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Featured researches published by David T. Kopp.


The New England Journal of Medicine | 1991

Effect of strict glycemic control on renal hemodynamic response to amino acids and renal enlargement in insulin-dependent diabetes mellitus

Katherine R. Tuttle; J. Lewis Bruton; Marie C. Perusek; Jack L. Lancaster; David T. Kopp; Ralph A. DeFronzo

BACKGROUND Many patients with insulin-dependent diabetes mellitus have an increase in the glomerular filtration rate and renal enlargement early in the course of their disease. Both these changes may be risk factors for the later development of diabetic nephropathy. Their cause is not known, but they could be due to augmented renal responses to the increase in plasma amino acid concentrations that occurs when dietary protein intake is high, a factor known to increase glomerular filtration and renal blood flow in normal subjects. METHODS We measured the glomerular filtration rate and renal plasma flow after an overnight fast and during an infusion of amino acids in 12 patients with insulin-dependent diabetes mellitus and 9 normal subjects. The diabetic patients were studied when they were hyperglycemic, when they were euglycemic after an insulin infusion for 36 hours, and after intensive insulin therapy for 3 weeks. Kidney volume was measured by ultrasonography before and after the period of intensive insulin therapy. RESULTS The glomerular filtration rate and renal plasma flow were normal after fasting when the patients were hyperglycemic (mean [+/- SE] fasting plasma glucose level, 11.5 +/- 0.7 mmol per liter). After the amino acid infusion, these values increased more in the patients (glomerular filtration rate, 2.65 +/- 0.07 ml per second per 1.73 m2 of body-surface area; renal plasma flow, 13.30 +/- 0.68 ml per second per 1.73 m2; P less than 0.05 for both) than in the normal subjects (2.25 +/- 0.08 and 11.20 +/- 0.65 ml per second per 1.73 m2, respectively). The 36-hour infusion of insulin in the diabetic patients did not alter the glomerular filtration rate or renal plasma flow either before or during the amino acid infusion. After three weeks of intensive insulin therapy (fasting plasma glucose level, 5.3 +/- 0.2 mmol per liter), the glomerular filtration rate and renal plasma flow after the amino acid infusion (2.33 +/- 0.03 and 11.30 +/- 0.43 ml per second per 1.73 m2, respectively) were similar to those in the normal subjects. The kidney volumes in the normal subjects and the patients with diabetes were 219 +/- 14 and 312 +/- 14 ml per 1.73 m2, respectively (P less than 0.01); the volume decreased to 267 +/- 22 ml per 1.73 m2 (P less than 0.001) in the diabetic patients after three weeks of intensive insulin therapy, which was not significantly different from the volume in the normal subjects (P = 0.1). CONCLUSIONS Conventionally treated diabetic patients who have normal renal function while fasting have augmented renal hemodynamic responses to increased plasma amino acid concentrations. The concomitant decrease in these hemodynamic responses and in kidney size with strict glycemic control suggests that these phenomena are related and influenced by the metabolic state.


Medical Physics | 1997

Rapid objective measurement of gamma camera resolution using statistical moments

Trish A. Hander; Jack L. Lancaster; David T. Kopp; John C. Lasher; Ralph Blumhardt; Peter T. Fox

An easy and rapid method for the measurement of the intrinsic spatial resolution of a gamma camera was developed. The measurement is based on the first and second statistical moments of regions of interest (ROIs) applied to bar phantom images. This leads to an estimate of the modulation transfer function (MTF) and the full-width-at-half-maximum (FWHM) of a line spread function (LSF). Bar phantom images were acquired using four large field-of-view (LFOV) gamma cameras (Scintronix, Picker, Searle, Siemens). The following factors important for routine measurements of gamma camera resolution with this method were tested: ROI placement and shape, phantom orientation, spatial sampling, and procedural consistency. A 0.2% coefficient of variation (CV) between repeat measurements of MTF was observed for a circular ROI. The CVs of less than 2% were observed for measured MTF values for bar orientations ranging from -10 degrees to +10 degrees with respect to the x and y axes of the camera acquisition matrix. A 256 x 256 matrix (1.6 mm pixel spacing) was judged sufficient for routine measurements, giving an estimate of the FWHM to within 0.1 mm of manufacturer-specified values (3% difference). Under simulated clinical conditions, the variation in measurements attributable to procedural effects yielded a CV of less than 2% in newer generation cameras. The moments method for determining MTF correlated well with a peak-valley method, with an average difference of 0.03 across the range of spatial frequencies tested (0.11-0.17 line pairs/mm, corresponding to 4.5-3.0 mm bars). When compared with the NEMA method for measuring intrinsic spatial resolution, the moments method was found to be within 4% of the expected FWHM.


Radiation Research | 2000

Measurement and Validation of Benchmark-Quality Thick-Target Tungsten X-Ray Spectra below 150 kVp

J. R. Mercier; David T. Kopp; William D. McDavid; Stephen B Dove; Jack L. Lancaster; D. M. Tucker

Abstract Mercier, J. R., Kopp, D. T., McDavid, W. D., Dove, S. B., Lancaster, J. L. and Tucker, D. M. Measurement and Validation of Benchmark-Quality Thick-Target Tungsten X-Ray Spectra below 150 kVp. Pulse-height distributions of two constant potential X-ray tubes with fixed anode tungsten targets were measured and unfolded. The measurements employed quantitative alignment of the beam, the use of two different semiconductor detectors (high-purity germanium and cadmium-zinc-telluride), two different ion chamber systems with beam-specific calibration factors, and various filter and tube potential combinations. Monte Carlo response matrices were generated for each detector for unfolding the pulse-height distributions into spectra incident on the detectors. These response matrices were validated for the low error bars assigned to the data. A significant aspect of the validation of spectra, and a detailed characterization of the X-ray tubes, involved measuring filtered and unfiltered beams at multiple tube potentials (30–150 kVp). Full corrections to ion chamber readings were employed to convert normalized fluence spectra into absolute fluence spectra. The characterization of fixed anode pitting and its dominance over exit window plating and/or detector dead layer was determined. An Appendix of tabulated benchmark spectra with assigned error ranges was developed for future reference.


Medical Physics | 2000

An improved method for rapid objective measurement of gamma camera resolution

Trish A. Hander; Jack L. Lancaster; William D. McDavid; David T. Kopp

An improved method for an easy, rapid measurement of the intrinsic spatial resolution of a gamma camera is presented. A simplified model was previously developed based solely on mean and standard deviation measurements taken from a region of interest in bar pattern images. This led to an estimate of the modulation transfer function and the full width at half maximum (FWHM) of a line spread function (LSF). The improved method involved expanding the simplified model to incorporate input modulation, square wave input versus the assumed sinusoidal input, aperture (pixel) size, and scatter from the plastic in the bar pattern. The input square wave modulation was calculated to be unity for the typical bar patterns used for gamma camera quality control assessment. For the typical range of bar sizes available, in combination with the typical resolving capabilities of gamma cameras, the sinusoidal approximation of the bar pattern was found to be valid (<1% contribution to the measured resolution from higher harmonic frequencies present in a square wave input with an effective input modulation greater than unity by a factor of 4/pi). The aperture correction factor was calculated for numerous bar and pixel size combinations. Applying the aperture correction factor results in an improvement in the accuracy of the calculated FWHM values, especially for large apertures (pixel sizes). For a camera with a specified FWHM value of 3.5 mm, the simplified model predicts values ranging from 3.2 to 4.1 mm, when the acquisition matrix varies from 128(2) to 512(2). When the expanded model is used with the aperture correction applied, this range was reduced to 3.6-3.9 mm. The scatter correction further improved the calculated FWHM (from 3.6 to 3.8 mm). It is suggested that the expanded model should be used when more accurate measurements are desired, such as in acceptance testing.


Health Physics | 2000

Using measured 30-150 kVp polychromatic tungsten x-ray spectra to determine ion chamber calibration factors, N(x) (Gy C -1 )

J. R. Mercier; David T. Kopp; William D. McDavid; Stephen B Dove; Jack L. Lancaster; D. M. Tucker

Two methods for determining ion chamber calibration factors (Nx) are presented for polychromatic tungsten x-ray beams whose spectra differ from beams with known Nx. Both methods take advantage of known x-ray fluence and kerma spectral distributions. In the first method, the x-ray tube potential is unchanged and spectra of differing filtration are measured. A primary standard ion chamber with known Nx for one beam is used to calculate the x-ray fluence spectrum of a second beam. Accurate air energy absorption coefficients are applied to the x-ray fluence spectra of the second beam to calculate actual air kerma and Nx. In the second method, two beams of differing tube potential and filtration with known Nx are used to bracket a beam of unknown Nx. A heuristically derived Nx interpolation scheme based on spectral characteristics of all three beams is described. Both methods are validated. Both methods improve accuracy over the current half value layer Nx estimating technique.


Medical Physics | 1988

Distance and depth measurements of radioactive objects utilizing rotating slant‐hole collimators

Jack L. Lancaster; David T. Kopp; John C. Lasher; Ralph Blumhardt

It is desirable to have an accurate method to determine the depth of various organs which are commonly imaged in nuclear medicine. The method presented here utilizes the geometrical characteristics of the rotating slant-hole collimator to calculate distances and depth. The accuracy of the calculated distance was evaluated for point sources in air separated by 11 cm. The reproducibility of the calculated distance was evaluated as a function of the extent of collimator rotation between observations for angular differences of 45 degrees, 90 degrees, 135 degrees, and 180 degrees. The theory of the method is discussed and the relative error in distance calculation analyzed mathematically as a function of (1) collimator rotation angle error, (2) collimator slant angle error, and (3) position calculation error. Our findings indicate this method to be accurate to within 2% with a reproducibility range of 3%-5% for point sources.


The Journal of Nuclear Medicine | 1975

67Gallium in 68 consecutive infection searches.

William C. Harvey; Donald A. Podoloff; David T. Kopp


The Journal of Nuclear Medicine | 1985

Effect of Errors in Reangulation on Planar and Tomographic Thallium-201 Washout Profile Curves

Jack L. Lancaster; Mark R. Starling; David T. Kopp; John C. Lasher; Ralph Blumhardt


The Journal of Nuclear Medicine | 1972

Further Observations on the Normal Radioactive Iodine Uptake

William C. Harvey; David T. Kopp; Warren W. Bovie


The Journal of Nuclear Medicine | 1985

Practical gamma camera quality control with a four-point phantom

Jack L. Lancaster; David T. Kopp; J. S. Lasher; Ralph Blumhardt

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Jack L. Lancaster

University of Texas Health Science Center at San Antonio

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Ralph Blumhardt

University of Texas Health Science Center at San Antonio

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John C. Lasher

University of Texas Health Science Center at San Antonio

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William D. McDavid

University of Texas Health Science Center at San Antonio

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D. M. Tucker

University of Texas Health Science Center at San Antonio

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J. R. Mercier

University of Texas Health Science Center at San Antonio

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Stephen B Dove

University of Texas Health Science Center at San Antonio

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Trish A. Hander

University of Texas Health Science Center at San Antonio

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William C. Harvey

Presbyterian Hospital of Dallas

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