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BioMed Central Page 1 of 2 (page number not for citation purposes) Journal of Cardiovascular Magnetic Resonance Open Access Poster presentation Prognostic role of CMR in acute myocardial infarction Lorenzo Monti*, Elena Corrada, Patrizia Presbitero, Renato Bragato, Mirko Curzi and Luca Balzarini Address: Istituto Clinico Humanitas, Rozzano, Italy * Corresponding author Introduction Cardiac Magnetic Resonance (CMR) provides a compre- hensive non-invasive characterization of acute myocardial infarction (MI). Purpose to test whether a single CMR study may improve the prog- nostic stratification of MI patients. Methods 29 patients were studied on day 3 ± 1 after a first MI, between June 2006 and April 2007. CMR included SSFP and T2 STIR sequences, first pass perfusion, Early (EGE: 1 to 2 minutes) and Late (LGE: 10 to 15 minutes) Gadolin- ium Enhancement. Subsequent clinical management was not affected from CMR results, and patients underwent the usual clinical and echocardiographic follow-up. In 2009 we tested the occurrence of the end-point of cardiac death or left ventricular (LV) remodelling (EDVi > 90 ml/ m 2 or LVEF < 50% at echocardiographic follow-up) in the studied population. Results At 23 ± 5 months follow-up, the endpoint was observed in 7 pts (25%): 1 cardiac death, 6 adverse LV remodeling. See Table 1 for the prognostic role of different CMR parameters: among the tested parameters, myocardial haemorrhage, observed in 8 pts (27%), has a unique 96,5% accuracy in predicting the endpoint, with a 100% NPV. Unexpectedly, LGE-based parameters such as total infarct mass and the presence MVO show prognostic accu- racy similar to the echocardiographic LVEF <50%. The 7 pts reaching the endpoint show both MVO (globally present in 15 pts -51%-) and Myocardial Haemorrhage. It seems that the assessment of MVO should keep in account the total amount and not only the mere presence of MVO: this hampers the usefulness of MVO, since the total amount changes over time. Conclusion T2-STIR images allow a long-term prognostic stratification of unrivalled accuracy during the acute phase of MI. The use of gadolinium do not significantly improve the prog- nostic accuracy of CMR. from 13th Annual SCMR Scientific Sessions Phoenix, AZ, USA. 21-24 January 2010 Published: 21 January 2010 Journal of Cardiovascular Magnetic Resonance 2010, 12(Suppl 1):P293 doi:10.1186/1532-429X-12-S1-P293 <supplement> <title> <p>Abstracts of the 13<sup>th </sup>Annual SCMR Scientific Sessions - 2010</p> </title> <note>Meeting abstracts - A single PDF containing all abstracts in this Supplement is available <a href="http://www.biomedcentral.com/content/files/pdf/1532-429X-11-S1-full.pdf">here</a>.</note> <url>http://www.biomedcentral.com/content/files/pdf/1532-429X-11-S1-info</url> </supplement> This abstract is available from: http://jcmr-online.com/content/12/S1/P293 © 2010 Monti et al; licensee BioMed Central Ltd.

Prognostic role of CMR in acute myocardial infarction

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Journal of Cardiovascular Magnetic Resonance

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Open AccePoster presentationPrognostic role of CMR in acute myocardial infarctionLorenzo Monti*, Elena Corrada, Patrizia Presbitero, Renato Bragato, Mirko Curzi and Luca Balzarini

Address: Istituto Clinico Humanitas, Rozzano, Italy

* Corresponding author

IntroductionCardiac Magnetic Resonance (CMR) provides a compre-hensive non-invasive characterization of acute myocardialinfarction (MI).

Purposeto test whether a single CMR study may improve the prog-nostic stratification of MI patients.

Methods29 patients were studied on day 3 ± 1 after a first MI,between June 2006 and April 2007. CMR included SSFPand T2 STIR sequences, first pass perfusion, Early (EGE: 1to 2 minutes) and Late (LGE: 10 to 15 minutes) Gadolin-ium Enhancement. Subsequent clinical management wasnot affected from CMR results, and patients underwentthe usual clinical and echocardiographic follow-up. In2009 we tested the occurrence of the end-point of cardiacdeath or left ventricular (LV) remodelling (EDVi > 90 ml/m2 or LVEF < 50% at echocardiographic follow-up) in thestudied population.

ResultsAt 23 ± 5 months follow-up, the endpoint was observedin 7 pts (25%): 1 cardiac death, 6 adverse LV remodeling.See Table 1 for the prognostic role of different CMRparameters: among the tested parameters, myocardialhaemorrhage, observed in 8 pts (27%), has a unique96,5% accuracy in predicting the endpoint, with a 100%NPV. Unexpectedly, LGE-based parameters such as totalinfarct mass and the presence MVO show prognostic accu-racy similar to the echocardiographic LVEF <50%. The 7

pts reaching the endpoint show both MVO (globallypresent in 15 pts -51%-) and Myocardial Haemorrhage. Itseems that the assessment of MVO should keep in accountthe total amount and not only the mere presence of MVO:this hampers the usefulness of MVO, since the totalamount changes over time.

ConclusionT2-STIR images allow a long-term prognostic stratificationof unrivalled accuracy during the acute phase of MI. Theuse of gadolinium do not significantly improve the prog-nostic accuracy of CMR.

from 13th Annual SCMR Scientific SessionsPhoenix, AZ, USA. 21-24 January 2010

Published: 21 January 2010

Journal of Cardiovascular Magnetic Resonance 2010, 12(Suppl 1):P293 doi:10.1186/1532-429X-12-S1-P293

<supplement> <title> <p>Abstracts of the 13<sup>th </sup>Annual SCMR Scientific Sessions - 2010</p> </title> <note>Meeting abstracts - A single PDF containing all abstracts in this Supplement is available <a href="http://www.biomedcentral.com/content/files/pdf/1532-429X-11-S1-full.pdf">here</a>.</note> <url>http://www.biomedcentral.com/content/files/pdf/1532-429X-11-S1-info</url> </supplement>

This abstract is available from: http://jcmr-online.com/content/12/S1/P293

© 2010 Monti et al; licensee BioMed Central Ltd.

Page 1 of 2(page number not for citation purposes)

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Table 1:

Patients n(%)

Positive Predictive Value % Negative Predictive Value % Accuracy %

LGE(>20% LV mass)

13 (44%) 53,8 93,8 72.4

MVO (present) 15 (51%) 46.7 100 72.4LVEF(< 50%)

14 (48%) 50.0 100 75.9

Area at risk (>40% LV mass) 9(31%)

55.5 90 79.3

Myocardial Haemorrhage 8(27%)

87.5 100 96.5

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