A direct comparison of decision rules for early discharge of suspected acute coronary syndromes in the era of high sensitivity troponin

Author:

Chew Pei Gee1,Frost Fredrick1,Mullen Liam1,Fisher Michael23,Zadeh Heidar2,Grainger Ruth4,Albouaini Khaled2,Dodd James5,Patel Bilal6,Velavan Periaswamy3,Kunadian Babu37,Rawat Anju1,Obafemi Toba1,Tong Sarah1,Jones Julia1,Khand Aleem138

Affiliation:

1. Aintree University Hospital NHS Trust, UK

2. Royal Liverpool University Hospital NHS Trust, UK

3. Institute for Cardiovascular Medicine and Science, Liverpool Heart and Chest Hospital NHS Trust, UK

4. Northwest Coast Strategic Clinical Networks, Warrington, UK

5. Liverpool Cancer and Clinical Trial Units, University of Liverpool, UK

6. Blackpool Teaching Hospitals NHS Foundation Trust, UK

7. Countess of Chester NHS Trust, Chester, UK

8. Institute of Aging and Chronic Diseases, University of Liverpool, UK

Abstract

Background: We tested the hypothesis that a single high sensitivity troponin at limits of detection (LOD HSTnT) (<5 ng/l) combined with a presentation non-ischaemic electrocardiogram is superior to low-risk Global Registry of Acute Coronary Events (GRACE) (<75), Thrombolysis in Myocardial Infarction (TIMI) (≤1) and History, ECG, Age, Risk factors and Troponin (HEART) score (≤3) as an aid to early, safe discharge for suspected acute coronary syndrome. Methods: In a prospective cohort study, risk scores were computed in consecutive patients with suspected acute coronary syndrome presenting to the Emergency Room of a large English hospital. Adjudication of myocardial infarction, as per third universal definition, involved a two-physician, blinded, independent review of all biomarker positive chest pain re-presentations to any national hospital. The primary and secondary outcome was a composite of type 1 myocardial infarction, unplanned coronary revascularisation and all cause death (MACE) at six weeks and one year. Results: Of 3054 consecutive presentations with chest pain 1642 had suspected acute coronary syndrome (52% male, median age 59 years, 14% diabetic, 20% previous myocardial infarction). Median time from chest pain to presentation was 9.7 h. Re-presentations occurred in eight hospitals with 100% follow-up achieved. Two hundred and eleven (12.9%) and 279 (17%) were adjudicated to suffer MACE at six weeks and one year respectively. Only HEART ≤3 (negative predictive value MACE 99.4%, sensitivity 97.6%, %discharge 53.4) and LOD HSTnT strategy (negative predictive value MACE 99.8%, sensitivity 99.5%, %discharge 36.9) achieved pre-specified negative predictive value of >99% for MACE at six weeks. For type 1 myocardial infarction alone the negative predictive values at six weeks and one year were identical, for both HEART ≤3 and LOD HSTnT at 99.8% and 99.5% respectively. Conclusion: HEART ≤3 or LOD HSTnT strategy rules out short and medium term myocardial infarction with ≥99.5% certainty, and short-term MACE with >99% certainty, allowing for early discharge of 53.4% and 36.9% respectively of suspected acute coronary syndrome. Adoption of either strategy has the potential to greatly reduce Emergency Room pressures and minimise follow-up investigations. Very early presenters (<3 h), due to limited numbers, are excluded from these conclusions.

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine,Critical Care and Intensive Care Medicine,General Medicine

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