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Letters to the Editor |
1 St Georges Hospital, London, UK
2 Helsinki University Hospital, Helsinki, Finland
3 Aarhus University Hospital (Aalborg), Aalborg, Denmark
4 University of Zagreb, Zagreb, Croatia
5 Innsbruck Medical University, Innsbruck, Austria
6 Kliniken Ludwigsburg-Bietigheim, Germany
7 University Hospital Maastricht, Maastricht, the Netherlands
8 Oulu University Hospital, Oulu, Finland
aAddress correspondence to this author at: Laboratory, Oulu University Hospital, PO Box 500, FIN-90029 OYS, Oulu, Finland, Fax: 358-8-3154474, e-mail paivi.h.laitinen@ppshp.fi
| The first 20% of the full text of this article appears below. |
To the Editor:
Evidence-based medicine is recognized as underlying good clinical practice. Similarly, evidence-based laboratory medicine should be used to guide and monitor laboratory testing. One area where laboratory testing has undergone a revolutionary change is in the diagnosis of acute coronary syndrome (ACS)1 , as underscored in the American College of Cardiology (ACC) and the European Society of Cardiology (ESC) consensus document on the definition of and diagnostic approach of myocardial infarction in 2000, updated in 2007. Since the original reports, the measurement of cTnT and cTnI has been recommended in many guidelines, (1)(2) and they have formed a part of the redefinition of myocardial infarction (3).
The CARdiac MArker Guideline Uptake in Europe study (CARMAGUE) was a pilot study to provide baseline data and validate a web-based audit tool to assess compliance of cardiac marker testing in current clinical practice. The study was sponsored by the European Federation
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