Association of accompanying dyspnoea with diagnosis and outcome of patients presenting with acute chest discomfort
Jazyk angličtina Země Velká Británie, Anglie Médium print
Typ dokumentu časopisecké články
Grantová podpora
Swiss National Science Foundation - Switzerland
PubMed
36917461
PubMed Central
PMC10243981
DOI
10.1093/ehjacc/zuad026
PII: 7077443
Knihovny.cz E-zdroje
- Klíčová slova
- 0/1h-algorithm, Diagnosis of MI, Dyspnoea, High-sensitivity cardiac troponin,
- MeSH
- akutní koronární syndrom * MeSH
- biologické markery MeSH
- bolesti na hrudi diagnóza etiologie MeSH
- dyspnoe diagnóza epidemiologie etiologie MeSH
- infarkt myokardu * diagnóza MeSH
- lidé MeSH
- prediktivní hodnota testů MeSH
- prognóza MeSH
- troponin T MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- biologické markery MeSH
- troponin T MeSH
AIMS: The presence of accompanying dyspnoea is routinely assessed and common in patients presenting with acute chest pain/discomfort to the emergency department (ED). We aimed to assess the association of accompanying dyspnoea with differential diagnoses, diagnostic work-up, and outcome. METHODS AND RESULTS: We enrolled patients presenting to the ED with chest pain/discomfort. Final diagnoses were adjudicated by independent cardiologists using all information including cardiac imaging. The primary diagnostic endpoint was the final diagnosis. The secondary diagnostic endpoint was the performance of high-sensitivity cardiac troponin (hs-cTn) and the European Society of Cardiology (ESC) 0/1h-algorithms for the diagnosis of myocardial infarction (MI). The prognostic endpoints were cardiovascular and all-cause mortality at two years. Among 6045 patients, 2892/6045 (48%) had accompanying dyspnoea. The prevalence of acute coronary syndrome (ACS) in patients with vs. without dyspnoea was comparable (MI 22.4% vs. 21.9%, P = 0.60, unstable angina 8.7% vs. 7.9%, P = 0.29). In contrast, patients with dyspnoea more often had cardiac, non-coronary disease (15.3% vs. 10.2%, P < 0.001). Diagnostic accuracy of hs-cTnT/I concentrations was not affected by the presence of dyspnoea (area under the curve 0.89-0.91 in both groups), and the safety of the ESC 0/1h-algorithms was maintained with negative predictive values >99.4%. Accompanying dyspnoea was an independent predictor for cardiovascular and all-cause death at two years [hazard ratio 1.813 (95% confidence intervals, 1.453-2.261, P < 0.01)]. CONCLUSION: Accompanying dyspnoea was not associated with a higher prevalence of ACS but with cardiac, non-coronary disease. While the safety of the diagnostic work-up was not affected, accompanying dyspnoea was an independent predictor for cardiovascular and all-cause death. CLINICAL TRIAL REGISTRATION: https://clinicaltrials.gov/ct2/show/NCT00470587, number NCT00470587.
BHF Centre for Cardiovascular Science University of Edinburgh Scotland United Kingdom
Department of Cardiac Surgery University Hospital Basel University of Basel Switzerland
Division of Internal Medicine University Hospital Basel University of Basel Switzerland
Emergency Department Hospital Clinic Barcelona Catalonia Spain
Emergency Department Kantonsspital Luzern Switzerland
Emergency Department University Hospital Basel University of Basel Switzerland
Emergency Department University Hospital Zurich Zurich Switzerland
Leipzig Heart Center Leipzig Germany
Servicio de Urgencias Hospital Clínico San Carlos Madrid Spain
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ClinicalTrials.gov
NCT00470587