Assessment of Myocardial Perfusion during Adenosine Stress Using Real Time Three-Dimensional and Two-Dimensional Myocardial Contrast Echocardiography: Comparison with Single-Photon Emission Computed Tomography
Objectives: To evaluate diagnostic accuracy of adenosine two‐dimensional and three‐dimensional myocardial contrast echocardiography (2D‐ and 3D‐MCE) compared with single‐photon emission computed tomography (SPECT) for assessing myocardial perfusion. Methods: From January through August 2007, patient...
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Veröffentlicht in: | Echocardiography (Mount Kisco, N.Y.) N.Y.), 2010-04, Vol.27 (4), p.421-429 |
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Zusammenfassung: | Objectives: To evaluate diagnostic accuracy of adenosine two‐dimensional and three‐dimensional myocardial contrast echocardiography (2D‐ and 3D‐MCE) compared with single‐photon emission computed tomography (SPECT) for assessing myocardial perfusion. Methods: From January through August 2007, patients with known or suspected CAD who were referred for SPECT underwent simultaneous adenosine 2D‐MCE and 3D‐MCE (live and full volume [FV]). Perfusion and wall motion in 17 segments in the left anterior descending, left circumflex, and right coronary artery territories were analyzed. Results: We studied 30 patients: mean (SD) age, 72.6 (8.2) years; 19 (63%) men. Perfusion by SPECT was abnormal in 13 patients (43%). When comparing MCE with SPECT, sensitivity was comparable for 2D‐MCE, 92%; live 3D‐MCE, 91%; and FV 3D‐MCE, 90%. Specificity was comparable for 2D‐MCE, 75%; live 3D‐MCE, 69%; and FV 3D‐MCE, 79%. Agreement between live 3D‐MCE and 2D‐MCE was 92% (κ[SE], 0.83 [0.17]) and between FV 3D‐MCE and 2D‐MCE, 88% (κ[SE], 0.76 [0.13]). For eight patients in whom SPECT showed reversible defects, live 3D‐MCE correctly identified defects in seven (88%), whereas FV 3D‐MCE correctly identified them in five (63%) (P = 0.57). Conclusion: Myocardial perfusion assessment is feasible by 3D‐MCE with the advantage of rapid, facile acquisition and offline image manipulation. (Echocardiography 2010;27:421‐429) |
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ISSN: | 0742-2822 1540-8175 |
DOI: | 10.1111/j.1540-8175.2009.01026.x |