32 research outputs found

    A Three-dimensional Deformable Brain Atlas for DBS Targeting. I. Methodology for Atlas Creation and Artifact Reduction.

    Get PDF
    BackgroundTargeting in deep brain stimulation (DBS) relies heavily on the ability to accurately localize particular anatomic brain structures. Direct targeting of subcortical structures has been limited by the ability to visualize relevant DBS targets.Methods and resultsIn this work, we describe the development and implementation, of a methodology utilized to create a three dimensional deformable atlas for DBS surgery. This atlas was designed to correspond to the print version of the Schaltenbrand-Bailey atlas structural contours. We employed a smoothing technique to reduce artifacts inherent in the print version.ConclusionsWe present the methodology used to create a three dimensional patient specific DBS atlas which may in the future be tested for clinical utility

    Work-worlds colliding: Self-reflexivity, power and emotion in organizational ethnography

    Get PDF
    While organizational ethnographers have embraced the concept of self-reflexivity, problems remain. In this article we argue that the prevalent assumption that self-reflexivity is the sole responsibility of the individual researcher limits its scope for understanding organizations. To address this, we propose an innovative method of collective reflection that is inspired by ideas from cultural and feminist anthropology. The value of this method is illustrated through an analysis of two ethnographic case studies, involving a ‘pair interview’ method. This collective approach surfaced self-reflexive accounts, in which aspects of the research encounter that still tend to be downplayed within organizational ethnographies, including emotion, intersubjectivity and the operation of power dynamics, were allowed to emerge. The approach also facilitated a second contribution through the conceptualization of organizational ethnography as a unique endeavour that represents a collision between one ‘world of work’: the university, with a second: the researched organization. We find that this ‘collision’ exacerbates the emotionality of ethnographic research, highlighting the refusal of ‘researched’ organizations to be domesticated by the specific norms of academia. Our article concludes by drawing out implications for the practice of self-reflexivity within organizational ethnography

    Determination of mean ionization potential using magnetic resonance imaging for the reduction of proton beam range uncertainties: theory and application.

    No full text
    The accurate determination of mean ionization potential (I m) has the potential to reduce range uncertainty based margins and therefore allow for more focal treatments in proton radiotherapy. Many methods have been proposed to reduce uncertainty in I m and stopping power ratios (SPR), each with varying degrees of accuracy and issues. In this work, we present a simple parameterized model to determine I m in human biological tissue, allowing for the computation of patient-specific I m at the voxel level using magnetic resonance imaging (MRI). The model requires the measurement of three parameters by MRI, with only two parameters, mass percent water content and mass percent hydrogen content in organic molecules, required for the special case of soft tissues. The accuracy of this I m determination method was evaluated in available 'standard' (ICRU Report #44, (ICRU 1989 Tissue Substitutes in Radiation Dosimetry and Measurement (Bethesda, MD: International Commission on Radiation Units and Measurements))) human tissues. The sensitivity of this I m determination method to in vivo perturbations was also tested by calculating the effect of 10% variations in the experimentally measurable parameters on I m and SPR. For the human tissues modeled in this work, a high level of accuracy with low susceptibility to perturbations in measurement error was achieved in the prediction of I m. Root-mean-square errors in I m were within 0.77% and 1.8% for both soft and bony tissues, and were 0.09% and 0.2% for the SPR of soft and bony tissues, respectively, assuming knowledge of electron density. Proof of principle MR measurements and model-based computations of I m and SPR were taken in phantom for a series of hydrogenous solutions and compared against expected I m and SPR calculations from known elemental composition. MR determined I m and SPR values in a known composition solution were determined to within 5% and 0.52%, respectively. We present a novel model to accurately calculate mean ionization potential from measurements acquirable by MRI and show its feasibility in a phantom

    On the molecular relationship between Hounsfield Unit (HU), mass density, and electron density in computed tomography (CT).

    No full text
    Accurate determination of physical/mass and electron densities are critical to accurate spatial and dosimetric delivery of radiotherapy for photon and charged particles. In this manuscript, the biology, chemistry, and physics that underly the relationship between computed tomography (CT) Hounsfield Unit (HU), mass density, and electron density was explored. In standard radiation physics practice, quantities such as mass and electron density are typically calculated based off a single kilovoltage CT (kVCT) scan assuming a one-to-one relationship between HU and density. It is shown that, in absence of mass density assumptions on tissues, the relationship between HU and density is not one-to-one with uncertainties as large as 7%. To mitigate this uncertainty, a novel multi-dimensional theoretical approach is defined between molecular (water, lipid, protein, and mineral) composition, HU, mass density, and electron density. Empirical parameters defining this relationship are x-ray beam energy/spectrum dependent and, in this study, two methods are proposed to solve for them including through a tissue mimicking phantom calibration process. As a proof of concept, this methodology was implemented in a separate in-house created tissue mimicking phantom and it is shown that sub 1% accuracy is possible for both mass and electron density. As molecular composition is not always known, the sensitivity of this model to uncertainties in molecular composition was investigated and it was found that, for soft tissue, sub 1% accuracy is achievable assuming nominal organ/tissue compositions. For boney tissues, the uncertainty in mineral content may lead to larger errors in mass and electron density compared with soft tissue. In this manuscript, a novel methodology to directly determine mass and electron density based off CT HU and knowledge of molecular compositions is presented. If used in conjunction with a methodology to determine molecular compositions, mass and electron density can be accurately calculated from CT HU
    corecore