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British Journal of Radiology (2005) 78, 422-427
© 2005 British Institute of Radiology
doi: 10.1259/bjr/32912696

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Full Paper

Investigation of optimum energies for chest imaging using film–screen and computed radiography

I D Honey, MSc A Mackenzie, MSc and D S Evans, MSc

Kings Centre for the Assessment of Radiological Equipment (KCARE), Kings College Hospital, London SE5 9RS, UK


    Abstract
 Top
 Abstract
 Introduction
 Theory
 Materials and methods
 Results
 Discussion
 Conclusions
 References
 
The purpose of the study was to compare the image quality of film–screen (FS) and computed radiography (CR) for adult chest examinations across a range of beam energies. A series of images of the CDRAD threshold contrast detail detection phantom were acquired for a range of tube potential and exposure levels with both CR and FS. The phantom was placed within 9 cm of Perspex to provide attenuation and realistic levels of scatter in the image. Hardcopy images of the phantom were scored from a masked light-box by two scorers. Threshold contrast indices were used to calculate a visibility index (VI). The relationships between dose and image quality for CR and for FS are fundamentally different. The improvements in VIs obtained using CR at 75 kVp and 90 kVp were found to be statistically significant compared with 125 kVp at matched effective dose levels. The relative performance of FS and CR varies as a function of energy owing to the different k-edges of each system. When changing from FS to CR, the use of lower tube potentials may allow image quality to be maintained whilst reducing effective dose. A tube voltage of 90 kVp is indicated by this work, but may require clinical verification.


    Introduction
 Top
 Abstract
 Introduction
 Theory
 Materials and methods
 Results
 Discussion
 Conclusions
 References
 
Digital imaging is gradually replacing the well established technology of conventional film–screen (FS) imaging. This is primarily due to the perceived advantages of digital image processing, electronic archiving, teleradiology and the potential for optimization of image acquisition and display independently. The wide dynamic range of digital systems make them particularly attractive for imaging the widely differing attenuating structures of the chest [1]. The Ionising Radiation (Medical Exposure) Regulations (2000) [2] require that radiographic techniques be optimized for each examination type. An optimization study should investigate tube voltage and the receptor dose required to achieve the minimal acceptable level of image quality.

The Council of European Communities have published guidelines on good radiographic technique for a range of standard FS imaging examinations [3]. The suggested posteroanterior chest technique is to use 125 kVp, 180 cm focus to film distance (FDD) with an antiscatter grid in place. There is no accepted guidance for digital radiography. Fundamental differences exist between FS imaging and computed radiography (CR) and the optimum technique may not necessarily be the same. First, CR has a wide dynamic range and the ability to perform image processing operations on details in the lung and mediastinum in order to enhance their visibility. This reduces the need to minimize the contrast between signals transmitted from lung to mediastinum by selection of a high tube voltage value, as is the practice for FS which has a narrow dynamic range. With digital systems such as CR the optimum tube voltage can be obtained by maximizing the signal to noise ratio whilst maintaining an effective dose level [46]. Second, photo-stimulable phosphor (PSP) plates have different absorption edge characteristics to rare-earth screens owing to their different elemental compositions (see Figure 1Go). In the diagnostic energy range BaF(Br0.85I0.15), which is the bulk constituent of the Agfa photo-stimulable phosphor plate (Agfa, Peissenberg, Germany) [7, 8], has a k-edge at ~37 keV, whilst Gd2O2S (used for rare earth screens) has a k-edge at ~50 keV. It can be seen from Figure 1Go that between these energies (37 keV to 50 keV) the attenuation performance of the photo-stimulable phosphor will be better relative to the FS than at other energies. For Figure 2Go, the fraction of the total incident transmitted beam photons, that interact with the detector, F, has been approximated using the following equation: Go


{780422E001}

where E=the maximum energy of the spectrum used; {varepsilon}=a discrete point in the energy spectrum; N({varepsilon})=the relative number of photons at a discrete energy level, {varepsilon}, in the primary beam after transmission through 10 cm of Perspex and 2.5 mm Al equivalent (obtained using Institute of Physics and Engineering in Medicine (IPEM) report 78 [9]); F({varepsilon})=the fraction of photons of an energy, {varepsilon}, that will interact within the detecting medium [10].



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Figure 1. The mass attenuation coefficients of Gd2O2S (thin solid line) and BaFB0.85I0.15 (thick solid line) as a function of energy [10].

 


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Figure 2. The fraction of photons interacting with a BaF(Br0.85I0.15) computed radiography (CR) plate (solid line) and a Gd2O2S phosphor screen (dashed line). The values were calculated using Equation 1Go, and published tables of data [9, 10]. Both curves have been normalized to their peak point.

 
The relative attenuation properties of the two systems will be dependent on the thickness of material used. Since details of the effective phosphor thickness are not well known, comparison of the magnitudes of the photon interaction fractions of the two detectors in Figure 2Go is not meaningful. However, the comparison of the variation of photon interaction fraction with energy for the two receptors is worthwhile. It can be seen that the variation in primary beam absorption fractions with tube voltage for the two systems is significantly different, with Gd2O2S maintaining its absorption efficiency better at higher energies than BaF(Br0.85I0.15).

It has been shown that for adult chest radiography, the performance of CR and FS is comparable [1114]. It should be noted that these studies did not use FS systems of the same speed. Conversely, for paediatric chest imaging where lower tube potential is used and the scatter contribution is less, it has been shown that a dose reduction of approximately 30% is possible with CR whilst maintaining the same image quality as with FS [15].

Studies of optimum tube voltage to be used for adult chest radiography using CR have resulted in somewhat conflicting results. When assessing the visibility of low contrast opacities in human volunteers [4] and low contrast disks within a phantom [16], in the range of 80–140 kVp, it was concluded that lower tube potential would result in significantly better image quality. Conversely, using anthropomorphic chest phantoms, signal to noise ratio and image quality assessed using the Commission of the European Communities (CEC) guidelines [3] were not significantly affected by tube voltage [5, 17]. It should be noted that as well as having different methods of assessing image quality these studies have different methods of matching dose at different tube potentials.

The variation of image quality with tube potential will be a complex function of the primary beam spectrum, the scatter spectrum and the variation of receptor absorption efficiency with energy. The aims of this work were to determine the optimum tube potential for chest imaging using CR, and to assess the comparative image quality of FS and CR as a function of tube voltage.


    Theory
 Top
 Abstract
 Introduction
 Theory
 Materials and methods
 Results
 Discussion
 Conclusions
 References
 
National guidelines for the assessment of radiological equipment [18] recommend the use of threshold contrast detail detection (TCDD) for the annual routine testing of image intensifiers. TCDD has been suggested for routine testing of CR [19, 20]. A TCDD test object consists of either a series of circular holes drilled into a material, or a series of circular objects positioned on a base material. Typically the number of details of each diameter visible in the image is recorded and used to calculate values of threshold contrast index, HT(A), Go


{780422E002}

where A is the detail area and CT is the minimum detectable contrast. CT must be calculated for the specific beam conditions used (energy and filtration). The threshold contrast index data can be viewed graphically, or summarized as a single quality index (QI) [21]. However, comparison of HT(A) values between images obtained at different tube potential values is not useful, since equal detail visibility would give rise to a superior HT(A) values at higher tube voltages. We propose to use a visibility index (VI) which is determined solely from the physical size of the detected objects rather than their radiographic contrasts, Go


{780422E003}

where N is the number of different groups of details with fixed diameters in the phantom used, d(A)ref is the smallest visible depth of hole for a given detail diameter in the reference image and d(A)image is the corresponding depth in the image of interest. Two similar depth-based image quality indices have been used in a study of chest radiographs [22]. The form of the visibility index is based on the quality index suggested by Gallacher et al [21]. The use of a reference curve taken from some "standard" image has the effect of normalizing both the quality index suggested by Gallacher and the visibility index suggested here, such that a value above 1.0 will be indicative of better-than-standard image quality.

For a quantum noise limited imaging system the detectable threshold contrast, CT, of holes of depth, d, in an otherwise uniform background is related to receptor dose, D, as follows, Go


{780422E004}

where Go


{780422E005}

where µ is the attenuation coefficient of air in the holes in the phantom. It follows that the threshold hole depth d is proportional to –ln D, and as a consequence VI must also be proportional to –ln D for a quantum noise limited detector. The mean VI value should be less affected by variations in the noise and observer performance than the individual d(A)image values. Also, it is simpler to compare two images using a single measure of image quality, rather than compare 10–15 values of d(A). However, it is still important to assess whether the system's relative performance is affected by detail size by examining the full TCDD curve.


    Materials and methods
 Top
 Abstract
 Introduction
 Theory
 Materials and methods
 Results
 Discussion
 Conclusions
 References
 
Tests were performed in a general X-ray room equipped with a Opti 150/30/50C tube and Polydoros LX50 generator (Siemens Medical Solutions, Erlangen, Germany), vertical bucky with moving antiscatter grid (focused at 1.50 m, 70 lines cm–1, grid ratio 7:1), and ADC Solo CR reader with MD10 phosphor plates (Agfa Healthcare, Peissenberg, Germany). A second set of tests were performed in a general X-ray room equipped with a ROT1750 tube and Optimus 50 generator (Philips Medical Systems, Eindhoven, The Netherlands), vertical bucky with a moving antiscatter grid (focused at 1.80 m, 36 lines cm–1, grid ratio 12:1), and a 400 speed HT-G film–screen cassette, processed using an Agfa CIC system.

Image quality was assessed using the CDRAD (University Hospital Nijmegen, St Radboud, The Netherlands) threshold contrast detail detectability test object. The CDRAD is a 1 cm thick Perspex plate containing circular holes of 15 different diameters (ranging from 0.3 mm to 8 mm) and 15 different depths (ranging from 0.3 mm to 8 mm) [23]. The detail depths are such that within a reasonable range of exposures some, but not all, of the details should be visible at all detail diameters.

The phantom was placed between 4 cm of Perspex (front) and 5 cm of Perspex (behind) to provide scatter and give attenuation similar to an adult chest. All exposures were made in the vertical bucky with a moving antiscatter grid, and a focal spot to detector distance of 180 cm (see Figure 3Go), as suggested in the CEC guidelines [3].



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Figure 3. A schematic diagram of the experimental setup used.

 
Images were obtained using both FS and CR at 75 kVp, 90 kVp and 125 kVp across a range of receptor doses spanning from approximately 0.5 µGy to approximately 20 µGy. The CR plates were read out using the setting 200 speed and "flat field" (without post processing). Before printing the images onto laser film, window and level were selected such that the visibility of the details appeared to be maximized and the background noise remained perceptible.

The images were scored using a masked light box and consistent low level ambient light conditions. The counting of "half visible" details was permitted, and this was accounted for in the analysis by taking a mean of the adjacent hole depths. VI values for each image were then calculated (Equation 2Go). The values from the 90 kVp CR automatic exposure control (AEC) images, with a receptor dose of 2.9 µGy, are used as the reference for calculating the VI values quoted throughout this report (N.B. this choice of normalization image is arbitrary). The images were scored by two experienced scorers, and the average of the two VI for each image was taken. Scoring was performed allowing variable viewing distance protocol, and standardized ambient light conditions.

Entrance surface dose was measured using a calibrated Radcal 2025 electrometer with 6 cm3 ionization chamber (Radcal Corporation, Monrovia, CA). The entrance surface doses and beam conditions were used to calculate effective doses for each set of exposure conditions (using the "Effdose" calculation package [24, 25]).

Receptor dose with the phantom in place was measured using a Dali 120 cm3 ion (PTW, Freiberg, Germany) chamber placed directly inside the bucky. Optical densities of the film–screen images were measured in a region away from any visible details using a Parry DT1405 densitometer (Parry, Newbury, UK).


    Results
 Top
 Abstract
 Introduction
 Theory
 Materials and methods
 Results
 Discussion
 Conclusions
 References
 
Figures 4Go and 5Go show the variation of VI with effective dose for the three tube potential values investigated with CR and FS, respectively. Table 1Go lists the receptor doses and optical densities of the points for the FS data. Figure 6Go plots the ratio of FS VI to CR VI for each tube voltage tested. With FS there is a point beyond which increasing exposure results in a decrease in detail visibility owing to optical density saturation. However, with CR at each tube potential the VI rises with exposure as lower contrast details to become more visible over the decreasing quantum noise. Consequently the image quality performance of FS relative to CR decreases beyond the peak associated with the optimum film blackening (Figure 6Go).



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Figure 4. Plot of visibility index (VI) versus effective dose for sets of computed radiography (CR) images obtained at 75 kVp (thick solid line with data points marked by horizontal lines), 90 kVp (dashed line with data points marked by crosses) and 125 kVp (thin solid line with data points marked by diamond shapes).

 


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Figure 5. Plot of visibility index (VI) versus effective dose for sets of film–screen (FS) images obtained at 75 kVp (thick solid line with data points marked by horizontal lines), 90 kVp (dashed line with data points marked by crosses) and 125 kVp (thin solid line with data points marked by diamond shapes).

 

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Table 1. The percentage difference in visibility index between film–screen (FS) and computed radiography (CR) at the dose level of the peak in FS image quality

 


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Figure 6. A plot of the ratio of film–screen (FS) visibility index (VI) trend-line to the computed radiography (CR) VI trend-line at 75 kVp (thick solid line), 90 kVp (dashed line) and 125 kVp (thin solid line).

 
Wilcoxen signed rank statistical tests were performed to assess the null hypotheses H1, H2 and H3, defined as follows:

The data were grouped into pairs of visibility indices obtained with approximately matched effective doses at different tube voltages. The data were matched such that for each pair the higher dose point was taken from the apparently lower image quality distribution (i.e. 125 kVp for H1 and H2, and 75 kVp for H3). Differences of up to 30% in dose were accepted for matched pairs. The results are summarized in Table 2Go. The Wilcoxen statistical test is not appropriate for testing the film–screen data, although clearly there is a strong tube voltage dependence shown in Figure 5Go.


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Table 2. Results of Wilcoxen signed rank test

 

    Discussion
 Top
 Abstract
 Introduction
 Theory
 Materials and methods
 Results
 Discussion
 Conclusions
 References
 
Comparison of FS with CR for chest imaging
It can be clearly seen from Figure 6Go that the difference between FS and CR is strongly dependent on beam energy. This should be considered when reviewing the results of comparative studies. For example the Hufton et al [15] study used tube voltages in the range 60–70 kVp for chest X-rays of infants, and assessed image quality against the CEC criteria. They concluded that dose reductions of the order of 30% were possible when using CR instead of 400 speed FS, whilst maintaining image quality. Conversely Cook et al [11] found no statistically significant difference between FS and CR at 125 kVp, for threshold contrast detail detectability phantoms with scatter conditions similar to an adult chest.

With FS it should be noted that the clinical details of interest in the lung and mediastinum will often not be displayed at the optimum optical density. Consequently the true performance of FS relative to CR will generally be poorer than indicated here, since CR VI improve relative to FS away from the peak of the FS curves (Figure 6Go).

Optimum tube voltage for CR chest examinations
Figure 4Go demonstrates that the image quality for the CR system was poorest at 125 kVp across the range of effective doses investigated. This is due to a combination of the variation of detector response with photon energy (see Figures 1Go and 2Go) and the decreased signal contrast at high tube voltage.

It can be seen from Figure 2Go that over the range of beam energies investigated in this study the photostimulable phosphor suffers a much greater reduction in primary beam absorption efficiency than the gadolinium oxysulphide screen. This is in broad agreement with the results of Fetterly and Handiandreou [26] who showed that the DQE of a Fuji CR system decreased with increasing tube voltage from 70 kVp to 95 kVp and 120 kVp. The different behaviour is due to the different k-edge positions of the two materials. The higher k-edge of Gd2O2S is beneficial for detecting high tube potential beams which have a greater percentage of photon energies above this threshold. It should be noted that the depth at which interactions occur in both the CR plate and intensifying screen will have some energy dependence. The efficiency of the transfer of light from the phosphors to either the film or the photomultiplier tube (in the case of CR) will be dependent on the depth of its origin. For CR, the average depth of interaction will be greater for the higher tube voltages, resulting in a greater spread of laser light and attenuation of photostimulated luminescence. For the FS system the relationship between depth of absorption and image quality is more complex owing to the dual screen geometry.

The sensitivity to the primary beam photons is a partial explanation for the comparatively poor performance of the CR system at high tube voltages. The scattered photon absorption efficiency of the two receptors should also be considered. Unfortunately this effect cannot be quantified as easily as the effect of the primary beam spectrum. Both detectors will in general be more sensitive to the scattered radiation incident on them than to the primary beam due to its lower energy. It can be seen from Figure 2Go that the sensitivity of the photostimulable phosphor increases more sharply with decreasing tube potential than the Gd2O2S screen. The scatter spectrum can be crudely considered to the equivalent to a beam of lower tube potential than the primary beam. At the higher energies the sensitivity to scatter and primary will be broadly similar for the Gd2O2S screen. For the photostimulable phosphor however, the sensitivity to scatter may be significantly higher than the primary beam.

The results of this study of the optimum tube voltage for CR support the results of other investigations [4, 16]. Both these studies used Fuji CR plates which use BaF(Br0.85I0.15) phosphors similar to that used by the Agfa system investigated in this work. These studies are therefore all comparable, and all suggest an improvement in detail visibility at tube voltages lower than the 125 kVp suggested for FS imaging [3]. It should be noted that the rationale behind the choice of high tube potential for FS is to maintain an acceptable range of radiographic densities across both the lung and mediastinum, rather than to maximize detail visibility in one or other of these regions. With CR the wide dynamic range and the ability to process data post acquisition suggest that minimization of contrast between mediastinum and lung should not be necessary [4]. The use of a tube voltage lower than 125 kVp is strongly suggested. The CEC guidelines require that chest exposures should be no longer than 20 ms to minimize cardiac motion artefact. It is recommended from the results of this work that a tube voltage in the range of 75 kVp to 90 kVp is used provided that the exposure time can be limited below 20 ms. Clinical trials a required to verify this result.


    Conclusions
 Top
 Abstract
 Introduction
 Theory
 Materials and methods
 Results
 Discussion
 Conclusions
 References
 
CR and FS have inherently different imaging characteristics; for example different energy response and responses to variations in exposure. It is therefore unlikely to be appropriate to acquire images using the same exposure factors for both systems. For chest imaging the results reported here indicate that CR produces optimum image quality in the range of 75 kVp to 90 kVp, rather than the higher energies which are often used in practice.


    Acknowledgments
 
The authors would like to acknowledge the Medicine and Healthcare products Regulatory Agency (MHRA) for funding this projects and the staff of the imaging departments for their assistance and co-operation in providing access to the imaging systems.


    Footnotes
 
Current address for D S Evans, Imaging and Medical Physics, University Hospital Birmingham NHS Trust, Birmingham, UK. Back

Received for publication January 30, 2004. Revision received September 23, 2004. Accepted for publication December 1, 2004.


    References
 Top
 Abstract
 Introduction
 Theory
 Materials and methods
 Results
 Discussion
 Conclusions
 References
 

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