Abstract

BackgroundFor two decades, bright-blood late gadolinium enhancement (LGE) cardiovascular magnetic resonance (CMR) has been considered the reference standard for the non-invasive assessment of myocardial viability. While bright-blood LGE can clearly distinguish areas of myocardial infarction from viable myocardium, it often suffers from poor scar-to-blood contrast, making subendocardial scar difficult to detect. Recently, we proposed a novel dark-blood LGE approach that increases scar-to-blood contrast and thereby improves subendocardial scar conspicuity. In the present study we sought to assess the clinical value of this novel approach in a large patient cohort with various non-congenital ischemic and non-ischemic cardiomyopathies on both 1.5 T and 3 T CMR scanners of different vendors.MethodsThree hundred consecutive patients referred for clinical CMR were randomly assigned to a 1.5 T or 3 T scanner. An entire short-axis stack and multiple long-axis views were acquired using conventional phase sensitive inversion recovery (PSIR) LGE with TI set to null myocardium (bright-blood) and proposed PSIR LGE with TI set to null blood (dark-blood), in a randomized order. The bright-blood LGE and dark-blood LGE images were separated, anonymized, and interpreted in a random order at different time points by one of five independent observers. Each case was analyzed for the type of scar, per-segment transmurality, papillary muscle enhancement, overall image quality, observer confidence, and presence of right ventricular scar and intraventricular thrombus.ResultsDark-blood LGE detected significantly more cases with ischemic scar compared to conventional bright-blood LGE (97 vs 89, p = 0.008), on both 1.5 T and 3 T, and led to a significantly increased total scar burden (3.3 ± 2.4 vs 3.0 ± 2.3 standard AHA segments, p = 0.015). Overall image quality significantly improved using dark-blood LGE compared to bright-blood LGE (81.3% vs 74.0% of all segments were of highest diagnostic quality, p = 0.006). Furthermore, dark-blood LGE led to significantly higher observer confidence (confident in 84.2% vs 78.4%, p = 0.033).ConclusionsThe improved detection of ischemic scar makes the proposed dark-blood LGE method a valuable diagnostic tool in the non-invasive assessment of myocardial scar. The applicability in routine clinical practice is further strengthened, as the present approach, in contrast to other recently proposed dark- and black-blood LGE techniques, is readily available without the need for scanner adjustments, extensive optimizations, or additional training.

Highlights

  • For two decades, bright-blood late gadolinium enhancement (LGE) cardiovascular magnetic resonance (CMR) has been considered the reference standard for the non-invasive assessment of myocardial viability

  • Complete conventional bright-blood and dark-blood LGE data sets were acquired in all subjects (n = 300)

  • Eight subjects (2.7%) had non-diagnostic bright-blood and/or dark-blood LGE image quality due to arrhythmia (n = 1), image artefacts (n = 6), or a combination of both (n = 1), and were excluded from further analysis. Exclusion of these eight patients was caused by non-diagnostic image quality in the brightblood LGE images only (n = 4), dark-blood LGE images only (n = 1), or both sets of images (n = 3)

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Summary

Introduction

Bright-blood late gadolinium enhancement (LGE) cardiovascular magnetic resonance (CMR) has been considered the reference standard for the non-invasive assessment of myocardial viability. While bright-blood LGE can clearly distinguish areas of myocardial infarction from viable myocardium, it often suffers from poor scar-to-blood contrast, making subendocardial scar difficult to detect. Since survivors of previous myocardial infarction (MI) face an increased risk of new cardiovascular events, there is great focus on detecting and accurately assessing the infarcted region [2]. Blood pool signal can mimic scar tissue and lead to false positive observations This makes subendocardial scar patterns difficult to detect and clearly delineate using conventional bright-blood LGE. Allowing additional time after contrast administration partly resolves this challenge, as due to contrast washout over time the scar and blood T1 values will start to diverge, thereby increasing scar-to-blood contrast This solution is unfavourable in daily clinical practice, where already long CMR examinations and high clinical demand result in significant timepressures

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