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Clinical recommendations for cardiovascular magnetic resonance mapping of T1, T2, T2* and extracellular volume: A consensus statement by the Society for Cardiovascular Magnetic Resonance (SCMR) endorsed by the European Association for Cardiovascular Imaging (EACVI)
Parametric mapping techniques provide a non-invasive tool for quantifying tissue alterations in myocardial disease in those eligible for cardiovascular magnetic resonance (CMR). Parametric mapping with CMR now permits the routine spatial visualization and quantification of changes in myocardial comp...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5633041/ https://www.ncbi.nlm.nih.gov/pubmed/28992817 http://dx.doi.org/10.1186/s12968-017-0389-8 |
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author | Messroghli, Daniel R. Moon, James C. Ferreira, Vanessa M. Grosse-Wortmann, Lars He, Taigang Kellman, Peter Mascherbauer, Julia Nezafat, Reza Salerno, Michael Schelbert, Erik B. Taylor, Andrew J. Thompson, Richard Ugander, Martin van Heeswijk, Ruud B. Friedrich, Matthias G. |
author_facet | Messroghli, Daniel R. Moon, James C. Ferreira, Vanessa M. Grosse-Wortmann, Lars He, Taigang Kellman, Peter Mascherbauer, Julia Nezafat, Reza Salerno, Michael Schelbert, Erik B. Taylor, Andrew J. Thompson, Richard Ugander, Martin van Heeswijk, Ruud B. Friedrich, Matthias G. |
author_sort | Messroghli, Daniel R. |
collection | PubMed |
description | Parametric mapping techniques provide a non-invasive tool for quantifying tissue alterations in myocardial disease in those eligible for cardiovascular magnetic resonance (CMR). Parametric mapping with CMR now permits the routine spatial visualization and quantification of changes in myocardial composition based on changes in T1, T2, and T2*(star) relaxation times and extracellular volume (ECV). These changes include specific disease pathways related to mainly intracellular disturbances of the cardiomyocyte (e.g., iron overload, or glycosphingolipid accumulation in Anderson-Fabry disease); extracellular disturbances in the myocardial interstitium (e.g., myocardial fibrosis or cardiac amyloidosis from accumulation of collagen or amyloid proteins, respectively); or both (myocardial edema with increased intracellular and/or extracellular water). Parametric mapping promises improvements in patient care through advances in quantitative diagnostics, inter- and intra-patient comparability, and relatedly improvements in treatment. There is a multitude of technical approaches and potential applications. This document provides a summary of the existing evidence for the clinical value of parametric mapping in the heart as of mid 2017, and gives recommendations for practical use in different clinical scenarios for scientists, clinicians, and CMR manufacturers. |
format | Online Article Text |
id | pubmed-5633041 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56330412017-10-17 Clinical recommendations for cardiovascular magnetic resonance mapping of T1, T2, T2* and extracellular volume: A consensus statement by the Society for Cardiovascular Magnetic Resonance (SCMR) endorsed by the European Association for Cardiovascular Imaging (EACVI) Messroghli, Daniel R. Moon, James C. Ferreira, Vanessa M. Grosse-Wortmann, Lars He, Taigang Kellman, Peter Mascherbauer, Julia Nezafat, Reza Salerno, Michael Schelbert, Erik B. Taylor, Andrew J. Thompson, Richard Ugander, Martin van Heeswijk, Ruud B. Friedrich, Matthias G. J Cardiovasc Magn Reson Review Parametric mapping techniques provide a non-invasive tool for quantifying tissue alterations in myocardial disease in those eligible for cardiovascular magnetic resonance (CMR). Parametric mapping with CMR now permits the routine spatial visualization and quantification of changes in myocardial composition based on changes in T1, T2, and T2*(star) relaxation times and extracellular volume (ECV). These changes include specific disease pathways related to mainly intracellular disturbances of the cardiomyocyte (e.g., iron overload, or glycosphingolipid accumulation in Anderson-Fabry disease); extracellular disturbances in the myocardial interstitium (e.g., myocardial fibrosis or cardiac amyloidosis from accumulation of collagen or amyloid proteins, respectively); or both (myocardial edema with increased intracellular and/or extracellular water). Parametric mapping promises improvements in patient care through advances in quantitative diagnostics, inter- and intra-patient comparability, and relatedly improvements in treatment. There is a multitude of technical approaches and potential applications. This document provides a summary of the existing evidence for the clinical value of parametric mapping in the heart as of mid 2017, and gives recommendations for practical use in different clinical scenarios for scientists, clinicians, and CMR manufacturers. BioMed Central 2017-10-09 /pmc/articles/PMC5633041/ /pubmed/28992817 http://dx.doi.org/10.1186/s12968-017-0389-8 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Messroghli, Daniel R. Moon, James C. Ferreira, Vanessa M. Grosse-Wortmann, Lars He, Taigang Kellman, Peter Mascherbauer, Julia Nezafat, Reza Salerno, Michael Schelbert, Erik B. Taylor, Andrew J. Thompson, Richard Ugander, Martin van Heeswijk, Ruud B. Friedrich, Matthias G. Clinical recommendations for cardiovascular magnetic resonance mapping of T1, T2, T2* and extracellular volume: A consensus statement by the Society for Cardiovascular Magnetic Resonance (SCMR) endorsed by the European Association for Cardiovascular Imaging (EACVI) |
title | Clinical recommendations for cardiovascular magnetic resonance mapping of T1, T2, T2* and extracellular volume: A consensus statement by the Society for Cardiovascular Magnetic Resonance (SCMR) endorsed by the European Association for Cardiovascular Imaging (EACVI) |
title_full | Clinical recommendations for cardiovascular magnetic resonance mapping of T1, T2, T2* and extracellular volume: A consensus statement by the Society for Cardiovascular Magnetic Resonance (SCMR) endorsed by the European Association for Cardiovascular Imaging (EACVI) |
title_fullStr | Clinical recommendations for cardiovascular magnetic resonance mapping of T1, T2, T2* and extracellular volume: A consensus statement by the Society for Cardiovascular Magnetic Resonance (SCMR) endorsed by the European Association for Cardiovascular Imaging (EACVI) |
title_full_unstemmed | Clinical recommendations for cardiovascular magnetic resonance mapping of T1, T2, T2* and extracellular volume: A consensus statement by the Society for Cardiovascular Magnetic Resonance (SCMR) endorsed by the European Association for Cardiovascular Imaging (EACVI) |
title_short | Clinical recommendations for cardiovascular magnetic resonance mapping of T1, T2, T2* and extracellular volume: A consensus statement by the Society for Cardiovascular Magnetic Resonance (SCMR) endorsed by the European Association for Cardiovascular Imaging (EACVI) |
title_sort | clinical recommendations for cardiovascular magnetic resonance mapping of t1, t2, t2* and extracellular volume: a consensus statement by the society for cardiovascular magnetic resonance (scmr) endorsed by the european association for cardiovascular imaging (eacvi) |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5633041/ https://www.ncbi.nlm.nih.gov/pubmed/28992817 http://dx.doi.org/10.1186/s12968-017-0389-8 |
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