Myocardial Infarction With Non-obstructive Coronary Arteries in Turkish Population

Cardiovascular Academy Society, Turkey16,026 enrolled

Overview

The objective of this study is to analyze the Demographics, Clinical Profiles, Management, in-Hospital and Long-Term Outcomes of Patients with Acute Coronary Syndrome Syndrome And Myocardial Infarction with Non-obstructive Coronary Artery Disease.

Acute coronary syndrome is leading causes of death worldwide. Although, \>90% of these patients had of culprit coronary lesion, a significant proportion of them had no any angiographic evidence of obstructive coronary arteries. Exact mechanism of the myocardial infarction remains unclear of these patients. However, MI registries have reported that the 5% to %10 of MI patients have no evidence of obstructive coronary artery disease. There is lack of any data regarding prevalence, demographics, patients' profile, management, and outcome of this clinical entity in Turkish population. This registry aims to obtain these data in Myocardial Infarction with Non-obstructive Coronary Artery Disease patients in Turkish population. Although there are huge data in this issue from different country and geographic areas, to date no any national data about prevalence, demographics, management and in-hospital outcomes of AF patients who admitting with cute coronary syndrome. With this rationale the registry also aims to obtain demographics, clinical profile, management, and in-hospital outcome of AF in Turkish Acute coronary syndrome population.

Study Type

OBSERVATIONAL

Enrollment

16,026

Conditions

Acute Coronary Syndrome Myocardial Infarction Atrial Fibrillation Diabetes Mellitus

Eligibility

Sex: ALLMin age: 18 YearsMax age: 90 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. Patients older than 18 years 2. Evidence of an MI as defined any one of the following criteria: Detection of a rise and/or fall of cardiac biomarker values \[preferably cardiac troponin (cTn)\] with at least one value above the 99th percentile upper reference limit (URL) and with at least one of the following: i. Symptoms of ischaemia. ii. New or presumed new signiﬁcant ST-segment-T wave (ST-T) changes or new left bundle branch block (LBBB). iii. Development of pathological Q waves in the ECG. iv. Imaging evidence of new loss of viable myocardium or new regional wall motion abnormality. v. Identiﬁcation of an intracoronary thrombus by angiography. 3. Invasive diagnostic coronary angiography (IDCA) findings to allow determination of the presence /absence of obstructive coronary artery disease 4. Signed informed consent form to trial participation Exclusion Criteria: 1. Inability/Refused to provide informed consent 2. Age below 18 years 3. Patients with unstable angina pectoris (ACS without increase and/or decrease of a cardiac biomarker, preferably high-sensitivity cardiac troponin, with at least one value above the 99th percentile of the upper reference limit) 4. Patients refused invasive diagnostic coronary angiography 5. Myocardial infarction associated with revascularization procedures

Locations (1)

Emin Alioğlu

Izmir, Turkey (Türkiye)

Outcomes

Primary Outcomes

Composites of Myocardial Infarction, Hospitalization, Revascularization, Death

Re-infarction, Any cause or Cardiovascular Hospitalization or Death

Time frame: 12 months

Secondary Outcomes

Atrial Fibrillation

Any type of atrial fibrillation

Time frame: 12 months

Heart failure

Acute decompensated heart failure with or without cardiogenic shock

Time frame: 12 months

Data from ClinicalTrials.gov

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