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Published on: August 9, 2024
Development of a Novel Risk-Prediction Tool for Emergency Department Patients with Symptoms of Coronary Artery
Andrew D McRae1,2, Aysha J Macci1,2, Jessalyn K Holodinsky1,2,3
1Department of Emergency Medicine, University of Calgary, Calgary, Alberta, Canada.
Insights
A new risk tool for chest pain patients in emergency departments can identify those unlikely to have acute coronary syndromes. This helps reduce unnecessary cardiac testing and improve healthcare efficiency.
Area of Science:
- Cardiology
- Emergency Medicine
- Health Services Research
Background:
- Over 600,000 Canadians visit the ED annually for chest pain, with 85% not having acute coronary syndromes (ACS).
- Many low-risk patients are referred for outpatient cardiac testing, leading to low-value care and limited access for high-risk individuals.
- Current risk tools, developed before high-sensitivity troponin assays, overestimate risk in ED patients with low troponin levels.
Purpose of the Study:
- To derive and validate a novel risk prediction tool for emergency department patients presenting with chest pain.
- To accurately identify low-risk patients who do not require further cardiac testing.
- To improve the appropriate referral of chest pain patients from the ED.
Main Methods:
- A multicentre prospective cohort study enrolling 6500 patients across 13 Canadian EDs.
- Prospective follow-up to ascertain major adverse cardiac events (MACE) within 30 days of the index ED encounter.
- Development and validation of a new risk prediction tool using data from enrolled patients.
Main Results:
- The study aims to develop a tool to differentiate low-risk from potentially higher-risk chest pain patients.
- The tool will be validated to ensure accuracy in predicting 30-day MACE.
- Expected outcome is a reliable instrument for guiding further cardiac testing decisions.
Conclusions:
- A novel risk prediction tool is needed to optimize the management of chest pain patients in the ED.
- The developed tool will guide safe and efficient referral decisions, reducing unnecessary testing.
- This will enhance healthcare resource utilization and patient access to appropriate cardiac evaluations.
Abstract:
Patients with chest pain and symptoms of acute coronary syndromes account for > 600,000 emergency department (ED) visits annually in Canada. Of these patients, 85% do not have acute coronary syndromes, and most are discharged from the ED after a thorough evaluation. However, a large proportion of these patients are referred for outpatient cardiac testing after ED discharge, even though their short-term risk of major adverse cardiac events (MACE), including death, new myocardial infarction, and need for revascularization, is very small. These referrals contribute to substantial low-value healthcare utilization, and limit access for those patients who are more likely to benefit from objective testing.Existing risk-prediction tools-developed prior to the advent of new high-sensitivity cardiac troponin assays-were derived in nonrepresentative populations, and when applied to ED patients with low cardiac troponin concentrations, systematically overestimate the short-term risk of MACE.This multicentre prospective cohort study will enroll ED patients with chest pain to derive and validate a novel risk prediction tool that distinguishes patients at low risk of MACE who do not require further cardiac testing from those who may benefit from additional cardiac testing. We will enroll 6500 patients in 13 Canadian EDs and prospectively follow them to ascertain a primary outcome of MACE within 30 days after their index ED encounter. The risk-prediction tool developed in this project will guide the safe, efficient, and appropriate referral of ED patients with chest pain.
Clinical Trial Registration:
NCT06743672.
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