Evidence map›Paper›PMID 39780838›Full record

ArticleJTCVS open2024

Five-year comparison of clinical and echocardiographic outcomes of pure aortic stenosis with pure aortic regurgitation or mixed aortic valve disease in the COMMENCE trial.

Vinod H Thourani, John D Puskas, Bartley Griffith, Lars G Svensson, Philippe Pibarot, Michael A Borger, David Heimansohn, Thomas Beaver, Eugene H Blackstone, Anna Liza M Antonio and 2 more

Registry-linked trialAbstract read
In one paragraph

Article in JTCVS open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01757665 (ProspeCtive, nOn-randoMized, MulticENter Clinical Evaluation of Edwards Pericardial Aortic and Mitral Bioprostheses), which is not on this map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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.

NCT01757665 nacompletednot on this map

ProspeCtive, nOn-randoMized, MulticENter Clinical Evaluation of Edwards Pericardial Aortic and Mitral Bioprostheses (Models 11000A and 11000M) With a New Tissue Treatment Platform (COMMENCE)

TypeinterventionalSponsorEdwards LifesciencesRan2012 to 2026Enrolled777ConditionsAortic Stenosis, Mitral Stenosis, Aortic Valve Insufficiency, Mitral Valve InsufficiencyArmsEdwards Aortic and Mitral Bioprostheses Models 11000A and 11000M
3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Review
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

12 authors.

Vinod H ThouraniDepartment of Cardiovascular Surgery, Marcus Valve Center, Piedmont Heart Institute, Atlanta, Ga.
John D PuskasDivision of Cardiothoracic Surgery, Emory University School of Medicine, Atlanta, Ga.
Bartley GriffithDepartment of Surgery, University of Maryland Medical Center, Baltimore, Md.
Lars G SvenssonDepartment of Thoracic and Cardiovascular Surgery, Cleveland Clinic, Cleveland, Ohio.
Philippe PibarotDepartment of Cardiology, Québec Heart and Lung Institute, Laval University, Quebec, Canada.
Michael A BorgerUniversity Department of Cardiac Surgery, Heart Center Leipzig, Leipzig, Germany.
David HeimansohnDepartment of Cardiothoracic Surgery, St. Vincent Heart Center of Indiana, Indianapolis, Ind.
Thomas BeaverDivision of Cardiovascular Surgery, University of Florida Health, Gainesville, Fla.
Eugene H BlackstoneDepartment of Thoracic and Cardiovascular Surgery, Cleveland Clinic, Cleveland, Ohio.
Anna Liza M AntonioEdwards Lifesciences, Irvine, Calif.
Joseph E BavariaDepartment of Cardiovascular Surgery, Jefferson Health, Philadelphia, Pa.
COMMENCE Trial Investigators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To compare outcomes of aortic valve replacement (AVR) in patients with pure aortic stenosis (Pure AS) and those with pure aortic regurgitation (Pure AR) or mixed AS and AR (MAVD) in the COMMENCE trial. Methods: Of 689 patients who underwent AVR in the COMMENCE trial, patients with moderate or severe AR with or without AS (Pure AR + MAVD; n = 135) or Pure AS (n = 323) were included. Inverse probability of treatment weighting Kaplan-Meier survival curves were used for time-to-event endpoints, and longitudinal changes in hemodynamics were evaluated using mixed-effects models. Echocardiographic outcomes were assessed by an echo core laboratory and clinical outcomes adjudicated by a clinical events committee. The mean duration of follow-up was 5.3 ± 2.2 years. Results: At 5 years, adjusted safety endpoints were not statistically different between groups; no structural valve deterioration (SVD) event occurred in either group. After adjustment, the Pure AR + MAVD group had a greater change in body surface area-corrected left ventricular (LV) mass reduction ( Conclusions: Patients with Pure AR + MAVD demonstrated similar clinical safety and freedom from SVD at 5 years compared to those with Pure AS. There was a significant difference in LV reverse remodeling in the Pure AR + MAVD group compared to the Pure AS group at 5 years. These favorable outcomes in patients with AR may reinforce the need for treatment before irreversible changes occur.

Indexed as

aortic regurgitationaortic stenosisaortic valve replacementclinical outcomesmixed aortic valve disease

Identifiers

PMID39780838
PMCPMC11704589

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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.