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Myocardial T1 mapping and extracellular volume quantification: a Society for Cardiovascular Magnetic Resonance (SCMR) and CMR Working Group of the European Society of Cardiology consensus statement
Rapid innovations in cardiovascular magnetic resonance (CMR) now permit the routine acquisition of quantitative measures of myocardial and blood T1 which are key tissue characteristics. These capabilities introduce a new frontier in cardiology, enabling the practitioner/investigator to quantify biol...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3854458/ https://www.ncbi.nlm.nih.gov/pubmed/24124732 http://dx.doi.org/10.1186/1532-429X-15-92 |
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author | Moon, James C Messroghli, Daniel R Kellman, Peter Piechnik, Stefan K Robson, Matthew D Ugander, Martin Gatehouse, Peter D Arai, Andrew E Friedrich, Matthias G Neubauer, Stefan Schulz-Menger, Jeanette Schelbert, Erik B |
author_facet | Moon, James C Messroghli, Daniel R Kellman, Peter Piechnik, Stefan K Robson, Matthew D Ugander, Martin Gatehouse, Peter D Arai, Andrew E Friedrich, Matthias G Neubauer, Stefan Schulz-Menger, Jeanette Schelbert, Erik B |
author_sort | Moon, James C |
collection | PubMed |
description | Rapid innovations in cardiovascular magnetic resonance (CMR) now permit the routine acquisition of quantitative measures of myocardial and blood T1 which are key tissue characteristics. These capabilities introduce a new frontier in cardiology, enabling the practitioner/investigator to quantify biologically important myocardial properties that otherwise can be difficult to ascertain clinically. CMR may be able to track biologically important changes in the myocardium by: a) native T1 that reflects myocardial disease involving the myocyte and interstitium without use of gadolinium based contrast agents (GBCA), or b) the extracellular volume fraction (ECV)–a direct GBCA-based measurement of the size of the extracellular space, reflecting interstitial disease. The latter technique attempts to dichotomize the myocardium into its cellular and interstitial components with estimates expressed as volume fractions. This document provides recommendations for clinical and research T1 and ECV measurement, based on published evidence when available and expert consensus when not. We address site preparation, scan type, scan planning and acquisition, quality control, visualisation and analysis, technical development. We also address controversies in the field. While ECV and native T1 mapping appear destined to affect clinical decision making, they lack multi-centre application and face significant challenges, which demand a community-wide approach among stakeholders. At present, ECV and native T1 mapping appear sufficiently robust for many diseases; yet more research is required before a large-scale application for clinical decision-making can be recommended. |
format | Online Article Text |
id | pubmed-3854458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38544582013-12-07 Myocardial T1 mapping and extracellular volume quantification: a Society for Cardiovascular Magnetic Resonance (SCMR) and CMR Working Group of the European Society of Cardiology consensus statement Moon, James C Messroghli, Daniel R Kellman, Peter Piechnik, Stefan K Robson, Matthew D Ugander, Martin Gatehouse, Peter D Arai, Andrew E Friedrich, Matthias G Neubauer, Stefan Schulz-Menger, Jeanette Schelbert, Erik B J Cardiovasc Magn Reson Position Statement Rapid innovations in cardiovascular magnetic resonance (CMR) now permit the routine acquisition of quantitative measures of myocardial and blood T1 which are key tissue characteristics. These capabilities introduce a new frontier in cardiology, enabling the practitioner/investigator to quantify biologically important myocardial properties that otherwise can be difficult to ascertain clinically. CMR may be able to track biologically important changes in the myocardium by: a) native T1 that reflects myocardial disease involving the myocyte and interstitium without use of gadolinium based contrast agents (GBCA), or b) the extracellular volume fraction (ECV)–a direct GBCA-based measurement of the size of the extracellular space, reflecting interstitial disease. The latter technique attempts to dichotomize the myocardium into its cellular and interstitial components with estimates expressed as volume fractions. This document provides recommendations for clinical and research T1 and ECV measurement, based on published evidence when available and expert consensus when not. We address site preparation, scan type, scan planning and acquisition, quality control, visualisation and analysis, technical development. We also address controversies in the field. While ECV and native T1 mapping appear destined to affect clinical decision making, they lack multi-centre application and face significant challenges, which demand a community-wide approach among stakeholders. At present, ECV and native T1 mapping appear sufficiently robust for many diseases; yet more research is required before a large-scale application for clinical decision-making can be recommended. BioMed Central 2013-10-14 /pmc/articles/PMC3854458/ /pubmed/24124732 http://dx.doi.org/10.1186/1532-429X-15-92 Text en Copyright © 2013 Moon et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. 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 | Position Statement Moon, James C Messroghli, Daniel R Kellman, Peter Piechnik, Stefan K Robson, Matthew D Ugander, Martin Gatehouse, Peter D Arai, Andrew E Friedrich, Matthias G Neubauer, Stefan Schulz-Menger, Jeanette Schelbert, Erik B Myocardial T1 mapping and extracellular volume quantification: a Society for Cardiovascular Magnetic Resonance (SCMR) and CMR Working Group of the European Society of Cardiology consensus statement |
title | Myocardial T1 mapping and extracellular volume quantification: a Society for Cardiovascular Magnetic Resonance (SCMR) and CMR Working Group of the European Society of Cardiology consensus statement |
title_full | Myocardial T1 mapping and extracellular volume quantification: a Society for Cardiovascular Magnetic Resonance (SCMR) and CMR Working Group of the European Society of Cardiology consensus statement |
title_fullStr | Myocardial T1 mapping and extracellular volume quantification: a Society for Cardiovascular Magnetic Resonance (SCMR) and CMR Working Group of the European Society of Cardiology consensus statement |
title_full_unstemmed | Myocardial T1 mapping and extracellular volume quantification: a Society for Cardiovascular Magnetic Resonance (SCMR) and CMR Working Group of the European Society of Cardiology consensus statement |
title_short | Myocardial T1 mapping and extracellular volume quantification: a Society for Cardiovascular Magnetic Resonance (SCMR) and CMR Working Group of the European Society of Cardiology consensus statement |
title_sort | myocardial t1 mapping and extracellular volume quantification: a society for cardiovascular magnetic resonance (scmr) and cmr working group of the european society of cardiology consensus statement |
topic | Position Statement |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3854458/ https://www.ncbi.nlm.nih.gov/pubmed/24124732 http://dx.doi.org/10.1186/1532-429X-15-92 |
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