3,336 research outputs found

    A note on the power divergence in lattice calculations of ΔI=1/2\Delta I = 1/2 K→ππK\to\pi\pi amplitudes at MK=MπM_{K}=M_{\pi}

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    In this note, we clarify a point concerning the power divergence in lattice calculations of ΔI=1/2\Delta I = 1/2 K→ππK\to\pi\pi decay amplitudes. There have been worries that this divergence might show up in the Minkowski amplitudes at MK=MπM_{K}=M_{\pi} with all the mesons at rest. Here we demonstrate, via an explicit calculation in leading-order Chiral Perturbation Theory, that the power divergence is absent at the above kinematic point, as predicted by CPS symmetry.Comment: 5 pages, 2 figure

    Finite-Volume Two-Pion Amplitudes in the I=0 Channel

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    We perform a calculation in one-loop chiral perturbation theory of the two-pion matrix elements and correlation functions of an I=0 scalar operator, in finite and infinite volumes for both full and quenched QCD. We show that major difficulties arise in the quenched theory due to the lack of unitarity. Similar problems are expected for quenched lattice calculations of K→ππK \to \pi \pi amplitudes with ΔI=1/2\Delta I=1/2. Our results raise the important question of whether it is consistent to study K→ππK\to\pi\pi amplitudes beyond leading order in chiral perturbation theory in quenched or partially quenched QCD.Comment: Version to appear on Phys. Lett. B, with only very minor and stylistic change

    A Fast and Accurate Diagnostic Test for Severe Sepsis Using Kernel Classifiers

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    Severe sepsis occurs frequently in the intensive care unit (ICU) and is a leading cause of admission, mortality, and cost. Treatment guidelines recommend early intervention, however gold standard blood culture test results may return in up to 48 hours. Insulin sensitivity (SI) is known to decrease with worsening condition and inflammatory response, and could thus be used to aid clinical treatment decisions. Some glycemic control protocols are able to accurately identify SI in real-time. A biomarker for severe sepsis was developed from retrospective SI and concurrent temperature, heart rate, respiratory rate, blood pressure, and SIRS score from 36 adult patients with sepsis. Patients were identified as having sepsis based on a clinically validated sepsis score (ss) of 2 or higher (ss = 0–4 for increasing severity). Kernel density estimates were used for the development of joint probability density profiles for ss = 2 and ss < 2 data hours (213 and 5858 respectively of 6071 total hours) and for classification. From the receiver operator characteristic (ROC) curve, the optimal probability cutoff values for classification were determined for in-sample and out-of-sample estimates. A biomarker including concurrent insulin sensitivity and clinical data for the diagnosis of severe sepsis (ss = 2) achieves 69–94% sensitivity, 75–94% specificity, 0.78–0.99 AUC, 3–17 LHR+, 0.06–0.4 LHR-, 9–38% PPV, 99–100% NPV, and a diagnostic odds ratio of 7–260 for optimal probability cutoff values of 0.32 and 0.27 for in-sample and out-of-sample data, respectively. The overall result lies between these minimum and maximum error bounds. Thus, the clinical biomarker shows good to high accuracy and may provide useful information as a real-time diagnostic test for severe sepsis

    Lorentz invariance of effective strings

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    Starting from a Poincar\'e invariant field theory of a real scalar field with interactions governed by a double-well potential in 2+1 dimensions, the Lorentz representation induced on the collective coordinates describing low-energy excitations about an effective string background is derived. In this representation, Lorentz transformations are given in terms of an infinite series, in powers of derivatives along the worldsheet. Transformations that act on the direction transverse to the string worldsheet involve a universal dimension −1-1 term. As a consequence, Lorentz invariance holds in this theory of long effective strings due to cancellations in the action between irrelevant terms and the dimension two term that describes free massless scalar fields in two dimensions. (in plain tex, no macropackages necessary)Comment: 9 page

    Strings in Homogeneous Background Spacetimes

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    The string equations of motion for some homogeneous (Kantowski-Sachs, Bianchi I and Bianchi IX) background spacetimes are given, and solved explicitly in some simple cases. This is motivated by the recent developments in string cosmology, where it has been shown that, under certain circumstances, such spacetimes appear as string-vacua. Both tensile and null strings are considered. Generally, it is much simpler to solve for the null strings since then we deal with the null geodesic equations of General Relativity plus some additional constraints. We consider in detail an ansatz corresponding to circular strings, and we discuss the possibility of using an elliptic-shape string ansatz in the case of homogeneous (but anisotropic) backgrounds.Comment: 25 pages, REVTE

    New Insights into Uniformly Accelerated Detector in a Quantum Field

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    We obtained an exact solution for a uniformly accelerated Unruh-DeWitt detector interacting with a massless scalar field in (3+1) dimensions which enables us to study the entire evolution of the total system, from the initial transient to late-time steady state. We find that the Unruh effect as derived from time-dependent perturbation theory is valid only in the transient stage and is totally invalid for cases with proper acceleration smaller than the damping constant. We also found that, unlike in (1+1)D results, the (3+1)D uniformly accelerated Unruh-DeWitt detector in a steady state does emit a positive radiated power of quantum nature at late-times, but it is not connected to the thermal radiance experienced by the detector in the Unruh effect proper.Comment: 6 pages, invited talk given by SYL at the conference of International Association for Relativistic Dynamics (IARD), June 2006, Storrs, Connecticut, US

    Fine Structure Discussion of Parity-Nonconserving Neutron Scattering at Epithermal Energies

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    The large magnitude and the sign correlation effect in the parity non-conserving resonant scattering of epithermal neutrons from 232^{232}Th is discussed in terms of a non-collective 2p−1h2p-1h local doorway model. General conclusions are drawn as to the probability of finding large parity violation effects in other regions of the periodic table.Comment: 6 pages, Tex. CTP# 2296, to appear in Z. Phys.

    Impact of glucocorticoids on insulin resistance in the critically ill

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    Glucocorticoids (GCs) have been shown to reduce insulin sensitivity in healthy individuals. Widely used in critical care to treat a variety of inflammatory and allergic disorders, they may inadvertently exacerbate stress-hyperglycaemia. This research uses model-based methods to quantify the reduction of insulin sensitivity from GCs in critically ill patients, and thus their impact on glycaemic control. A clinically validated model-based measure of insulin sensitivity (SI) was used to quantify changes between two matched cohorts of 40 intensive care unit (ICU) patients who received GCs and a control cohort who did not. All patients were admitted to the Christchurch hospital ICU between 2005 and 2007 and spent at least 24 hours on the SPRINT glycaemic control protocol. A 31% reduction in whole-cohort median insulin sensitivity was seen between the control cohort and patients receiving glucocorticoids with a median dose equivalent to 200mg/day of hydrocortisone per patient. Comparing percentile-patients as a surrogate for matched patients, reductions in median insulin sensitivity of 20, 25, and 21% were observed for the 25th, 50th and 75th-percentile patients. All these cohort and per-patient reductions are less than or equivalent to the 30-62% reductions reported in healthy subjects especially when considering the fact that the GC doses in this study are 1.3-4 times larger than those in studies of healthy subjects. This reduced suppression of insulin sensitivity in critically ill patients could be a result of saturation due to already increased levels of catecholamines and cortisol common in critically illness. Virtual trial simulation showed that reductions in insulin sensitivity of 20-30% associated with glucocorticoid treatment in the ICU have limited impact on glycaemic control levels within the context of the SPRINT protocol
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