Volume 13 Supplement 1

Abstracts of the 2011 SCMR/Euro CMR Joint Scientific Sessions

Open Access

Endsystolic versus enddiastolic scar imaging for transmurality assessment

  • Andreas Schuster1,
  • Amedeo Chiribiri1,
  • Geraint Morton1,
  • Masaki Ishida1,
  • Kalpa De Silva1,
  • Matthias Paul1,
  • Shazia Hussain1,
  • Divaka Perera1 and
  • Eike Nagel1
Journal of Cardiovascular Magnetic Resonance201113(Suppl 1):P158

https://doi.org/10.1186/1532-429X-13-S1-P158

Published: 2 February 2011

Objective

To investigate the influence of endsystolic scar imaging over routine enddiastolic scar imaging on transmurality.

Background

The late gadolinium enhancement (LGE) technique has been an important achievement in cardiovascular magnetic resonance (CMR) and is widely used to precisely localize and determine the amount of necrosis and fibrosis. The percentage of transmurality of LGE is inversely related to the likelihood of functional recovery after revascularisation. LGE imaging is usually performed in enddiastole as recommended by current guidelines of the SCMR. Whether or not endsystolic imaging would significantly influence transmurality in patients with ischemic scarring remains unclear.

Methods

107 segments with moderate hypokinesia or more severe wall motion abnormalities were studied in 20 patients with established coronary artery disease referred for viability assessment (33% of all segments). We used a SSFP standard 4-chamber view to determine the endsystolic and enddiastolic position in the cardiac cycle. LGE imaging was performed with patient specific trigger delays to obtain enddiastolic (LGEed) and endsystolic (LGEes) images. Enddiastolic and endsystolic wall thickness (WTed and WTes), thickness of the remaining viable rim (RIMed and RIMes) and thickness of scar in enddiastole was measured manually.

Results

Evidence of LGE was 84% in all dysfunctional segments with a mean scar of 3.4±2.5 mm. Total wall thickness and the thickness of the remaining viable myocardium increased from diastole to systole (WTed 7.9±1.9 versus WTes 8.4±2.2, p<0.001 ; RIMed 4.5±3.1 versus RIMes 5±3.4, p<0.001). There was a difference between the transmurality of scar measured in enddiastole and endsystole (LGEed 46±33% versus LGEes 44±33%, p<0.001). This difference was most pronounced in a subgroup of segments (n=50) between 25 and 75% transmurality of LGE (LGEed 57±18% versus LGEes 53±18%, p<0.001). Reduced transmurality was inversely correlated with increased thickness of the remaining viable rim between diastole and systole (r=-0.73).

Conclusion

Transmurality of scar changes little with varying acquisition times in the cardiac cycle. However there is a statistically significant difference between transmuralities derived from enddiastolic and endsystolic LGE imaging mainly due to the function of the remaining viable rim. Clinically this might not impact on decision making but clearly shows the importance of standardized imaging protocols especially in research studies.
Figure 1

Differences between transmurality in enddiastole and endsystole. Red area indicates transmurality above 75% and green area below 25%.

Figure 2

Differences between transmurality in enddiastole and endsystole. Especially in segments with intermediate transmurality this difference can be more extensive.

Table 1

Enddiastolic versus endsystolic LGE imaging and segmental transmurality

p

All segments (n=107)

LGEed 46±33% versus LGEes 44±33%,

<0.001

Segments with up to 25% transmurality (n=25)

LGEed 25±9% versus LGEes 22±8%

<0.001

Segments with 25% and 75% transmurality (n=50)

LGEed 57±18% versus LGEes 53±18%

<0.001

Segments with transmural scar (n=15)

LGEed 99±1% versus LGEes 99±2%

0.55

Authors’ Affiliations

(1)
King's College London

Copyright

© Schuster et al; licensee BioMed Central Ltd. 2011

This article is published under license to BioMed Central Ltd. 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.

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