Noninvasive evaluation of mitral regurgitation by analysis of left atrial signal loss in cine magnetic resonance.

Magnetic resonance imaging that uses shallow flip angles, short repetition times, and gradient refocused echoes results in multiple images throughout the cardiac cycle in which the blood pool has high signal intensity. In cine magnetic resonance images, disturbed (high velocity) blood flow produces a loss of signal intensity within the intracavitary blood pool, which makes this technique potentially useful for evaluating valvular disease. Multilevel cine magnetic resonance imaging was performed in 26 patients with mitral regurgitation (MR) documented and graded for severity by Doppler echocardiography or contrast ventriculography. Intracavitary left atrial signal intensity was analyzed in order to derive parameters that reflect the severity of the lesion. Seven normal volunteers were studied for comparison. All regurgitant lesions were visualized in cine magnetic resonance images as discrete regions of systolic signal loss extending from the mitral valve into the left atrium. The extent and degree of signal loss correlated well with severity. In patients with mild MR, signal loss was seen in 3.3 +/- 1.2 (+/- SD) anatomic levels compared to 4.9 +/- 1.4 levels in patients with moderate MR (p = NS), and in 7.0 +/- 1.4 levels in patients with severe MR (p less than 0.001 versus mild MR). The total area of maximal systolic left atrial signal loss seen in all levels was 10 +/- 6 cm2 in mild versus 31 +/- 17 cm2 in moderate (p less than 0.001) and 96 +/- 30 cm2 in severe MR (p less than 0.001).(ABSTRACT TRUNCATED AT 250 WORDS)

Quantification of regional myocardial function by rapid cine MR imaging.

The capability of rapid (cine) MR imaging to quantitate left ventricular function was assessed in 13 normal subjects and in 15 patients with ischemic heart disease and regional wall-motion abnormalities proved by echocardiography and/or by contrast ventriculography. Fifteen to 20 MR images/cardiac cycle were acquired by using partial flip angles, short repetition times, and gradient-refocused echoes. Regional wall motion was assessed qualitatively in the equatorial left ventricular section by using the cine display and quantitatively by measuring myocardial thickness at end-diastole and at end-systole in six left ventricular segments in this plane. In normal volunteers wall motion was normal in all segments. Heterogeneity of systolic wall thickening was observed in normal subjects, ranging from 33% +/- 17% in the posteroseptal segment to 66% +/- 29% in the posterior segment. Overall systolic wall thickening was 48% +/- 28%. From the cinematic display of MR images, abnormal wall motion was observed in 40 of 90 segments in patients with ischemic heart disease, which correlated well with results of echocardiography or contrast ventriculography. Twenty-one segments were hypokinetic, 15 were akinetic, and four were dyskinetic. In patients with ischemic heart disease, percentage systolic wall thickening was 43% +/- 31% in the segments with normal wall motion, 6% +/- 18% in hypokinetic segments, -4% +/- 24% in akinetic segments, and -13% +/- 25% in dyskinetic zones. Absolute systolic wall thickening was less than 2 mm in 31 of 40 abnormal segments and was greater than 2 mm in only three. Rapid acquisition, improved temporal resolution, and the capacity for cine display make this new MR technique potentially useful not only for qualitative assessment of cardiac wall motion, but also for quantification of regional myocardial function.

Evaluation of pulmonary blood supply by nuclear magnetic resonance imaging in patients with pulmonary atresia.

Nuclear magnetic resonance (NMR) imaging defines the blood pool without the need for contrast medium. Consequently, it may be useful for defining the pulmonary circulation in patients with pulmonary atresia, in whom opacification of these vessels can be problematic. Ten patients with pulmonary atresia were evaluated by gated NMR imaging. The morphology of the right ventricular outflow tract, the size and the course of the central pulmonary vessels and the source of the collateral supply to the lung were assessed. Central pulmonary arteries were identified and measured in 9 of the 10 patients. One patient had no detectable central pulmonary arteries. Angiography confirmed the NMR findings in all but two patients, in whom NMR scanning visualized a main pulmonary artery that was not seen on angiography. Collateral arteries arising from the aorta or the arch vessels, as well as intracardiac malformations and aortic arch anomalies, were identified in all 10 patients. In six patients with palliative surgery, NMR imaging correctly demonstrated all patent shunts. Nuclear magnetic resonance imaging appears to be an effective noninvasive technique for evaluating patients with pulmonary atresia. However, tomographic thickness and spatial resolution are still limiting factors for this technique in infants.

MR imaging of the thoracic aorta in Marfan patients.

A characteristic shape of the ascending aorta has been reported in patients with Marfan syndrome. To evaluate the capability of magnetic resonance (MR) imaging to distinguish between marfanoid and other aortic aneurysms, 11 Marfan patients (group 1), eight patients with ascending aorta enlargement (group 2), and 20 normal subjects (group 3) had transverse and sagittal MR of the thoracic aorta. Aortic diameter was measured at the sinuses of Valsalva (SV), the caudal portion of the ascending aorta, the prearch region (PA), the middle arch, and the descending aorta. The ratio SV/PA was significantly greater (p less than 0.001) in group 1 compared with groups 2 and 3. The SV/PA in all Marfan patients exceeded 1.4 but was less than 1.3 in subjects of groups 2 and 3. Magnetic resonance imaging provides definitive measurements of aortic dimensions and is potentially the method of choice for establishing the diagnosis of aortic involvement in Marfan syndrome and monitoring the course of aortic enlargement.

MR imaging of congenital anomalies of the aortic arch.

Eighteen patients with congenital aortic arch anomalies were evaluated by ECG-gated MR imaging. Transverse images encompassing the heart and thoracic aorta were available in all patients; sagittal or coronal studies were available in 12 patients. Visualization of the aortic arch, its orientation, and the origin and course of the arch vessels was assessed. Associated intracardiac abnormalities were noted, and the effect of aberrant vessels on the trachea or esophagus was determined. Thirteen patients had a right aortic arch. Mirror-image branching was found in 10 cases, and an aberrant left subclavian artery was found in three of these. Three patients had a left aortic arch with aberrant right subclavian artery, and two patients had a double arch. Tracheal compression caused by vascular rings was found in two patients with respiratory symptoms. Corroborating studies (angiography, surgery, CT, and autopsy) in 16 patients confirmed the MR diagnoses in all but one. We conclude that MR could substitute for other techniques as an effective, noninvasive method for the evaluation of congenital aortic arch anomalies.