LOng-Term Fate of Moderate Aortic Regurgitation Left Untreated at the Time of Mitral Valve Surgery

Sponsor
Michele De Bonis (Other)
Overall Status
Completed
CT.gov ID
NCT05774795
Collaborator
(none)
183
1
7
795.7

Study Details

Study Description

Brief Summary

Multivalvular heart disease is a highly prevalent clinical condition that comprises 14.6% of the patients undergoing valvular surgery. Specifically, aortic valve regurgitation (AR) can be present in a considerable proportion of patients undergoing mitral valve (MV) surgery. In the Society of Thoracic Surgeons database, con- comitant aortic and mitral surgery accounted for 57.8% of the total multivalvular procedures with an unadjusted mortality rate of 10.7%.

When both the aortic and MVs exhibit severe disease, con- comitant valve surgery is well-accepted by the surgical commu- nity and supported by current guidelines. On the other hand, when the aortic valve (AV) shows only moderate regurgita- tion, which would not be surgically treated if singly present, the appropriate management of the AV pathology at the time of MV surgery is still under debate.

The American College of Cardiology guidelines state that aortic valve replacement (AVR) is reasonable (class IIa) in patients with moderate AR (stage B) while undergoing surgery on the ascend- ing aorta, a coronary artery bypass graft or MV surgery (level of evidence: C). Conversely, the latest European Society of Cardiology guidelines on valvular heart disease define as con- troversial the decision to treat the AV in patients with moderate AR who undergo MV surgery, considering the slow progression of this disease. In this group of patients, they advocate a heart team approach that will take into account the aetiology of AR, the life expectancy of the patient, the operative risk and other clinical factors.

This disagreement may lead to uncertainty about how patients with less than severe AR should be managed during MV surgery, especially considering the burden of double-valve surgical procedures.

The goal of this study is to evaluate the immediate and long- term outcomes, including the need for a new procedure on the AV, in patients with moderate AR at the time of MV surgery.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Mitral valve surgery
  • Procedure: Aortic valve surgery

Study Design

Study Type:
Observational
Actual Enrollment :
183 participants
Observational Model:
Case-Control
Time Perspective:
Cross-Sectional
Official Title:
LOng-Term Fate of Moderate Aortic Regurgitation Left Untreated at the Time of Mitral Valve Surgery
Actual Study Start Date :
Mar 24, 2021
Actual Primary Completion Date :
Mar 31, 2021
Actual Study Completion Date :
Mar 31, 2021

Arms and Interventions

Arm Intervention/Treatment
Mitral valve surgery only

Procedure: Mitral valve surgery
Mitral valve repair or replacement to treat mitral regurgitation

Mitral valve surgery + Aortic valve surgery

Procedure: Mitral valve surgery
Mitral valve repair or replacement to treat mitral regurgitation

Procedure: Aortic valve surgery
Aortic valve replacement to treat aortic regurgitation

Outcome Measures

Primary Outcome Measures

  1. Mortality [through study completion, an average of 12 years]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

General criteria for both groups

  • Adult patients;

  • Patients undergoing mitral valve surgery, with moderate-grade AR, as assessed by preoperative echocardiography;

Specific criteria Group 1 (study group) - Patients who have not undergone aortic valve surgery in conjunction with mitral valve surgery

Specific criteria Group 2 (control group)

  • Patients undergoing aortic valve surgery in conjunction with mitral valve surgery
Exclusion Criteria:
  • Patients who have not undergone mitral surgery

  • Patients undergoing multivalvular surgery other than mitro-aortic surgery

Contacts and Locations

Locations

Site City State Country Postal Code
1 IRCCS Ospedale San Raffaele Milan Italy 20132

Sponsors and Collaborators

  • Michele De Bonis

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Michele De Bonis, Chief of Cardiac Surgery of the Advanced and Research Therapies, Ospedale San Raffaele
ClinicalTrials.gov Identifier:
NCT05774795
Other Study ID Numbers:
  • LOTMAR
First Posted:
Mar 20, 2023
Last Update Posted:
Mar 20, 2023
Last Verified:
Mar 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 20, 2023