Rapid isotropic diffusion mapping without susceptibility artifacts: whole brain studies using diffusion-weighted single-shot STEAM MR imaging.

A subsecond magnetic resonance imaging (MRI) technique for isotropic diffusion mapping is described which, in contrast to echo-planar imaging (EPI), is insensitive to resonance offsets, i.e., tissue susceptibility differences, magnetic field inhomogeneities, and chemical shifts. It combines a diffusion-weighted (DW) spin-echo preparation period and a high-speed stimulated echo acquisition mode (STEAM) MRI sequence and yields single-shot images within measuring times of 559 msec (80 echoes). Here, diffusion encoding involved one scan without DW, three DW scans with b = 490 sec mm(-2), and three DW scans with b = 1000 sec mm(-2) (orthogonal gradient orientations). An automated on-line evaluation resulted in isotropic DW images as well as ADC maps (trace of the diffusion tensor). Experiments at 2.0 T covered the brain of healthy subjects in 20 contiguous sections of 6 mm thickness and 2.0 x 2.0 mm(2) in-plane resolution within a total measuring time of 78 sec. High-resolution studies at 1.0 x 1.0 mm(2) (interpolated from 2.0 x 1.0 mm(2) acquisitions) were obtained within 5 min 13 sec using four averages. In comparison with EPI, DW single-shot STEAM MRI exhibits only about half the SNR, but completely avoids regional signal losses, high intensity artifacts, and geometric distortions.     

Single breath-hold volumetric imaging of the heart using magnetization-prepared 3-dimensional segmented echo planar imaging

We show the feasibility of single breath-hold volumetric imaging of the heart using a three-dimensional (3D) segmented echo planar Imaging (EPI) pulse sequence. Fifteen healthy subjects were evaluated using three magnetization preparation schemes: (a) a driven equilibrium T2-weighted preparation for bright blood and dark myocardium; (b) a STEAM magnetization preparation for dark blood; and (c) fat suppression for coronary artery Imaging. An interleaved EPI trajectory encoding six echoes per Interleave with a 1090 Hz/pixel readout bandwidth was used to collect a 126 × 256 matrix in 22 heartbeats with data acquisition windows per cardiac cycle of 71–285 msec for 8–32 sections. Multiplanar reconstructions could be used if thin (1–3 mm) sections were acquired. Breath-hold volumetric imaging with 3D segmented EPI holds promise for rapid volumetric evaluation of cardiac anatomy.     

Single-breathhold 3D-trueFISP cine cardiac imaging.

Cardiac MRI function measurements are typically based on multiple breathhold 2D sequences to acquire images of the entire heart. In the present study, the feasibility of a cine 3D TrueFISP technique in which several complete volumetric measurements may be obtained during a single breathhold is demonstrated. In contrast to 3D FLASH, the TrueFISP sequence offers an excellent contrast between the myocardium and the intraventricular cavity without the use of contrast agent. An ECG-gated 3D cine TrueFISP sequence was implemented with a repetition time of 2.4-2.8 ms, which allows imaging of the complete heart within a single breathhold throughout 20-46 heartbeats with a 3D frame rate of 8-13 volumes per cardiac cycle and a spatial resolution of about 1.5 x 3.5 x 3.5 mm(3). Breathhold volumetric cine imaging with the 3D TrueFISP technique holds promise for rapid and accurate evaluation of the cardiac regional wall motion and the calculation of cardiac volume and ejection fraction.     

Mixed echo train acquisition displacement encoding with stimulated echoes: an optimized DENSE method for in vivo functional imaging of the human heart.

Mixed echo train acquisition displacement encoding with stimulated echoes (meta-DENSE) is a phase-based displacement mapping technique suitable for imaging myocardial function. This method has been optimized for use with patients who have a history of myocardial infarction. The total scan time is 12-14 heartbeats for an in-plane resolution of 2.8 x 2.8 mm2. Myocardial strain is mapped at this resolution with an accuracy of 2% strain in vivo. Compared to standard stimulated echo (STE) methods, both data acquisition speed and resolution are improved with inversion-recovery FID suppression and the meta-DENSE readout scheme. Data processing requires minimal user intervention and provides a rapid quantitative feedback on the MRI scanner for evaluating cardiac function. Published 2001 Wiley-Liss, Inc.     

High-speed STEAM MRI of the human heart.

High-speed STEAM MR images of the normal human heart were obtained from single cardiac cycles using a 2.0-T whole-body system equipped with conventional 10 mT m-1 gradients. The single-shot 90 degrees-TE/2-90 degrees-TM-(alpha-TE/2-Acq)n pulse sequence acquires n differently phase-encoded stimulated echoes. Measuring times of 127-254 ms were achieved using a "repetition time" of 3.96 ms in conjunction with data matrices of 32-64 x 128 pixels covering a field-of-view of 250-350 mm. The sequence provides easy access to anatomical short-axis and long-axis views of the heart by single and double oblique rotation of the image orientation. STEAM images resemble the features of spin-echo images with respect to chemical shifts, susceptibilities, and flow. Thus, no additional techniques are required for the suppression of blood signals. EKG-triggered acquisitions demonstrate that slice-selective STEAM sequences using short TM intervals allow an unambiguous delineation of those parts of the myocardium that remain stationary within the selected plane throughout the entire imaging process. Neither spins leaving nor entering the slice defined by the initial 90 degrees RF pulses give rise to a stimulated echo and therefore do not contribute to the resulting image.     

Implementation of helical computed tomography in magnetic resonance imaging

PURPOSE: To provide a rapid sequence for volumetric imaging of large fields of view. MATERIALS AND METHODS: The volumetric imaging principles of x-ray helical computed tomograpy (CT) were implemented here on an MRI scanner. However, using the advantages offered by MRI, spiral trajectories in K-space were incorporated to make the helical scan more efficient. Thus, data acquisition and interpolations were conducted in K-space and images reconstructed by gridding and applying the inverse Fourier transform. The rapid spiral helical (RASH) imaging method was evaluated by computer simulations, by scanning phantoms and an in vitro heart, and by comparison to conventional multislice interleaved spirals (MSIS) imaging. RESULTS: A significant time saving (61.4% to 85.9%) relative to MSIS was achieved without significant degradation in image quality. Volume assessment and in-plane resolution by RASH were almost identical to the MSIS pulse sequence. The corresponding increase in effective slice width was estimated to range (for the values studied here) from 1.31 to 2.5 according to the selection of the helical pitch and the slice thickness used for imaging. CONCLUSION: The suggested method offers the advantages provided by x-ray helical CT and can be useful in MRI volumetric scanning of large objects.     

TrueFISP: assessment of accuracy for measurement of left ventricular mass in an animal model

PURPOSE: To test the accuracy of a high performance true fast imaging with steady-state precession (TrueFISP) pulse sequence for the assessment of left ventricular (LV) mass in a large animal model on 1.5-T scanners. MATERIALS AND METHODS: We imaged dogs (N = 10) on a clinical 1.5-T clinical scanner using electrocardiogram (ECG)-gated TrueFISP. In all animals, contiguous segmented k-space cine images were acquired from base to apex (in-plane resolution 1 x 1 mm(2), slice thickness 5 mm, TR = 4.8 msec, TE = 1.6 msec) during repeated breath-holds. In nine of the 10 animals, single-shot images gated to end-diastole were also acquired from base to apex in a single breath-hold (in-plane resolution 1 x 1 mm(2), slice thickness 5 mm, TR = 3.2 msec, TE = 1.6 msec). After imaging, animals were killed, the left ventricle was isolated, and the true mass of the left ventricle (free wall and septum) was determined. Independently, two observers blinded to the post-mortem results computed LV masses based on analysis of the magnetic resonance (MR) images. RESULTS: Comparison of the computed LV mass using TrueFISP to the actual mass showed excellent agreement. Cine-systole was the most accurate technique (mass = 98.6% +/- 4.5% actual, bias = 1.2 +/- 3.4 g) followed by cine-diastole (mass = 97.9% +/- 5.3% actual, bias = 1.8 +/- 4.1 g) and single shot (mass = 94.7% +/- 7.9% actual, bias = 4.2 +/- 6.3 g). Inter- and intra-observer variabilities were low (5.8% +/- 7.1% and 0.4% +/- 4.8%, respectively). CONCLUSION: We conclude that TrueFISP imaging is an accurate, rapid method to determine ventricular mass. In single-shot mode, TrueFISP requires only one breath-hold to estimate the mass of the heart within 6% of the actual value, whereas the segmented k-space implementation measured LV mass to within 3% of the true value.     

Radial single-shot STEAM MRI.

Rapid MR imaging using the stimulated echo acquisition mode (STEAM) technique yields single-shot images without any sensitivity to resonance offset effects. However, the absence of susceptibility-induced signal voids or geometric distortions is at the expense of a somewhat lower signal-to-noise ratio than EPI. As a consequence, the achievable spatial resolution is limited when using conventional Fourier encoding. To overcome the problem, this study combined single-shot STEAM MRI with radial encoding. This approach exploits the efficient undersampling properties of radial trajectories with use of a previously developed iterative image reconstruction method that compensates for the incomplete data by incorporating a priori knowledge. Experimental results for a phantom and human brain in vivo demonstrate that radial single-shot STEAM MRI may exceed the resolution obtainable by a comparable Cartesian acquisition by a factor of four.     

Dynamic contrast-enhanced myocardial perfusion imaging using saturation-prepared TrueFISP

PURPOSE: To develop and test a saturation-recovery TrueFISP (SR-TrueFISP) pulse sequence for first-pass myocardial perfusion imaging. MATERIALS AND METHODS: First-pass magnetic resonance imaging (MRI) of Gd-DTPA (2 mL) kinetics in the heart was performed using an SR-TrueFISP pulse sequence (TR/TE/alpha = 2.6 msec/1.4 msec/55 degrees ) with saturation preparation TD = 30 msec before the TrueFISP readout. Measurements were also performed with a conventional saturation-recovery TurboFLASH (SRTF) pulse sequence for comparison. RESULTS: SR-TrueFISP images were of excellent quality and demonstrated contrast agent wash-in more clearly than SRTF images. The signal increase in myocardium was higher in SR-TrueFISP than in SRTF data. Precontrast SNR and peak CNR were not significantly different between both sequences despite 57% improved spatial resolution for SR-TrueFISP. CONCLUSION: SR-TrueFISP first-pass MRI of myocardial perfusion leads to a substantial improvement of image quality and spatial resolution. It is well suited for first-pass myocardial perfusion studies at cardiovascular MR systems with improved gradient hardware.     

Diffusion tensor imaging using partial Fourier STEAM MRI with projection onto convex subsets reconstruction.

Diffusion-weighted single-shot STEAM MRI allows for diffusion mapping of the human brain without sensitivity to resonance offset effects. In order to compensate for its inherently lower SNR and speed than echo-planar imaging, this work describes the use of partial Fourier encoding in combination with image reconstruction by the projection onto convex subsets algorithm. The method overcomes phase distortions in diffusion-weighted partial Fourier acquisitions that disturb the conjugate complex symmetry of k-space and preclude the use of respective reconstruction techniques. In comparison with full Fourier encoding and a static flip angle for the STEAM readout pulses, experimental results at 2.9 T demonstrate a gain in relative SNR per unit time by 20% for 5/8 phase encoding with optimized variable flip angles. Simultaneously, the imaging time is reduced from about 670 ms (80 echoes) to 440 ms (50 echoes). Current implementations at 2 x 2 mm2 in-plane resolution comprise a protocol for clinical anisotropy studies (12 diffusion-encoding gradient directions at 1000 s mm(-2)) covering 18 sections of 4-mm thickness within a measurement time of 8.5 min (5 averages) and a version optimized for fiber tracking using 24 gradient directions and 38 sections of 2-mm thickness yielding a measurement time of 29.5 min (4 averages).     

Multislice dark-blood carotid artery wall imaging: a 1.5 T and 3.0 T comparison

PURPOSE: To compare two multislice turbo spin-echo (TSE) carotid artery wall imaging techniques at 1.5 T and 3.0 T, and to investigate the feasibility of higher spatial resolution carotid artery wall imaging at 3.0 T. MATERIALS AND METHODS: Multislice proton density-weighted (PDW), T2-weighted (T2W), and T1-weighted (T1W) inflow/outflow saturation band (IOSB) and rapid extended coverage double inversion-recovery (REX-DIR) TSE carotid artery wall imaging was performed on six healthy volunteers at 1.5 T and 3.0 T using time-, coverage-, and spatial resolution-matched (0.47 x 0.47 x 3 mm3) imaging protocols. To investigate whether improved signal-to-noise ratio (SNR) at 3.0 T could allow for improved spatial resolution, higher spatial resolution imaging (0.31 x 0.31 x 3 mm3) was performed at 3.0 T. Carotid artery wall SNR, carotid lumen SNR, and wall-lumen contrast-to-noise ratio (CNR) were measured. RESULTS: Signal gain at 3.0 T relative to 1.5 T was observed for carotid artery wall SNR (223%) and wall-lumen CNR (255%) in all acquisitions (P < 0.025). IOSB and REX-DIR images were found to have different levels of SNR and CNR (P < 0.05) with IOSB values observed to be larger. Normalized to a common imaging time, the higher spatial resolution imaging at 3.0 T and the lower spatial resolution imaging at 1.5 T provided similar levels of wall-lumen CNR (P = NS). CONCLUSION: Multislice carotid wall imaging at 3.0 T with IOSB and REX-DIR benefits from improved SNR and CNR relative to 1.5 T, and allows for higher spatial resolution carotid artery wall imaging.     

Myocardial tissue tracking with two-dimensional cine displacement-encoded MR imaging: development and initial evaluation

A breath-hold two-dimensional cine magnetic resonance (MR) pulse sequence based on displacement encoding with stimulated echoes (DENSE) for quantitative myocardial motion tracking was developed and evaluated. In the sequence, complementary spatial modulation of magnetization was used for time-independent artifact suppression, and echo-planar imaging was used for rapid data sampling. Twelve healthy volunteers underwent cine DENSE MR imaging, and six of them also underwent conventional MR imaging myocardial tagging. The circumferential shortening component of strain (E(cc)) was measured on cine DENSE MR images and conventional tagged MR images. With complementary spatial modulation of magnetization, 10% or less of the total cine DENSE MR image energy was attributed to an artifact-generating echo during systolic imaging. Two-dimensional intramyocardial displacement and strain were measured at cine DENSE MR imaging with spatial resolution and temporal resolution of 2.7 x 2.7 mm and 60 msec, respectively. E(cc) measured at cine DENSE MR imaging correlated well with that measured at conventional MR imaging tagging (slope = 0.88, intercept = 0.00, R = 0.87).     

The straight and narrow path to good head and spine MRI

The path to good head and spine images is narrow and treacherous. We have attempted to give the traveller a small but important set of basic rules, enabling him to cross with success. 1. Averaging can be used to achieve sufficient SNR for thin sections, but the cost in terms of scan time is high. Zooming the image (reducing the field of view) should generally be avoided, as the price in terms of SNR is very high. 2. Rectangular pixels and half-Fourier imaging are two methods for decreasing scan time. HFI, which produces high spatial resolution images, can be used when the SNR is not a limiting factor. Rectangular pixels improve the SNR, but decrease resolution. 3. To achieve good T1 contrast with spin echo imaging, set TE less than or equal to 20 msec. and TR less than or equal to 600 msec. For T2 weighted images, a TR between 2.0 and 3.0 sec. is preferred, typically with two echoes: for example, TEs of 25 and 90 msec. 4. Better slice profiles or gaps between slices can be used to combat slice-to-slice interference. This results in improved SNR on T1 weighted images and improved contrast on T2 weighted images. 5. Low bandwidth techniques may be used to improve the SNR on both T1 and T2 weighted images. Chemical shift artifact puts a finite limit on the extent to which this can be applied. 6. Motion compensating gradients are a tremendous boon to MRI and should be utilized in all possible head and spine applications. These reduce image degradation from CSF and vessel pulsation, as well as from involuntary motion. 7. Fast imaging techniques can be used in 2-D multislice mode to decrease scan time. Unfortunately the T2 contrast with this approach is far inferior to that of spin echo technique. 3-D FLASH, with 1 mm. sections, T1 contrast superior to spin echo technique, and the potential for high resolution reformatted images, may replace conventional 2-D, T1 weighted, spin echo imaging. Pulse techniques that combine all the advantages mentioned lie in the future. For example, one possible approach is a T2 weighted head screen that incorporates low bandwidth technique and HFI. This would produce high resolution images with reasonable SNR in approximately half the present scan time. Despite any further new developments, the trade-off between image quality and scan time will likely always remain.(ABSTRACT TRUNCATED AT 400 WORDS)     

Multislice breath-hold spiral magnetic resonance coronary angiography in patients with coronary artery disease: effect of intravascular contrast medium

PURPOSE: First, to apply a breath-hold multislice 2D spiral magnetic resonance (MR) approach in patients acquiring within 16 heartbeats (acquisition window, 116 msec) a 10-mm-thick stack of four slices (resolution, 1.3 x 1.3 mm(2)); and second, to evaluate the effect of an intravascular Fe-based contrast medium (CM) on a signal-to-noise ratio (SNR) and a contrast-to-noise ratio (CNR). MATERIALS AND METHODS: In each patient one or two coronary arteries were imaged prior to and following cumulative doses of 0.25, 0.5, and 0.75 mg of Fe/kg of body weight (bw) of an intravascular CM (CLARISCAN trade mark, Nycomed-Amersham, Princeton, NJ, USA) containing ultrasmall superparamagnetic iron oxide (USPIO) particles. RESULTS: On precontrast maximum intensity projection (MIP) images generated from the stack of slices, 10 and 11 stenoses of 12 stenoses confirmed by coronary angiography were detected by readers 1 and 2, respectively. SNR and CNR in the coronary arteries peaked at 0.50 mg of Fe/kg of bw, yielding a slight increase of 15.5% and 18.4%, respectively (P < 0.05 vs. precontrast), which did not improve detection of coronary artery stenoses. CONCLUSION: The presented multislice spiral approach allows display of coronary anatomy in MIP formats for convenient display of coronary stenoses. The pulse sequence did not benefit from an intravascular USPIO-based CM, since little improvement in SNR and CNR was achieved.     

MR imaging in carotid artery atherosclerosis plaque characterization.

AIM: To evaluate the potential role of carotid artery atherosclerosis plaque magnetic resonance (MR) microimaging as magnetic resonance imaging (MRI) marker, ex vivo MR images were acquired at optimized parameters on 9.4T Bruker animal imager for occluded tissue resected by carotid endarterectomy (CEA) and corresponding histopathological analysis was made. METHODS AND MATERIALS: For imaging, CEA tissues of size 2-6 cm long and 0.5-1.5 cm wide, were transferred to 15 ml co-polymer laboratory culture tubes containing either 10% formalin in phosphate buffered saline (PBS) or in 50% glycerol in PBS. Imaging protocol was set at TE=30 ms, TR=1.5 s, matrix size=265 x 512, NEX=128, slice thickness=1 mm and in-plane resolution=0.1 mm for total sample size 2.5 cm. Soon after imaging done, carotid artery tissues were cut into 5-mm segments and processed for histological section for successive 5-micrometer slices. To compare morphology of 5 mum thin CEA section with that of 1 mm MR slices, registration was obtained between histologic sections and MR slices. Contrast and magnetic resonance relaxation characteristics were analyzed. RESULTS: Total carotid artery area computed by MR imaging was correlated with areas determined from histologic sections (r(2)=0.989, p=0.0001). For the lumen area, the correlation between MR images and histologic area was (r(2)=0.942, p=0.0001). Relaxation times and T(2) parametric images of different plaque components were determinant for contrast resolution. Scan parameters were optimized for fibrous cap and atheroma. Scan parameters were characteristic for comparison at 1.5T and 9.4T MR imagers. CONCLUSION: The observed correlation validated MR microimaging to assess morphological features of carotid artery plaques and contrast resolution highlighted the potential of in vivo MR imaging as non-invasive MRI marker to monitor carotid artery plaque morphometry and plaque composition.     

Diffusion tensor mapping of the human brain using single-shot line scan imaging

A recently developed single-shot line scan imaging technique for diffusion measurements (Finsterbusch and Frahm, Magn Reson Med 1999;42:772-778) was extended to full diffusion tensor mapping of the human brain. Because the sequence acquires stimulated echoes from individual columns of magnetization ("lines"), the approach is affected neither by spatial aliasing when studying inner volumes nor by resonance offset effects or T2* dephasing as in diffusion-weighted echoplanar imaging. Experiments on healthy subjects were performed at 2.0 T using 31 single-shot images (5b values, 6 orientations, 520 msec each) at 1.5 x 1.5 mm2resolution (interpolated) and 6.0 mm section thickness. Apart from calculated images with isotropic diffusion weighting, the results include maps of the six independent diffusion tensor components, the apparent diffusion coefficient, the relative anisotropy, and the main diffusion direction. The achievable signal-to-noise ratio and resolution allow the identification of differently oriented nerve fibers in the brain stem. J. Magn. Reson. Imaging 2000;12:388-394.     

Localized echo-volume imaging methods for functional MRI

To perform true three-dimensional activation experiments in the human brain, dedicated localized echo-volume imaging (L-EVI) methods were developed. Three-dimensional acquisition allows generation of activation maps with minimal vascular enhancement related to inflow effects. The rapid acquisition of the L-EVI (～100 msec) reduces signal instabilities caused by motion, facilitating the detection of the small intensity changes expected with brain activation. Single-shot L-EVI was performed on normal volunteers at 1.5 T, imaging a three-dimensional predefined volume (240 × 45 × 45 mm³) in the superior portion of the brain with a spatial resolution of 3.75 × 5 × 5 mm³. Increased brain coverage was achieved with a multi-volume imaging (three-shot) version, which simultaneously achieved effective suppression of signals from cerebrospinal fluid. In addition, both asymmetric spin-echo (ASE) and spin-echo (SE) versions of the technique were used to detect blood oxygenation level dependent (BOLD) signal changes in the motor cortex with a finger-tapping paradigm. Images obtained by the L-EVI sequence were qualitatively comparable to standard multislice two-dimensional echo-planar images. Both ASE and SE functional MRI (fMRI) experiments showed consistent activation in the contralateral primary sensorimotor cortex. Furthermore, significant differences in location and magnitude of activation was observed between the two methods, confirming theoretical predictions.     

A pulse sequence for rapid in vivo spin-locked MRI

PURPOSE: To develop a novel pulse sequence called spin-locked echo planar imaging (EPI), or (SLEPI), to perform rapid T1rho-weighted MRI. MATERIALS AND METHODS: SLEPI images were used to calculate T1rho maps in two healthy volunteers imaged on a 1.5-T Sonata Siemens MRI scanner. The head and extremity coils were used for imaging the brain and blood in the popliteal artery, respectively. RESULTS: SLEPI-measured T1rho was 83 msec and 103 msec in white (WM) and gray matter (GM), respectively, 584 msec in cerebrospinal fluid (CSF), and was similar to values obtained with the less time-efficient sequence based on a turbo spin-echo readout. T1rho was 183 msec in arterial blood at a spin-lock (SL) amplitude of 500 Hz. CONCLUSION: We demonstrate the feasibility of the SLEPI pulse sequence to perform rapid T1rho MRI. The sequence produced images of higher quality than a gradient-echo EPI sequence for the same contrast evolution times. We also discuss applications and limitations of the pulse sequence.     

Limits of 8-Tesla magnetic resonance imaging spatial resolution of the deoxygenated cerebral microvasculature

PURPOSE: To quantify the minimum magnetic resonance imaging (MRI) spatial resolution of the visible deoxygenated microscopic vessels of the human brain at 8 T. MATERIALS AND METHODS: This study compared 8-T gradient echo (GE) images of a human cadaver brain having an in-plane resolution of 195 x 195 microm to corresponding digital photographs of 205 cryomicrotome sections of the same cadaver brain, along with summed images of 25 contiguous cryomicrotome sections. One-millimeter-thick GE images of a 1-cm-thick unfixed whole coronal brain section were acquired using techniques similar to those commonly utilized for 8-T human imaging in vivo. RESULTS: There was excellent MR visualization of the deoxygenated microscopic vessels within the brain down to a resolution of approximately 100 microm. CONCLUSION: By taking advantage of magnetic susceptibility-based blood oxygenation level-dependent (BOLD) contrast, deoxygenated microscopic blood vessels smaller than the pixel dimensions used for imaging can be visualized using a whole-body 8-T MRI system.     

MRCP imaging at 3.0 T vs. 1.5 T: preliminary experience in healthy volunteers

PURPOSE: To evaluate the impact of magnetic resonance cholangiopancreatography (MRCP) imaging at 1.5T and 3.0T on image quality. MATERIALS AND METHODS: Fourteen volunteers were examined at both 1.5T and 3.0T using MRCP imaging performed with a breath-held two-dimensional (2D) half-Fourier acquired single-shot turbo spin-echo (HASTE) thick-slab sequence, a free-breathing navigator-triggered three-dimensional (3D) turbo spin-echo (TSE) sequence with prospective acquisition correction, and a heavily T2-weighted (T2W) sequence with breath-held multislice HASTE. All images were scored for visualization of the biliary and pancreatic ducts, severity of artifacts, image noise, and overall image quality. RESULTS: MRCP imaging at 3.0T yielded a significant improvement in overall image quality compared to 1.5T. We found a trend for superior visualization of the biliary and pancreatic ducts at 3.0T. Heavily T2W imaging with thin sections (1.4 mm) at 3.0T provided diagnostic images and better visualization of the biliary and pancreatic ducts than heavily T2W imaging with standard sections (2.8 mm) at 3.0T. CONCLUSION: Our experience suggests that MRCP imaging at 3.0T has the potential to provide excellent images. High-resolution heavily T2W imaging with a small voxel size (1.3 x 1.3 x 1.4 mm) at 3.0T can provide diagnostic images and allow evaluation of small pathologies of the bile and pancreatic ducts, which 1.5T MRI cannot sufficiently visualize.