Modification of the GRACE Risk Score for Risk Prediction in Patients With Acute Coronary Syndromes

Author:

Georgiopoulos Georgios123,Kraler Simon4,Mueller-Hennessen Matthias56,Delialis Dimitrios1,Mavraganis Georgios1,Sopova Kateryna26789,Wenzl Florian A.4,Räber Lorenz10,Biener Moritz5,Stähli Barbara E.11,Maneta Eleni1,Spray Luke9,Iglesias Juan F.12,Coelho-Lima Jose2,Tual-Chalot Simon13,Muller Olivier14,Mach François12,Frey Norbert56,Duerschmied Daniel6715,Langer Harald F.6715,Katus Hugo56,Roffi Marco12,Camici Giovanni G.4,Mueller Christian16,Giannitsis Evangelos5,Spyridopoulos Ioakim29,Lüscher Thomas F.417,Stellos Konstantinos67813,Stamatelopoulos Kimon12

Affiliation:

1. Department of Clinical Therapeutics, Alexandra Hospital, National and Kapodistrian University of Athens Medical School, Athens, Greece

2. Translational and Clinical Research Institute, Vascular Biology and Medicine Theme, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom

3. Department of Cardiovascular Imaging, School of Biomedical Engineering and Imaging Sciences, Guy’s and St Thomas’ NHS Foundation Trust, London, United Kingdom

4. Center for Molecular Cardiology, University of Zurich, Zurich, Switzerland

5. Department of Cardiology, University Hospital Heidelberg, University of Heidelberg, Heidelberg, Germany

6. German Centre for Cardiovascular Research (DZHK), Partner Site Heidelberg/Mannheim, Mannheim, Germany

7. Department of Cardiology, Angiology, Hemostaseology and Medical Intensive Care, University Medical Centre Mannheim, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany

8. Department of Cardiovascular Research, European Center for Angioscience, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany

9. Department of Cardiology, Freeman Hospital, Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, United Kingdom

10. Department of Cardiology, Swiss Heart Center, Inselspital Bern, Bern, Switzerland

11. Department of Cardiology, University Heart Center, University Hospital Zurich, Zurich, Switzerland

12. Department of Cardiology, Geneva University Hospitals, Geneva, Switzerland

13. Biosciences Institute, Vascular Biology and Medicine Theme, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom

14. Department of Cardiology, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland

15. European Center for Angioscience, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany

16. Cardiovascular Research Institute Basel and University Hospital of Basel, Basel, Switzerland

17. Royal Brompton and Harefield Hospitals and Imperial College and Kings College, London, United Kingdom

Abstract

ImportanceThe Global Registry of Acute Coronary Events (GRACE) risk score, a guideline-recommended risk stratification tool for patients presenting with acute coronary syndromes (ACS), does not consider the extent of myocardial injury.ObjectiveTo assess the incremental predictive value of a modified GRACE score incorporating high-sensitivity cardiac troponin (hs-cTn) T at presentation, a surrogate of the extent of myocardial injury.Design, Setting, and ParticipantsThis retrospectively designed longitudinal cohort study examined 3 independent cohorts of 9803 patients with ACS enrolled from September 2009 to December 2017; 2 ACS derivation cohorts (Heidelberg ACS cohort and Newcastle STEMI cohort) and an ACS validation cohort (SPUM-ACS study). The Heidelberg ACS cohort included 2535 and the SPUM-ACS study 4288 consecutive patients presenting with a working diagnosis of ACS. The Newcastle STEMI cohort included 2980 consecutive patients with ST-elevation myocardial infarction treated with primary percutaneous coronary intervention. Data were analyzed from March to June 2023.ExposuresIn-hospital, 30-day, and 1-year mortality risk estimates derived from an updated risk score that incorporates continuous hs-cTn T at presentation (modified GRACE).Main Outcomes and MeasuresThe predictive value of continuous hs-cTn T and modified GRACE risk score compared with the original GRACE risk score. Study end points were all-cause mortality during hospitalization and at 30 days and 1 year after the index event.ResultsOf 9450 included patients, 7313 (77.4%) were male, and the mean (SD) age at presentation was 64.2 (12.6) years. Using continuous rather than binary hs-cTn T conferred improved discrimination and reclassification compared with the original GRACE score (in-hospital mortality: area under the receiver operating characteristic curve [AUC], 0.835 vs 0.741; continuous net reclassification improvement [NRI], 0.208; 30-day mortality: AUC, 0.828 vs 0.740; NRI, 0.312; 1-year mortality: AUC, 0.785 vs 0.778; NRI, 0.078) in the derivation cohort. These findings were confirmed in the validation cohort. In the pooled population of 9450 patients, modified GRACE risk score showed superior performance compared with the original GRACE risk score in terms of reclassification and discrimination for in-hospital mortality end point (AUC, 0.878 vs 0.780; NRI, 0.097), 30-day mortality end point (AUC, 0.858 vs 0.771; NRI, 0.08), and 1-year mortality end point (AUC, 0.813 vs 0.797; NRI, 0.056).Conclusions and RelevanceIn this study, using continuous rather than binary hs-cTn T at presentation, a proxy of the extent of myocardial injury, in the GRACE risk score improved the mortality risk prediction in patients with ACS.

Publisher

American Medical Association (AMA)

Subject

Cardiology and Cardiovascular Medicine

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