In vivo, in utero microscopic magnetic resonance imaging: application in a rat model of diaphragmatic hernia.

This article presents a microscopic MR technique for imaging small mammalian fetuses in utero and in vivo which can be used as a tool for studying normal and abnormal development in small animal fetal models, for targeting in utero intervention in such models, and for following development serially. This new method is applied to a rat model of congenital diaphragmatic hernia (CDH). Pregnant Sprague-Dawley rats were fed nitrofen at 9.5 days postcoitus to induce CDH in the fetuses. The dams were imaged to identify fetuses with CDH for targeted in utero intervention, which consisted of fetal tracheal ligation. Following tracheal ligation, the fetuses were followed serially with our MR technique. For MR imaging, the dam was anesthetized with intramuscular ketamine and intraperitoneal pentobarbital. In utero imaging was performed on a 4 Tesla MRI system using a multislice, fast spin echo sequence with a long TR and short effective TE. These results were validated by examining individual fetuses postmortem using high-resolution MR and anatomic dissection. The in utero, in vivo MR technique is highly accurate for diagnosing CDH and following the effects of surgical intervention, and shows promise as a tool for the study of embryogenesis in small animal models. Magn Reson Med 44:331-335, 2000.

A MRI bolus tagging method for observing helical flow in the descending aorta.

We present a MRI bolus tagging method for exploring the helical nature of blood flow in the aorta. Two image series are collected, the first to quantify longitudinal flow (coronal/sagittal imaging plane-transverse saturation plane), the second to measure rotational flow (transverse imaging plane-coronal/sagittal saturation plane). The experimental protocol has been established in healthy adult volunteers and children with normal vasculature. Our results permit immediate visualization of the unique nature of helical flow in each volunteer. We demonstrate evidence of rapid helical twist, no helical twist, and reversal of twist.

Continuous inversion angiography.

A subtractive time-of-flight technique for magnetic resonance angiography is described. In this approach, the arterial supply to an organ is inverted in a steady-state fashion by applying off-resonance irradiation in the presence of a linear magnetic field gradient. An angiogram is formed by subtracting an image acquired with arterial inversion from a control image acquired with no arterial inversion. A single coil is used to apply both the inversion and observation pulses. Intracranial angiograms obtained from normal volunteers using a two-dimensional projective implementation of this technique at 1.5 T illustrate excellent small vessel detail and background suppression.

Circumferential myocardial shortening in the normal human left ventricle. Assessment by magnetic resonance imaging using spatial modulation of magnetization.

BACKGROUND: Conventional cardiac imaging methods do not depict true segmental myocardial shortening, since they cannot determine segment length between fixed points in the myocardium. METHODS AND RESULTS: We used electrocardiographically gated magnetic resonance imaging with spatial modulation of magnetization to noninvasively "tag" the myocardium with dark stripes at uniform 7-mm intervals center to center at end diastole. We then determined end-systolic stripe separation and thereby calculated circumferential shortening. When end systole was not reached in the first image series, a second temporally overlapped series starting in late systole was used to determine late-systolic shortening. Septal, anterior, lateral, and inferior segments were assessed at endocardium, midwall, and epicardium on five midventricular short-axis sections each in 10 normal volunteers. A transmural gradient in circumferential shortening was observed, with the percentage of endocardial segment shortening consistently greater than epicardial segment shortening (epicardial, 22 +/- 5%; midwall, 30 +/- 6%; and endocardial, 44 +/- 6%; p less than 0.0001 by analysis of variance). Circumferential shortening varied from apex to base with slices closer to the base of the left ventricle showing less shortening at the midwall (28 +/- 9%) and endocardium (39 +/- 6%) than more apical slices at the midwall (34 +/- 13%) and endocardium (49 +/- 9%) (p less than 0.05 and p less than 0.01, respectively, by analysis of variance). CONCLUSIONS: Transmural and longitudinal heterogeneity of circumferential shortening is present in the normal human left ventricle. Magnetic resonance imaging with spatial modulation of magnetization is a powerful new tool for assessment of circumferential shortening and provides information unobtainable with conventional imaging methods.

Multiple-hospital survey of ejection-fraction variability using a cardiac phantom.

A dynamic cardiac phantom was used to provide identical input data at 11 different nuclear medicine laboratories throughout the Philadelphia area, and the variability in the resulting calculations of ejection fraction (EF) was assessed. The variability observed between different operators using the same computer system averaged 3 EF units, which was similar to that between different observers using different types of computers. In the range of low ejection fractions, however, there was a suggestion that EFs calculated with an MDS computer were slightly lower than those from a DEC computer.

A method for localization of sources of human cerebral potentials evoked by sensory stimuli.

A method based on potential field theory is described for assessing the location and orientation of dipole generators of the human scalp-recorded sensory evoked potential (EP). The method assumes that the EP at a given moment is due to a single dipole source and that the head can be modeled by a homogeneous conductive sphere (brain) surrounded by inner (skull) and outer (scalp) shells of differing conductivity (three-sphere model). Solution for source location and orientation from the surface potential field is given for the case of a single homogeneous sphere (one-sphere model). It is then shown that a unique solution for the three-sphere model can be derived from the one-sphere solution. Solutions are obtained by application of an iterative procedure which minimizes the error between calculated and empirical potential fields. A test of the method is described in which the calculated location and orientation of a dipole was in good agreement with the known source of an early component of the human somatosensory EP.