315 research outputs found

    Search for CP Violation in the Decay Z -> b (b bar) g

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    About three million hadronic decays of the Z collected by ALEPH in the years 1991-1994 are used to search for anomalous CP violation beyond the Standard Model in the decay Z -> b \bar{b} g. The study is performed by analyzing angular correlations between the two quarks and the gluon in three-jet events and by measuring the differential two-jet rate. No signal of CP violation is found. For the combinations of anomalous CP violating couplings, h^b=h^AbgVbh^VbgAb{\hat{h}}_b = {\hat{h}}_{Ab}g_{Vb}-{\hat{h}}_{Vb}g_{Ab} and hb=h^Vb2+h^Ab2h^{\ast}_b = \sqrt{\hat{h}_{Vb}^{2}+\hat{h}_{Ab}^{2}}, limits of \hat{h}_b < 0.59and and h^{\ast}_{b} < 3.02$ are given at 95\% CL.Comment: 8 pages, 1 postscript figure, uses here.sty, epsfig.st

    A Novel Dimeric Inhibitor Targeting Beta2GPI in Beta2GPI/Antibody Complexes Implicated in Antiphospholipid Syndrome

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    Background: b2GPI is a major antigen for autoantibodies associated with antiphospholipid syndrome (APS), an autoimmune disease characterized by thrombosis and recurrent pregnancy loss. Only the dimeric form of b2GPI generated by anti-b2GPI antibodies is pathologically important, in contrast to monomeric b2GPI which is abundant in plasma. Principal Findings: We created a dimeric inhibitor, A1-A1, to selectively target b2GPI in b2GPI/antibody complexes. To make this inhibitor, we isolated the first ligand-binding module from ApoER2 (A1) and connected two A1 modules with a flexible linker. A1-A1 interferes with two pathologically important interactions in APS, the binding of b2GPI/antibody complexes with anionic phospholipids and ApoER2. We compared the efficiency of A1-A1 to monomeric A1 for inhibition of the binding of b2GPI/antibody complexes to anionic phospholipids. We tested the inhibition of b2GPI present in human serum, b2GPI purified from human plasma and the individual domain V of b2GPI. We demonstrated that when b2GPI/antibody complexes are formed, A1-A1 is much more effective than A1 in inhibition of the binding of b2GPI to cardiolipin, regardless of the source of b2GPI. Similarly, A1-A1 strongly inhibits the binding of dimerized domain V of b2GPI to cardiolipin compared to the monomeric A1 inhibitor. In the absence of anti-b2GPI antibodies, both A1-A1 and A1 only weakly inhibit the binding of pathologically inactive monomeric b2GPI to cardiolipin. Conclusions: Our results suggest that the approach of using a dimeric inhibitor to block b2GPI in the pathologica

    Antiphospholipid syndrome; its implication in cardiovascular diseases: a review

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    Antiphospholipid syndrome (APLS) is a rare syndrome mainly characterized by several hyper-coagulable complications and therefore, implicated in the operated cardiac surgery patient. APLS comprises clinical features such as arterial or venous thromboses, valve disease, coronary artery disease, intracardiac thrombus formation, pulmonary hypertension and dilated cardiomyopathy. The most commonly affected valve is the mitral, followed by the aortic and tricuspid valve. For APLS diagnosis essential is the detection of so-called antiphospholipid antibodies (aPL) as anticardiolipin antibodies (aCL) or lupus anticoagulant (LA). Minor alterations in the anticoagulation, infection, and surgical stress may trigger widespread thrombosis. The incidence of thrombosis is highest during the following perioperative periods: preoperatively during the withdrawal of warfarin, postoperatively during the period of hypercoagulability despite warfarin or heparin therapy, or postoperatively before adequate anticoagulation achievement. Cardiac valvular pathology includes irregular thickening of the valve leaflets due to deposition of immune complexes that may lead to vegetations and valve dysfunction; a significant risk factor for stroke. Patients with APLS are at increased risk for thrombosis and adequate anticoagulation is of vital importance during cardiopulmonary bypass (CPB). A successful outcome requires multidisciplinary management in order to prevent thrombotic or bleeding complications and to manage perioperative anticoagulation. More work and reporting on anticoagulation management and adjuvant therapy in patients with APLS during extracorporeal circulation are necessary

    Value of hospital antimicrobial stewardship programs [ASPs]:a systematic review

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    Abstract Background Hospital antimicrobial stewardship programs (ASPs) aim to promote judicious use of antimicrobials to combat antimicrobial resistance. For ASPs to be developed, adopted, and implemented, an economic value assessment is essential. Few studies demonstrate the cost-effectiveness of ASPs. This systematic review aimed to evaluate the economic and clinical impact of ASPs. Methods An update to the Dik et al. systematic review (2000–2014) was conducted on EMBASE and Medline using PRISMA guidelines. The updated search was limited to primary research studies in English (30 September 2014–31 December 2017) that evaluated patient and/or economic outcomes after implementation of hospital ASPs including length of stay (LOS), antimicrobial use, and total (including operational and implementation) costs. Results One hundred forty-six studies meeting inclusion criteria were included. The majority of these studies were conducted within the last 5 years in North America (49%), Europe (25%), and Asia (14%), with few studies conducted in Africa (3%), South America (3%), and Australia (3%). Most studies were conducted in hospitals with 500–1000 beds and evaluated LOS and change in antibiotic expenditure, the majority of which showed a decrease in LOS (85%) and antibiotic expenditure (92%). The mean cost-savings varied by hospital size and region after implementation of ASPs. Average cost savings in US studies were 732perpatient(range:732 per patient (range: 2.50 to $2640), with similar trends exhibited in European studies. The key driver of cost savings was from reduction in LOS. Savings were higher among hospitals with comprehensive ASPs which included therapy review and antibiotic restrictions. Conclusions Our data indicates that hospital ASPs have significant value with beneficial clinical and economic impacts. More robust published data is required in terms of implementation, LOS, and overall costs so that decision-makers can make a stronger case for investing in ASPs, considering competing priorities. Such data on ASPs in lower- and middle-income countries is limited and requires urgent attention

    Measurement of the W-pair cross section in e+ee^+ e^- collisions at 172 GeV

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    The e+e- --> W+W- cross section is measured in a data sample collected by ALEPH at a mean centre--of--mass energy of 172.09 GEV, corresponding to an integrated luminosity of 10.65 pb-1. Cross sections are given for the three topologies, fully leptonic, semi-leptonic and hadronic of a W-pair decay. Under the assumption that no other decay modes are present, the W-pair cross section is measured to be 11.7 +- 1.2 (stat.) +- 0.3 (syst.) pb. The existence of the triple gauge boson vertex of the Standard Model is clearly preferred by the data. The decay branching ratio of the W boson into hadrons is measured to be B(W --> hadrons) = 67.7 +- 3.1 (stat.) +- 0.7 (syst.)%, allowing a determination of the CKM matrix element |Vcs|= 0.98 +- 0.14 (stat.) +- 0.03 (syst.)

    Measurement of the tau lepton lifetime with the three-dimensional impact parameter method.

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    A new method is presented for the measurement of the mean τ\tau lepton lifetime using events in which τ\tau's are pair-produced and both τ\tau's decay to hadrons and ντ\nu_\tau. Based on the correlation between the two τ\tau's produced at a symmetric e+ee^+ e^- collider, the 3DIP method relies on the three-dimensional information from a double-sided vertex detector and on kinematic constraints for the precise measurement of the τ\tau decay angles. Using the data collected from 1992 to 1994 with the ALEPH detector at LEP, a τ\tau lifetime of 288.0±3.1±1.3288.0 \pm 3.1 \pm 1.3 \fs is obtained from the sample in which both τ\tau's decay to one charged track, and 292.8±5.6±3.0292.8 \pm 5.6 \pm 3.0 \fs from the sample in which one τ\tau decays to one prong and the other to three prongs. The results show small statistical correlations with those derived from other methods. When combined with the previously published ALEPH measurements, the resulting τ\tau lifetime is 291.2±2.0±1.2291.2 \pm 2.0 \pm 1.2 \fs

    Measurement of the tau lepton lifetime with the three-dimensional impact parameter method.

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    A new method is presented for the measurement of the mean τ\tau lepton lifetime using events in which τ\tau's are pair-produced and both τ\tau's decay to hadrons and ντ\nu_\tau. Based on the correlation between the two τ\tau's produced at a symmetric e+ee^+ e^- collider, the 3DIP method relies on the three-dimensional information from a double-sided vertex detector and on kinematic constraints for the precise measurement of the τ\tau decay angles. Using the data collected from 1992 to 1994 with the ALEPH detector at LEP, a τ\tau lifetime of 288.0±3.1±1.3288.0 \pm 3.1 \pm 1.3 \fs is obtained from the sample in which both τ\tau's decay to one charged track, and 292.8±5.6±3.0292.8 \pm 5.6 \pm 3.0 \fs from the sample in which one τ\tau decays to one prong and the other to three prongs. The results show small statistical correlations with those derived from other methods. When combined with the previously published ALEPH measurements, the resulting τ\tau lifetime is 291.2±2.0±1.2291.2 \pm 2.0 \pm 1.2 \fs

    Measurement of the tau lepton lifetime with the three-dimensional impact parameter method.

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    A new method is presented for the measurement of the mean τ\tau lepton lifetime using events in which τ\tau's are pair-produced and both τ\tau's decay to hadrons and ντ\nu_\tau. Based on the correlation between the two τ\tau's produced at a symmetric e+ee^+ e^- collider, the 3DIP method relies on the three-dimensional information from a double-sided vertex detector and on kinematic constraints for the precise measurement of the τ\tau decay angles. Using the data collected from 1992 to 1994 with the ALEPH detector at LEP, a τ\tau lifetime of 288.0±3.1±1.3288.0 \pm 3.1 \pm 1.3 \fs is obtained from the sample in which both τ\tau's decay to one charged track, and 292.8±5.6±3.0292.8 \pm 5.6 \pm 3.0 \fs from the sample in which one τ\tau decays to one prong and the other to three prongs. The results show small statistical correlations with those derived from other methods. When combined with the previously published ALEPH measurements, the resulting τ\tau lifetime is 291.2±2.0±1.2291.2 \pm 2.0 \pm 1.2 \fs

    Measurement of the tau lepton lifetime with the three-dimensional impact parameter method.

    No full text
    A new method is presented for the measurement of the mean τ\tau lepton lifetime using events in which τ\tau's are pair-produced and both τ\tau's decay to hadrons and ντ\nu_\tau. Based on the correlation between the two τ\tau's produced at a symmetric e+ee^+ e^- collider, the 3DIP method relies on the three-dimensional information from a double-sided vertex detector and on kinematic constraints for the precise measurement of the τ\tau decay angles. Using the data collected from 1992 to 1994 with the ALEPH detector at LEP, a τ\tau lifetime of 288.0±3.1±1.3288.0 \pm 3.1 \pm 1.3 \fs is obtained from the sample in which both τ\tau's decay to one charged track, and 292.8±5.6±3.0292.8 \pm 5.6 \pm 3.0 \fs from the sample in which one τ\tau decays to one prong and the other to three prongs. The results show small statistical correlations with those derived from other methods. When combined with the previously published ALEPH measurements, the resulting τ\tau lifetime is 291.2±2.0±1.2291.2 \pm 2.0 \pm 1.2 \fs

    Measurement of the tau lepton lifetime with the three-dimensional impact parameter method.

    No full text
    A new method is presented for the measurement of the mean τ\tau lepton lifetime using events in which τ\tau's are pair-produced and both τ\tau's decay to hadrons and ντ\nu_\tau. Based on the correlation between the two τ\tau's produced at a symmetric e+ee^+ e^- collider, the 3DIP method relies on the three-dimensional information from a double-sided vertex detector and on kinematic constraints for the precise measurement of the τ\tau decay angles. Using the data collected from 1992 to 1994 with the ALEPH detector at LEP, a τ\tau lifetime of 288.0±3.1±1.3288.0 \pm 3.1 \pm 1.3 \fs is obtained from the sample in which both τ\tau's decay to one charged track, and 292.8±5.6±3.0292.8 \pm 5.6 \pm 3.0 \fs from the sample in which one τ\tau decays to one prong and the other to three prongs. The results show small statistical correlations with those derived from other methods. When combined with the previously published ALEPH measurements, the resulting τ\tau lifetime is 291.2±2.0±1.2291.2 \pm 2.0 \pm 1.2 \fs
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