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The value of stress perfusion cardiovascular magnetic resonance imaging for patients referred from the adult congenital heart disease clinic: 5-year experience at the Toronto General Hospital

Published online by Cambridge University Press:  18 September 2013

Djeven P. Deva
Affiliation:
Department of Medical Imaging, Peter Munk Cardiac Centre, Toronto General Hospital, University of Toronto, Ontario, Canada
Felipe S. Torres
Affiliation:
Radiology Department, Hospital de Clínicas de Porto Alegre, Porto Alegre, Rio Grande do Sul, Brazil
Rachel M. Wald
Affiliation:
Division of Cardiology, Peter Munk Cardiac Centre, Toronto General Hospital, University of Toronto, Ontario, Canada
S. Lucy Roche
Affiliation:
Division of Cardiology, Peter Munk Cardiac Centre, Toronto General Hospital, University of Toronto, Ontario, Canada
Laura Jimenez-Juan
Affiliation:
Department of Medical Imaging, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada
Erwin N. Oechslin
Affiliation:
Division of Cardiology, Peter Munk Cardiac Centre, Toronto General Hospital, University of Toronto, Ontario, Canada
Andrew M. Crean*
Affiliation:
Department of Medical Imaging, Peter Munk Cardiac Centre, Toronto General Hospital, University of Toronto, Ontario, Canada Division of Cardiology, Peter Munk Cardiac Centre, Toronto General Hospital, University of Toronto, Ontario, Canada
*
Correspondence to: Dr A. Crean, Division of Cardiology and Department of Medical Imaging, 1c-544 NCSB, Toronto General Hospital, 585, University Ave, Toronto, Canada M5G 2N2. Tel: +1 647 928 6616; Fax: +1 416-593-0502; E-mail: andrew.crean@uhn.ca
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Abstract

Background: Vasodilator stress perfusion cardiovascular magnetic resonance imaging is a clinically useful tool for detection of clinically significant myocardial ischaemia in adults. We report our 5-year retrospective experience with perfusion cardiovascular magnetic resonance in a large, quarternary adult congenital heart disease centre. Methods: We reviewed all cases of perfusion cardiovascular magnetic resonance in patients referred from the adult congenital heart disease service. Dipyridamole stress perfusion cardiovascular magnetic resonance was undertaken on commercially available 1.5 and 3 T cardiovascular magnetic resonance scanners. Late gadolinium enhancement imaging was performed 8–10 minutes after completion of the rest perfusion sequence. Navigator whole-heart coronary magnetic resonance angiography was also performed where feasible. Results of stress cardiovascular magnetic resonance were correlated with complementary imaging studies, surgery, and clinical outcomes. Results: Over 5 years, we performed 34 stress perfusion cardiovascular magnetic resonance examinations (11 positive). In all, 84% of patients had further investigations for ischaemia in addition to cardiovascular magnetic resonance. Within a subgroup of 19 patients who had definitive alternative assessment of their coronary arteries, stress perfusion cardiovascular magnetic resonance demonstrated a sensitivity of 82% and specificity of 100%. Of the 34 studies, two were false negatives, in which the aetiology of ischaemia was extrinsic arterial compression rather than intrinsic coronary luminal narrowing. Coronary abnormalities were identified in 71% of cases who had coronary magnetic resonance angiography. Conclusion: Stress perfusion cardiovascular magnetic resonance is a useful and accurate tool for investigation of myocardial ischaemia in an adult congenital heart disease population with suspected non-atherosclerotic coronary abnormalities.

Information

Type
Original Articles
Copyright
Copyright © Cambridge University Press 2013 
Figure 0

Figure 1 Adult congenital heart disease stress perfusion CMR imaging protocol. The basic stress CMR protocol can be completed in an hour. Optional sequences can be added in between segments of the basic protocol as shown in the example above. Coronary magnetic resonance angiography is usually performed after late gadolinium enhancement imaging, when all the gadolinium has been delivered, to maximise T1 signal from coronary arteries. CMR = cardiovascular magnetic resonance.

Figure 1

Table 1 Population characteristics.

Figure 2

Table 2 Indication for stress cardiovascular magnetic resonance.

Figure 3

Figure 2 Proximal occlusion of ALCAPA repair with subsequent collateralisation – dipyridamole stress perfusion cardiovascular magnetic resonance. Images from dipyridamole stress perfusion cardiovascular magnetic resonance of a 23-year-old man who had previously had repair of ALCAPA. Stress perfusion sequences (a) demonstrate reversible subendocardial perfusion defects in the LAD and circumflex territories (solid arrows) not seen on the rest perfusion sequence (b) and significantly greater in volume than small subendocardial anterior wall and anterolateral papillary muscle infarcts (dotted arrows) on late gadolinium enhancement sequences (c). There is also mild peri-infarct ischaemia (dashed arrow) in the anterior wall (a). These stress perfusion defects were demonstrated to be secondary to restricted flow to the left anterior descending coronary artery and circumflex territories via a complex network of narrow calibre collaterals from the right coronary artery. Curved multiplanar reconstruction images from gated contrast-enhanced coronary computed tomography (d) demonstrate absence of the left main coronary artery due to remote occlusion following ALCAPA repair. A complex network of narrow calibre collaterals connect a dilated conus branch of the right coronary artery to the distal LAD supplying the LAD territory and circumflex territories retrogradely. ALCAPA = anomalous left coronary from pulmonary artery; Co = collaterals; Conus = conus branch; LAD = left anterior descending coronary artery; LCx = circumflex coronary artery; OM = large calibre obtuse marginal; RCA = right coronary artery; RSV = right sinus of Valsalva; RV = right ventricle; SoV = sinus of Valsalva.

Figure 4

Figure 3 RCA territory stress perfusion defect in a patient with Kawasaki disease and proximal RCA aneurysm. Images from dipyridamole stress perfusion cardiovascular magnetic resonance of a 30-year-old male with Kawasaki disease and known aneurysm of the proximal RCA demonstrating a reversible RCA territory perfusion defect (white solid arrow) on stress perfusion sequences (a) with no defect on rest perfusion sequences (b) or evidence of infarct on late gadolinium sequences (c). The proximal right coronary artery aneurysm (dotted arrow) is visualised on cine steady-state free precession imaging (d). RCA = right coronary artery.

Figure 5

Figure 4 Coronary compression in repaired TOF-APV and free pulmonary regurgitation and extrinsic compression of left main coronary artery by aneurysmal main pulmonary artery – false negative stress perfusion CMR. Stress CMR, invasive coronary angiograms, coronary CT, and exercise tolerance test in a 56-year-old male with repaired TOF-APV and free pulmonary regurgitation who presented with angina on exertion. Axial cine steady-state free precession sequences from a single axial level demonstrate the origin of the left main coronary artery (black arrow) in diastole (a) and its displacement by a dilated main pulmonary artery (black star) in systole (b). The main pulmonary artery (black star) dilated significantly from 47 mm in diastole to 57 mm in systole. Normal stress perfusion CMR study with no perfusion defect at stress (c) or rest (d). Invasive coronary angiography demonstrating a normal calibre proximal left main coronary artery (black arrow) in diastole (e) and subsequent compression by the dilated main pulmonary artery during systole (f). Maximum intensity projection images from gated CT angiogram acquired throughout the cardiac cycle in an oblique plane in diastole (g) and systole (h) demonstrating the significant systolic dilation of the main pulmonary artery (black star) causing compression of the proximal left main coronary artery (black arrow) against the left sinus of Valsalva (asterisk). Exercise tolerance test with sample electrocardiograms at rest (i), and at peak exercise (j) in the period of worst ST depression during which the patient experienced typical angina. CMR = cardiovascular magnetic resonance; CT = computed tomography; TOF-APV = tetralogy of Fallot with absent pulmonary valve.

Figure 6

Table 3 Diagnostic performance of vasodilator stress CMR.

Figure 7

Figure 5 Kawasaki aneurysms with mural thrombus and transmural infarction due to distal embolisation of thrombus. Curved multiplanar reconstruction (a) and axial (e) images from gated navigator steady-state free precession whole-heart coronary magnetic resonance angiogram in a 20-year-old male with Kawasaki disease-related fusiform aneurysms in the proximal and mid-circumflex coronary artery (asterisk). The axial, curved multiplanar reconstruction images and short-axis sections through the vessel (b–d) reveal mural thrombus (white solid arrow) and eccentric wall calcification (black dashed arrow) in the mid-circumflex artery aneurysm on this contrast-enhanced study. Cardiac short-axis cine steady-state free precession (f) and late gadolinium enhancement images (h) demonstrate thinning and transmural circumflex territory infarction (black arrows) likely because of distal embolisation of thrombus from the aneurysm. The stress perfusion cardiovascular magnetic resonance image demonstrates a matched perfusion defect (g) due to the infarction. Note that the aneurysmal circumflex coronary artery (asterisk) is almost as large as the descending thoracic aorta (star). LA = left atrium; LAD = left anterior descending coronary artery; LM = left main coronary artery; LV = left ventricle; RA = right atrium; RCA = right coronary artery; SoV = sinuses of Valsalva.

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