14 research outputs found
Entanglement Rate for Gaussian Continuous Variable Beams
We derive a general expression that quantifies the total entanglement
production rate in continuous variable systems, where a source emits two
entangled Gaussian beams with arbitrary correlators.This expression is
especially useful for situations where the source emits an arbitrary frequency
spectrum,e.g. when cavities are involved. To exemplify its meaning and
potential, we apply it to a four-mode optomechanical setup that enables the
simultaneous up- and down-conversion of photons from a drive laser into
entangled photon pairs. This setup is efficient in that both the drive and the
optomechanical up- and down-conversion can be fully resonant.Comment: 18 pages, 6 figure
Pattern phase diagram for 2D arrays of coupled limit-cycle oscillators
Arrays of coupled limit-cycle oscillators represent a paradigmatic example
for studying synchronization and pattern formation. They are also of direct
relevance in the context of currently emerging experiments on nano- and
optomechanical oscillator arrays. We find that the full dynamical equations for
the phase dynamics of such an array go beyond previously studied Kuramoto-type
equations. We analyze the evolution of the phase field in a two-dimensional
array and obtain a "phase diagram" for the resulting stationary and
non-stationary patterns. The possible observation in optomechanical arrays is
discussed briefly
Geometric phases in astigmatic optical modes of arbitrary order
The transverse spatial structure of a paraxial beam of light is fully
characterized by a set of parameters that vary only slowly under free
propagation. They specify bosonic ladder operators that connect modes of
different order, in analogy to the ladder operators connecting
harmonic-oscillator wave functions. The parameter spaces underlying sets of
higher-order modes are isomorphic to the parameter space of the ladder
operators. We study the geometry of this space and the geometric phase that
arises from it. This phase constitutes the ultimate generalization of the Gouy
phase in paraxial wave optics. It reduces to the ordinary Gouy phase and the
geometric phase of non-astigmatic optical modes with orbital angular momentum
states in limiting cases. We briefly discuss the well-known analogy between
geometric phases and the Aharonov-Bohm effect, which provides some
complementary insights in the geometric nature and origin of the generalized
Gouy phase shift. Our method also applies to the quantum-mechanical description
of wave packets. It allows for obtaining complete sets of normalized solutions
of the Schr\"odinger equation. Cyclic transformations of such wave packets give
rise to a phase shift, which has a geometric interpretation in terms of the
other degrees of freedom involved.Comment: final versio
Rotationally induced vortices in optical cavity modes
We show that vortices appear in the modes of an astigmatic optical cavity
when it is put into rotation about its optical axis. We study the properties of
these vortices and discuss numerical results for a specific realization of such
a set-up. Our method is exact up to first order in the time-dependent paraxial
approximation and involves bosonic ladder operators in the spirit of the
quantum-mechanical harmonic oscillator.Comment: 8 pages, 5 figures. Accepted for publication in a special issue
(singular optics 2008) of Journal of Optics A: Pure and Applied Optic
Rotational stabilization and destabilization of an optical cavity
We investigate the effects of rotation about the axis of an astigmatic
two-mirror cavity on its optical properties. This simple geometry is the first
example of an optical system that can be destabilized and, more surprisingly,
stabilized by rotation. As such, it has some similarity with both the Paul trap
and the gyroscope. We illustrate the effects of rotational (de)stabilization of
a cavity in terms of the spatial structure and orbital angular momentum of its
modes.Comment: 5 pages, 3 figures. Accepted for publication in Physical Review
Practical robustness evaluation in radiotherapy - A photon and proton-proof alternative to PTV-based plan evaluation
Background and purpose: A planning target volume (PTV) in photon treatments aims to ensure that the clinical target volume (CTV) receives adequate dose despite treatment uncertainties. The underlying static dose cloud approximation (the assumption that the dose distribution is invariant to errors) is problematic in intensity modulated proton treatments where range errors should be taken into account as well. The purpose of this work is to introduce a robustness evaluation method that is applicable to photon and proton treatments and is consistent with (historic) PTV-based treatment plan evaluations. Materials and methods: The limitation of the static dose cloud approximation was solved in a multi-scenario simulation by explicitly calculating doses for various treatment scenarios that describe possible errors in the treatment course. Setup errors were the same as the CTV-PTV margin and the underlying theory of 3D probability density distributions was extended to 4D to include range errors, maintaining a 90% confidence level. Scenario dose distributions were reduced to voxel-wise minimum and maximum dose distributions; the first to evaluate CTV coverage and the second for hot spots. Acceptance criteria for CTV D98 and D2 were calibrated against PTV-based criteria from historic photon treatment plans. Results: CTV D98 in worst case scenario dose and voxel-wise minimum dose showed a very strong correlation with scenario average D98 (R-2 > 0.99). The voxel-wise minimum dose visualised CTV dose conformity and coverage in 3D in agreement with PTV-based evaluation in photon therapy. Criteria for CTV D98 and D2 of the voxel-wise minimum and maximum dose showed very strong correlations to PTV D98 and D2 (R-2 > 0.99) and on average needed corrections of -0.9% and +2.3%, respectively. Conclusions: A practical approach to robustness evaluation was provided and clinically implemented for PTV-less photon and proton treatment planning, consistent with PTV evaluations but without its static dose cloud approximation. (C) 2019 The Authors. Published by Elsevier B.V
Effect of angiotensin-converting enzyme inhibitor and angiotensin receptor blocker initiation on organ support-free days in patients hospitalized with COVID-19
IMPORTANCE Overactivation of the renin-angiotensin system (RAS) may contribute to poor clinical outcomes in patients with COVID-19.
Objective To determine whether angiotensin-converting enzyme (ACE) inhibitor or angiotensin receptor blocker (ARB) initiation improves outcomes in patients hospitalized for COVID-19.
DESIGN, SETTING, AND PARTICIPANTS In an ongoing, adaptive platform randomized clinical trial, 721 critically ill and 58 non–critically ill hospitalized adults were randomized to receive an RAS inhibitor or control between March 16, 2021, and February 25, 2022, at 69 sites in 7 countries (final follow-up on June 1, 2022).
INTERVENTIONS Patients were randomized to receive open-label initiation of an ACE inhibitor (n = 257), ARB (n = 248), ARB in combination with DMX-200 (a chemokine receptor-2 inhibitor; n = 10), or no RAS inhibitor (control; n = 264) for up to 10 days.
MAIN OUTCOMES AND MEASURES The primary outcome was organ support–free days, a composite of hospital survival and days alive without cardiovascular or respiratory organ support through 21 days. The primary analysis was a bayesian cumulative logistic model. Odds ratios (ORs) greater than 1 represent improved outcomes.
RESULTS On February 25, 2022, enrollment was discontinued due to safety concerns. Among 679 critically ill patients with available primary outcome data, the median age was 56 years and 239 participants (35.2%) were women. Median (IQR) organ support–free days among critically ill patients was 10 (–1 to 16) in the ACE inhibitor group (n = 231), 8 (–1 to 17) in the ARB group (n = 217), and 12 (0 to 17) in the control group (n = 231) (median adjusted odds ratios of 0.77 [95% bayesian credible interval, 0.58-1.06] for improvement for ACE inhibitor and 0.76 [95% credible interval, 0.56-1.05] for ARB compared with control). The posterior probabilities that ACE inhibitors and ARBs worsened organ support–free days compared with control were 94.9% and 95.4%, respectively. Hospital survival occurred in 166 of 231 critically ill participants (71.9%) in the ACE inhibitor group, 152 of 217 (70.0%) in the ARB group, and 182 of 231 (78.8%) in the control group (posterior probabilities that ACE inhibitor and ARB worsened hospital survival compared with control were 95.3% and 98.1%, respectively).
CONCLUSIONS AND RELEVANCE In this trial, among critically ill adults with COVID-19, initiation of an ACE inhibitor or ARB did not improve, and likely worsened, clinical outcomes.
TRIAL REGISTRATION ClinicalTrials.gov Identifier: NCT0273570
The TRENDY multi-center randomized trial on hepatocellular carcinoma - Trial QA including automated treatment planning and benchmark-case results
Background and purpose: The TRENDY trial is an international multi-center phase-II study, randomizing hepatocellular carcinoma (HCC) patients between transarterial chemoembolization (TACE) and stereotactic body radiation therapy (SBRT) with a target dose of 48-54 Gy in six fractions. The radiotherapy quality assurance (QA) program, including prospective plan feedback based on automated treatment planning, is described and results are reported. Materials and methods: Scans of a single patient were used as a benchmark case. Contours submitted by nine participating centers were compared with reference contours. The subsequent planning round was based on a single set of contours. A total of 20 plans from participating centers, including 12 from the benchmark case, 5 from a clinical pilot and 3 from the first study patients, were compared to automatically generated VMAT plans. Results: For the submitted liver contours, Dice Similarity Coefficients (DSC) with the reference delineation ranged from 0.925 to 0.954. For the GTV, the DSC varied between 0.721 and 0.876. For the 12 plans on the benchmark case, healthy liver normal-tissue complication probabilities (NTCPs) ranged from 0.2% to 22.2% with little correlation between NCTP and PTV-D95% (R-2 <0.3). Four protocol deviations were detected in the set of 20 treatment plans. Comparison with co-planar autoVMAT QA plans revealed these were due to too high target dose and suboptimal planning. Overall, autoVMAT resulted in an average liver NTCP reduction of 2.2 percent point (range: 16.2 percent point to -1.8 percent point, p = 0.03), and lower doses to the healthy liver (p <0.01) and gastrointestinal organs at risk (p <0.001). Conclusions: Delineation variation resulted in feedback to participating centers. Automated treatment planning can play an important role in clinical trials for prospective plan QA as suboptimal plans were detected. (c) 2017 Elsevier B.V. All rights reserve