6 research outputs found

    Demonstration of a simple entangling optical gate and its use in Bell-state analysis

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    We demonstrate a new architecture for an optical entangling gate that is significantly simpler than previous realisations, using partially-polarising beamsplitters so that only a single optical mode-matching condition is required. We demonstrate operation of a controlled-Z gate in both continuous-wave and pulsed regimes of operation, fully characterising it in each case using quantum process tomography. We also demonstrate a fully-resolving, nondeterministic optical Bell-state analyser based on this controlled-Z gate. This new architecture is ideally suited to guided optics implementations of optical gates.Comment: 4 pages, 3 figures. v2: additional author, improved data and figures (low res), some other minor changes. Accepted for publication in PR

    Minimum error discrimination of Pauli channels

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    We solve the problem of discriminating with minimum error probability two given Pauli channels. We show that, differently from the case of discrimination between unitary transformations, the use of entanglement with an ancillary system can strictly improve the discrimination, and any maximally entangled state allows to achieve the optimal discrimination. We also provide a simple necessary and sufficient condition in terms of the structure of the channels for which the ultimate minimum error probability can be achieved without entanglement assistance. When such a condition is satisfied, the optimal input state is simply an eigenstate of one of the Pauli matrices.Comment: 8 pages, no figure

    Quantum teleportation and entanglement swapping with linear optics logic gates

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    We report on the usage of a linear optics phase gate for distinguishing all four Bell states simultaneously in a quantum teleportation and entanglement swapping protocol. This is demonstrated by full state tomography of the one and two qubit output states of the two protocols, yielding average state fidelities of about 0.83 and 0.77, respectively. In addition, the performance of the teleportation channel is characterised by quantum process tomography. The non classical properties of the entanglement swapping output states are further confirmed by the violation of a CHSH-type Bell inequality of 2.14 on average.Comment: 11 pages, 3 figure

    Ezetimibe added to statin therapy after acute coronary syndromes

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    BACKGROUND: Statin therapy reduces low-density lipoprotein (LDL) cholesterol levels and the risk of cardiovascular events, but whether the addition of ezetimibe, a nonstatin drug that reduces intestinal cholesterol absorption, can reduce the rate of cardiovascular events further is not known. METHODS: We conducted a double-blind, randomized trial involving 18,144 patients who had been hospitalized for an acute coronary syndrome within the preceding 10 days and had LDL cholesterol levels of 50 to 100 mg per deciliter (1.3 to 2.6 mmol per liter) if they were receiving lipid-lowering therapy or 50 to 125 mg per deciliter (1.3 to 3.2 mmol per liter) if they were not receiving lipid-lowering therapy. The combination of simvastatin (40 mg) and ezetimibe (10 mg) (simvastatin-ezetimibe) was compared with simvastatin (40 mg) and placebo (simvastatin monotherapy). The primary end point was a composite of cardiovascular death, nonfatal myocardial infarction, unstable angina requiring rehospitalization, coronary revascularization ( 6530 days after randomization), or nonfatal stroke. The median follow-up was 6 years. RESULTS: The median time-weighted average LDL cholesterol level during the study was 53.7 mg per deciliter (1.4 mmol per liter) in the simvastatin-ezetimibe group, as compared with 69.5 mg per deciliter (1.8 mmol per liter) in the simvastatin-monotherapy group (P<0.001). The Kaplan-Meier event rate for the primary end point at 7 years was 32.7% in the simvastatin-ezetimibe group, as compared with 34.7% in the simvastatin-monotherapy group (absolute risk difference, 2.0 percentage points; hazard ratio, 0.936; 95% confidence interval, 0.89 to 0.99; P = 0.016). Rates of pre-specified muscle, gallbladder, and hepatic adverse effects and cancer were similar in the two groups. CONCLUSIONS: When added to statin therapy, ezetimibe resulted in incremental lowering of LDL cholesterol levels and improved cardiovascular outcomes. Moreover, lowering LDL cholesterol to levels below previous targets provided additional benefit
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