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1.
AJR Am J Roentgenol ; 182(4): 849-59, 2004 Apr.
Article in English | MEDLINE | ID: mdl-15039151

ABSTRACT

OBJECTIVE: Our aim was to formulate appropriate MDCT chest and abdominopelvic CT scan protocols for pediatric patients. MATERIALS AND METHODS: Surface radiation dose measurements from a set of anthropomorphic phantoms (nominal 1 year old, 5 year old, and 10 year old) and an adult phantom were compared with standard CT dose index measurements. Image-noise values on axial 5-mm-thick anthropomorphic phantom images were obtained as a measure of image quality. RESULTS: Peripheral CT dose index values obtained with the standard 16-cm acrylic phantom were within approximately 10% of the CT surface dose measurements for the pediatric anthropomorphic phantoms for both chest and abdominopelvic scan protocols. The noise value for the adult phantom image acquired using a typical clinical CT technique was identified, and targeting this level of noise for pediatric CT examinations resulted in a decrease in dose of 60-90%. Initially, 80 kVp was selected for use with very small children; however, beam-hardening artifacts were severe enough to cause us to abandon this option. Current pediatric protocols at M. D. Anderson Cancer Center rely on 100- and 120-kVp settings. The display field-of-view parameter can be used as a surrogate for patient size to develop clinical pediatric CT protocol charts. CONCLUSION: CT dose index measurements obtained using the 16-cm standard acrylic phantom are sufficiently accurate for estimating chest and abdominopelvic CT entrance exposures for pediatric patients of the same approximate size as the anthropomorphic phantoms used in this study. Image-noise measurements can be used to adjust chest and abdominopelvic CT techniques for pediatric populations, resulting in a decrease in measured entrance dose by 60-90%.


Subject(s)
Pelvis/diagnostic imaging , Radiography, Abdominal/methods , Radiography, Thoracic/methods , Tomography, X-Ray Computed/methods , Adult , Child , Child, Preschool , Humans , Infant , Phantoms, Imaging , Radiation Dosage , Scintillation Counting , Skin , Tomography, X-Ray Computed/instrumentation
2.
Med Phys ; 30(7): 1768-75, 2003 Jul.
Article in English | MEDLINE | ID: mdl-12906194

ABSTRACT

The purpose of this study was to evaluate the use of digital x-ray imaging detectors for the measurement of diagnostic x-ray tube focal spot size using a slit camera. Slit camera images of two focal spots for a radiographic x-ray tube were acquired with direct-exposure film (DF) (as specified by the National Electrical Manufacturers Association [NEMA] Standards Publication No. XR 5, 1992), computed radiography (CR) imaging plates, and an a-Si:H/CsI:Tl-based flat-panel (FP) detector. Images obtained with the CR and the FP were acquired over a broad range of detector entrance exposure levels. The DF slit images were evaluated according to NEMA specifications (visually, using a 7x magnifying glass with reticule) by six medical physicists. Additionally, the DF images were digitized and the focal spot sizes obtained from the digital profiles of the slit. The CR and the FP images were analyzed in a manner similar to the digitized DF images. It took less than 20 minutes for a complete CR or FP measurement of focal spot size in two dimensions. In comparison, a typical DF measurement with visual evaluation takes at least 60 minutes, in our experience. In addition to a great reduction in measurement time achieved by using digital detectors, the tube loading requirements were reduced to approximately 20 mAs compared with approximately 1000 mAs when using the DF technique. The calculated focal spot sizes for CR and FP differed from those of digitized DF by -2.4% to +4.8% (sigma=2.5%), far less than the -16.6% to +9.3% (sigma=8.1%) variability introduced by the visual evaluation of the slit image. In addition, the calculated focal spot sizes for the CR and the FP images maintained a coefficient of variation <1.0% over the broad range of exposure levels. Based upon these results, we conclude that (1) FP and CR detectors yield consistent results in measurements of x-ray tube focal spot sizes, (2) compared to DF, CR and FP significantly reduce measurement time and tube loading requirements, (3) CR and FP readily permit digital profile analysis, thereby eliminating observer error, and (4) unlike DF, CR and FP are independent of exposure level.


Subject(s)
Calibration/standards , Equipment Failure Analysis/instrumentation , Equipment Failure Analysis/methods , Film Dosimetry/instrumentation , Radiographic Image Enhancement/methods , Radiographic Image Enhancement/standards , Transducers , X-Ray Intensifying Screens , Equipment Failure Analysis/standards , Film Dosimetry/methods , Radiometry/instrumentation , Radiometry/methods , Radiometry/standards , Reproducibility of Results , Sensitivity and Specificity , Tomography, X-Ray Computed/instrumentation , Tomography, X-Ray Computed/methods , United States
3.
Med Phys ; 29(9): 2052-61, 2002 Sep.
Article in English | MEDLINE | ID: mdl-12349926

ABSTRACT

Amorphous silicon/cesium iodide (a-Si:H/CsI:Tl) flat-panel (FP)-based full-field digital mammography systems have recently become commercially available for clinical use. Some investigations on physical properties and imaging characteristics of these types of detectors have been conducted and reported. In this perception study, a phantom containing simulated microcalcifications (microCs) of various sizes was imaged with four detector systems: a FP system, a small field-of-view charge coupled device (CCD) system, a high resolution computed radiography (CR) system, and a conventional mammography screen/film (SF) system. The images were reviewed by mammographers as well as nonradiologist participants. Scores reflecting confidence ratings were given and recorded for each detection task. The results were used to determine the average confidence-rating scores for the four imaging systems. Receiver operating characteristics (ROC) analysis was also performed to evaluate and compare the overall detection accuracy for the four detector systems. For calcifications of 125-140 microm in size, the FP system was found to have the best performance with the highest confidence-rating scores and the greatest detection accuracy (Az = 0.9) in the ROC analysis. The SF system was ranked second while the CCD system outperformed the CR system. The p values obtained by applying a Student t-test to the results of the ROC analysis indicate that the differences between any two systems are statistically significant (p<0.005). Differences in microC detectability for the large (150-160 microm) and small (112-125 microm) size microC groups showed a wider range of p values (not all p values are smaller than 0.005, ranging from 0.6 to <0.001) compared to the p values obtained for the medium (125-140 microm) size microC group. Using the p values to assess the statistical significance, the use of the average confidence-rating scores was not as significant as the use of the ROC analysis p value for p value.


Subject(s)
Breast Neoplasms/diagnostic imaging , Calcinosis/diagnostic imaging , Mammography/instrumentation , Radiographic Image Enhancement/instrumentation , Data Display , Equipment Failure Analysis , Female , Humans , Mammography/methods , Observer Variation , Phantoms, Imaging , ROC Curve , Reproducibility of Results , Sensitivity and Specificity , Video Recording/instrumentation
4.
J Digit Imaging ; 15 Suppl 1: 27-32, 2002.
Article in English | MEDLINE | ID: mdl-12105694

ABSTRACT

The aim of this work was to implement the DICOM Grayscale Standard Display Function (GSDF) at all stages of image presentation for computed radiography (CR) and direct digital radiography (DR) modalities. Cathode-ray tubes (CRT) were calibrated according to vendor procedures. Printer look-up-tables (LUT) were measured. Custom LUTs were created and loaded. Fuji CR gradation processing parameters were adjusted to accommodate a GSDF printer LUT. Conformance to the GSDF for hard-copy and soft-copy displays was measured with DICOM Part 14 procedures. One system was intended to completely incorporate the GSDF, although the hard-copy result was correct. The CR systems required creation of custom GSDF printer LUTs, adjustment of gradation processing parameters, and/or calibration of CRT luminance response at the quality control station. The picture archiving and communication system workstations from one vendor required third-party software for calibration. Current implementations of DICOM GSDF by vendors may be inconsistent or nonexistent. Significant effort by in-house staff must be expended to properly incorporate the GSDF.


Subject(s)
Data Display/standards , Radiology Information Systems/standards , Humans , Radiography, Thoracic , Software , Tomography, X-Ray Computed
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