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180702 r ||| eng |
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|a Ho, Chuong
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|a Point-of-care troponin testing in patients with symptoms suggestive of acute coronary syndrome: A health technology assessment
|h Elektronische Ressource
|c clinical authors, Chuong Ho, Karen Cimon, Laura Weeks, Monika Mierzwinski-Urban, Lesley Dunfield, economic authors, Lesley Soril, Fiona Clement, Mohammed Jabr
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|a Health technology assessment
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|a Ottawa (ON)
|b Canadian Agency for Drugs and Technologies in Health
|c 2016, [March 2016]
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|a 1 PDF file (ix, 133 pages)
|b illustrations
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|a Includes bibliographical references
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|a Troponin T / therapeutic use
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|a Point-of-Care Systems / standards
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|a Cost-Benefit Analysis
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|a Acute Coronary Syndrome / diagnosis
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|a Troponin I / therapeutic use
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|a Canadian Agency for Drugs and Technologies in Health
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|a eng
|2 ISO 639-2
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|b NCBI
|a National Center for Biotechnology Information
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|a CADTH optimal use report
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|a "PROSPERO Registration Number: CRD42015023442."
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|u https://www.ncbi.nlm.nih.gov/books/NBK362840
|3 Volltext
|n NLM Bookshelf Books
|3 Volltext
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|a 610
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|a Testing of cardiac biomarkers, such as cardiac troponin I or cardiac troponin T, has an important role in the diagnostic workup for acute coronary syndrome (ACS) (including acute myocardial infarction [AMI] and unstable angina), and in patients presenting with acute chest pain and a non-diagnostic electrocardiogram (ECG). Bedside testing of cardiac troponins (cTn) using point-of-care (POC) assays was developed to reduce the turnaround time of the standard tests performed in a central laboratory, and to expedite treatment. Given the introduction and increasing diffusion of POC cTn use, a review of its clinical and economic evidence is needed to inform decisions about its acquisition and use in emergency rooms and other in-hospital settings, as well as in rural health care centres and remote settings
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