Valutazione della sensibilità diagnostica per l’infarto miocardico senza sopraslivellamento del tratto ST (NSTEMI) di due metodi ad alta sensibilità per la troponina cardiaca
Articolo
Data di Pubblicazione:
2011
Citazione:
Valutazione della sensibilità diagnostica per l’infarto miocardico senza sopraslivellamento del tratto ST (NSTEMI) di due metodi ad alta sensibilità per la troponina cardiaca / F. Braga, A. Dolci, A. Cavallero, A. Ghezzi, I. Infusino, M. Milano, M. Rubino, G. Marenzi, M. Panteghini. - In: BIOCHIMICA CLINICA. - ISSN 0393-0564. - 35:3(2011), pp. 186-189.
Abstract:
Evaluation of the sensitivity of two highly sensitive troponin assays for early detection of non ST-elevation myocardial infarction (NSTEMI). The major clinical role for the cardiac troponin in the myocardial infarction diagnosis is in patients with non diagnostic initial electrocardiogram (ECG) (suspected NSTEMI). The aim of this study was to evaluate the clinical sensitivity of two highly sensitive last generation troponin assays (Siemens Advia TnI-Ultra and
Roche Diagnostics hsTnT) in the diagnosis of patients presenting with recent NSTEMI in comparison to conventional troponin assays. The study group consisted of 150 patients admitted to the Emergency Department with suspected acute coronary syndrome, to whom serial blood samples were taken every 3 h throughout the first 6 h after hospital
admission. After evaluation of clinical history, ECG, and standard troponin results, obtained blinded to results of tested
troponin assays, 31 patients were diagnosed as NSTEMI. Positive results were considered values >40 ng/L for TnIUltra and >15 ng/L for hsTnT, respectively. Sensitivities for NSTEMI were 81%, 87%, and 58% at admission and 100%,100%, and 94% after 6 h for TnI-Ultra, hsTnT, and conventional assays, respectively. Interestingly, with both highly
sensitive assays the maximal 100% sensitivity was already reached 3 h after admission. New highly sensitive troponin
assays may significantly shorten the time to rule out NSTEMI. Although preliminary, our data suggest that the observation period of patients with suspected myocardial damage can be reduced from the conventional 12 h from hospital admission to only 3 h. Accordingly, a new protocol, sampling at presentation and 3 h later, could be
recommended
Tipologia IRIS:
01 - Articolo su periodico
Elenco autori:
F. Braga, A. Dolci, A. Cavallero, A. Ghezzi, I. Infusino, M. Milano, M. Rubino, G. Marenzi, M. Panteghini
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