThe Royal Wolverhampton NHS Trust · GB

Funding

British Heart Foundation PG/14/74/31056
6 · The paper itself

Abstract

backgroundThe optimal management of chronic severe primary degenerative mitral regurgitation (MR) is to repair the valve but identification of the optimal timing of surgery remains challenging. Current guidelines suggest 'watchful waiting' until the onset of symptoms or left ventricular (LV) dysfunction but these have been challenged as promoting 'rescue surgery'. Better predictors are required to inform decision-making in relation to the necessity and timing of surgery. Chronic volume overload is a stimulus for adverse adaptive LV remodelling. Subclinical reduction in LV strain before mitral repair predicts a fall in LV ejection fraction following surgery and is thought to reflect the development of myocardial fibrosis in response to chronic volume overload. Myocardial fibrosis can be detected non-invasively using cardiac magnetic resonance (CMR) imaging techniques as an expansion of the extracellular volume (ECV). METHODS/

designThis study investigates whether: 1) patients with above median ECV will have smaller reduction in end-systolic volume index (as a measure of the degree of reverse LV remodelling) on CMR following mitral valve repair, compared to those with below median ECV; and 2) higher ECV on CMR, validated through histology, adversely impacts upon post-operative complications and symptomatic improvement following surgery. This is a multi-centre, prospective, cross-sectional comparison of patients prior to and 9 months following surgery for chronic severe primary degenerative MR. To establish the natural history of ECV in MR, an additional cohort of patients with asymptomatic MR who do not wish to consider early repair will be followed. Investigations include CMR, cardiopulmonary exercise test, stress echocardiography, signal-averaged electrocardiogram, 24-h electrocardiogram monitoring, laboratory tests and patient-reported outcome measures. Patients undergoing surgery will have cardiac biopsies performed at the time of mitral valve repair for histological quantification of fibrosis. DISCUSSION: This study will advance our understanding of ventricular remodelling in MR, its impact on patient symptoms and ventricular response following surgery. Establishing the link between myocardial fibrosis (measured on CMR and validated through histology), with early ventricular dysfunction, will offer physicians a novel non-invasive biomarker that can further inform the timing of surgery.

trial registrationThis trial was registered at ClinicalTrials.gov ( NCT02355418 ) on 30th November 2015.

Indexed as

AdultBiomarkersCross-Sectional StudiesEchocardiography, StressElectrocardiography, AmbulatoryExercise TestFibrosisHeartHumansMagnetic Resonance ImagingMitral ValveMitral Valve InsufficiencyMyocardiumPostoperative ComplicationsProspective StudiesResearch DesignBiomarkersArrhythmia riskCardiac MRIExercise capacityExtracellular volumeMyocardial fibrosisPrimary mitral regurgitationTiming of surgeryVentricular reverse remodelling

Identifiers

PMID29166877
PMCPMC5700678
OpenAlexW2768340323

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.