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Short Term Outcome of Primary Precutaneous Coronary Intervention in Ostial Versus Non Ostial Culprit Proximal Left Anterior Descending Artery Acute Myocardial Infraction

A

Assiut University

Status

Unknown

Conditions

Acute Myocardial Infarction

Study type

Observational

Funder types

Other

Identifiers

NCT04104048
acute myocardial infraction

Details and patient eligibility

About

To compare short-term clinical outcomes of primary PCI between the ostial LAD-AMI and the non-ostial LAD-AMI. The primary endpoint was the major cardiovascular events (MACE) defined as being the composite of cardiac death, AMI, stent thrombosis

Full description

Current guidelines recommend percutaneous coronary intervention (PCI) for most patients with ST segment elevation acute myocardial infarction (STEMI) or with non ST segment elevation acute coronary syndrome (NSTEACS) (1), (2). In STEMI patients, PCI is advised in all patients in the first 12 hours after onset of symptoms, the earlier the better (1).

Coronary revascularization does not always lead to coronary reperfusion. The development of devices and procedure has improved clinical outcomes of percutaneous coronary intervention (PCI) to the culprit of acute myocardial infarction (AMI) (3-5).

However, proximal left anterior descending artery (LAD)-AMI has still been associated with high morbidity and mortality because of the broad ischemic area (6, 7). In fact, clinical outcomes were significantly worse in the proximal LAD-AMI as compared with the mid LAD-AMI.5) Moreover, the proximal LAD disease in stable angina was closely associated with early revascularization following optimal medical therapy (8). Therefore, clinical guidelines regarding coronary revascularization have discriminated the proximal LAD disease from other LAD diseases (9).

In terms of coronary revascularization, the ostial LAD disease requires special attention in the proximal LAD disease, because percutaneous coronary interventions (PCI) can be more complex in the ostial LAD disease than in the non-ostial proximal LAD disease (10) even in the setting of AMI, left-main-trunk (LMT)-to-LAD crossover stenting was frequently required in the ostial LAD disease (11).

Enrollment

300 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients who were diagnosed as Anterior STEMI according to criteria developed by the European Society of Cardiology.
  2. Onset of maximal intensity of chest pain within 12 hours before procedure

Exclusion criteria

  1. Patients presenting with Previous PCI to LAD.
  2. Patients presenting with Previous CABG.
  3. Patients presenting with NSTEMI ACS.

Trial design

300 participants in 1 patient group

patients who were diagnosed as Anterior STEMI
Description:
1. Patients who were diagnosed as Anterior STEMI according to criteria developed by the European Society of Cardiology. 2. Onset of maximal intensity of chest pain within 12 hours before procedure

Trial contacts and locations

0

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Central trial contact

yehia taha, professor; khaled mohammed, lecturer

Data sourced from clinicaltrials.gov

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