To the Editor:
Vriend et al (1) outlined in their letter to the editor that the capabilities of MRI are not only limited to a detailed imaging of the entire aorta but also allow functional flow measurements. Therefore, they favor MRI over helical CT scanning in the follow-up of patients with coarctation of the aorta. We totally agree that new functional measurements performed with MRI can contribute to the diagnostic workup of coarctation patients and that it might be even more cost-effective to perform MRI without echocardiography in the regular follow-up. (2) But, at the moment, the availability and experience for MRI in congenital cardiology are very limited to a small number of centers worldwide.
We wanted to point out in our study (3) that both helical CT scanning and MRI are highly useful for the imaging of the thoracic aorta in patients with coarctation, but measurements obtained from different methods in sequential studies should be interpreted with care. The following attributes favor helical CT scanning: better resolution; less investigation time; no disturbance with pacemakers; better compatibility with intensive care monitoring; and, generally, greater availability. Other attributes favor MRI, like the possibility of additional functional studies, the lack of ionizing radiation, and, maybe, the lack of need for contrast media. Therefore, the optimal imaging method should be selected for every individual patient. Shifts between methods should be avoided.
From a scientific point of view, there is no doubt that MRI measurement of collateral flow, (4) the elastic properties of the aorta, (5) flow profiles at different sites of the arterial vessels, and many other functional questions are compelling issues of coarctation research, as coarctation seems to be not only a local defect, but also a systemic vessel disease with alterations in the vessel wall (6-8) and in the vascular response. (9) However, this was not the primary aim of our study.
Alfred Hager, MD
Harald Kaemnaerer, MD, VMD
John Hess, MD
Technische Universitat Munchen
Munchen, Germany
Reproduction of this article is prohibited without written permission from the American College of Chest Physicians (www.chestjournal. org/misc/reprints.shtml).
Correspondence to: Alfred Hager, MD, Klinik fur Kinderkardiologie und angeborene Herzfehler, Deutsches Herzzentrum Munchen, Technische Universitat Munchen, Lazarettstr 36, D-80636 Munchen, Germany; e-mail: hager@dhm.ndm.de
REFERENCES
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(8) Smith Maia MM, Cortes TM, Parga JR, et al. Evolutional aspects of children and adolescents with surgically corrected aortic coarctation: clinical, echocardiographic, and magnetic resonance image analysis of 113 patients. J Thorac Cardiovasc Surg 2004; 127:712-720
(9) Aggoun Y, Sidi D, Bonnet D. Arterial dysfunction after treatment of coarctation of the aorta. Arch Mal Coeur Vaiss 2001; 94:785-789
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