Optimal Timing of Coronary Artery Bypass Grafting in Hemodynamically Stable Patient After Myocardial Infarction and Definition of Poor Prognostic Factors. Pilot Study

NCT ID: NCT03863158

Last Updated: 2019-03-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

476 participants

Study Classification

OBSERVATIONAL

Study Start Date

2007-01-01

Study Completion Date

2019-02-28

Brief Summary

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Acute coronary syndromes (ACS) represent the leading cause of death in France. Their incidence is increasing due to population aging and to the persistence of cardiovascular risk factors. Currently, revascularization surgery remains outside the emergency treatment, because early performed, it tends to lead to extension and hemorrhage of the infarcted area, because of the CPB, aortic clamping, cardioplegia, and other heart manipulation.

However, CABG are indicated as an emergency in some situations of STEMI: Threat of infarction of an extended territory without favorable anatomy to angioplasty, anatomy not favorable to angioplasty associated with cardiogenic shock or persistent ischemia, acute complications of myocardial infarction (massive mitral insufficiency, interventricular communication, parietal rupture) requiring surgery under CPB with concomitant bypass surgery or failure of angioplasty (proximal coronary dissection).

Operative mortality is high; 15 to 20% for patients operated 12 to 48 hours after AMI and 4-5% for those operated after 48 hours.

Nevertheless, it seems legitimate to study if there would be a place for primary surgical revascularization in case of patient with hemodynamically stable ACS, in order to limit myocardial ischemia, spread of necrosis, to limit the risk of recurrence, and the consequences of low cardiac output. Performing a complete early surgical revascularization could limit the ischemia-reperfusion syndrome and anticipate the occurrence of cardiogenic shock.

Detailed Description

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Trial on medical records only

Conditions

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Cardiac Surgery

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Interventions

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No intervention

No intervention / medical records only

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients presenting acute myocardial infarction with hemodynamic stability at the diagnosis
* Patients undergoing coronary artery bypass in Dijon University hospital

Exclusion Criteria

* Patients with Acute pulmonary oedema
* Patients with cardiorespiratory arrest before coronary angiography
* hemodynamically unstable patient at diagnosis
* patients requiring combined surgery
* patients with unstable angina
Minimum Eligible Age

18 Years

Maximum Eligible Age

99 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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BOUCHOT Olivier

UNKNOWN

Sponsor Role collaborator

LAUBRIET-JAZAYERI Aline

UNKNOWN

Sponsor Role collaborator

Centre Hospitalier La Chartreuse

OTHER

Sponsor Role lead

Responsible Party

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MORGANT Marie-Catherine

Principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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CCVT-ChloéBernard 2019

Identifier Type: -

Identifier Source: org_study_id

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