Quality control in mammography: The American College of Radiology's Mammography Screening Accreditation Program.
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Biomedical subjects
Publications and source records attributed to R E Hendrick.
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This paper presents an analysis of signal-to-noise and contrast-to-noise ratios from small tip angle, gradient reversal (FLASH) imaging. Analytic and numerical techniques are used to determine the delay times and tip angles that maximize signal-to-noise per unit time from a single tissue. Similar procedures are used to determine the delay times and tip angles that maximize both T1-induced and T-2*-induced contrast-to-noise per unit time for a pair of tissues as a function of tissue characteristics and pulse sequence sampling times. The advantage of optimized FLASH imaging over optimized spin-echo imaging is quantitated by comparing signal-to-noise and contrast-to-noise ratios per unit time from the two sequences. Images are used to confirm these numerical results, to compare noise levels resulting from gradient reversals versus 180 degrees rephasing pulses and to assess the possible adverse effects of static magnetic field inhomogeneities on FLASH imaging.
This work discusses the effect of sampling time on noise, signal-to-noise and contrast-to-noise ratios in magnetic resonance imaging. A simple imaging experiment is performed to demonstrate the effect of sampling time on noise, confirming theoretical expectations that doubling the sampling time while decreasing the read gradient strength by a factor of two reduces statistical noise to 1/square root 2 of its original level. This result suggests that sampling time should be maximized within the constraints of the pulse sequence: namely, that sampling time should be increased and read gradient strength decreased as TE is increased. Revised expressions for signal-to-noise and contrast-to-noise ratios are presented based on the assumption that sampling time increases linearly with echo delay time above a certain minimum TE value. The revised expressions are then used to derive new predictions of the interpulse delay times that maximize signal-to-noise and contrast-to-noise ratios in spin-echo imaging. It is demonstrated that sampling times are critical in determining whether T1-weighted or T2-weighted sequences produce superior tissue contrast in spin-echo imaging.
The influence of signal averaging (n), repetition time (TR), and echo delay (TE) on systematic noise (cardiac, vascular, respiratory, and peristaltic ghost artifacts) and statistical noise (thermal effects) was determined in eight healthy volunteers and 57 patients. Systematic noise was the dominant factor degrading abdominal magnetic resonance (MR) images. Signal averaging was the primary determinant of both statistical and systematic image noise, fitting a power function (n)b with b = 0.44 and -0.42, respectively, close to the expected b = -0.5 power function. All types of ghosting showed the same sensitivity to signal averaging. Normalized systematic noise increased slightly with TR (b = 0.16) and increased markedly with TE (b = 0.40). These data indicate that the short TR, short TE technique is a powerful method for reducing motion artifacts on breathhold images and can be combined with signal averaging to further suppress artifacts, improve signal-to-noise ratio, and maximize anatomic resolution.
The relative efficacies of different spin-echo pulse sequences at 1.5 T were evaluated in the detection of focal hepatic disease. Pulse sequences compared were spin-echo with a repetition time (TR) of 200 msec and echo time (TE) of 20 msec, with six excitations; TR = 300 msec, TE = 20 msec, with 16 excitations (T1-weighted sequences); and a double spin-echo with TR = 2500 and TE = 25 and 70, with two excitations (proton-density-weighted and T2-weighted pulse sequences, respectively). Respiratory-motion compensation, which involved a recording of the phase-encoding gradients (Exorcist), was used for the last two sequences. Spin-echo with TR = 2500 msec and TE = 70 msec was superior in lesion detection and contrast-to-noise ratio. The proton-density-weighted and T2-weighted sequences with respiratory compensation produced better artifact suppression than did the short TR, short TE T1-weighted sequence with temporal averaging. In contradistinction to prior results at 0.6 T, T2-weighted pulse sequences appear superior to T1-weighted pulse sequences with multiple excitations for both lesion detection and artifact suppression at 1.5 T.
The pulse-sequence equations for spin-echo magnetic resonance imaging were used to determine interpulse delay times that give the highest signal-to-noise ratio from a single tissue. This theoretical result was then verified experimentally using 1-, 2-, and 5-mM/l copper sulfate solutions imaged on a 0.15-T resistive system. Theoretical analysis determined the spin-echo interpulse delay times that maximize the signal-to-noise ratio from a single tissue as TEopt = TEmin, the minimum echo delay time permitted by the system, and, to a good approximation, TRopt = 1.27 T1 + 1.90 TEmin, with T1 the longitudinal magnetic relaxation time of the tissue. Phantom measurements of the signal-to-noise ratio in a typical imaging system confirmed the theoretically determined TRopt values to within 7%.
Magnetic resonance imaging demands that tissue contrast and signal-to-noise advantages be sought in each component of the imaging system. One component of magnetic resonance imaging in which contrast and signal-to-noise ratios are easily manipulated is in the choice of pulse sequences and interpulse delay times. This article provides a general method for determining the best choices of interpulse delay times in pulse sequences and applies that method to saturation recovery, inversion recovery, and spin-echo sequences. Saturation recovery and inversion recovery sequences with rephasing pulses, and tissues with unequal hydrogen densities are considered. Optimization of pulse sequences is carried out for the two distinct cases of (a) a fixed number of sequence repetitions and (b) a fixed total imaging time. Analytic expressions are derived or approximate expressions are provided for the interpulse delay times that optimize contrast-to-noise ratios in each pulse sequence. The acceptable range of interpulse delay times to obtain reasonable contrast using each pulse sequence is discussed.
Several recent articles have assessed the relative efficiency of nuclear magnetic resonance (NMR) pulse sequences. One consideration that has received little attention is the effect on image contrast of displaying images without information on the sign of the reconstructed signals. The radiofrequency receivers currently used on most NMR imaging systems are quadrature detectors that preserve both the magnitude and sign of the NMR signal. Usually, however, sign or phase information is not used in the final image presentation. We point out that in imaging sequences that may have negative signals, such as inversion recovery, this loss of sign information produces a reduction in contrast between some tissues in an NMR image. We discuss the tissue parameters and interpulse delay times that result in contrast loss in inversion recovery and indicate the extent of contrast loss. We point out that for some tissues with unequal hydrogen spin densities, the region of contrast loss coincides with the region where maximum contrast would occur if sign information were preserved.
The importance of spin density [N(H)] and spin-lattice (T1) and spin-spin (T2) relaxation in the characterization of tissue by nuclear magnetic resonance (NMR) is clearly recognized. This work considers which optimized pulse sequences provide the best tissue discrimination between a given pair of tissues. The effects of tissue spin density and machine-imposed minimum rephasing echo times (TEMIN) for achieving maximum signal tissue contrast are discussed. A long TEMIN sacrifices T1-dependent contrast in saturation recovery (SR) and inversion recovery (IR) pulse sequences so that spin-echo (SE) becomes the optimum sequence to provide tissue contrast, due to T2 relaxation. Pulse sequences providing superior performance may be selected based on spin density and T1 and T2 ratios for a given pair of tissues. Selection of the preferred pulse sequence and interpulse delay times to produce maximum tissue contrast is strongly dependent on knowledge of tissue spin densities as well as T1 and T2 characteristics. As the spin density ratio increases, IR replaces SR as the preferred sequence and SE replaces IR and SR as the pulse sequence providing superior contrast. To select the optimal pulse sequence and interpulse delay times, an accurate knowledge of tissue spin density, T1 and T2 must be known for each tissue.
This review summarizes the physical basis of magnetic resonance (MR) imaging contrast agents, including both T1 agents, such as gadolinium-DTPA (diethylenetriaminepentaacetic acid), and T2 or T2* agents, such as superparamagnetic iron oxides. The maximization of image contrast and lesion visibility with contrast agents is described, and the use of contrast agents in MR angiography and perfusion imaging is discussed.
BACKGROUND: We investigated whether liver-minus-spleen (L-S) attenuation differences can accurately diagnose fatty infiltration of the liver on contrast-enhanced computed tomography (CT). METHODS: A group of 78 patients administered a fast injection (90-s duration) of 150 mL 60% ionic contrast was compared with 81 patients given a slow injection (152.5 s). The presence or absence of fatty infiltration of the liver was diagnosed by noncontrast CT. RESULTS: The L-S attenuation differences varied significantly, depending on both injection rate and timing of measurements. For the fast-injection group, the optimal L-S threshold for diagnosing fatty infiltration ranged from -43 to -33 Hounsfield units (HU) for early (79 s) and late measurements (106 s), respectively. For the slow-injection group, the optimal threshold ranged from -31 to -25 HU (80 and 112 s, respectively). In addition, sensitivity was not very high (range = 0.54-0.71) for either injection protocol at any measurement time because of significant overlap of L-S values between normal and fatty infiltration patients. Moderate and severe fatty infiltration were more reliably diagnosed than mild fatty infiltration by this method. CONCLUSIONS: Contrast injection rate and timing of measurements significantly influence the optimal L-S threshold for diagnosing fatty liver. This limits the clinical usefulness of such measurements.
Noninvasive evaluation of the human body has become an essential tool in the diagnosis of disease processes. Recent developments in nuclear magnetic resonance imaging (MRI) have extended a powerful chemical analytic technique to the medical imaging field. This article presents the fundamental principles of MRI in terms of the concept of transmission and reception of energy. A selected bibliography directs the reader to a more detailed discussion of the pertinent physics.