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dc.contributor.authorPuntmann, VOen_US
dc.contributor.authorValbuena, Sen_US
dc.contributor.authorHinojar, Ren_US
dc.contributor.authorPetersen, SEen_US
dc.contributor.authorGreenwood, JPen_US
dc.contributor.authorKramer, CMen_US
dc.contributor.authorKwong, RYen_US
dc.contributor.authorMcCann, GPen_US
dc.contributor.authorBerry, Cen_US
dc.contributor.authorNagel, Een_US
dc.contributor.authorSCMR Clinical Trial Writing Groupen_US
dc.date.accessioned2018-09-24T09:33:31Z
dc.date.available2018-08-05en_US
dc.date.issued2018-09-20en_US
dc.date.submitted2018-09-23T19:56:07.439Z
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/45024
dc.description.abstractCardiovascular disease remains a leading cause of morbidity and mortality globally. Changing natural history of the disease due to improved care of acute conditions and ageing population necessitates new strategies to tackle conditions which have more chronic and indolent course. These include an increased deployment of safe screening methods, life-long surveillance, and monitoring of both disease activity and tailored-treatment, by way of increasingly personalized medical care. Cardiovascular magnetic resonance (CMR) is a non-invasive, ionising radiation-free method, which can support a significant number of clinically relevant measurements and offers new opportunities to advance the state of art of diagnosis, prognosis and treatment. The objective of the SCMR Clinical Trial Taskforce was to summarizes the evidence to emphasize where currently CMR-guided clinical care can indeed translate into meaningful use and efficient deployment of resources results in meaningful and efficient use. The objective of the present initiative was to provide an appraisal of evidence on analytical validation, including the accuracy and precision, and clinical qualification of parameters in disease context, clarifying the strengths and weaknesses of the state of art, as well as the gaps in the current evidence This paper is complementary to the existing position papers on standardized acquisition and post-processing ensuring robustness and transferability for widespread use. Themed imaging-endpoint guidance on trial design to support drug-discovery or change in clinical practice (part II), will be presented in a follow-up paper in due course. As CMR continues to undergo rapid development, regular updates of the present recommendations are foreseen.en_US
dc.format.extent67 - ?en_US
dc.languageengen_US
dc.language.isoenen_US
dc.relation.ispartofJ Cardiovasc Magn Resonen_US
dc.rightsThis 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.
dc.subjectBiomarkeren_US
dc.subjectCardiac magnetic resonanceen_US
dc.subjectImagingen_US
dc.subjectPosition paperen_US
dc.subjectSCMRen_US
dc.titleSociety for Cardiovascular Magnetic Resonance (SCMR) expert consensus for CMR imaging endpoints in clinical research: part I - analytical validation and clinical qualification.en_US
dc.typeArticle
dc.rights.holder© The Author(s). 2018.
dc.identifier.doi10.1186/s12968-018-0484-5en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/30231886en_US
pubs.issue1en_US
pubs.notesNot knownen_US
pubs.publication-statusPublished onlineen_US
pubs.volume20en_US
dcterms.dateAccepted2018-08-05en_US


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