Thirty-five patients with congenital obstruction of the right ventricular outflow tract underwent magnetic resonance (MR) imaging for evaluation of the pulmonary arteries. All patients underwent cardiac catheterization, and 33 underwent two-dimensional Doppler echocardiography. Results of the three imaging studies were compared. With regard to the presence of a pulmonary confluence, results of MR imaging and angiography were in agreement in 31 of the 35 patients (89%), results of echocardiography and MR imaging were in agreement in 27 of 33 patients (82%), and results of echocardiography and angiography were in agreement in 27 of 33 patients (82%). There was good correlation of measurements of main pulmonary artery size among all three methods and of right and left pulmonary artery size obtained at MR imaging and angiography. Echocardiographic measurements of right and left pulmonary artery size correlated poorly with those obtained at MR imaging and angiography. Results indicated that MR imaging is useful in evaluating the pulmonary arteries in patients with congenital heart disease.
To evaluate the use of magnetic resonance (MR) imaging in the detection of coronary artery bypass grafts (CABGs), 20 patients with grafts underwent electrocardiographic-gated MR study. The number and location of CABGs in each patient were not known at the time of study. The number of grafts seen with MR imaging was compared with the actual number of grafts determined from the operative or angiographic report. On the prospective review of the images, 54 of 64 grafts (84%) were detected, with three false-positive results. When the images were reevaluated with knowledge of the type and number of grafts in each patient, 56 of 64 grafts (88%) were detected. Forty-one of the 46 (89%) left grafts, 15 of the 18 (83%) right grafts, and five of the 11 (45%) internal mammary grafts were detected. Although resolution was not adequate to determine the presence of graft stenosis, this early experience indicates that patent CABGs can be seen with MR imaging.
The authors describe a child with Budd-Chiari syndrome secondary to membranous obstruction of the hepatic veins and a web in the inferior vena cava. Transhepatic catheter venography demonstrated the occlusion, which was recanalized and dilated percutaneously via a transhepatic approach. Hepatomegaly and ascites decreased promptly and the prothrombin time became normal.
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