Re-engineering the Clinical Approach to Suspected Cardiac Chest Pain Assessment in the Emergency Department by Expediting Evidence to Practice Using Artificial Intelligence - RAPIDxAI

Contribution To Literature:

The RAPIDxAI trial showed that in patients with elevated hs-cTn, an AI-based clinical decision support tool did not improve 6-month CV outcomes but improved rates of evidence-based care without an increased risk of adverse events.

Description:

The goal of the trial was to determine the efficacy and safety of an artificial intelligence (AI)-based clinical decision support tool compared with usual care in the diagnosis and management of emergency department (ED) patients with elevated high-sensitivity cardiac troponin (hs-cTn).

Study Design

  • Multicenter
  • Cluster-randomized

Twelve South Australian EDs (6 urban, 6 rural) underwent stratified randomization to use an AI-based decision support tool (n = 1,568) or standard care (n = 1,461) in the evaluation of patients with elevated hs-cTn of suspected primary cardiac etiology.

  • Total number of enrollees: 3,029
  • Duration of follow-up: 6 months
  • Mean patient age: 75 years
  • Percentage female: 58%

Inclusion criteria:

  • Age ≥18 years
  • ≥1 hs-cTn value ≥99th percentile of the upper reference limit
  • Suspected cardiac cause of elevated hs-cTn

Principal Findings:

The primary efficacy outcome, composite of cardiovascular (CV) death, myocardial infarction (MI), and unplanned CV readmission at 6 months, for AI vs. control, was: 26.0% vs. 26.4% (hazard ratio 0.99, 95% confidence interval 0.86-1.14, p = 0.872).

The primary safety outcome, composite of all-cause death or MI at 30 days, for AI vs. control, was: 0.86% vs. 1.1% (p for noninferiority < 0.001).

Secondary outcomes for AI vs. control:

  • Invasive coronary angiography if not classified as type 1 MI: 5.2% vs. 9.4%
  • Statin use if classified as type 1 MI: 81.8% vs. 68.0%

Interpretation:

In ED patients with elevated hs-cTn and suspected myocardial injury, 6-month clinical outcomes were similar when initial evaluation and management was assisted by an AI algorithm compared with usual care. The algorithm, based on the Fourth Universal Definition of MI, provided diagnostic probabilities of type 1 versus 2 MI and acute versus chronic myocardial injury, associated prognostic assessments, and evidence-based management recommendations. No increase in short-term adverse events was noted despite lower rates of invasive angiography in patients not classified as type 1 MI, suggesting the relative safety of the tool when used to support independent clinical assessment.

Importantly, although event rates were similar between groups, there were higher rates of evidence-based therapies such as statins and antiplatelet agents in the AI arm. The overall rate of antiplatelet use in type 1 MI-classified patients was still relatively low, which may reflect subsequent reclassification based on additional diagnostic data. Nonetheless, the current data suggest that AI-based decision support tools may reinforce adherence to guideline-directed medical therapies in critical diagnoses such as type 1 MI without an increased risk for harm. It is likely that these AI algorithms will get refined over time. Cost-effectiveness and scalability also need to be evaluated in future studies.

References:

Presented by Dr. Derek Chew at the European Society of Cardiology Congress, London, UK, September 2, 2024.

Keywords: Artificial Intelligence, Myocardial Infarction, Troponin, ESC Congress, ESC24


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