70 research outputs found

    Isovector axial vector and pseudoscalar transition form factors of Δ\Delta in QCD

    Full text link
    We investigate the isovector axial vector and pseudoscalar form factors of Δ\Delta baryon by employing light-cone QCD sum rules. Numerical calculations show that the form factors can be well fitted by the exponential form. We make a comparison with the predictions of Lattice QCD, Chiral Perturbation Theory and Quark Model.Comment: 9 pages, 9 figures. arXiv admin note: text overlap with arXiv:1405.533

    Sigma-meson and omega-rho mixing effects in omega --> pi^+ pi^- gamma decay

    Full text link
    We calculate the branching ratio of omega --> pi^+ pi^- gamma decay in a phenomenological framework in which the contributions of VMD, chiral loops, sigma-meson intermediate state amplitudes and the effects of omega-rho mixing are considered. We conclude that the sigma-meson intermediate state amplitude and omega-rho mixing make substantial contribution to the branching ratio.Comment: 10 pages RevTex, 4 Figures, to be published in Acta Phys. Pol.

    PMC51 MEDICATION ADHERENCE: A CONCEPTUAL REVIEW

    Get PDF

    RACE-IT - Rapid Acute Coronary Syndrome Exclusion using the Beckman Coulter Access high-sensitivity cardiac troponin I: A stepped-wedge cluster randomized trial

    Get PDF
    Background: Protocols utilizing high-sensitivity cardiac troponin (hs-cTn) assays for the evaluation of suspected acute coronary syndrome (ACS) in the emergency department (ED) have been gaining popularity across the US and the world. These protocols more rapidly rule-out ACS and more accurately identify the presence of acute myocardial injury. At this time, few randomized trials have evaluated the safety and operational impact of these assays, resulting in limited evidence to guide the use and implementation of hs-cTn in the ED. Objective: The main study objective is to test the effectiveness of a rapid ACS rule-out pathway using hs-cTnI in safely discharging patients from the ED for whom clinical suspicion for ACS exists. Design: This prospective, implementation trial (n = 11,070) will utilize a stepped wedge cluster randomized trial design. The design will allow for all participating sites to capture benefit from the implementation of the hs-cTnI pathway while providing data evaluating the effectiveness in providing safe and rapid evaluation of patients with clinical suspicion for ACS. Summary: Demonstrating that clinical pathways using hs-cTnI can be effectively implemented to rapidly rule-out ACS while conserving costly hospital resources has significant implications for the care of patients with possible acute cardiac conditions in EDs across the US. Clinicaltrialsgov identifier: NCT04488913
    • …
    corecore