37,252 research outputs found

    How Will Comparative Effectiveness Research Affect the Quality of Health Care?

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    Outlines how the use of comparative effectiveness research on the relative merits of a healthcare intervention compared with others could improve quality of care and outcomes. Presents challenges in enhancing CE research and expanding its adoption

    Accelerated Cardiac Diffusion Tensor Imaging Using Joint Low-Rank and Sparsity Constraints

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    Objective: The purpose of this manuscript is to accelerate cardiac diffusion tensor imaging (CDTI) by integrating low-rankness and compressed sensing. Methods: Diffusion-weighted images exhibit both transform sparsity and low-rankness. These properties can jointly be exploited to accelerate CDTI, especially when a phase map is applied to correct for the phase inconsistency across diffusion directions, thereby enhancing low-rankness. The proposed method is evaluated both ex vivo and in vivo, and is compared to methods using either a low-rank or sparsity constraint alone. Results: Compared to using a low-rank or sparsity constraint alone, the proposed method preserves more accurate helix angle features, the transmural continuum across the myocardium wall, and mean diffusivity at higher acceleration, while yielding significantly lower bias and higher intraclass correlation coefficient. Conclusion: Low-rankness and compressed sensing together facilitate acceleration for both ex vivo and in vivo CDTI, improving reconstruction accuracy compared to employing either constraint alone. Significance: Compared to previous methods for accelerating CDTI, the proposed method has the potential to reach higher acceleration while preserving myofiber architecture features which may allow more spatial coverage, higher spatial resolution and shorter temporal footprint in the future.Comment: 11 pages, 16 figures, published on IEEE Transactions on Biomedical Engineerin

    Lessons learned from the financial crisis for financial stability and banking supervision

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    The financial crisis that began in 2007 has revealed a need for a new supervisory and regulatory approach aimed at strengthening the system and containing the risk of future financial and economic disruptions. Three ingredients are needed to ensure financial stability: robust analysis, better regulation, and international cooperation. First, financial stability analysis must be improved to take full account of the different sources of systemic risk. Data coverage of the balance sheets of both non-bank financial institutions and the non-financial sectors should be increased. Moreover, to address the problems raised by the interconnections among financial institutions more granular and timely information on their exposures is needed. There must be further integration of macro- and micro-information and an upgrading of financial stability models. The second ingredient is the design of robust regulatory measures. Under the auspices of the G20 and the Financial Stability Board, the Basel Committee on Banking Supervision recently put forward substantial proposals on capital and liquidity. They will result in more robust capital base, lower leverage, less cyclical capital rules and better control of liquidity risk. Finally, the third ingredient is strong international cooperation. Ensuring more effective exchanges of information among supervisors in different jurisdictions and successful common actions is key in preserving financial integration, while avoiding negative cross-border spill-overs. Better resolution regimes are part of the efforts to ensure that the crisis of one institution does not impair the ability of the financial markets to provide essential services to the economy.financial crisis, international cooperation, macroprudential analysis, procyclicality, prudential regulation, stress tests

    A review of the literature concerning anxiety for educational assessments

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    Doctor of Philosophy

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    dissertationAggressive random testing tools, or fuzzers, are impressively effective at finding bugs in compilers and programming language runtimes. For example, a single test-case generator has resulted in more than 460 bugs reported for a number of production-quality C compilers. However, fuzzers can be hard to use. The first problem is that failures triggered by random test cases can be difficult to debug because these tests are often large. To report a compiler bug, one must often construct a small test case that triggers the bug. The existing automated test-case reduction technique, delta debugging, is not sufficient to produce small, reportable test cases. A second problem is that fuzzers are indiscriminate: they repeatedly find bugs that may not be severe enough to fix right away. Third, fuzzers tend to generate a large number of test cases that only trigger a few bugs. Some bugs are triggered much more frequently than others, creating needle-in-the-haystack problems. Currently, users rule out undesirable test cases using ad hoc methods such as disallowing problematic features in tests and filtering test results. This dissertation investigates approaches to improving the utility of compiler fuzzers. Two components, an aggressive test-case reducer and a tamer, are added to the fuzzing workflow to make the fuzzer more user friendly. We introduce C-Reduce, an aggressive test-case reducer for C/C++ programs, which exploits rich domain-specific knowledge to output test cases nearly as good as those produced by skilled humans. This reducer produces outputs that are, on average, more than 30 times smaller than those produced by the existing reducer that is most commonly used by compiler engineers. Second, this dissertation formulates and addresses the fuzzer taming problem: given a potentially large number of random test cases that trigger failures, order them such that diverse, interesting test cases are highly ranked. Bug triage can be effectively automated, relying on techniques from machine learning to suppress duplicate bug-triggering test cases and test cases triggering known bugs. An evaluation shows the ability of this tool to solve the fuzzer taming problem for 3,799 test cases triggering 46 bugs in a C compiler

    Process of designing robust, dependable, safe and secure software for medical devices: Point of care testing device as a case study

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    This article has been made available through the Brunel Open Access Publishing Fund.Copyright © 2013 Sivanesan Tulasidas et al. This paper presents a holistic methodology for the design of medical device software, which encompasses of a new way of eliciting requirements, system design process, security design guideline, cloud architecture design, combinatorial testing process and agile project management. The paper uses point of care diagnostics as a case study where the software and hardware must be robust, reliable to provide accurate diagnosis of diseases. As software and software intensive systems are becoming increasingly complex, the impact of failures can lead to significant property damage, or damage to the environment. Within the medical diagnostic device software domain such failures can result in misdiagnosis leading to clinical complications and in some cases death. Software faults can arise due to the interaction among the software, the hardware, third party software and the operating environment. Unanticipated environmental changes and latent coding errors lead to operation faults despite of the fact that usually a significant effort has been expended in the design, verification and validation of the software system. It is becoming increasingly more apparent that one needs to adopt different approaches, which will guarantee that a complex software system meets all safety, security, and reliability requirements, in addition to complying with standards such as IEC 62304. There are many initiatives taken to develop safety and security critical systems, at different development phases and in different contexts, ranging from infrastructure design to device design. Different approaches are implemented to design error free software for safety critical systems. By adopting the strategies and processes presented in this paper one can overcome the challenges in developing error free software for medical devices (or safety critical systems).Brunel Open Access Publishing Fund
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