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<title>European Journal of Echocardiography - current issue</title>
<link>http://ejechocard.oxfordjournals.org</link>
<description>European Journal of Echocardiography - RSS feed of current issue</description>
<prism:eIssn>1532-2114</prism:eIssn>
<prism:coverDisplayDate>May 2008</prism:coverDisplayDate>
<prism:publicationName>European Journal of Echocardiography</prism:publicationName>
<prism:issn>1525-2167</prism:issn>
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<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/317?rss=1">
<title><![CDATA[Multidisciplinary approach in a case of successful surgical treatment of a voluminous intracardiac fungal mass in an infant]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/317?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Troise, D. E., Guarnieri, G. F., Laforgia, N., Tagliente, M. R., Pirolo, T., Arciprete, P., de Luca Tupputi Schinosa, L.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1093/ejechocard/jen119</dc:identifier>
<dc:title><![CDATA[Multidisciplinary approach in a case of successful surgical treatment of a voluminous intracardiac fungal mass in an infant]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>318</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>317</prism:startingPage>
<prism:section>LETTERS TO THE EDITOR</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/319?rss=1">
<title><![CDATA[Echocardiographic selection of candidates for cardiac resynchronization therapy: the lack of evidence!]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/319?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Soliman, O. I.I., Geleijnse, M. L., ten Cate, F. J.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1093/ejechocard/jen010</dc:identifier>
<dc:title><![CDATA[Echocardiographic selection of candidates for cardiac resynchronization therapy: the lack of evidence!]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>320</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>319</prism:startingPage>
<prism:section>LETTERS TO THE EDITOR</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/319-a?rss=1">
<title><![CDATA[Multidisciplinary approach in a case of successful surgical treatment of a voluminous intracardiac fungal mass in an infant: reply]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/319-a?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Correale, M., Ieva, R., Rinaldi, M., Rinaldi, G., Di Biase, M.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1093/ejechocard/jen118</dc:identifier>
<dc:title><![CDATA[Multidisciplinary approach in a case of successful surgical treatment of a voluminous intracardiac fungal mass in an infant: reply]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>319</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>319</prism:startingPage>
<prism:section>LETTERS TO THE EDITOR</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/320?rss=1">
<title><![CDATA[Echocardiographic selection of candidates for cardiac resynchronization therapy: the lack of evidence! Reply]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/320?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Vitarelli, A.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1093/ejechocard/jen021</dc:identifier>
<dc:title><![CDATA[Echocardiographic selection of candidates for cardiac resynchronization therapy: the lack of evidence! Reply]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>321</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>320</prism:startingPage>
<prism:section>LETTERS TO THE EDITOR</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/321?rss=1">
<title><![CDATA[Determination of stenotic mitral valve area: new, old, and gold standards]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/321?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Flachskampf, F. A., Klinghammer, L.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1093/ejechocard/jen037</dc:identifier>
<dc:title><![CDATA[Determination of stenotic mitral valve area: new, old, and gold standards]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>321</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>321</prism:startingPage>
<prism:section>LETTERS TO THE EDITOR</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/321-a?rss=1">
<title><![CDATA[Reply to the letter to the editor by F. A. Flachskampf et al. Determination of stenotic mitral valve area: new, old, and gold standards]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/321-a?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[de Isla, L. P.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1093/ejechocard/jen038</dc:identifier>
<dc:title><![CDATA[Reply to the letter to the editor by F. A. Flachskampf et al. Determination of stenotic mitral valve area: new, old, and gold standards]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>322</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>321</prism:startingPage>
<prism:section>LETTERS TO THE EDITOR</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/323?rss=1">
<title><![CDATA[A Statement on Ethics From the HEART Group]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/323?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1093/ejechocard/jen139</dc:identifier>
<dc:title><![CDATA[A Statement on Ethics From the HEART Group]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>325</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>323</prism:startingPage>
<prism:section>HEART GROUP STATEMENT</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/326?rss=1">
<title><![CDATA[Doppler myocardial imaging in the diagnosis of early systolic left ventricular dysfunction in diabetic rats]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/326?rss=1</link>
<description><![CDATA[
<sec><st>Aim</st>
<p>To find out if Doppler myocardial imaging (DMI) can detect early signs of left ventricular (LV) dysfunction in a rat model of diabetic cardiomyopathy.</p>
</sec>
<sec><st>Methods</st>
<p>Eight control and 12 Streptozotocin (STZ)-induced diabetic rats underwent transthoracic echocardiography with high-resolution technology at baseline and 2, 4, 8, 12, and 16 weeks after STZ injection. Radial function was analysed using conventional M-mode, and velocity, strain and strain rate imaging. Longitudinal function was analysed using pulsed Doppler imaging of the mitral annulus.</p>
</sec>
<sec><st>Results</st>
<p>In the diabetic rats, a significant increase in LV end diastolic and end systolic diameter was measured when compared with controls (<I>P</I> &lt; 0.001). Fractional shortening and LV ejection fraction remained unchanged in both groups. Using DMI, diabetic rats demonstrated a decrease in radial systolic velocity (rate of change: +0.01 vs. &ndash;0.003 week<sup>&ndash;1</sup>; <I>P</I> &lt; 0.01) and radial systolic strain rate (+0.003 vs. &ndash;0.205 week<sup>&ndash;1</sup>; <I>P</I> = 0.08) of the anteroseptal wall. Histologic examination revealed dilated cardiomyopathy with no signs of fibrosis.</p>
</sec>
<sec><st>Conclusion</st>
<p>Although LV ejection fraction remained preserved, velocity and strain rate imaging was able to detect radial systolic dysfunction in diabetic rats. The absence of histological signs of fibrosis suggests that other mechanisms play a role in the development of diabetic cardiomyopathy.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Weytjens, C., Franken, P. R., D'hooge, J., Droogmans, S., Cosyns, B., Lahoutte, T., Van Camp, G.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1093/ejechocard/jen123</dc:identifier>
<dc:title><![CDATA[Doppler myocardial imaging in the diagnosis of early systolic left ventricular dysfunction in diabetic rats]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>333</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>326</prism:startingPage>
<prism:section>EXPERIMENTAL PAPERS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/334?rss=1">
<title><![CDATA[Measurement of cardiac output by real-time 3D echocardiography in patients undergoing assessment for cardiac transplantation]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/334?rss=1</link>
<description><![CDATA[
<sec><st>Aims</st>
<p>Heart transplant assessment includes cardiac output calculation by right heart catheterisation. Real-time 3D echocardiography (RT-3DE), unlike 2D echocardiography, can measure stroke volume without inaccurate geometrical assumptions. The purpose of this study was to assess the feasibility and accuracy of non-invasive RT-3DE cardiac output calculation.</p>
</sec>
<sec><st>Methods and results</st>
<p>Forty consecutive patients referred for transplant assessment underwent transthoracic RT-3DE. Full volume 3DE data sets were acquired from apical views with the iE33 ultrasound system (Philips Ultrasound, Bothell, USA). Four patients were excluded due to poor image quality. The remaining 36 patients had end-diastolic (LVEDV) and end-systolic (LVESV) left ventricular volumes manually traced, using endocardial detection software. Cardiac output was subsequently calculated: [(LVEDV &ndash; LVESV) <FONT FACE="arial,helvetica">x</FONT> heart rate]. Thermodilution derived cardiac outputs, under the same haemodynamic conditions, were used as reference for comparison. There was close correlation between RT-3DE and catheter derived cardiac outputs (<I>r</I> = 0.91, <I>y</I> = 0.86x + 0.45, SEE 0.39 L/min, mean difference from reference &ndash;0.06 L/min, SD 0.40 L/min). RT-3DE data analysis took 3 min per case.</p>
</sec>
<sec><st>Conclusion</st>
<p>This study shows RT-3DE is an accurate method for calculating cardiac output. In patients requiring serial evaluation of cardiac function, this non-invasive test may be preferable to invasive right heart catheterisation.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Hoole, S. P., Boyd, J., Ninios, V., Parameshwar, J., Rusk, R. A.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1016/j.euje.2007.03.033</dc:identifier>
<dc:title><![CDATA[Measurement of cardiac output by real-time 3D echocardiography in patients undergoing assessment for cardiac transplantation]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>337</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>334</prism:startingPage>
<prism:section>CLINICAL/ORIGINAL PAPERS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/338?rss=1">
<title><![CDATA[Determinants of an abnormal response to exercise in patients with asymptomatic valvular aortic stenosis]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/338?rss=1</link>
<description><![CDATA[
<sec><st>Aim</st>
<p>Patients with asymptomatic aortic stenosis (AS) and abnormal haemodynamic responses to exercise testing are at increased risk of cardiac events. This study assesses the Doppler echocardiographic determinants of a positive exercise test in a cohort of asymptomatic patients with AS.</p>
</sec>
<sec><st>Methods and results</st>
<p>One hundred and twenty-eight patients with AS underwent quantitative Doppler echocardiographic measurements at rest and during exercise test. Of these patients, 60 had an abnormal response to exercise. Two independent determinants of an abnormal exercise response were selected in multivariate analysis: a larger increase in mean transaortic pressure gradient (<I>P</I> = 0.00014) and a limited contractile reserve&mdash;latent left ventricular dysfunction&mdash;as indicated by smaller changes in ejection fraction (<I>P</I> = 0.0002). Limiting symptoms were associated with greater increase in mean transaortic pressure gradient, smaller changes in systolic blood pressure and a lower ejection fraction at peak exercise. The increase in pressure gradient was associated with smaller exercise-induced changes in aortic valve area and in ejection fraction and new or worsening mitral regurgitation during exercise.</p>
</sec>
<sec><st>Conclusion</st>
<p>Abnormal responses to exercise in asymptomatic AS patients are mediated by a larger increase in mean transaortic pressure gradient and/or a limited contractile reserve characterized by an inadequate increase in ejection fraction at exercise.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Lancellotti, P., Karsera, D., Tumminello, G., Lebois, F., Pierard, L. A.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1016/j.euje.2007.04.005</dc:identifier>
<dc:title><![CDATA[Determinants of an abnormal response to exercise in patients with asymptomatic valvular aortic stenosis]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>343</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>338</prism:startingPage>
<prism:section>CLINICAL/ORIGINAL PAPERS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/344?rss=1">
<title><![CDATA[Myocardial contraction properties along the long and short axes of the left ventricle in isolated left ventricular non-compaction: pulsed tissue Doppler echocardiography]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/344?rss=1</link>
<description><![CDATA[
<sec><st>Aim</st>
<p>Our objective was to evaluate regional systolic myocardial contraction properties along the long and short axes of the left ventricle (LV) in patients with isolated LV non-compaction (IVNC).</p>
</sec>
<sec><st>Methods and results</st>
<p>Pulsed tissue Doppler imaging (TDI) was used to record myocardial velocities along these axes in 25 patients with IVNC (10 asymptomatic&ndash;LV ejection fraction [LVEF] &ge; 50%; 15 symptomatic&ndash;LVEF &lt; 50%) and 15 healthy controls. In all cases, the systolic velocity pattern featured 2 distinct peaks (SW1, SW2). These peak velocities and the intervals from the electrocardiographic Q wave to each peak (Q-SW1, Q-SW2) were recorded for each axis, and group means were calculated. The asymptomatic group displayed significantly higher long axis SW2 and significantly longer long axis Q-SW1 than the controls. The symptomatic group had significantly lower SW1 and SW2 on both axes and significantly longer short axis Q-SW1 than the asymptomatic group and the controls. Long axis Q-SW1 and short axis Q-SW1 in the symptomatic group were significantly longer than the corresponding control findings, but were not significantly different from the corresponding asymptomatic group findings.</p>
</sec>
<sec><st>Conclusion</st>
<p>In conclusion, patients with IVNC exhibit distinct systolic myocardial shortening velocities along the long and short axes of the LV. Further, these pulsed TDI findings suggest that asymptomatic patients (those with normal LVEF) have subclinical myocardial dysfunction.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Tufekcioglu, O., Aras, D., Yildiz, A., Topaloglu, S., Maden, O.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1016/j.euje.2007.05.001</dc:identifier>
<dc:title><![CDATA[Myocardial contraction properties along the long and short axes of the left ventricle in isolated left ventricular non-compaction: pulsed tissue Doppler echocardiography]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>350</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>344</prism:startingPage>
<prism:section>CLINICAL/ORIGINAL PAPERS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/351?rss=1">
<title><![CDATA[Three methods for evaluation of left atrial volume]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/351?rss=1</link>
<description><![CDATA[
<sec><st>Aim</st>
<p>To compare and contrast 3 different echocardiographic methods used to measure left atrial (LA) volume: biplane area length (AL), biplane modified Simpson (SIMP), and prolate ellipse (PE) methods.</p>
</sec>
<sec><st>Methods and results</st>
<p>A review of consecutive patients who presented to our outpatient echocardiography laboratory for a resting transthoracic study between April 2006 and May 2006 was performed. Echocardiograms were reexamined and LA volume measured using the AL, SIMP, and PE methods. Of 102 consecutive patients evaluated, 97 had a measure of LA volume using all 3 methods. A significant difference in the measurement of mean &plusmn; SD LA volume was noted among the 3 different methods: 37 &plusmn; 16 mL/m<sup>2</sup> for AL, 34 &plusmn; 14 mL/m<sup>2</sup> for SIMP, and 27 &plusmn; 12 mL/m<sup>2</sup> for PE. The PE method yielded routinely smaller values compared with either the AL or SIMP method (<I>P</I> &lt; 0.001). Differences increased with increased LA volume. The SIMP method derived consistently smaller (&lt;5 mL/m<sup>2</sup>) values than those of the AL method, consistent across the full range of LA volumes.</p>
</sec>
<sec><st>Conclusion</st>
<p>Significant differences exist among these 3 commonly used methods for measuring LA volume. Standardization of the measurement of LA volume is recommended.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Jiamsripong, P., Honda, T., Reuss, C. S., Hurst, R. T., Chaliki, H. P., Grill, D. E., Schneck, S. L., Tyler, R., Khandheria, B. K., Lester, S. J.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1016/j.euje.2007.05.004</dc:identifier>
<dc:title><![CDATA[Three methods for evaluation of left atrial volume]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>355</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>351</prism:startingPage>
<prism:section>CLINICAL/ORIGINAL PAPERS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/356?rss=1">
<title><![CDATA[The left atrial function index: a rhythm independent marker of atrial function]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/356?rss=1</link>
<description><![CDATA[
<sec><st>Aims</st>
<p>This study evaluates a simple echocardiographic rhythm independent expression of left atrial (LA) function, &lsquo;the left atrial function index&rsquo; (LAFI).</p>
</sec>
<sec><st>Background</st>
<p>Quantitation of LA function is challenging and often established parameters including peak A are limited to sinus rhythm (SR). We hypothesized that atrial function could be characterized independent of rhythm by combining analogues of LA volume, reservoir function and LV stroke volume.</p>
</sec>
<sec><st>Methods</st>
<p>Seventy-two patients with chronic atrial fibrillation (CAF) were followed for six months post cardioversion (CV). Thirty-seven age matched healthy subjects were controls. The LAFI = LAEF <FONT FACE="arial,helvetica">x</FONT> LVOT-VTI/LAESVI (LAEF = LA emptying fraction, LAESVI = maximal LA volume indexed to BSA, LVOT-VTI = outflow tract velocity time integral).</p>
</sec>
<sec><st>Results</st>
<p>The LAFI pre-CV in the CAF group was depressed vs controls (0.10 &plusmn; 0.05 vs 0.54 &plusmn; 0.17; <I>P</I> = 0.0001). Post-CV, LAFI was lower in persistent AF than in those restored to SR (AF vs SR: 0.08 &plusmn; 0.03 vs 0.15 &plusmn; 0.08; <I>P</I> = 0.0001), improved progressively in SR and was unchanged when AF persisted.</p>
</sec>
<sec><st>Conclusion</st>
<p>The LAFI, a simple, rhythm independent expression of atrial function, appears sensitive to differences between individuals in AF and those restored to SR and justifies clinical and investigative applications.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Thomas, L., Hoy, M., Byth, K., Schiller, N. B.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1016/j.euje.2007.06.002</dc:identifier>
<dc:title><![CDATA[The left atrial function index: a rhythm independent marker of atrial function]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>362</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>356</prism:startingPage>
<prism:section>CLINICAL/ORIGINAL PAPERS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/363?rss=1">
<title><![CDATA[Transthoracic Doppler echocardiography assessment of left anterior descending artery flow in patients with previous anterior myocardial infarction]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/363?rss=1</link>
<description><![CDATA[
<sec><st>Aim</st>
<p>We tested the hypothesis that shortening of diastolic pressure half time (PHT) of left anterior descending (LAD) coronary flow in patients with old reperfused anterior myocardial infarction (MI) is related to the presence of permanent myocardial damage of the reperfused area.</p>
</sec>
<sec><st>Methods and results</st>
<p>We studied 49 patients divided into: group A: 15 patients with previous anterior MI and evidence of myocardial scar; group B: 10 patients with previous anterior MI and no evidence of myocardial scar and group C: 24 patients without anterior MI. All patients underwent coronary angiography at least 6 months after an index event and any reperfusion procedure. Group A patients had lower PHT (199 &plusmn; 62 ms) than group C (377 &plusmn; 103 ms, <I>p</I> = 0.0001) and group B (316 &plusmn; 154 ms, <I>p</I> = 0.029) patients. No other LAD flow velocity parameter differed among the 3 groups. A PHT value of 265 ms discriminated patients with scarred anteriorwallwith a sensitivity of 79% and a specificity of 94% (0.88, <I>p</I> &lt; 0.001).</p>
</sec>
<sec><st>Conclusion</st>
<p>Shortening of the LAD flow diastolic PHT in patients with remote, reperfused anterior MI reflects scarred myocardial tissue in the anteroapical wall while patients who maintain diastolic wall thickness after an acute coronary syndrome have PHT similar to patients without anterior MI.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Karatasakis, G., Leontiadis, E., Papadakis, E., Koutsogiannis, N., Athanassopoulos, G., Spargias, K., Poldermans, D., Karagiannis, S. E., Cokkinos, D. V.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1016/j.euje.2007.06.001</dc:identifier>
<dc:title><![CDATA[Transthoracic Doppler echocardiography assessment of left anterior descending artery flow in patients with previous anterior myocardial infarction]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>367</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>363</prism:startingPage>
<prism:section>CLINICAL/ORIGINAL PAPERS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/368?rss=1">
<title><![CDATA[Tissue Doppler echocardiography reliably reflects severity of iron overload in pediatric patients with {beta} thalassemia]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/368?rss=1</link>
<description><![CDATA[
<sec><st>Aims</st>
<p>Tissue Doppler imaging has been recently used to evaluate ventricular function in patients with &beta; thalassemia. In clinical practice, serum ferritin is commonly used to assess the severity of iron overload. The aim of this study was to determine which Doppler findings correlated with serum ferritin.</p>
</sec>
<sec><st>Methods and results</st>
<p>Thirty-one pediatric patients with transfusion-dependent &beta; thalassemia with normal LVFS were evaluated. Seven patients with serum ferritin &lt;2500 ng/ mL, 13 patients with serum ferritin 2500&ndash;5000 ng/mL, and 11 patients with serum ferritin &gt;5000 ng/mL were studied. Diastolic dysfunction was absent in all patients with serum ferritin &lt;2500 ng/mL, and was present in all patients with serum ferritin &gt;5000 ng/mL. Deceleration time (DT) has a significant correlation with serum ferritin (<I>r</I> = &ndash;0.59, <I>p</I> &lt; 0.0001). Difference of pulmonary vein atrial reversal flow and mitral valve A wave duration (PVAR &ndash; MVA) and early ventricular filling velocity to early diastolic myocardial velocity ratio (<I>E</I>/<I>E</I>m) significantly correlated with serum ferritin (<I>r</I> = 0.49, <I>p</I> = 0.006; <I>r</I> = 0.56, <I>p</I> = 0.001, respectively).</p>
</sec>
<sec><st>Conclusion</st>
<p>Decreased DT, increased PVAR-MVA duration, and increased <I>E</I>/<I>E</I>m ratio reliably reflected severe iron overload in pediatric patients with &beta; thalassemia. Systolic and diastolic LV function is preserved in patients who have serum ferritin &lt;2500 ng/mL.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Silvilairat, S., Sittiwangkul, R., Pongprot, Y., Charoenkwan, P., Phornphutkul, C.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1016/j.euje.2007.06.003</dc:identifier>
<dc:title><![CDATA[Tissue Doppler echocardiography reliably reflects severity of iron overload in pediatric patients with {beta} thalassemia]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>372</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>368</prism:startingPage>
<prism:section>CLINICAL/ORIGINAL PAPERS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/373?rss=1">
<title><![CDATA[An intensive interactive course for 3D echocardiography: is 'crop till you drop' an effective learning strategy?]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/373?rss=1</link>
<description><![CDATA[
<sec><st>Background</st>
<p>Three-dimensional echocardiography (3DE) appears to show incremental benefit over two-dimensional echocardiography (2DE), but it's uptake has been slow. We tested attendees before and after an intensive interactive training course to identify its efficacy.</p>
</sec>
<sec><st>Methods</st>
<p>Attendees (<I>n</I> = 35, 23 cardiologists, 12 sonographers) were shown how to use 3DE review software and asked to identify the pathology of five patients (wall motion abnormality, peri-prosthetic mitral regurgitation, subaortic membrane, small ventricular septal defect, submitral stenosis) on 2D and 3D images. In the following one and a half-day interactive teaching course, brief presentations on application of 3DE for assessment of wall motion, valve and congenital abnormalities were followed by review of 3D datasets, during which the attendees made their own interpretations before being shown the optimal viewing strategy. Test cases were not discussed and the test was repeated at the end of the course.</p>
</sec>
<sec><st>Results</st>
<p>Most attendees (57%) had access but with little or no use of a 3DE system. Three-dimensional echocardiography had no incremental value before training. After training, overall correct responses significantly improved compared with baseline interpretation, although improvement was not the same for all diagnoses. All groups (cardiologists vs. sonographers, inexperienced vs. moderately experienced reviewers) improved similarly.</p>
</sec>
<sec><st>Conclusions</st>
<p>Incorporation of 3DE into standard practice may be limited by inexperience. An interactive teaching course with rehearsal and direct mentoring appears to overcome this limitation and may improve the uptake of this technique.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Jenkins, C., Monaghan, M., Shirali, G., Guraraja, R., Marwick, T. H.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1016/j.euje.2007.06.011</dc:identifier>
<dc:title><![CDATA[An intensive interactive course for 3D echocardiography: is 'crop till you drop' an effective learning strategy?]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>380</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>373</prism:startingPage>
<prism:section>CLINICAL/ORIGINAL PAPERS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/381?rss=1">
<title><![CDATA[Hand carried echocardiography screening for LV systolic dysfunction in a pulmonary function laboratory]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/381?rss=1</link>
<description><![CDATA[
<sec><st>Aims</st>
<p>Dyspnea is a common indication for pulmonary evaluation but also a common symptom in heart failure. Identification of dyspneic patients with significant LV systolic dysfunction is critical because of high morbidity of untreated heart failure. We sought to determine whether screening patients referred for pulmonary function testing (PFT) using a hand carried ultrasound (HCU) device could identify LV systolic dysfunction.</p>
</sec>
<sec><st>Methods</st>
<p>Forty-nine subjects were recruited from a pulmonary function lab to undergo a brief echocardiographic examination by an internist using a HCU device. All subjects also received an examination with a full-featured echocardiogram machine as a gold standard.</p>
</sec>
<sec><st>Results</st>
<p>All subjects with normal PFT had normal LV systolic function. Among subjects with abnormal PFT, 6 (15%) had LV systolic dysfunction and the remainder had normal LV systolic function. No subjects with LV systolic dysfunction by full-featured echocardiograms were missed by the HCU (sensitivity 100%, specificity 95%, negative predictive value 100%, positive predictive value 75%).</p>
</sec>
<sec><st>Conclusions</st>
<p>LV systolic dysfunction is prevalent among patients with pulmonary disease and can be accurately screened for by a physician using a hand carried ultrasound device with subsequent confirmation with complete echocardiography.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Kirkpatrick, J. N., Ghani, S. N., Spencer, K. T.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1016/j.euje.2007.06.013</dc:identifier>
<dc:title><![CDATA[Hand carried echocardiography screening for LV systolic dysfunction in a pulmonary function laboratory]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>383</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>381</prism:startingPage>
<prism:section>CLINICAL/ORIGINAL PAPERS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/384?rss=1">
<title><![CDATA[Subaortic dynamic obstruction: a contributing factor to haemodynamic instability in tako-tsubo syndrome?]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/384?rss=1</link>
<description><![CDATA[
<p>We present a case of transient apical ballooning with haemodynamic instability in a female patient with normal coronaries and a history of poorly controlled systemic arterial hypertension. There was dynamic obstruction of the outflow tract and moderate secondary mitral regurgitation at presentation. These were due to systolic anterior motion of the mitral valve, which normalised gradually with the recovery of left ventricular function, and to a &lsquo;sigmoid&rsquo; septum. Mid-cavity obstruction is potentially an important contributory factor to the haemodynamic instability sometimes encountered in this syndrome.</p>
]]></description>
<dc:creator><![CDATA[Ionescu, A.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1016/j.euje.2006.11.011</dc:identifier>
<dc:title><![CDATA[Subaortic dynamic obstruction: a contributing factor to haemodynamic instability in tako-tsubo syndrome?]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>385</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>384</prism:startingPage>
<prism:section>CASE REPORTS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/386?rss=1">
<title><![CDATA[Endocarditis complicating a congenital quadricuspid aortic valve]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/386?rss=1</link>
<description><![CDATA[
<p>The most common aortic valve congenital abnormality is observed in bicuspid aortic valve. Only a few cases of aortic valve quadricuspidy have been reported in the literature. We report a new case of endocarditis complicating a congenital quadricuspid aortic valve.</p>
]]></description>
<dc:creator><![CDATA[Bauer, F., Litzler, P.-Y., Tabley, A., Cribier, A., Bessou, J.-P.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1016/j.euje.2006.12.001</dc:identifier>
<dc:title><![CDATA[Endocarditis complicating a congenital quadricuspid aortic valve]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>387</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>386</prism:startingPage>
<prism:section>CASE REPORTS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/388?rss=1">
<title><![CDATA[Complete regression of massive cardiac involvement associated with acute T cell leukemia following chemotheraphy]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/388?rss=1</link>
<description><![CDATA[
<p>Adult T cell leukemia/lymphomas are aggressive disorders, which infiltrate not only the bone marrow but extensively the visceral organs as well. A case with left ventricular systolic dysfunction with myocardial infiltration and massive pericardial effusion which was demonstrated with echocardiography is discussed. The patient responded well to pericardial drainage and subsequent chemotherapy. The dramatic improvement in echocardiographic findings after chemotherapy gave a clue to investigate suspected patients with aggressive leukemia and lymphomas for exclusion of leukemic infiltration of myocardium.</p>
]]></description>
<dc:creator><![CDATA[Arat, N., Bakanay, S. M., Yildiz, E., Tufekcioglu, O., Golbasi, Z.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1016/j.euje.2006.12.006</dc:identifier>
<dc:title><![CDATA[Complete regression of massive cardiac involvement associated with acute T cell leukemia following chemotheraphy]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>390</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>388</prism:startingPage>
<prism:section>CASE REPORTS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/391?rss=1">
<title><![CDATA[Multiple cardiac metastases from a malignant melanoma]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/391?rss=1</link>
<description><![CDATA[
<p>Metastatic tumors in the pericardium or the heart are more common than primary tumors and their incidence has increased during the last decades due to the prolonged survival of patients with cancer and the increased prevalence of the disease in the general population. We present the case of a 36-year-old patient admitted to our hospital due to fatigue, dyspnea, and episodes of dizziness and fainting during the last month. He had a history of a malignant skin melanoma surgically removed 4 years ago. The echo study identified multiple metastases in the heart involving the pericardium, the myocardium and the right atrium, where the tumor was mobile creating mechanical tricuspid valve stenosis. Malignant metastasis was confirmed by pericardiocentesis and, although treatment with chemotherapy was promptly initiated, the patient died 4 months later. Despite the difficulty in clinical diagnosis of cardiac melanoma, early detection has important therapeutic and prognostic implications. Echocardiography is the most common diagnostic modality and transesophageal approach may be the technique of choice to image intracardiac metastatic tumors.</p>
]]></description>
<dc:creator><![CDATA[Chrissos, D. N., Stougiannos, P. N., Mytas, D. Z., Katsaros, A. A., Andrikopoulos, G. K., Kallikazaros, I. E.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1016/j.euje.2006.12.008</dc:identifier>
<dc:title><![CDATA[Multiple cardiac metastases from a malignant melanoma]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>392</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>391</prism:startingPage>
<prism:section>CASE REPORTS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/393?rss=1">
<title><![CDATA[Intracardiac metastasis of malignant melanoma]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/393?rss=1</link>
<description><![CDATA[
<sec><st>Aim</st>
<p>To report a case of intracardiac metastasis of malignant melanoma with multiple mobile, large masses in left atrium (LA), left ventricle (LV) and right atrium (RA).</p>
</sec>
]]></description>
<dc:creator><![CDATA[Samiei, N., Farahani, M. M., Sadeghipour, A., Mozaffari, K., Maleki, M.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1016/j.euje.2007.01.001</dc:identifier>
<dc:title><![CDATA[Intracardiac metastasis of malignant melanoma]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>394</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>393</prism:startingPage>
<prism:section>CASE REPORTS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/395?rss=1">
<title><![CDATA[Multiple pseudo-abscesses following aortic valve replacement]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/395?rss=1</link>
<description><![CDATA[
<p>Prosthetic aortic valve endocarditis is associated with valve ring abscess, conduction abnormalities and a grave prognosis. Aortic root abscess is a serious complication of infective endocarditis with high mortality. We report a case of a patient who had echocardiographic features resembling aortic root abscess along with severe aortic regurgitation, 6 weeks following aortic valve replacement. Valvular dehiscence led to perivalvular abscess like appearance. Infective endocarditis was exluded. He underwent a successful redo aortic valve surgery with slow recovery.</p>
]]></description>
<dc:creator><![CDATA[Attar, M.N., Moore, R.K.G., Khan, S.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1016/j.euje.2007.01.003</dc:identifier>
<dc:title><![CDATA[Multiple pseudo-abscesses following aortic valve replacement]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>396</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>395</prism:startingPage>
<prism:section>CASE REPORTS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/397?rss=1">
<title><![CDATA[Left atrial appendage thrombus outside of a 'successful' ligation]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/397?rss=1</link>
<description><![CDATA[
<p>A 79-year-old woman with severe aortic stenosis underwent aortic valve replacement surgery, and had ligation of the left atrial appendage (LAA) using an epicardial approach. On a post-operative echocardiographic evaluation, the distal portion of the LAA was excluded, leaving no communication with the left atrium. The proximal portion of the LAA, however, was in continuity with the circulation and a large thrombus was present within it. While previous reports of incomplete LAA ligation have involved disruption of the suture line, this present report describes a case of incomplete ligation due to persistence of the proximal portion of the appendage. Thus, thrombus formation occurred despite a &lsquo;successful&rsquo; epicardial exclusion of the distal LAA.</p>
]]></description>
<dc:creator><![CDATA[Donnino, R., Tunick, P. A., Kronzon, I.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1016/j.euje.2007.01.006</dc:identifier>
<dc:title><![CDATA[Left atrial appendage thrombus outside of a 'successful' ligation]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>398</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>397</prism:startingPage>
<prism:section>CASE REPORTS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/399?rss=1">
<title><![CDATA[An unusual case of late bioprosthetic mitral valve thrombosis successfully managed with anticoagulation]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/399?rss=1</link>
<description><![CDATA[
<p>In this report, we present the case of a patient with hemodynamically significant thrombosis of a mitral bioprosthesis occurring 11 years after valve replacement. The diagnosis was suspected on the basis of a subacute increase in the transvalvular gradient seen on transthoracic echocardiography and was con- firmed by transesophageal echocardiography which disclosed unusual features. A hypercoagulable work up showed raised plasma factor VIII levels. The patient was successfully managed with oral anticoagulation.</p>
]]></description>
<dc:creator><![CDATA[Aminian, A., Lefebvre, P., Delmotte, P., Friart, A.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1016/j.euje.2007.02.001</dc:identifier>
<dc:title><![CDATA[An unusual case of late bioprosthetic mitral valve thrombosis successfully managed with anticoagulation]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>400</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>399</prism:startingPage>
<prism:section>CASE REPORTS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/401?rss=1">
<title><![CDATA[Loffler's endocarditis: the hypereosinophic syndrome]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/401?rss=1</link>
<description><![CDATA[
<p>In the present study we describe two similar severe cases of L&ouml;ffler's endocarditis in which eosinophilic infiltrations obliterated the entire right ventricular cavity and caused severe right ventricular dysfunction.</p>
]]></description>
<dc:creator><![CDATA[Ostovan, M. A., Aslani, A.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1016/j.euje.2007.02.008</dc:identifier>
<dc:title><![CDATA[Loffler's endocarditis: the hypereosinophic syndrome]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>402</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>401</prism:startingPage>
<prism:section>CASE REPORTS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/403?rss=1">
<title><![CDATA[Severe calcification of the lateral mitral annulus in constrictive pericarditis: a potential pitfall for the use of echocardiographic tissue Doppler imaging]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/403?rss=1</link>
<description><![CDATA[
<p>According to the guidelines of the European Society of Cardiology on the diagnosis and management of pericardial diseases, tissue Doppler imaging (TDI) is proposed to be part of the diagnostic work-up in patients with suspected constrictive pericarditis (CP). We describe a case which illustrates that TDI analysis may be misleading in patients with severe pericardial calcifications of the lateral mitral annulus. Multi-slice computed tomography (MSCT) data in this case contributed much to a better understanding of the impact of heterogeneous calcification patterns on the results of TDI assessment in CP.</p>
]]></description>
<dc:creator><![CDATA[Butz, T., Langer, C., Scholtz, W., Jategaonkar, S., Bogunovic, N., Horstkotte, D., Faber, L.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1016/j.euje.2007.02.006</dc:identifier>
<dc:title><![CDATA[Severe calcification of the lateral mitral annulus in constrictive pericarditis: a potential pitfall for the use of echocardiographic tissue Doppler imaging]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>405</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>403</prism:startingPage>
<prism:section>CASE REPORTS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/406?rss=1">
<title><![CDATA[Acute pulmonary embolus in pregnancy: a case study highlighting the value of TTE]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/406?rss=1</link>
<description><![CDATA[
<p>In pregnancy, the incidence of pulmonary embolism (PE) is increased fivefold when compared to non-pregnant women of the same age, and PE is one of the leading causes of death during pregnancy. However, the diagnosis of PE among pregnant women is complicated by concerns regarding radiation exposure. We report the case of a 36-year-old woman at 9 weeks gestation with an acute PE that highlights the value of transthoracic echocardiography in diagnosis, for initial and on-going treatment in such a setting, while keeping doses of radiation low.</p>
]]></description>
<dc:creator><![CDATA[Stoodley, P., Cooper, M., Thomas, L.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1016/j.euje.2007.03.024</dc:identifier>
<dc:title><![CDATA[Acute pulmonary embolus in pregnancy: a case study highlighting the value of TTE]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>409</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>406</prism:startingPage>
<prism:section>CASE REPORTS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/410?rss=1">
<title><![CDATA[Acquired coronary fistula after left ventricular de-airing by apical needle aspiration]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/410?rss=1</link>
<description><![CDATA[
<p>Acquired coronary fistula is uncommon, but has been reported to occur after several surgical procedures, acute myocardial infarction, endomyocardial biopsy, coronary angioplasty, and thoracic trauma. We describe the occurrence of a left coronary to left ventricular cavity fistula following resection of a left atrial myxoma, with spontaneous closure in the following weeks. The fistula was likely caused by a needle inserted into the left ventricular apex, a procedure routinely used to ensure left ventricular de-airing.</p>
]]></description>
<dc:creator><![CDATA[Unger, P., Moreels, M., Stoupel, E., de Canniere, D.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1016/j.euje.2007.03.028</dc:identifier>
<dc:title><![CDATA[Acquired coronary fistula after left ventricular de-airing by apical needle aspiration]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>411</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>410</prism:startingPage>
<prism:section>CASE REPORTS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/412?rss=1">
<title><![CDATA[Functional mitral stenosis: a rare complication of the Impella assist device]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/412?rss=1</link>
<description><![CDATA[
<p>In patients with left ventricular output failure, the Impella left ventricular assist device increases total cardiac output despite a drop in output provided by the left ventricle itself. We present a patient with cardiogenic shock after myocardial infarction in whom an Impella recover 2.5 was implanted. Correct placement was ensured by fluoroscopy, pressure and current signals displayed on the console of the system, and transthoracic echocardiography. On follow-up, the Impella device was dislocated with the shaft of the device lying on the anterior mitral leaflet causing a functional mitral stenosis evident by an increased transmitral diastolic flow gradient. After removing the device, the patients' haemodynamics improved within minutes. Other than a mild regurgitation, mitral valve was without pathological findings. Although infrequent, this case shows a possible complication of the Impella ventricular assist device and highlights the importance of periodical echocardiographic surveillance, especially in patients who show a poor response to therapy.</p>
]]></description>
<dc:creator><![CDATA[Toggweiler, S., Jamshidi, P., Erne, P.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1093/ejechocard/jen029</dc:identifier>
<dc:title><![CDATA[Functional mitral stenosis: a rare complication of the Impella assist device]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>413</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>412</prism:startingPage>
<prism:section>ELECTRONIC PAPERS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/414?rss=1">
<title><![CDATA[Aortic valve fibroelastoma causing cerebral infarction]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/414?rss=1</link>
<description><![CDATA[
<p>We report incidental findings of aortic valve fibroelastoma in a patient with embolic complications during routine transthoracic echocardiography.</p>
]]></description>
<dc:creator><![CDATA[Hansen, A., Oel, W.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1093/ejechocard/jen019</dc:identifier>
<dc:title><![CDATA[Aortic valve fibroelastoma causing cerebral infarction]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>414</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>414</prism:startingPage>
<prism:section>ELECTRONIC PAPERS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/415?rss=1">
<title><![CDATA[Ockham's razor or Hickam's dictum: a right atrial mass following excision of left atrial myxoma]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/415?rss=1</link>
<description><![CDATA[
<p>We report a case of a 54-year-old man presenting with a right atrial mass 7 months after undergoing a left atrial myxoma excision surgery. The differential diagnosis included recurrent myxoma or thrombus. The patient underwent repeat open sternotomy on cardiopulmonary bypass. Histopathological evaluation of the mass revealed an organizing thrombus. This report is, to our knowledge, the first that demonstrates right atrial thrombus shortly following excision of left atrial myxoma.</p>
]]></description>
<dc:creator><![CDATA[Abramowitz, Y., Perlman, G., Levy, E., Beeri, R., Chajek-Shaul, T., Leibowitz, D.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1093/ejechocard/jen023</dc:identifier>
<dc:title><![CDATA[Ockham's razor or Hickam's dictum: a right atrial mass following excision of left atrial myxoma]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>416</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>415</prism:startingPage>
<prism:section>ELECTRONIC PAPERS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/417?rss=1">
<title><![CDATA[Free floating thrombus exiting the left ventricle]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/417?rss=1</link>
<description><![CDATA[
<p>A 75-year-old man with a history of previous myocardial infarction underwent two-dimensional transthoracic echocardiography as part of a routine follow-up evaluation. During the examination, a free-floating thrombus was identified in the left ventricular (LV) cavity. After a number of cardiac cycles, the thrombus suddenly flowed free out of the LV outflow tract into the aorta.</p>
]]></description>
<dc:creator><![CDATA[Kim, H., Cho, Y.-K., Nam, C.-W., Hur, S.-H.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1093/ejechocard/jen024</dc:identifier>
<dc:title><![CDATA[Free floating thrombus exiting the left ventricle]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>418</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>417</prism:startingPage>
<prism:section>ELECTRONIC PAPERS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/419?rss=1">
<title><![CDATA[Aorta-atrial fistula, a rare complication of prosthetic valve endocarditis]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/419?rss=1</link>
<description><![CDATA[
<p>A 51-year-old male with a history of a mechanical Carbomedics aortic and mitral valve replacement in 2003 and several re-operations because of endocarditis of the mitral valve in 2007 presented with heart failure 68 days after operation. Echocardiography confirmed the presence of a fistulous connection between the aorta and the left atrium. Because of the multiple surgical interventions and high operative risk, an initial conservative medical treatment was initiated and the clinical course was uneventful to this date.</p>
]]></description>
<dc:creator><![CDATA[Dewilde, W., Kurvers, M., Jaarsma, W.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1093/ejechocard/jen025</dc:identifier>
<dc:title><![CDATA[Aorta-atrial fistula, a rare complication of prosthetic valve endocarditis]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>421</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>419</prism:startingPage>
<prism:section>ELECTRONIC PAPERS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/422?rss=1">
<title><![CDATA[Right atrial myxoma: echocardiographic appearance]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/422?rss=1</link>
<description><![CDATA[
<p>A 67-year-old asymptomatic male was admitted for evaluation of his arterial hypertension. The routine echocardiographic study revealed a large tumour in the dilated right atrium. The mass appeared to arise from the posterior wall of the right atrium. After infusion of a contrast agent, the mass appeared to fill with the contrast agent, ruling out the possibility of the mass being a clot.</p>
<p>Transesophageal study revealed a round mass arising from the posterior right atrial wall just adjacent to the extrusion of the superior vena cava. The patient subsequently underwent cardiac surgery and a cardiac tumour was excised that proved to be a cardiac myxoma. In this case we present echocardiographic images and the macro- and microscopic view of the right atrial myxoma.</p>
]]></description>
<dc:creator><![CDATA[Patrianakos, A. P., Parthenakis, F. I., Nyktari, E., Kochiadakis, G. E., Koutsopoulos, A. V., Vardas, P. E.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1093/ejechocard/jen028</dc:identifier>
<dc:title><![CDATA[Right atrial myxoma: echocardiographic appearance]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>423</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>422</prism:startingPage>
<prism:section>ELECTRONIC PAPERS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/424?rss=1">
<title><![CDATA[An unusual case of isolated non-compacted right ventricular myocardium]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/424?rss=1</link>
<description><![CDATA[
<p>Isolated ventricular non-compaction is a rare type of cardiomyopathy resulting from arrested myocardial development during embryogenesis. This rare entity can be easily diagnosed by characteristic appearance of prominent myocardial trabeculations and deep inter-trabecular spaces. The clinical manifestations include heart failure signs, ventricular arrhythmias, and cardio-embolic events. Although the usual site of involvement is the left ventricle, the right ventricle (RV) can rarely be affected. Here, we report a case of 23-year-old male patient with isolated RV non-compaction.</p>
]]></description>
<dc:creator><![CDATA[Gomathi, S. B., Makadia, N., Ajit, S. M.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1093/ejechocard/jen016</dc:identifier>
<dc:title><![CDATA[An unusual case of isolated non-compacted right ventricular myocardium]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>425</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>424</prism:startingPage>
<prism:section>ELECTRONIC PAPERS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/426?rss=1">
<title><![CDATA[Cardiac complications in Whipple's disease]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/426?rss=1</link>
<description><![CDATA[
<p>Whipple's disease or intestinal lipodystrophy is an infection induced by <I>Tropheryma whipplei</I>. It is rare with an estimated incidence of 0.4 per million. Symptoms are arthropathy, weight loss, and diarrhoea, but other organs notably the central nervous system may be affected. We demonstrate a case of cardiac complications in Whipple's disease. The patient presented with endocardial infiltrations on TEE examinations and heart failure and improved after antibiotic treatment.</p>
]]></description>
<dc:creator><![CDATA[Hansen, A., Mereles, D.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1093/ejechocard/jen022</dc:identifier>
<dc:title><![CDATA[Cardiac complications in Whipple's disease]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>427</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>426</prism:startingPage>
<prism:section>ELECTRONIC PAPERS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/428?rss=1">
<title><![CDATA[Cardiac tamponade because of left atrium direct invasion by a large cell neuroendocrine metastatic carcinoma of the lung]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/428?rss=1</link>
<description><![CDATA[
<p>A 53-year-old man presented with cardiac tamponade due to direct invasion of left atrium by a large cell neuroendocrine metastatic lung adenocarcinoma. Direct invasion of left atrial cavity by this type of lung tumour is rare. When cardiac involvement is suspected, two-dimensional echocardiography is the first-line diagnostic tool. Computerized tomography and magnetic resonance imaging can provide additional anatomical information and, as in this case, further delineation of the relation between intracavity masses and normal structures, including the mural site of attachment and tumour extension.</p>
]]></description>
<dc:creator><![CDATA[Lysitsas, D. N., Banerjee, P., Shiu, M. F.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1093/ejechocard/jen027</dc:identifier>
<dc:title><![CDATA[Cardiac tamponade because of left atrium direct invasion by a large cell neuroendocrine metastatic carcinoma of the lung]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>429</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>428</prism:startingPage>
<prism:section>ELECTRONIC PAPERS</prism:section>
</item>

<item rdf:about="http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/430?rss=1">
<title><![CDATA[Prolapsing left atrial myxoma: preoperative diagnosis using a multimodal imaging approach with magnetic resonance imaging and real-time three-dimensional echocardiography]]></title>
<link>http://ejechocard.oxfordjournals.org/cgi/content/short/9/3/430?rss=1</link>
<description><![CDATA[
<p>Real-time three-dimensional echocardiography (RT3DE) is a new promising technique for the evaluation of intracardiac masses. We present the diagnostic work-up using a multimodal-imaging approach in a 74-year-old patient with a prolapsing tumour in the left atrium suggestive of a myxoma, causing severe congestive heart failure attributable to dynamic left ventricular inflow obstruction, and mimicking severe mitral valve stenosis. Real-time three-dimensional echocardiography allowed to accurately image the entire volume of the myxoma, and to analyse the dynamic left ventricular inflow obstruction. The size of the lobulated mass as assessed by RT3DE was 65 <FONT FACE="arial,helvetica">x</FONT> 25 <FONT FACE="arial,helvetica">x</FONT> 22 mm.</p>
<p>The mass was surgically removed, histology was diagnostic for myxoma, and the patient had an uneventful recovery.</p>
<p>Real-time three-dimensional echocardiography images the entire volume of a mass allowing for accurate measurements in multiple planes, and allowing for real-time evaluation of obstructive effects on ventricular in- or outflow. This case shows how RT3DE and other non-invasive imaging modalities may be used as complementary techniques for evaluation of intracardiac masses.</p>
]]></description>
<dc:creator><![CDATA[Butz, T., Scholtz, W., Korfer, J., Maleszka, A., Jategaonkar, S., Meissner, A., Trappe, H.J., Korfer, R., Horstkotte, D., Kleikamp, G., Faber, L.]]></dc:creator>
<dc:date>2008-04-28</dc:date>
<dc:identifier>info:doi/10.1093/ejechocard/jen026</dc:identifier>
<dc:title><![CDATA[Prolapsing left atrial myxoma: preoperative diagnosis using a multimodal imaging approach with magnetic resonance imaging and real-time three-dimensional echocardiography]]></dc:title>
<dc:publisher>European Society of Cardiology</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>9</prism:volume>
<prism:endingPage>432</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>430</prism:startingPage>
<prism:section>ELECTRONIC PAPERS</prism:section>
</item>

</rdf:RDF>