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Dive into the research topics where Stephen R. Bunker is active.

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Featured researches published by Stephen R. Bunker.


Clinical Nuclear Medicine | 1984

Biliary scintigraphy. The "hot rim" sign.

Michael A. Cawthon; Debra M. Brown; Michael F. Hartshorne; Robert D. Karl; John M. Bauman; William H. Howard; Stephen R. Bunker

A new cholescintigraphic finding, the “hot rim” sign, is reported in a case of acute cholecystitis. Local inflammation in the gallbladder fossa may be the cause of this phenomenon.


Clinical Nuclear Medicine | 1985

Optimal technetium-99m RBC labeling for gastrointestinal hemorrhage study.

Al Landry; Michael F. Hartshorne; Stephen R. Bunker; John M. Bauman; Michael A. Cawthon; Robert D. Karl; William H. Howard

Four methods of Tc-99m red blood cell labeling were tested for labeling efficiency and kinetics in normal adults. From a perspective of the gastrointestinal hemorrhage study, the in vivo method was least appropriate because of extravascular loss of pertechnetate. The modified in vitro method was disadvantageous because of long labeling intervals in a syringe fixed to the patients forearm (45 minutes). The pure in vitro methods produced the highest labeling efficiency (95% +) and are preferred by the authors.


Clinical Nuclear Medicine | 1985

A false-negative Xenon-133 study in focal fatty infiltration of the liver

Michael F. Hartshorne; Lida Crooks; William F. Bennett; Hector Ramirez; Stephen R. Bunker; Michael A. Cawthon; Robert D. Karl; John M. Bauman

A Xe-133 hepatic study was misleading when the absence of Xe-133 localization in an area of low CT numbers was considered to be negative for a diagnosis of focal fatty infiltration.


Clinical Nuclear Medicine | 1982

Fourier phase analysis in non-cyclic dynamic studies.

Michael F. Hartshorne; Stephen R. Bunker; Jack L. Lancaster; Robert J. Telepak; Craig S. Hammes; Robert D. Karl; Michael A. Cawthon; William H. Howard

Single harmonic Fourier amplitude and phase (FA/P) analyses of 129 radionuclide angiographic (RNA) studies were found to reflect accurately the sequence and quantity of perfusion determined in the independently interpreted RNA studies. In addition, the anatomic detailing in peripheral studies (hands, feet, etc.) was considered superior to that obtained in RNA studies.


Clinical Nuclear Medicine | 1985

Dual isotope scanning with gallium-67 citrate and technetium-99m radiopharmaceuticals

Robert D. Karl; Michael F. Hartshorne; Michael A. Cawthon; John M. Bauman; William H. Howard; Stephen R. Bunker

The interpretation of Ga-67 scans is limited by the complex anatomic and physiologic distribution of Ga-67 and by the low resolution possible with this isotope. The use of a second isotope Tc-99m, tagged to an appropriate pharmaceutical allows the identification of anatomic landmarks. Computer acquisition of both the Ga-67 and Tc-99m images allows for subtraction of the Tc-99m images from the Ga-67 images and leads to precise localization of abnormal Ga-67 accumulations. Only a small percentage of the counts in the Tc-99m window are due to Ga-67 scatter and do not degrade the Tc-99m images. Cases illustrating the value of the dual-isotope technique are presented.


Clinical Nuclear Medicine | 1985

False aneurysm of ascending aorta.

Michael F. Hartshorne; Stephen R. Bunker; John M. Bauman; Michael A. Cawthon; William H. Howard; Robert D. Karl

An unsuspected false aneurysm of the ascending aorta was discovered during a first pass, left-to-right shunt study.


Clinical Nuclear Medicine | 1984

Chest radionuclide angiography in the evaluation of pulmonary masses

Michael F. Hartshorne; John M. Bauman; Robert J. Telepak; Robert D. Karl; Michael A. Cawthon; William H. Howard; Stephen R. Bunker

A retrospective analysis of 104 chest radionuclude angiography (CRNA) studies establishes the utility of this procedure in the evaluation of pulmonary malignancies and benign masses. Remarkable abnormalities in the perfusion of the lungs were identified in 36 (58%) of 62 cases that were not predictably normal or predictably abnormal form the clinical setting. While 60 of these 62 cases involved malignancy being evaluated for metastases, only 21 (34%) had metastases Identified by radionuclide bone or liver-spleen scintigraphy. In addition to diagnosis of superior vena cava obstruction, the CRNA may have a more frequent application as an adjunct to routine scintigraphic studies directed to the identification of metastatic disease.


Clinical Nuclear Medicine | 1984

LEFT VENTRICULAR VOLUMES FROM SINGLE PHOTON EMISSION COMPUTED TOMOGRAPHY (SPECT)

Stephen R. Bunker; Michael F. Hartshorne; William P. Schmidt; William H. Howard; John M. Bauman; Michael A. Cawthon; Robert D. Karl

A prospective study was performed in 25 patients, comparing SPECT left ventricular (LV) end-diastolic (ED) volume (V) to that of contrast ventriculography (ANGIO). SPECT examination utilized 25 mCi Tc-99m RBC labeled in vivo. Sixty images were acquired with a Picker Dyna Camera 5 over 180° from RAO to LPO utilizing a 50 msec ED window. The 30-second images were preprocessed using a 5x5 spatial filter with a cutoff of 0.10 and then reconstructed into transaxial slices by filtered back-projection utilizing a low resolution proprietary filter. The apex and base of the LV were determined by review of additional long-axis and short-axis slice reconstructions. LVEDV was subsequently calculated from count-corrected regions of interest (ROIs) generated about the transaxial LV slices. All patients underwent contrast ventriculography (ANGIO) within 72 hours of the SPECT study. The correlation coefficient between SPECT and ANGIO LVEDV over a range of 87 to 506 cc was 0.97 with a standard error of the estimate (SEE) of 23 cc. We conclude that SPECT allows for noninvasive and accurate determination of LVEDV without the need for blood sample counting or assumptions about LV geometry and chest wall attenuation.


Clinical Nuclear Medicine | 1982

Computer edge displays for cardiac wall motion evaluation.

Robert J. Telepak; Michael F. Hartshorne; Stephen R. Bunker

Several computer display techniques in both black and white and color are described. Use of such techniques improves the qualitative evaluation of ECG-gated cardiac blood pool studies, especially by less experienced observers. Detection of wall motion at the interface between the myocardial wall and the labeled blood within the cardiac chambers is greatly enhanced. No additional equipment nor computer processing time is required to use these display schemes.


American Heart Journal | 1982

Noninvasive diagnosis of cardiac amyloidosis by technetium-99m-pyrophosphate myocardial scintigraphy

Samuel M. Sobol; Jerry M. Brown; Stephen R. Bunker; Jijibhoy Patel; Robert J. Lull

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Michael F. Hartshorne

University of Texas Health Science Center at San Antonio

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Robert J. Lull

Letterman Army Medical Center

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Jack L. Lancaster

University of Texas Health Science Center at San Antonio

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Jerry M. Brown

Letterman Army Medical Center

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Robert J. Telepak

Letterman Army Medical Center

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Jijibhoy Patel

Letterman Army Medical Center

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John C. Lasher

University of Texas Health Science Center at San Antonio

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