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Effect of Significant Ischemic Mitral Regurgitation on the Outcome of ST Segment Elevation Myocardial Infarction Patients Treated With Primary Percutaneous Coronary Intervention

A

Assiut University

Status

Unknown

Conditions

Ischemic Mitral Regurgitation

Study type

Observational

Funder types

Other

Identifiers

NCT04106648
Ischemic mitral regurgitation

Details and patient eligibility

About

The goal of the study is to correlate the effect of ischemic mitral regurgitation on the outcome of STEMI patients treated with successful primary PCI using clinical data and echocardiography on presentation and during short term follow up after 3 months

Full description

  • IMR is defined as mitral regurgitation (MR) caused by chronic changes of LV structure and function due to ischemic heart disease. It is not a valve disease but represents the valvular consequences of increased tethering forces and reduced closing forces. It is reported in approximately one-fifth of patients following acute myocardial infarction (MI) and one-half of those with congestive heart failure. IMR is a frequent complication of coronary artery disease and it worsens the prognosis.
  • It is important to distinguish between primary MR due to organic disease of one or more components of the mitral valve apparatus and secondary MR which is not a valve disease, but represents LV disease. Secondary MR is defined as functional MR, due to LV remodeling by cardiomyopathy or coronary artery disease. In the latter clinical setting, secondary functional MR is called IMR. There are some limitations in this definition of functional IMR. Recent studies have revealed evidence of structural changes in the mitral leaflets in response to tethering on them by LV pathological remodeling. The leaflet adaptation includes enlargement and increased stiffness.
  • Aim of the work :

To correlate the effect of ischemic mitral regurgitation on the outcome of STEMI patients treated with successful primary PCI using clinical data and echocardiography on presentation and during short term follow up after 3 months

Enrollment

134 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Subjects with first presentation
  2. Subjects with Acute STEMI
  3. Subjects undergoing Primary PCI with Successful reperfusion
  4. Subjects with significant IMR Grade (III/IV) to (IV/IV)
  5. Subjects with acute STEMI with no or non-significant MR undergoing Primary PCI undergoing primary PCI with successful reperfusion (as control)

Exclusion criteria

  1. Rheumatic mitral regurge
  2. Valvular mitral regurge
  3. IMR Grade (II/IV)
  4. Cardiomyopathies
  5. Associated other valvular heart diseases

Trial contacts and locations

0

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Central trial contact

Fady Usama Kostandy, Msc

Data sourced from clinicaltrials.gov

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