Biomedical subjects

J G Pipe

Publications and source records attributed to J G Pipe.

27 records · Page 2Linked to original sources

PubMed1995

Spatial encoding and reconstruction in MRI with quadratic phase profiles.

Application of a slice-selective frequency modulated radiofrequency excitation pulse in a magnetic resonance (MR) imaging experiment creates a quadratic phase profile along the direction of slice selection. This quadratic phase profile inherently localizes the signal contribution to its vertex, which can be shifted with the application of a linear magnetic field gradient. Different methods for reconstruction of the spatial profile are discussed. The point spread functions of these reconstructions are similar to that of conventional Fourier transforms; one important difference is the elimination of aliasing at the expense of MR signal amplitude when performing 'local,' or limited, reconstruction. Limited reconstruction together with spatially limited excitation combines some of the advantages of both three-dimensional phase-encoded and two-dimensional multislice techniques in appropriate situations. Applications discussed are three-dimensional gradient echo experiments applied to time of flight MR angiography and T2(+)-weighted data collection.

Computer Simulation↗

PubMed1995

Analytical resolution and noise characteristics of linearly reconstructed magnetic resonance data with arbitrary k-space sampling.

The effects of time-varying readout gradients and data sampling with variable dwell times in magnetic resonance imaging are examined. General reconstruction formulas are given for linear reconstruction with even k-space weighting. Closed analytic expressions for estimator variance are given for data sampling during arbitrary gradient waveforms with both uniform kx step size and nonuniform kx step size. It is shown that estimator variance increases (the signal-to-noise ratio decreases) for nonconstant gradient waveforms. It is also shown that estimator variance is greater for constant k-space sampling strategies than for constant time sampling at the Nyquist rate. Data collected during a triangular readout gradient waveform, with either constant time or constant k-space sampling, versus conventional (constant gradient) collection confirms theoretical predictions for estimator variance. The benefits of collecting data while the readout gradient is ramping up from and down to zero are discussed.

Algorithms↗

PubMed1995

Magnetic-resonance imaging techniques for detection of elasticity variation.

The relative success of manual palpation in the detection of breast cancer would suggest that a method for remote palpation resulting in a measurement of tissue elasticity could provide a diagnostic tool for detecting cancerous lesions deeper within the breast. This presumption is based in part on the excellent contrast between neoplastic and normal tissue due to the large (orders of magnitude) relative variation in the shear elastic modulus. By comparison, the bulk deformational modulus maintains the same value to within 20% for most soft tissues. A specific method of magnetic-resonance imaging (MRI) which measures tissue displacements has been used in experiments with a phantom containing regions of increased Young's modulus as a demonstration. The spatial modulation of magnetization technique uses the displacement of a spatial grid pattern caused by spin saturation to track regional motion. Mathematical reconstruction of the distribution of elastic moduli is shown for select examples. Any modality, e.g., MRI, ultrasound, etc., which can detect local tissue motion with sufficient spatial resolution can be used and therefore the results presented here should give an indication of the utility of such motion tracking techniques to future measurement of tissue elasticity.

Biophysical Phenomena↗

PubMed1995

In vivo MR determination of water diffusion coefficients and diffusion anisotropy: correlation with structural alteration in gliomas of the cerebral hemispheres.

PURPOSE: To determine whether a relationship exists between water diffusion coefficients or diffusion anisotropy and MR-defined regions of normal or abnormal brain parenchyma in patients with cerebral gliomas. METHODS: In 40 patients with cerebral gliomas, diffusion was characterized in a single column of interest using a motion-insensitive spin-echo sequence that was applied sequentially at two gradient strength settings in three orthogonal directions. Apparent diffusion coefficients (ADCs) were derived for the three orthogonal axes at 128 points along the column. An average ADC and an index of diffusion anisotropy (IDA = diffusion coefficientmax-min/diffusionmean) was than calculated for any of nine MR-determined regions of interest within the tumor or adjacent parenchyma. RESULTS: In cerebral edema, mean ADC (all ADCs as 10(-7) cm2/s) was 138 +/- 24 (versus 83 +/- 6 for normal white matter) with mean IDA of 0.26 +/- 0.14 (versus 0.45 +/- 0.17 for normal white matter). Solid enhancing central tumor mean ADC was 131 +/- 25 with mean IDA of 0.15 +/- 0.10. Solid enhancing tumor margin mean ADC was 131 +/- 25, with IDA of 0.25 +/- 0.20. Cyst or necrosis mean ADC was 235 +/- 35 with IDA of 0.07 +/- 0.04. CONCLUSION: In cerebral gliomas ADC and IDA determinations provide information not available from routine MR imaging. ADC and IDA determinations allow distinction between normal white matter, areas of necrosis or cyst formation, regions of edema, and solid enhancing tumor. ADCs can be quickly and reliably characterized within a motion-insensitive column of interest with standard MR hardware.

Adolescent↗

PubMed1991

Quantitative measurement of tissue perfusion and diffusion in vivo.

Magnetic resonance imaging techniques designed for sensitivity to microscopic motions of water diffusion and blood flow in the capillary network are also exceptionally sensitive to bulk motion properties of the tissue, which may lead to contrast artifact and large quantitative errors. The magnitude of bulk motion error that exists in human brain perfusion/diffusion imaging and the inability of cardiac gating to adequately control this motion are demonstrated by direct measurement of phase stability of voxels localized in the brain. Two methods are introduced to reduce bulk motion phase error. The first, a postprocessing phase correction algorithm, reduces coarse phase error but is inadequate by itself for quantitative perfusion/diffusion MRI. The second method employs orthogonal slice selection gradients to define a column of tissue in the object, from which echoes may be combined in a phase-insensitive manner to measure more reliably the targeted signal attenuation. Applying this acquisition technique and a simplistic model of perfusion and diffusion signal attenuations yields an estimated perfusion fraction of 3.4 +/- 1.1% and diffusion coefficient of 1.1 +/- 0.2 x 10(-5) cm2/s in the white matter of one normal volunteer. Successful separation of perfusion and diffusion effects by this technique is supported in a dynamic study of calf muscle. Periods of normal blood flow, low flow, and reactive hyperemia are clearly distinguished in the quantitative perfusion results, whereas measured diffusion remained nearly constant.

Algorithms↗

PubMed1991

A progressive gradient moment nulling design technique.

A method is presented for designing motion-compensated gradients in a progressive manner. The method is easily applicable to many types of waveforms, and can compensate for any order of motion. It can be implemented graphically or numerically. Underlying theory and examples of its application are provided.

Humans↗

PubMed1991

Effect of bulk tissue motion on quantitative perfusion and diffusion magnetic resonance imaging.

The effect of irreproducible bulk tissue motions upon quantification of tissue perfusion and diffusion was studied via computer simulation of random phase error in conventional phase-encoded perfusion/diffusion MRI. Simulations using acquisition parameters typical for human brain studies demonstrate that bulk motion irreproducibility of approximately 60 microns/s can produce phase instability on the order of 20 degrees which overwhelms estimates of perfusion fraction and produces significant errors in diffusion values. Bulk tissue motion control of the human brain via cardiac gating and substantial head restraint was studied by direct measurement of voxel phase stability. Phase instability of 10 degrees to 20 degrees was observed from right-to-left and anterior-to-posterior motions and significantly greater phase variability from superior-to-inferior motion. The spatial pattern of phase variability indicates the source is likely a mixture of cardiac pulsation and respiration.

Brain↗

PubMed1991

Method for measuring three-dimensional motion with tagged MR imaging.

Recent methods of magnetic resonance imaging involve the placement of a grid of planes of saturation over the imaging plane; distortion of the grid corresponds to tissue displacement in two dimensions. An extension to this method that allows measurement of motion in the third dimension involves a second acquisition that tilts the grid, allowing analysis of motion normal to the imaging plane. A rotating phantom was used to verify the accuracy of the motion measurements, and the technique was applied to the heart wall and skeletal muscle. Phantom results show that the measure of z motion can be as accurate as that of x and y motion. Three-dimensional displacements of heart-wall and skeletal muscle are shown. With an accurate measure of three-dimensional motion, more complete analysis of heart-wall motion and contraction is possible.

Humans↗

PubMed1990

Anisotropic diffusion in human white matter: demonstration with MR techniques in vivo.

Quantitative measurements of perfusion and molecular diffusion were made in human white matter in two orientations of the motion-sensitization gradient to document anisotropy of these parameters. Measurements were localized to a 10 X 10-mm tissue column oriented in an anterior-to-posterior direction in the left cerebral hemisphere just above the body of the left ventricle. This region was selected because of the relatively high directionality of white matter fibers. In this study of five healthy volunteers, strong diffusion anisotropy was observed in all cases. Twofold or greater anisotropy was commonly observed, with the higher diffusion value associated with motion sensitivity along the fiber directions. By combining data from both gradient orientations in all cases, diffusion values of solid tissue ranged from 0.38 X 10(-3) mm2/sec to 1.12 X 10(-3) mm2/sec, and measured perfusion fractions were in the range of 2%-5% (excluding areas highly contaminated by cerebrospinal fluid). Little or no perfusion-fraction anisotropy was observed; however, perfusion measurements were limited by noise. Data were collected without cardiac gating by using a technique that offers good immunity to bulk tissue motion artifacts.

Adult↗