Early Exclusion of Major Adverse Cardiac Events in Emergency Department Chest Pain Patients: A Prospective

Yuk-Ki Leung1, Nga-Man Cheng1, Cangel Pui-Yee Chan1

  • 1Accident and Emergency Medicine Academic Unit, Main Clinical Block and Trauma Centre, Prince of Wales Hospital, Shatin, New Territories, Hong Kong.

Insights

A modified TIMI score of 0 or HEART score of ≤ 2 effectively identifies low-risk patients for early discharge. These scores, using a single cardiac troponin T measurement, rule out major adverse cardiac events within 30 days.

Area of Science:

  • Cardiology
  • Emergency Medicine
  • Biomarker Research

Background:

  • Evaluating chest pain in the emergency department (ED) for acute coronary syndrome (ACS) is often prolonged.
  • Current protocols rely on serial troponin measurements, increasing ED wait times.

Purpose of the Study:

  • To validate the diagnostic accuracy of the Thrombolysis in Myocardial Infarction (TIMI) score with a single high-sensitive cardiac troponin T (hs-cTnT) measurement.
  • To compare the TIMI score's effectiveness against combinations of heart-type fatty acid binding protein (H-FABP) and a modified HEART score for ruling out 30-day major adverse cardiac events (MACE).

Main Methods:

  • Recruited 602 adult patients presenting to the ED with chest pain and suspected ACS.
  • Assessed TIMI and HEART scores, and performed point-of-care H-FABP testing for each patient.

Main Results:

  • A modified TIMI score of 0 (11% of patients) and a HEART score ≤ 2 (16% of patients) identified individuals with no 30-day MACE, achieving 100% sensitivity.
  • Combining TIMI and HEART scores enhanced specificity to 22.0% without compromising sensitivity.
  • Early H-FABP measurement (> 7 μg/L) showed 91.1% specificity for predicting 30-day MACE.

Conclusions:

  • A modified TIMI score of 0 or a HEART score of ≤ 2, utilizing a single hs-cTnT level, can reliably identify low-risk patients.
  • These scores facilitate early discharge from the ED within 2 hours for patients with low risk of 30-day MACE.
Abstract

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