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In-depth CMR training is not readily available.
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Good practice regarding clinical trial design, conduct, analysis and reporting is essential in CMR trials, and training in these areas will be required for CMR practitioners who are involved with clinical trials.
Knowledge of the adverse events associated with regadenoson perfusion CMR has implications for patient safety and staff training.
For EMP and EMP-CMR methods, the SOI is absent in the training data.
The SOI is not present in the training data when using EMP and EMP-CMR methods.
Insufficient numbers of adequately trained physicians limit utilisation and dissemination of CMR.
Study managers (NMM and ER) who report to the chief investigator (CMR) and are employed by the sponsor (Griffith University), provide initial training and ongoing support to the research nurses and site investigators, and monitor data quality and site processes, at least monthly.
Knowledge of adverse events associated with regadenoson perfusion cardiac magnetic resonance (CMR) and patient tolerability has implications for patient safety and staff training.
The training set was reviewed for consensus by another experienced clinician (HA with 20 years of CMR experience).
Manual segmentation was performed for all slices in end-diastole and end-systole in both the training set and the test set by an experienced clinician (ErH with 14 years of CMR experience).
In addition, both lack of knowledge as well as insufficient training of both the GPs as well as the pharmacists hinder the implementation of CMRs.
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