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      Rationale and design of the Clinical Evaluation of Magnetic Resonance Imaging in Coronary heart disease 2 trial (CE-MARC 2): A prospective, multicenter, randomized trial of diagnostic strategies in suspected coronary heart disease

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      , BSc, MBChB a , , MSc b , , MSc b , , MA a , , MSc, MA c , , PhD c , , MBChB, MD d , , MBChB, PhD e , , MD, PhD a , , MBChB, PhD a , *
      American Heart Journal
      Mosby

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          Abstract

          Background

          A number of investigative strategies exist for the diagnosis of coronary heart disease (CHD). Despite the widespread availability of noninvasive imaging, invasive angiography is commonly used early in the diagnostic pathway. Consequently, approximately 60% of angiograms reveal no evidence of obstructive coronary disease. Reducing unnecessary angiography has potential financial savings and avoids exposing the patient to unnecessary risk. There are no large-scale comparative effectiveness trials of the different diagnostic strategies recommended in international guidelines and none that have evaluated the safety and efficacy of cardiovascular magnetic resonance.

          Trial Design

          CE-MARC 2 is a prospective, multicenter, 3-arm parallel group, randomized controlled trial of patients with suspected CHD (pretest likelihood 10%-90%) requiring further investigation. A total of 1,200 patients will be randomized on a 2:2:1 basis to receive 3.0-T cardiovascular magnetic resonance–guided care, single-photon emission computed tomography–guided care (according to American College of Cardiology/American Heart Association appropriate-use criteria), or National Institute for Health and Care Excellence guidelines–based management. The primary (efficacy) end point is the occurrence of unnecessary angiography as defined by a normal (>0.8) invasive fractional flow reserve. Safety of each strategy will be assessed by 3-year major adverse cardiovascular event rates. Cost-effectiveness and health-related quality-of-life measures will be performed.

          Conclusions

          The CE-MARC 2 trial will provide comparative efficacy and safety evidence for 3 different strategies of investigating patients with suspected CHD, with the intension of reducing unnecessary invasive angiography rates. Evaluation of these management strategies has the potential to improve patient care, health-related quality of life, and the cost-effectiveness of CHD investigation.

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          Most cited references19

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          Single photon-emission computed tomography.

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            Third universal definition of myocardial infarction.

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              A simple approximation for calculating sample sizes for comparing independent proportions.

              A simple approximation is provided to the formula for the sample sizes needed to detect a difference between two binomial probabilities with specified significance level and power. The formula for equal sample sizes was derived by Casagrande, Pike and Smith (1978, Biometrics 34 , 483-486) and can be easily generalized to the case of unequal sample sizes. It is shown that over fairly wide ranges of parameter values and ratios of sample sizes, the percentage error which results from using the approximation is no greater than 1%. The approximation is especially useful for the inverse problem of estimating power when the sample sizes are given.
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                Author and article information

                Contributors
                Journal
                Am Heart J
                Am. Heart J
                American Heart Journal
                Mosby
                0002-8703
                1097-6744
                1 January 2015
                January 2015
                : 169
                : 1
                : 17-24.e1
                Affiliations
                [a ]Multidisciplinary Cardiovascular Research Centre (MCRC) & Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK
                [b ]Leeds Institute of Clinical Trials Research, University of Leeds, Leeds, UK
                [c ]Centre for Health Economics, University of York, York, UK
                [d ]Department of Cardiovascular Sciences, University of Leicester, and the National Institute of Health Research Leicester Cardiovascular Biomedical Research Unit, Leicester, UK
                [e ]BHF Glasgow Cardiovascular Research Centre, Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK
                Author notes
                [* ]Reprint requests: John P. Greenwood, MBChB, PhD, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, LS2 9JT, UK. j.greenwood@ 123456leeds.ac.uk
                Article
                S0002-8703(14)00614-0
                10.1016/j.ahj.2014.10.008
                4277294
                25497243
                1f9bcc52-4fc8-4859-8e71-ed5b9bad2741
                © 2014 The Authors

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/).

                History
                : 26 April 2014
                : 10 October 2014
                Categories
                Trial Design

                Cardiovascular Medicine
                Cardiovascular Medicine

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