Wide variations in patient dose for the same examinations have been demonstrated by several studies throughout Europe. By investigating patient dose, variations can be acknowledged, causal agents sought and the necessary adjustments made. Diagnostic reference levels (DRLs) provide a framework with which dose levels from individual hospitals are compared, and when exceeded, corrective actions can be taken where appropriate. This study aimed to establish DRLs for barium enema and barium meal examinations in Ireland. Measurements were recorded using a dose-area product meter in 12 hospitals representing 33% of relevant hospitals. Results demonstrated wide mean hospital dose variation, by up to a factor of 7.8 and 4.2 for barium enema and barium meal examinations, respectively. Minimum and maximum individual patient dose values varied by a factor of 45 for barium enemas and 90 for barium meal examinations. Reasons for dose variations were complex, but major factors for both examinations were fluoroscopy time, secondary radiation grid type and level of filtration. Some examination-specific factors were also noted. DRLs, established using the quantity dose-area product, were calculated to be 47 Gy cm(2) for barium enemas and 17 Gy cm(2) for barium meal examinations. Although the DRL value for barium meals was the same as the reference value established in the UK for that examination in 1996, the barium enema DRL in this study was 45% higher than the relevant UK value.

With the introduction of Council Directive 97/43/Euratom, all member states should establish relevant diagnostic reference levels for X-ray examinations. Diagnostic reference levels help to facilitate standardisation and optimisation within departments and attempt to reduce dose variations between hospitals. High variation of individual patient doses for plain-film examinations by up to a factor of 75 was demonstrated by a previous Irish study, which highlighted the necessity for further investigation into other examinations in Ireland. The current work aimed to establish reference values for intravenous urography (IVU) examinations, an important contributor to collective dose. Eleven Irish hospitals were randomly selected, representing 30% of the total number of hospitals. Dose-area product (DAP) readings for IVUs were recorded along with technical and procedural details. Resultant data demonstrated mean hospital and individual patient DAP variations of a factor of 4 and 58, respectively. Stepwise regression analysis demonstrated that number of images taken, method of image acquisition and patient weight were the main causal agents for dose variations recorded. A proposed diagnostic reference level of 12 Gy cm(2) was established at the level of the third-quartile value of the mean hospital DAP values. This article provides evidence of large variations in DAP values for IVU examinations. It is hoped that application of the proposed DRL of 12 Gy cm(2 )will reduce the size of these variations.

Four hospitals have been studied, intra- and inter-hospital variations examined and the mean DAP values recorded for barium enemas and barium meals. Mean DAP values for barium meals and barium enemas at 11.4 Gy x cm2 and 20.1 Gy x cm2 respectively have been shown. Differences between individual examinations for barium meals varied by up to a factor of 185 and for barium enemas, up to a factor of 19, with hospital means for barium meal and enema examinations each differing by up to a factor of 3. The data provided by this study have suggested that large variations in patient dose do exist in Ireland for barium meal and barium enema examinations. Fluoroscopy time was shown to be a major contributor to the variations reported, with number of images playing a minor role. Results have demonstrated the need for standardisation of technique throughout the country for these examinations.

In this paper we present a methodology for data accesses when solving batches of Tridiagonal and Pentadiagonal matrices that all share the same left-hand-side (LHS) matrix. The intended application is to the numerical solution of Partial Differential Equations via the finite-difference method, although the methodology is applicable more broadly. By only storing one copy of this matrix, a significant reduction in storage overheads is obtained, together with a corresponding decrease in compute time. Taken together, these two performance enhancements lead to an overall more efficient implementation over the current state of the art algorithms cuThomasBatch and cuPentBatch, allowing for a greater number of systems to be solved on a single GPU. We demonstrate the methodology in the case of the Diffusion Equation, Hyperdiffusion Equation, and the Cahn-Hilliard Equation, all in one spatial dimension. In this last example, we demonstrate how the method can be used to perform 2 20 independent simulations of phase separation in one dimension. In this way, we build up a robust statistical description of the coarsening phenomenon which is the defining behavior of phase separation. We anticipate that the method will be of further use in other similar contexts requiring statistical simulation of physical systems.

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