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Published in: BMC Cardiovascular Disorders 1/2012

Open Access 01-12-2012 | Study protocol

Hypotheses, rationale, design, and methods for prognostic evaluation of cardiac biomarker elevation after percutaneous and surgical revascularization in the absence of manifest myocardial infarction. A comparative analysis of biomarkers and cardiac magnetic resonance. The MASS-V Trial

Authors: Whady Hueb, Bernard J Gersh, Paulo Cury Rezende, Cibele Larrosa Garzillo, Eduardo Gomes Lima, Ricardo D'Oliveira Vieira, Rosa Maria Rahmi Garcia, Desiderio Favarato, Carlos Alexandre W Segre, Alexandre Costa Pereira, Paulo Rogério Soares, Expedito Ribeiro, Pedro Lemos, Marco A Perin, Célia Cassaro Strunz, Luis AO Dallan, Fabio B Jatene, Noedir AG Stolf, Alexandre Ciappina Hueb, Ricardo Dias, Fabio A Gaiotto, Leandro Menezes Alves da Costa, Fernando Teiichi Costa Oikawa, Rodrigo Morel Vieira de Melo, Carlos Vicente Serrano Junior, Luiz Francisco Rodrigues de Ávila, Alexandre Volney Villa, José Rodrigues Parga Filho, César Nomura, José AF Ramires, Roberto Kalil Filho, The MASS-V Study Group

Published in: BMC Cardiovascular Disorders | Issue 1/2012

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Abstract

Background

Although the release of cardiac biomarkers after percutaneous (PCI) or surgical revascularization (CABG) is common, its prognostic significance is not known. Questions remain about the mechanisms and degree of correlation between the release, the volume of myocardial tissue loss, and the long-term significance. Delayed-enhancement of cardiac magnetic resonance (CMR) consistently quantifies areas of irreversible myocardial injury. To investigate the quantitative relationship between irreversible injury and cardiac biomarkers, we will evaluate the extent of irreversible injury in patients undergoing PCI and CABG and relate it to postprocedural modifications in cardiac biomarkers and long-term prognosis.

Methods/Design

The study will include 150 patients with multivessel coronary artery disease (CAD) with left ventricle ejection fraction (LVEF) and a formal indication for CABG; 50 patients will undergo CABG with cardiopulmonary bypass (CPB); 50 patients with the same arterial and ventricular condition indicated for myocardial revascularization will undergo CABG without CPB; and another 50 patients with CAD and preserved ventricular function will undergo PCI using stents. All patients will undergo CMR before and after surgery or PCI. We will also evaluate the release of cardiac markers of necrosis immediately before and after each procedure. Primary outcome considered is overall death in a 5-year follow-up. Secondary outcomes are levels of CK-MB isoenzyme and I-Troponin in association with presence of myocardial fibrosis and systolic left ventricle dysfunction assessed by CMR.

Discussion

The MASS-V Trial aims to establish reliable values for parameters of enzyme markers of myocardial necrosis in the absence of manifest myocardial infarction after mechanical interventions. The establishments of these indices have diagnostic value and clinical prognosis and therefore require relevant and different therapeutic measures. In daily practice, the inappropriate use of these necrosis markers has led to misdiagnosis and therefore wrong treatment. The appearance of a more sensitive tool such as CMR provides an unprecedented diagnostic accuracy of myocardial damage when correlated with necrosis enzyme markers. We aim to correlate laboratory data with imaging, thereby establishing more refined data on the presence or absence of irreversible myocardial injury after the procedure, either percutaneous or surgical, and this, with or without the use of cardiopulmonary bypass.
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Metadata
Title
Hypotheses, rationale, design, and methods for prognostic evaluation of cardiac biomarker elevation after percutaneous and surgical revascularization in the absence of manifest myocardial infarction. A comparative analysis of biomarkers and cardiac magnetic resonance. The MASS-V Trial
Authors
Whady Hueb
Bernard J Gersh
Paulo Cury Rezende
Cibele Larrosa Garzillo
Eduardo Gomes Lima
Ricardo D'Oliveira Vieira
Rosa Maria Rahmi Garcia
Desiderio Favarato
Carlos Alexandre W Segre
Alexandre Costa Pereira
Paulo Rogério Soares
Expedito Ribeiro
Pedro Lemos
Marco A Perin
Célia Cassaro Strunz
Luis AO Dallan
Fabio B Jatene
Noedir AG Stolf
Alexandre Ciappina Hueb
Ricardo Dias
Fabio A Gaiotto
Leandro Menezes Alves da Costa
Fernando Teiichi Costa Oikawa
Rodrigo Morel Vieira de Melo
Carlos Vicente Serrano Junior
Luiz Francisco Rodrigues de Ávila
Alexandre Volney Villa
José Rodrigues Parga Filho
César Nomura
José AF Ramires
Roberto Kalil Filho
The MASS-V Study Group
Publication date
01-12-2012
Publisher
BioMed Central
Published in
BMC Cardiovascular Disorders / Issue 1/2012
Electronic ISSN: 1471-2261
DOI
https://doi.org/10.1186/1471-2261-12-65

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