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Development and validation of a prognostic score integrating remote heart failure symptoms and clinical variables in mortality risk prediction after myocardial infarction: the PragueMi score
P. Wohlfahrt, D. Jenča, V. Melenovský, J. Stehlik, J. Mrázková, M. Šramko, M. Kotrč, M. Želízko, V. Adámková, J. Piťha, J. Kautzner
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, validační studie
Grantová podpora
NV 19-09-00125
Ministry of Health of the Czech Republic
LX22NPO5104
National Institute for Research of Metabolic and Cardiovascular Diseases
European Union-Next Generation EU
PubMed
38497201
DOI
10.1093/eurjpc/zwae114
Knihovny.cz E-zdroje
- MeSH
- časové faktory MeSH
- hodnocení rizik MeSH
- infarkt myokardu * mortalita diagnóza MeSH
- lidé středního věku MeSH
- lidé MeSH
- metody pro podporu rozhodování MeSH
- prediktivní hodnota testů MeSH
- prognóza MeSH
- prospektivní studie MeSH
- reprodukovatelnost výsledků MeSH
- rizikové faktory MeSH
- senioři MeSH
- srdeční selhání * mortalita diagnóza patofyziologie MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- validační studie MeSH
AIMS: While heart failure (HF) symptoms are associated with adverse prognosis after myocardial infarction (MI), they are not routinely used for patients' stratification. The primary objective of this study was to develop and validate a score to predict mortality risk after MI, combining remotely recorded HF symptoms and clinical risk factors, and to compare it against the guideline-recommended Global Registry of Acute Coronary Events (GRACE) score. METHODS AND RESULTS: A cohort study design using prospectively collected data from consecutive patients hospitalized for MI at a large tertiary heart centre between June 2017 and September 2022 was used. Data from 1135 patients (aged 64 ± 12 years, 26.7% women), were split into derivation (70%) and validation cohort (30%). Components of the 23-item Kansas City Cardiomyopathy Questionnaire and clinical variables were used as possible predictors. The best model included the following variables: age, HF history, admission creatinine and heart rate, ejection fraction at hospital discharge, and HF symptoms 1 month after discharge including walking impairment, leg swelling, and change in HF symptoms. Based on these variables, the PragueMi score was developed. In the validation cohort, the PragueMi score showed superior discrimination to the GRACE score for 6 months [the area under the receiver operating curve (AUC) 90.1, 95% confidence interval (CI) 81.8-98.4 vs. 77.4, 95% CI 62.2-92.5, P = 0.04) and 1-year risk prediction (AUC 89.7, 95% CI 83.5-96.0 vs. 76.2, 95% CI 64.7-87.7, P = 0.004). CONCLUSION: The PragueMi score combining HF symptoms and clinical variables performs better than the currently recommended GRACE score.
1st Medical School Charles University Katerinska 1660 32 Prague 120 00 Czech Republic
3rd Medical School Charles University Prague Czech Republic
Department of Cardiology Institute for Clinical and Experimental Medicine Prague Czech Republic
Division of Cardiovascular Medicine University of Utah School of Medicine Salt Lake City UT USA
Experimental Medicine Centre Institute for Clinical and Experimental Medicine Prague Czech Republic
Medical and Dentistry School Palacký University Olomouc Czech Republic
Citace poskytuje Crossref.org
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