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3T contrast-enhanced whole heart coronary MRA using 32-channel cardiac coils for the detection of coronary artery disease
Journal of Cardiovascular Magnetic Resonance volume 11, Article number: O5 (2009)
Introduction
In recent years, improved gradient performance and radiofrequency (RF) receiving coils and advanced data acquisition techniques including navigator gating and parallel imaging allowed non-invasive whole-heart coronary imaging. Previous studies have shown that 3.0 T is a promising platform for the detection of significant coronary artery stenoses with contrast-enhanced data acquisition. However, the imaging time (~10 minutes) and spatial resolution (1.3 × 1.3 × 1.3 mm3) remain major limitations [1]. Newly developed 32-channel cardiac coils allow greater acceleration factors and thus reduced imaging time and higher spatial resolution [2].
Purpose
To evaluate the feasibility and diagnostic accuracy of 3 T contrast-enhanced whole-heart coronary MRA using 32-channel cardiac coils. The imaging time, image quality score, and diagnostic accuracy were evaluated in consecutive patients with suspected coronary artery disease.
Methods
20 patients with suspected coronary artery disease who were scheduled for x-ray coronary angiography (mean age 68 ± 14 years, 11 males) underwent MRA at 3 T (MAGNETOM Tim Trio, Siemens) after informed consent was obtained. Contrast-enhanced coronary MRA was also performed in 5 patients who were scheduled for 64-slice coronary CTA. The imaging technique was an ECG-triggered, navigator-gated, inversion-recovery, segmented gradient-echo sequence. A 32-channel matrix coil was used for data acquisition. To reduce imaging time, parallel acquisition (GRAPPA) was used in the phase-encoding direction with an acceleration factor of three. Imaging parameters included: voxel size 0.55 × 0.55 × 0.65 mm3 (interpolated from 1.1 × 1.1 × 1.3 mm3), TR/TE = 3.3/1.5 msec, flip angle = 20°, bandwidth = 700 Hz/pixel. Contrast agent (0.15 mmol/kg body weight, Multihance, Bracco Imaging SpA, Italy) was intravenously administered at a rate of 0.3 ml/sec. The diagnostic accuracy of MRA in detecting significant stenoses (≥ 50%) with the intention to diagnose method was evaluated on a per-segment basis using x-ray angiography as the reference, non-assessable segments were considered to be false-negative or false-positive, respectively.
Results
Whole-heart coronary MRA was successfully completed in 19 of 20 (95%) patients who were scheduled for x-ray coronary angiography and in 5 patients who were scheduled for 64-slice coronary CTA. The averaged imaging time with 32-channel cardiac coils was 6.2 ± 1.3 min. The sensitivity, specificity, positive predictive value, and negative predictive value of coronary MRA for detecting significant stenoses were 81% (62–94%), 96% (92–98%), 71% (52–86%), 98% (94–99%), respectively, on a per-segment basis. Figure 1.
Conclusion
Combined with dedicated 32-channel cardiac coils, parallel imaging with higher acceleration factors allows improvements in imaging speed, study success rate, and reduced dose of the contrast agent when compared with conventional 12-channel coils. Higher study success rate achieved by 32-channel coils substantially improved overall accuracy of coronary MRA in detecting coronary artery disease when using the intention to diagnose method.
References
Qi Yang, Li DB, et al: #2917 Proceedings of 16th annual ISMRM, Toronto. 2008
Niendorf T, et al: Magn Reson Med. 2006, 56: 167-176. 10.1002/mrm.20923.
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Open Access This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution 2.0 International License (https://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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Yang, Q., Li, K., Bi, X. et al. 3T contrast-enhanced whole heart coronary MRA using 32-channel cardiac coils for the detection of coronary artery disease. J Cardiovasc Magn Reson 11 (Suppl 1), O5 (2009). https://doi.org/10.1186/1532-429X-11-S1-O5
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DOI: https://doi.org/10.1186/1532-429X-11-S1-O5