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Radiology Department, Stoke Mandeville Hospital, Mandeville Road, Aylesbury, Buckinghamshire HP21 8AL, UK
| Abstract |
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| Introduction |
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Following the implementation of dose reduction strategies in the late 1980s, the annual collective effective dose from CT at this hospital was previously reported as 3.9 manSv (2210 examinations) in 1991 for a conventional axial CT scanner (GE 9000 HP; General Electric Medical Systems, Milwaukee, WI) [3]. In the present study we have calculated the annual collective effective dose following installation of a helical CT scanner (Siemens Somatom Plus 4; Siemens Aktiengesellschaft, Erlangen, Germany), and again approximately 2 years later, after adjustment of clinical scan protocols, in the first iteration of our work towards optimization of patient dose and image quality.
| Method |
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For each type of scan, agreement was achieved between all reporting radiologists on the scanned volume, with a check being made to ensure that European quality criteria for diagnostic images were met in this respect [4]. This process was led by one radiologist with a special interest in CT. In an iterative procedure, tube current (mA) and/or rotation time were then gradually reduced, and slice width and/or pitch were gradually adjusted, under the supervision of a consultant radiologist. It is essential that such adjustments are made in an incremental fashion in order that unacceptable deterioration in image quality is detected and avoided. Throughout this gradual process of protocol adjustment, CT images were assessed against the image criteria given in the European working document to ensure that diagnosticity was not compromised. In general, the lowest mAs values have been achieved in areas where there is high inherent contrast, e.g. chest, spine and imaging for renal calculi. In almost all body scan protocols it has been possible to adopt a pitch of at least 1.5 and a tube potential of 120 kV. For head scan protocols (all at 140 kV), where higher spatial resolution is required, sequence scanning or a pitch of 1.0 is normally used, together with smaller slice widths. The scanner can also be operated at 80 kV, although to date this tube potential setting has not been used clinically.
Thus, standardized low dose protocols were derived for a range of scanned volumes and pathologies. Table 1
shows four of our current protocols for some common examinations, namely standard brain, chest, abdomen and pelvis, for this particular model of CT scanner, although in fact there are now over 30 pathology-specific protocols in clinical use. Each pathology-specific protocol defines the pre- and post-contrast scan volumes, slice width, tube potential, tube current and scan time. It has been proposed elsewhere that scan protocols have limited usefulness in determining individual patient doses, as clinical practice may vary to suit individual patients in terms of size and clinical indication [5]. However, because we have developed an extended range of protocols tailored to specific clinical indications, deviations from the protocols only occur in relation to patient size, i.e. tube current is increased for an obese patient, or decreased for a paediatric patient. Our pathology-specific protocols, which relate to all average adult patients, are therefore useful in determining representative patient doses that enable comparison of different scan protocols. Our current scan protocols are now felt to be approaching the optimum, and any further attempts at dose reduction will necessitate a more in-depth analysis of image quality.
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Effective doses were calculated using the commercially available software CTDOSE for both the original and current protocols [7]. Pre- and post-contrast scan volumes were defined for all protocols, therefore effective doses for both components of a given examination were calculated and then combined to give the total effective dose per examination. CTDOSE uses normalized organ dose data sets, together with measured values of free-in-air axial dose for particular models of scanner, and details of the clinical technique for each type of examination [8]. These organ dose data sets were derived using Monte Carlo calculations in an anthropomorphic phantom representing a 70 kg hermaphrodite adult and currently relate to a previous generation of axial CT scanners, but details of appropriate matches for newer scanners to the original data sets have been produced by ImPACT (a Medical Devices Agency evaluation group) [9]. For the Somatom Plus 4 CT scanner, data set 1 was used for head scans and data set 16 for body scans at both 120 kVp and 140 kVp.
The CTDOSE software requires the following input parameters: scanned volume (in terms of baseline in the phantom and number of slices), slice width, couch increment (axials), effective mAs and CT dose index per mAs (CTDI). CTDI is a measure of the total dose from a single slice irradiation. The European working document gives the following formula for CTDI [4]:
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where Z1 and Z2 are the limits of integration, D(z) is the single slice dose profile and T is the nominal slice thickness in centimeters. Integration distances and the phantom in which the measurement is made are identified in suffix notation, e.g. CTDI
Z,phantom, where the suffix
Z is the integration distance, and "phantom" denotes measurement in a specified phantom or air.
The CTDI10cm,air values used in the dose calculations are shown in Table 2
and were obtained from measurements using a pencil ion chamber (active length 10 cm) and dosemeter (type 35050A; Keithley Instruments Inc., Cleveland, OH). The measurements were made free-in-air, with the chamber on the scanner central axis. Because the organ dose data are expressed in terms of absorbed dose to ICRU muscle, these measured values of dose-in-air were converted to dose-to-ICRU muscle using appropriate conversion factors before input into the program [10].
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Some inaccuracies were introduced for scans with gantry tilt, namely all scans that use a coronal projection (sinuses, facial bones, orbits and petrous bone), as CTDOSE does not cater for this projection. Effective dose for corresponding axial scans was used as an approximation in these instances, with inevitable loss of accuracy. Gantry tilt is also used on a small percentage of lumbar spine scans, where the clinical aim is identification of a pars defect, therefore some loss of accuracy is to be expected here also. It has been shown elsewhere that the approximation of an angled projection to an axial slice can result in errors of up to 20% [11].
The quantity doselength product (DLP) was then derived for all scan protocols using the methods described in the European working document, for comparison against the four proposed diagnostic reference levels relating to head, chest, abdomen and pelvis [4]. The quantity DLP uses a weighted CTDI, (CTDIw (mGy)). CTDIw is an approximation to the average dose over a single slice and is derived from a combination of measurements at the surface and centre of a defined set of Perspex phantoms, according to the equation:
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where CTDI10cm,c is the CTDI measured at the centre of the phantom and CTDI10cm,p is the CTDI measured at the periphery of the phantom.
The European working document gives the following formulae for DLP:
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where i represents each scan sequence forming part of an examination, nCTDIw is the normalized weighted CTDI in the phantom (mGy mAs-1), N is the number of slices, T is the slice thickness, C is the radiographic exposure in mAs, A is the tube current (mA) and t is the total acquisition time for the sequence. The nCTDIw values used for the scanner in this study are given in Table 2
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Data on patient attendances for a 12-month period from April 1999 to April 2000 were obtained from the Radiology Information System (RIS), in which CT examinations are allocated to Korner categories [12]. The number of examinations that included a contrast run could be readily determined from the data, as these were logged into separate categories. The Korner data were then used together with the data on effective doses to determine annual collective effective doses for each Korner category. Of a total of 6149 examinations, 100 limb examinations were excluded from the analysis as limbs are not included within the software phantom used by CTDOSE. The effective dose from this category of scan will be comparatively small (<0.1 mSv) and the contribution to collective effective dose is likely to be less than 0.01 manSv. Table 3
shows how the remaining 6049 examinations in 19992000 were allocated to the various Korner categories. Again, some loss of accuracy accompanies this process, as about half the Korner categories contain several different scan protocols. For example, the Korner category "spine" includes patients for cervical, thoracic and lumbar spine, each of which has a different effective dose owing to the different organs irradiated. Furthermore, the exact protocol used depends on the pathology. As the majority of these examinations were T or L spine, the average effective dose for these two examinations was used in determining the collective effective dose in this category. Similarly, other Korner categories, e.g. chest and abdomen, contain scans carried out using a variety of protocols according to pathology. For such Korner categories it was possible to derive approximate effective doses per category by taking a simple average of the effective doses for all the scan protocols within that category.
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| Results |
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Indicative image noise levels, obtained using a selection of the original and current protocols to scan Perspex phantoms, are shown in Table 7
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| Discussion |
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The DLP of 1253 mGy cm for a brain scan with contrast is above the proposed reference level of 1050 mGy cm for head scans. Calzado et al [13] have shown that the correlation between image quality score and DLP is not straightforward for CT of the brain. In that study, higher DLP values were not always associated with greater fulfilment of some specific EC image quality criteria, for which fulfilment was uniformly low across all scanners tested. The highest score against these particular criteria was attributed to reconstruction algorithm rather than tohigher dose. Similarly, another criterion on twoscanners attracted low scores attributable to pathology, anatomical variants or motion artefact. Mean DLP values in the range 4801018 mGy cm were reported, with the highest overall image quality score associated with the scanner giving a mean DLP of 1018 mGy cm. However, this scanner, despite having the highest image score and highest dose, gave the worst performance for two of the criteria. Because of these complex relationships, detailed analysis of our brain scans will be required to determine whether dose reduction without compromising diagnosticity is feasible.
Image noise is represented by the statistical variation of measured values of Hounsfield units when scanning a homogeneous object such as a Perspex phantom. A 2-fold increase in noise might be expected from a 4-fold decrease in dose, and this has been borne out to some extent in our standard chest examinations, where the dose has been halved, giving an observed increase of 90% in noise [4]. Decreases in dose were less dramatic for other scan protocols, and this is reflected in the smaller increases observed in noise levels.
The continual appraisal of images against the EC quality criteria during this first iteration in the optimization process has brought us to the stage where further dose reduction will require more detailed analysis of image quality, which will probably be on a smaller scale. There may be some scope for dose reduction in the future, arising from the use of alternative modalities, although currently the shift tends to be in the opposite direction, reflecting the national situation. CT scans for suspected pulmonary embolus and renal calculi are examples of such pathologies, formerly referred for examination by nuclear medicine and intravenous urography (IVU), respectively. We have effectively removed much of the excess dose caused by our CT practice, achieving a collective dose saving of 5.6 manSv per year, and leaving a smaller margin in which more detailed optimization of practice can be pursued.
The CT scanner at this site uses solid state detector technology. Zeman et al [14] have reported that the use of solid state detectors allows a theoretical dose reduction of approximately 30% in comparison with equivalent scanners with gas detectors. It follows that similar models of scanner with gas detectors might operate optimally at about 14 manSv for a similar patient workload. Similarly, extrapolating our average patient examination dose of 1.8 mSv per scan to an equivalent scanner with gas detectors, an average "optimized" examination dose of around 2.3 mSv might be expected.
With CT being such a major contributor to UK collective effective dose, it is crucially important that exposure from this source is justified for every patient, and once justified, that it is optimized. Manufacturers of CT scanners can assist in the process of optimization by further development of dose-saving design features, and by promoting and promulgating lower dose scan parameters during applications training after installation.
Received for publication July 14, 2000. Revision received January 12, 2001. Accepted for publication April 4, 2001.
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