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      Accuracy of advanced versus strictly conventional 12-lead ECG for detection and screening of coronary artery disease, left ventricular hypertrophy and left ventricular systolic dysfunction

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          Abstract

          Background

          Resting conventional 12-lead ECG has low sensitivity for detection of coronary artery disease (CAD) and left ventricular hypertrophy (LVH) and low positive predictive value (PPV) for prediction of left ventricular systolic dysfunction (LVSD). We hypothesized that a ~5-min resting 12-lead advanced ECG test ("A-ECG") that combined results from both the advanced and conventional ECG could more accurately screen for these conditions than strictly conventional ECG.

          Methods

          Results from nearly every conventional and advanced resting ECG parameter known from the literature to have diagnostic or predictive value were first retrospectively evaluated in 418 healthy controls and 290 patients with imaging-proven CAD, LVH and/or LVSD. Each ECG parameter was examined for potential inclusion within multi-parameter A-ECG scores derived from multivariate regression models that were designed to optimally screen for disease in general or LVSD in particular. The performance of the best retrospectively-validated A-ECG scores was then compared against that of optimized pooled criteria from the strictly conventional ECG in a test set of 315 additional individuals.

          Results

          Compared to optimized pooled criteria from the strictly conventional ECG, a 7-parameter A-ECG score validated in the training set increased the sensitivity of resting ECG for identifying disease in the test set from 78% (72-84%) to 92% (88-96%) (P < 0.0001) while also increasing specificity from 85% (77-91%) to 94% (88-98%) (P < 0.05). In diseased patients, another 5-parameter A-ECG score increased the PPV of ECG for LVSD from 53% (41-65%) to 92% (78-98%) (P < 0.0001) without compromising related negative predictive value.

          Conclusion

          Resting 12-lead A-ECG scoring is more accurate than strictly conventional ECG in screening for CAD, LVH and LVSD.

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          Most cited references38

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          Statistical pattern recognition: a review

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            ACC/AHA 2002 guideline update for exercise testing: summary article. A report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Committee to Update the 1997 Exercise Testing Guidelines).

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              Coronary microvascular dysfunction is highly prevalent in women with chest pain in the absence of coronary artery disease: results from the NHLBI WISE study.

              Chest pain in the absence of obstructive coronary artery disease (CAD) is common in women; it is frequently associated with debilitating symptoms and repeated evaluations and may be caused by coronary microvascular dysfunction. However, the prevalence and determinants of microvascular dysfunction in these women are uncertain. We measured coronary flow velocity reserve (coronary velocity response to intracoronary adenosine) to evaluate the coronary microvasculature and risk factors for atherosclerosis in 159 women (mean age, 52.9 years) with chest pain and no obstructive CAD. All women were referred for coronary angiography to evaluate their chest pain as part of the Women's Ischemia Syndrome Evaluation (WISE) study. Seventy-four (47%) women had subnormal (<2.5) coronary flow velocity reserve suggestive of microvascular dysfunction (mean, 2.02 +/- 0.38); 85 (53%) had normal reserve (mean, 3.13 +/- 0.64). Demographic characteristics, blood pressure, ventricular function, lipid levels, and reproductive hormone levels were not significantly different between women with normal and those with abnormal microvascular function. Postmenopausal hormone use within 3 months was significantly less prevalent among those with microvascular dysfunction (40% vs 60%, P =.032). Age and number of years past menopause correlated with flow velocity reserve (r = -0.18, P =.02, and r = -0.30, P <.001, respectively). No significant associations were identified between flow velocity reserve and lipid and hormone levels, blood pressure, and left ventricular ejection fraction. Coronary microvascular dysfunction is present in approximately one half of women with chest pain in the absence of obstructive CAD and cannot be predicted by risk factors for atherosclerosis and hormone levels. Therefore, the diagnosis of coronary microvascular dysfunction should be considered in women with chest pain not attributable to obstructive CAD.
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                Author and article information

                Journal
                BMC Cardiovasc Disord
                BMC Cardiovascular Disorders
                BioMed Central
                1471-2261
                2010
                16 June 2010
                : 10
                : 28
                Affiliations
                [1 ]Human Adaptation and Countermeasures Division, NASA Johnson Space Center, Houston, TX, USA
                [2 ]Department of Electrical Engineering, Arkansas Tech University, Russellville, AR, USA
                [3 ]Department of Engineering, Colorado State University, Pueblo, CO, USA
                [4 ]Institute of Physiology, School of Medicine, University of Ljubljana, Ljubljana, Slovenia
                [5 ]Division of Cardiovascular Medicine, University of Texas Health Science Center, Houston, TX, USA
                [6 ]Biostatistics, School of Nursing, Johns Hopkins University, Baltimore, MD, USA
                [7 ]Division of Cardiology, University of Texas Health Science Center, San Antonio, TX, USA
                [8 ]Heart and Lung Treatment and Transplant Center, Texas Heart Institute, Houston, TX, USA
                [9 ]Cardiac Catheterization Laboratory, Thomas Memorial Hospital, Charleston, WV, USA
                [10 ]Instituto de Investigaciones Cardiovasculares, Universidad de los Andes, Mérida, Venezuela
                [11 ]Grupo de Ingenieria Biomedica, Universidad de Los Andes, Mérida, Venezuela
                [12 ]Department of Clinical Physiology, Lund University Hospital, Lund, Sweden
                Article
                1471-2261-10-28
                10.1186/1471-2261-10-28
                2894002
                20565702
                9dde8f8e-b9e8-48d8-a123-b6f4180f6ad4
                Copyright ©2010 Schlegel et al; licensee BioMed Central Ltd.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 8 December 2009
                : 16 June 2010
                Categories
                Research article

                Cardiovascular Medicine
                Cardiovascular Medicine

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