116 research outputs found
Optimal control of transitions between nonequilibrium steady states
Biological systems fundamentally exist out of equilibrium in order to
preserve organized structures and processes. Many changing cellular conditions
can be represented as transitions between nonequilibrium steady states, and
organisms have an interest in optimizing such transitions. Using the
Hatano-Sasa Y-value, we extend a recently developed geometrical framework for
determining optimal protocols so that it can be applied to systems driven from
nonequilibrium steady states. We calculate and numerically verify optimal
protocols for a colloidal particle dragged through solution by a translating
optical trap with two controllable parameters. We offer experimental
predictions, specifically that optimal protocols are significantly less costly
than naive ones. Optimal protocols similar to these may ultimately point to
design principles for biological energy transduction systems and guide the
design of artificial molecular machines.Comment: Accepted for publication at PLoS ON
Antioxidantienstatus bei Patienten mit Magenkarzinom vor und nach operativer Intervention
Bei 59 Patienten mit einem Magenkarzinom ersfolgte vor operativer Resektion sowie am 2., 5. und 11. postoperativen Tag die Bestimmung von Selen, Glutathionperoxidase, Superoxiddismutase, Glutathion, Vitamin E und C, Zink, Magnesium, Kupfer, Eisen, Calcium im Blut und bei einigen Parametern auch im Urin. Als Meßparameter der oxidativen Belastung diente die Bestimmung der TBARS im Blut und im Urin. Die Ergebnisse zeigen, dass der Antioxidantienstatus bei Patienten mit Magenkarzinom bereits vor der Therapieeinleitung von Gesunden abweicht, dass Unterscheide in Abhänigkeit vom bestehenden Veränderungen weiter verstärkt und dass bei Auftreten von postoperativen Komplikationen signifikante Veränderungen des Antioxidantienstatus nachweisbar sind
Quantizing Horava-Lifshitz Gravity via Causal Dynamical Triangulations
We extend the discrete Regge action of causal dynamical triangulations to
include discrete versions of the curvature squared terms appearing in the
continuum action of (2+1)-dimensional projectable Horava-Lifshitz gravity.
Focusing on an ensemble of spacetimes whose spacelike hypersurfaces are
2-spheres, we employ Markov chain Monte Carlo simulations to study the path
integral defined by this extended discrete action. We demonstrate the existence
of known and novel macroscopic phases of spacetime geometry, and we present
preliminary evidence for the consistency of these phases with solutions to the
equations of motion of classical Horava-Lifshitz gravity. Apparently, the phase
diagram contains a phase transition between a time-dependent de Sitter-like
phase and a time-independent phase. We speculate that this phase transition may
be understood in terms of deconfinement of the global gravitational Hamiltonian
integrated over a spatial 2-sphere.Comment: 24 pages; 10 figure
The geometry of thermodynamic control
A deeper understanding of nonequilibrium phenomena is needed to reveal the
principles governing natural and synthetic molecular machines. Recent work has
shown that when a thermodynamic system is driven from equilibrium then, in the
linear response regime, the space of controllable parameters has a Riemannian
geometry induced by a generalized friction tensor. We exploit this geometric
insight to construct closed-form expressions for minimal-dissipation protocols
for a particle diffusing in a one dimensional harmonic potential, where the
spring constant, inverse temperature, and trap location are adjusted
simultaneously. These optimal protocols are geodesics on the Riemannian
manifold, and reveal that this simple model has a surprisingly rich geometry.
We test these optimal protocols via a numerical implementation of the
Fokker-Planck equation and demonstrate that the friction tensor arises
naturally from a first order expansion in temporal derivatives of the control
parameters, without appealing directly to linear response theory
Inter-rater reliability of the EPUAP pressure ulcer classification system using photographs
Background. Many classification systems for grading pressure ulcers are discussed in the literature. Correct identification and classification of a pressure ulcer is important for accurate reporting of the magnitude of the problem, and for timely prevention. The reliability of pressure ulcer classification systems has rarely been tested. Aims and objectives. The purpose of this paper is to examine the inter-rater reliability of classifying pressure ulcers according to the European Pressure Ulcer Advisory Panel classification system when using pressure ulcer photographs.Design. Survey was among pressure ulcer experts.Methods. Fifty-six photographs were presented to 44 pressure ulcer experts. The experts classified the lesions as normal skin, blanchable erythema, pressure ulcer (four grades) or incontinence lesion. Inter-rater reliability was calculated.Results. The multirater-Kappa for the entire group of experts was 0.80 (P < 0.001).Various groups of experts obtained comparable results. Differences in classifications are mainly limited to 1 degree of difference. Incontinence lesions are most often confused with grade 2 (blisters) and grade 3 pressure ulcers (superficial pressure ulcers).Conclusions. The inter-rater reliability of the European Pressure Ulcer Advisory Panel classification appears to be good for the assessment of photographs by experts. The difference between an incontinence lesion and a blister or a superficial pressure ulcer does not always seem clear.Relevance to clinical practice. The ability to determine correctly whether a lesion is a pressure ulcer lesion is important to assess the effectiveness of preventive measures. In addition, the ability to make a correct distinction between pressure ulcers and incontinence lesions is important as they require different preventive measures. A faulty classification leads to mistaken measures and negative results. Photographs can be used as a practice instrument to learn to discern pressure ulcers from incontinence lesions and to get to know the different grades of pressure ulcers. The Pressure Ulcer Classification software package has been developed to facilitate learning
Phase II Trial with Carboplatin and Bendamustine in Patients with Extensive Stage Small-Cell Lung Cancer
Background:Bendamustine is an alkylating agent with hybrid activity and proven efficacy in small-cell lung cancer associated with a favorable toxicity rate. This phase II study of carboplatin/bendamustine was conducted to evaluate the efficacy of this combination in patients with extensive disease small-cell lung cancer (ED-SCLC).Methods:Fifty-six untreated patients with ED-SCLC were enrolled. Their median age was 63 years. Sixty-seven percent of patients were male and 18% had a World Health Organization performance status of 2. Bendamustine was administered as a 30- to 60-minute infusion at a dose of 80 mg/m2 on days 1 and 2, and carboplatin was given at an area under the curve of 5 on day 1 of a 21-day cycle.Results:Fifty-five patients were assessable for response and toxicity. The overall response rate was 72.7% (95% confidence interval: 59%–84%), with one complete remission (1.8%). The median time to progression was 5.2 months (95% confidence interval: 4.2–5.6). At the time of evaluation, 71% of the patients had died. The median survival time reached 8.3 months (95% confidence interval: 6.6–9.9). The major toxicity of this regimen was myelosuppression, including grade 3 or 4 neutropenia (46%), thrombopenia (26%), anemia (15%), and infections (11%). Toxic death was recorded in two patients (3.6%).Conclusions:The carboplatin/bendamustine regimen is a well-tolerated cytostatic combination in ED-SCLC with activity comparable with that of other platinum-based regimens. Further investigations, such as a phase III trial, are currently planned
Development of the interRAI Pressure Ulcer Risk Scale (PURS) for use in long-term care and home care settings
<p>Abstract</p> <p>Background</p> <p>In long-term care (LTC) homes in the province of Ontario, implementation of the Minimum Data Set (MDS) assessment and The Braden Scale for predicting pressure ulcer risk were occurring simultaneously. The purpose of this study was, using available data sources, to develop a bedside MDS-based scale to identify individuals under care at various levels of risk for developing pressure ulcers in order to facilitate targeting risk factors for prevention.</p> <p>Methods</p> <p>Data for developing the interRAI Pressure Ulcer Risk Scale (interRAI PURS) were available from 2 Ontario sources: three LTC homes with 257 residents assessed during the same time frame with the MDS and Braden Scale for Predicting Pressure Sore Risk, and eighty-nine Ontario LTC homes with 12,896 residents with baseline/reassessment MDS data (median time 91 days), between 2005-2007. All assessments were done by trained clinical staff, and baseline assessments were restricted to those with no recorded pressure ulcer. MDS baseline/reassessment samples used in further testing included 13,062 patients of Ontario Complex Continuing Care Hospitals (CCC) and 73,183 Ontario long-stay home care (HC) clients.</p> <p>Results</p> <p>A data-informed Braden Scale cross-walk scale using MDS items was devised from the 3-facility dataset, and tested in the larger longitudinal LTC homes data for its association with a future new pressure ulcer, giving a c-statistic of 0.676. Informed by this, LTC homes data along with evidence from the clinical literature was used to create an alternate-form 7-item additive scale, the interRAI PURS, with good distributional characteristics and c-statistic of 0.708. Testing of the scale in CCC and HC longitudinal data showed strong association with development of a new pressure ulcer.</p> <p>Conclusions</p> <p>interRAI PURS differentiates risk of developing pressure ulcers among facility-based residents and home care recipients. As an output from an MDS assessment, it eliminates duplicated effort required for separate pressure ulcer risk scoring. Moreover, it can be done manually at the bedside during critical early days in an admission when the full MDS has yet to be completed. It can be calculated with established MDS instruments as well as with the newer interRAI suite instruments designed to follow persons across various care settings (interRAI Long-Term Care Facilities, interRAI Home Care, interRAI Palliative Care).</p
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