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      Can left ventricular function parameters be determined within half of the time with MRI?

      editorial
      The International Journal of Cardiovascular Imaging
      Springer Netherlands

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          Abstract

          Accurate determination of left ventricular mass and left ventricular systolic volume and function is important for assessment of prognosis and therapeutic options in patients with hypertensive heart disease, coronary heart disease and congestive heart failure [1, 2]. In patients with hypertension, left ventricular hypertrophy increases the relative risk of mortality by twofold in those patients who also have coronary artery disease and by fourfold in those patients with normal coronary arteries [3]. Because of the low cost, M-mode echocardiography is the most widely used method to determine left ventricular mass [4]. However, there is considerable variability for repeated measurements. Two-dimensional and 3-dimensional echocardiography is more used for determination of left ventricular volumes and left ventricular ejection fraction, with an excellent intra-observer variability but worse inter-observer variability [5]. Additionally, not in all patients high quality images can be obtained, which permit precise assessment of left ventricular volumes and function. Because of its high spatial and temporal resolution, MRI is the best technique for assessment of right and left ventricular function. For determination of left ventricular function one can either use the Simpson’s rule or the area-length method. With the Simpson’s rule left ventricular volumes are calculated by summing the endocardial area within multiple short axis slices from base to apex of the heart and multiplying each area by the slice thickness [6]. Left ventricular volumes and left ventricular mass using this technique have been validated with cast measurements and cadaver studies and show an excellent correlation. Intra- and inter-observer variability of the measurements of left ventricular volume, ejection fraction and left ventricular mass are very low [7, 8]. Because of this high reproducibility, in clinical trials, only limited number of patients are needed to detect a change of left ventricular volume, ejection fraction or left ventricular mass. Studies, that use MR, require sample sizes that are 80–90% smaller than other imaging methods [9]. For calculation left ventricular mass endocardial and epicardial contours have to be drawn from base to apex and multiplied by slice thickness [10]. Manually, tracing of all contours is cumbersome and time consuming. Also with automated contour detection using commercially available software correct analysis remains time consuming. In this issue of the International Journal of Cardiac Imaging, Lubbers et al. demonstrate, that by tracing every second slice decreases accuracy for left ventricular ejection fraction with only 1.7% and for left ventricular mass with 4.1%. For left ventricular volume one has to be aware, however that tracing half of the slices gives half the accuracy compared to true volume. In clinical studies, this could imply the need of more patients for comparison. For normal patient care the method suggested by Lubbers satisfies completely and could become the standard procedure for measurement of left ventricular mass, volume and function. However, in clinical studies one can better rely on the better accuracy of tracing all slices.

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          Most cited references6

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          Left ventricular measurements with cine and spin-echo MR imaging: a study of reproducibility with variance component analysis.

          The authors studied the reproducibility of repeated measurements of left ventricular volumes, weight, and wall stress as determined with cine and spin-echo magnetic resonance (MR) imaging. Two observers analyzed 40 serial MR imaging examinations twice, yielding a total of 160 repeated measurements. Estimates of 95% ranges for change were ejection fraction, 10% and 12%; wall mass, 16% and 21%; and wall stress, 22% and 20%, for measurements derived from cine MR imaging and spin-echo MR imaging, respectively. Reproducibility was not significantly different between cine and spin-echo MR imaging. Intraobserver, interobserver, and interexamination errors were quantitated with variance component analysis. Interexamination variability was the single most important contributor to total variance. Reproducibility of left ventricular chamber volume measurements with MR imaging is superior to that of other imaging modalities. In addition, MR imaging can provide reliable estimates of wall mass and wall stress. Efforts to improve reproducibility should be aimed at lowering interexamination variability.
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            Dimensional accuracy of magnetic resonance in studies of the heart.

            Magnetic resonance (MR) can provide high-resolution tomographic images of the heart at any part of the cardiac cycle. Tests on static and dynamic phantoms showed that the technique can give accurate measurements of ventricular wall thickness, cavity volume, and stroke volume. In 20 patients with angina pectoris, electrocardiographically gated MR images of the left ventricle were compared with X-ray contrast ventriculograms. There was good correlation with the anteroposterior ventriculogram, but poorer correlation in the lateral projection because of difficulty in locating the aortic valve precisely on the ventriculogram. In 20 normal subjects, left and right ventricular volumes at end-diastole and end-systole were measured by summing the areas of the cavities in multiple contiguous sections. Stroke volumes and ejection fractions were thus calculated, and the ratio of left to right ventricular stroke volume was very close to the theoretical value of 1, in all cases. In any individual volume measurement, the error was approximately 2%. MR therefore provides an accurate non-invasive method of studying cardiac dimensions and function.
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              Diversity of patterns of hypertrophy in patients with systemic hypertension and marked left ventricular wall thickening.

              In selected patients with systemic hypertension it may be difficult to ascertain whether left ventricular (LV) hypertrophy is a secondary end-organ consequence of long-term elevations in blood pressure or, alternatively, a manifestation of a coexistent primary hypertrophic cardiomyopathy. To address this issue and better characterize LV hypertrophy in systemic hypertension, 2-dimensional echocardiography was used to define the patterns of LV hypertrophy in 102 patients with sustained systemic hypertension and marked degrees of wall thickening. Patients ranged in age from 31 to 88 years (mean 61) and were predominantly female (58%); all were black. By selection, each patient had a maximal LV wall thickness of greater than 15 mm (range 16 to 29). Distribution of hypertrophy was judged to be symmetric (i.e., concentric) in most patients (67 of 102, 66%). However, a substantial proportion (35 patients, 34%) demonstrated nonuniform, asymmetric patterns of hypertrophy in which at least 1 segment of the LV wall was at least 1.5 times the thickness of any other. In these 35 patients, the distribution of hypertrophy was similar to that characteristic of the morphologic spectrum of hypertrophic cardiomyopathy, with thickening of portions of both the ventricular septum and free wall in 16 patients, anterior and posterior ventricular septum alone in 11 patients and segmental involvement of only the anterior ventricular septum in 8. Patients with asymmetric patterns of wall thickening did not differ from the patients with symmetric hypertrophy with regard to age, sex or clinical findings. Asymmetric LV hypertrophy appears to represent an important feature of the morphologic spectrum of severe hypertensive heart disease.(ABSTRACT TRUNCATED AT 250 WORDS)
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                Author and article information

                Contributors
                lbr01@atriummc.nl
                Journal
                Int J Cardiovasc Imaging
                The International Journal of Cardiovascular Imaging
                Springer Netherlands (Dordrecht )
                1569-5794
                1875-8312
                25 July 2007
                February 2008
                : 24
                : 2
                : 193-194
                Affiliations
                Department of Cardiology, Atrium Medical Centre Parkstad, Henri Dunantstreet 5, 6401 CX Heerlen, The Netherlands
                Article
                9250
                10.1007/s10554-007-9250-8
                2198937
                17653612
                89832ec6-c483-438b-9ebd-870f7b969770
                © Springer Science+Business Media B.V. 2007
                History
                : 30 June 2007
                : 4 July 2007
                Categories
                Editorial Comment
                Custom metadata
                © Springer Science+Business Media B.V. 2008

                Cardiovascular Medicine
                Cardiovascular Medicine

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