39 research outputs found
Quantum numbers of the state and orbital angular momentum in its decay
Angular correlations in decays, with , and , are used to measure
orbital angular momentum contributions and to determine the value of
the meson. The data correspond to an integrated luminosity of 3.0
fb of proton-proton collisions collected with the LHCb detector. This
determination, for the first time performed without assuming a value for the
orbital angular momentum, confirms the quantum numbers to be .
The is found to decay predominantly through S wave and an upper limit
of at C.L. is set on the fraction of D wave.Comment: 16 pages, 4 figure
Observation of Z production in proton-lead collisions at LHCb
The first observation of Z boson production in proton-lead collisions at a centre-of-mass energy per proton-nucleon pair of root(s) N N = 5TeV is presented. The data sample corresponds to an integrated luminosity of 1.6 nb(-1) collected with the LHCb detector. The Z candidates are reconstructed from pairs of oppositely charged muons with pseudorapidities between 2.0 and 4.5 and transverse momenta above 20 GeV/c. The invariant dimuon mass is restricted to the range 60-120 GeV/c. The Z production cross-section is measured to be sigma(Z ->mu+mu-) (fwd) = 13.5(-4.0)(+5.4)(stat.) +/- 1.2(syst.) nb in the direction of the proton beam and sigma(Z ->mu+mu-) (bwd) = 10.7(-5.1)(+8.4)(stat.) +/- 1.0(syst.) nb in the direction of the lead beam, where the first uncertainty is statistical and the second systematic
Measurement of Upsilon production in pp collisions at \sqrt{s} = 7 TeV
The production of Upsilon(1S), Upsilon(2S) and Upsilon(3S) mesons in
proton-proton collisions at the centre-of-mass energy of sqrt(s)=7 TeV is
studied with the LHCb detector. The analysis is based on a data sample of 25
pb-1 collected at the Large Hadron Collider. The Upsilon mesons are
reconstructed in the decay mode Upsilon -> mu+ mu- and the signal yields are
extracted from a fit to the mu+ mu- invariant mass distributions. The
differential production cross-sections times dimuon branching fractions are
measured as a function of the Upsilon transverse momentum pT and rapidity y,
over the range pT < 15 GeV/c and 2.0 < y < 4.5. The cross-sections times
branching fractions, integrated over these kinematic ranges, are measured to be
sigma(pp -> Upsilon(1S) X) x B(Upsilon(1S)->mu+ mu-) = 2.29 {\pm} 0.01 {\pm}
0.10 -0.37 +0.19 nb, sigma(pp -> Upsilon(2S) X) x B(Upsilon(2S)->mu+ mu-) =
0.562 {\pm} 0.007 {\pm} 0.023 -0.092 +0.048 nb, sigma(pp -> Upsilon(3S) X) x
B(Upsilon(3S)->mu+ mu-) = 0.283 {\pm} 0.005 {\pm} 0.012 -0.048 +0.025 nb, where
the first uncertainty is statistical, the second systematic and the third is
due to the unknown polarisation of the three Upsilon states.Comment: 22 pages, 7 figure
Evidence for CP violation in time-integrated D0 -> h-h+ decay rates
A search for time-integrated CP violation in D0 -> h-h+ (h=K, pi) decays is
presented using 0.62 fb^-1 of data collected by LHCb in 2011. The flavor of the
charm meson is determined by the charge of the slow pion in the D*+ -> D0 pi+
and D*- -> D0bar pi- decay chains. The difference in CP asymmetry between D0 ->
K-K+ and D0 -> pi-pi+, Delta ACP = ACP(K-K+) - ACP(pi-pi+), is measured to be
[-0.82 \pm 0.21(stat.) \pm 0.11(syst.)]%. This differs from the hypothesis of
CP conservation by 3.5 standard deviations.Comment: 8 pages, 3 figures, 2 tables; v2 minor updates after journal revie
Economic consequences of investing in anti-HCV antiviral treatment from the Italian NHS perspective : a real-world-based analysis of PITER data
OBJECTIVE:
We estimated the cost consequence of Italian National Health System (NHS) investment in direct-acting antiviral (DAA) therapy according to hepatitis C virus (HCV) treatment access policies in Italy.
METHODS:
A multistate, 20-year time horizon Markov model of HCV liver disease progression was developed. Fibrosis stage, age and genotype distributions were derived from the Italian Platform for the Study of Viral Hepatitis Therapies (PITER) cohort. The treatment efficacy, disease progression probabilities and direct costs in each health state were obtained from the literature. The break-even point in time (BPT) was defined as the period of time required for the cumulative costs saved to recover the Italian NHS investment in DAA treatment. Three different PITER enrolment periods, which covered the full DAA access evolution in Italy, were considered.
RESULTS:
The disease stages of 2657 patients who consecutively underwent DAA therapy from January 2015 to December 2017 at 30 PITER clinical centres were standardized for 1000 patients. The investment in DAAs was considered to equal âŹ25 million, âŹ15 million, and âŹ9 million in 2015, 2016, and 2017, respectively. For patients treated in 2015, the BPT was not achieved, because of the disease severity of the treated patients and high DAA prices. For 2016 and 2017, the estimated BPTs were 6.6 and 6.2 years, respectively. The total cost savings after 20 years were âŹ50.13 and âŹ55.50 million for 1000 patients treated in 2016 and 2017, respectively.
CONCLUSIONS:
This study may be a useful tool for public decision makers to understand how HCV clinical and epidemiological profiles influence the economic burden of HCV