Development of Clinical Decision Support System to Define 30 Day Adverse Clinical Events (Non Fatal Myocardial Infarction, Cardiac Related Death or Coronary Intervention) for Patients Presenting to Emergency Department With Acute Coronary Syndrome
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Acute Coronary Syndrome
- Sponsor
- Turkish Ministry of Health Izmir Teaching Hospital
- Enrollment
- 400
- Locations
- 1
- Primary Endpoint
- Non fatal myocardial infarction, cardiac related death or coronary intervention in 30 days
- Last Updated
- 8 years ago
Overview
Brief Summary
Acute coronary syndromes are among main complains for patients presenting to emergency department. Risk classification systems are used to classify patients to appropriate risks and help physicians manage diagnosis strategies and treatments. Purpose of this study is to develop a clinical decision support system for patients presenting to emergency department with the help of statistical machine learning.
Detailed Description
Acute coronary syndromes are among main complains for patients presenting to emergency department and create a burden to emergency departments and hospitals. Risk classification systems were developed and used to classify patients to appropriate risk groups. According to risk classification, different diagnosis and treatment modalities can be used and help physicians manage diagnosis strategies and treatments. Purpose of this study is to develop a clinical decision support system for patients presenting to emergency department with the help of statistical machine learning.
Investigators
Serhat Akay
M.D.
Turkish Ministry of Health Izmir Teaching Hospital
Eligibility Criteria
Inclusion Criteria
- •Presenting to emergency department with acute chest pain consistent with acute coronary syndrome
Exclusion Criteria
- •Patients with less than 18 years old
- •Patients presenting with ST-segment elevation myocardial infarction
- •Patients presenting with other causes of acute chest pain (pneumothorax, pulmonary -embolism, aortic dissection
- •Decline to participate in study
Outcomes
Primary Outcomes
Non fatal myocardial infarction, cardiac related death or coronary intervention in 30 days
Time Frame: 30 days
Patients will be screened for 30 days for Non fatal myocardial infarction, cardiac related death or coronary intervention (coronary angiogram, coronary artery bypass surgery)