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Prediction of adverse events after acute myocardial infarction: derivation and external validation of an extended CHA2DS2-VASc score model
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Disciplinary Domain of Medicine and Pharmacy, research centers etc., Centre for Clinical Research, County of Västmanland.ORCID iD: 0000-0003-1433-0329
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Disciplinary Domain of Medicine and Pharmacy, research centers etc., Centre for Clinical Research, County of Västmanland.ORCID iD: 0000-0002-1355-0250
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Sciences, Cardiology.ORCID iD: 0000-0001-9116-8084
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2025 (English)In: BMJ Open, E-ISSN 2044-6055, Vol. 15, no 11, article id e097267Article in journal (Refereed) Published
Abstract [en]

BACKGROUND: The CHA2DS2-VASc score predicts poor prognosis in patients with acute myocardial infarction (AMI), with or without atrial fibrillation. In this observational study, we aimed to evaluate the CHA2DS2-VASc score by itself and extended with clinical data to predict adverse events in patients after AMI.

METHODS: In this longitudinal observational study, we used a cohort of 955 patients hospitalised for AMI at Västmanland County Hospital, Västerås, Sweden, to derive prediction models. The CHA2DS2-VASc score alone and combined with clinical data (systolic blood pressure, creatinine level, ST-segment elevation and diuretic use at discharge) was analysed using Cox regression to evaluate the risk of major adverse events (MAE), defined as all-cause death or hospitalisation due to recurrent MI, heart failure or ischaemic stroke. Discriminatory performance was presented as the time-dependent area under the curve (tdAUC). The prediction models were validated in 416 patients with AMI hospitalised at Uppsala University Hospital, Uppsala, Sweden.

RESULTS: During a median of 2.5 years, 287 (30.1%) patients experienced MAE. CHA2DS2-VASc scores of 2, 4 and 6 were associated with fourfold, ninefold and 18-fold increases in the relative risk of MAE, respectively, with a tdAUC of 0.76 at a 2-year follow-up. Extending the CHA2DS2-VASc score with clinical data significantly improved the prediction model (p<0.001), yielding a tdAUC of 0.81. The models performed well in the validation cohort, with satisfactory calibration and tdAUC values of 0.70-0.78.

CONCLUSION: The addition of clinical data to the CHA2DS2-VASc score was superior to a model with CHA2DS2-VASc alone in predicting adverse events in patients after AMI, and the model performed well in external validation.

Place, publisher, year, edition, pages
BMJ Publishing Group Ltd, 2025. Vol. 15, no 11, article id e097267
Keywords [en]
CARDIOLOGY, Ischaemic heart disease, Myocardial infarction
National Category
Cardiology and Cardiovascular Disease
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URN: urn:nbn:se:uu:diva-572436DOI: 10.1136/bmjopen-2024-097267ISI: 001620604500001PubMedID: 41263845Scopus ID: 2-s2.0-105022516109OAI: oai:DiVA.org:uu-572436DiVA, id: diva2:2018152
Available from: 2025-12-02 Created: 2025-12-02 Last updated: 2026-03-23Bibliographically approved

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Leppert, JerzySelmeryd, JonasChristersson, ChristinaHedberg, Pär

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