Dataset Information

Inhomogeneity correction and the analytic anisotropic algorithm.

ABSTRACT: The ability of the analytic anisotropic algorithm (AAA), a superposition- convolution algorithm implemented in the Eclipse (Varian Medical Systems, Palo Alto, CA) treatment planning system (TPS), to accurately account for the presence of inhomogeneities in simple geometries is examined. The goal of 2% accuracy, as set out by the American Association of Physicists in Medicine Task Group 65, serves as a useful benchmark against which to evaluate the inhomogeneity correction capabilities of this treatment planning algorithm. A planar geometry phantom consisting of upper and lower layers of Solid Water (Gammex rmi, Middleton, WI) separated by a heterogeneity region of variable thickness, is modeled within the Eclipse TPS. Results obtained with the AAA are compared with experimental measurements. Seven different materials, spanning the range from air to aluminum, constitute the inhomogeneity layer. In general, the AAA overpredicts dose beyond low-density regions and underpredicts dose distal to volumes of high density. In many cases, the deviation between the AAA and experimental results exceeds the Task Group 65 target of 2%. The source of these deviations appears to arise from an inability of the AAA to correctly account for altered attenuation along primary ray paths.

SUBMITTER: Robinson D

PROVIDER: S-EPMC5721710 | biostudies-literature | 2008 May

REPOSITORIES: biostudies-literature

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Inhomogeneity correction and the analytic anisotropic algorithm.

Robinson Don D

Journal of applied clinical medical physics 20080501 2

The ability of the analytic anisotropic algorithm (AAA), a superposition- convolution algorithm implemented in the Eclipse (Varian Medical Systems, Palo Alto, CA) treatment planning system (TPS), to accurately account for the presence of inhomogeneities in simple geometries is examined. The goal of 2% accuracy, as set out by the American Association of Physicists in Medicine Task Group 65, serves as a useful benchmark against which to evaluate the inhomogeneity correction capabilities of this tr ...[more]

PMID: 18714283

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Project description:Purpose[Formula: see text] mapping is a powerful tool for studying osteoarthritis (OA) changes and bilateral imaging may be useful in investigating the role of between-knee asymmetry in OA onset and progression. The quantitative double-echo in steady-state (qDESS) can provide fast simultaneous bilateral knee [Formula: see text] and high-resolution morphometry for cartilage and meniscus. The qDESS uses an analytical signal model to compute [Formula: see text] relaxometry maps, which require knowledge of the flip angle (FA). In the presence of [Formula: see text] inhomogeneities, inconsistencies between the nominal and actual FA can affect the accuracy of [Formula: see text] measurements. We propose a pixel-wise [Formula: see text] correction method for qDESS [Formula: see text] mapping exploiting an auxiliary [Formula: see text] map to compute the actual FA used in the model.MethodsThe technique was validated in a phantom and in vivo with simultaneous bilateral knee imaging. [Formula: see text] measurements of femoral cartilage (FC) of both knees of six healthy participants were repeated longitudinally to investigate the association between [Formula: see text] variation and [Formula: see text].ResultsThe results showed that applying the [Formula: see text] correction mitigated [Formula: see text] variations that were driven by [Formula: see text] inhomogeneities. Specifically, [Formula: see text] left-right symmetry increased following the [Formula: see text] correction ([Formula: see text] = 0.74 > [Formula: see text] = 0.69). Without the [Formula: see text] correction, [Formula: see text] values showed a linear dependence with [Formula: see text]. The linear coefficient decreased using the [Formula: see text] correction (from 24.3 ± 1.6 ms to 4.1 ± 1.8) and the correlation was not statistically significant after the application of the Bonferroni correction (p value > 0.01).ConclusionThe study showed that [Formula: see text] correction could mitigate variations driven by the sensitivity of the qDESS [Formula: see text] mapping method to [Formula: see text], therefore, increasing the sensitivity to detect real biological changes. The proposed method may improve the robustness of bilateral qDESS [Formula: see text] mapping, allowing for an accurate and more efficient evaluation of OA pathways and pathophysiology through longitudinal and cross-sectional studies.

Dataset Information

Inhomogeneity correction and the analytic anisotropic algorithm.

Publications

Inhomogeneity correction and the analytic anisotropic algorithm.

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