165 research outputs found

    A CFD-based mixing model for vegetated flows

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    This paper provides a CFD‐based modelling framework for predicting flow field, turbulence and mixing characteristics within vegetated environments such as ponds and wetlands. The framework has been implemented within a commercial CFD code – ANSYS Fluent 19 – via a set of user‐defined‐functions. Following the approach outlined by King et al. (2012), the standard k‐Δ turbulence closure model has been modified to capture the energy transfer at the vegetation/clear flow shear interface and within the vegetation. The implementation assumes that vegetation is vertical, but non‐orthogonal flow in the horizontal plane is accounted for. Values for the drag coefficient and the mixing coefficients are estimated based on the vegetation stem diameter and density. Following Tanino and Nepf (2008), a switch has been incorporated to account for the fact that the relevant length scale changes from stem diameter to stem spacing as stem density increases. A set of model parameters is proposed, based on a re‐evaluation of previously published laboratory data and theoretical analysis. Five different experimental data sets are used to demonstrate that the model is able to predict mixing within fully‐vegetated systems and due to both vertical and horizontal shear layers. The framework was developed to provide a practical prediction tool for engineering purposes, in particular for the estimation of residence time distributions in real partially‐vegetated stormwater management ponds. Its implementation here within a commercial CFD package potentially facilitates application to complex pond geometries, including patches of different types of vegetation with different bulk stem diameter and density characteristics

    Effect of mean void fraction correlations on a shell-and-tube evaporator dynamic model performance

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    In this paper, the influence of different mean void fraction correlations on a shell-and-tube evaporator dynamic model performance has been evaluated. The model proposed is based on the moving boundary approach and includes the expansion valve modelling. Several transient tests, using R134a as working fluid, have been carried out varying refrigerant mass flow, inlet enthalpy and secondary fluid flow. Then, the model performance, using different mean void fractions, is analysed from the system model outputs (evaporating pressure, refrigerant outlet temperature and condensing water outlet temperature). The slip ratio expressions selected are: homogenous, momentum flux model, Zivi's, Chisholm's and Smith's correlations. The results of the comparison between experimental and model predictions depend on the transient characteristics and there is not a single slip ratio correlation that provides the best performance in all the cases analysed.Navarro-EsbrĂ­, J.; MiliĂĄn SĂĄnchez, V.; Mota Babiloni, A.; MolĂ©s Ribera, F.; VerdĂș MartĂ­n, GJ. (2015). Effect of mean void fraction correlations on a shell-and-tube evaporator dynamic model performance. Science and Technology for the Built Environment. 21(7):1057-1072. doi:10.1080/23744731.2015.1034594S1057107221

    Psychosocial Treatment of Children in Foster Care: A Review

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    A substantial number of children in foster care exhibit psychiatric difficulties. Recent epidemiologi-cal and historical trends in foster care, clinical findings about the adjustment of children in foster care, and adult outcomes are reviewed, followed by a description of current approaches to treatment and extant empirical support. Available interventions for these children can be categorized as either symptom-focused or systemic, with empirical support for specific methods ranging from scant to substantial. Even with treatment, behavioral and emotional problems often persist into adulthood, resulting in poor functional outcomes. We suggest that self-regulation may be an important mediat-ing factor in the appearance of emotional and behavioral disturbance in these children

    International Lower Limb Collaborative (INTELLECT) study : a multicentre, international retrospective audit of lower extremity open fractures

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    A novel formulation of inhaled sodium cromoglicate (PA101) in idiopathic pulmonary fibrosis and chronic cough: a randomised, double-blind, proof-of-concept, phase 2 trial

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    Background Cough can be a debilitating symptom of idiopathic pulmonary fibrosis (IPF) and is difficult to treat. PA101 is a novel formulation of sodium cromoglicate delivered via a high-efficiency eFlow nebuliser that achieves significantly higher drug deposition in the lung compared with the existing formulations. We aimed to test the efficacy and safety of inhaled PA101 in patients with IPF and chronic cough and, to explore the antitussive mechanism of PA101, patients with chronic idiopathic cough (CIC) were also studied. Methods This pilot, proof-of-concept study consisted of a randomised, double-blind, placebo-controlled trial in patients with IPF and chronic cough and a parallel study of similar design in patients with CIC. Participants with IPF and chronic cough recruited from seven centres in the UK and the Netherlands were randomly assigned (1:1, using a computer-generated randomisation schedule) by site staff to receive PA101 (40 mg) or matching placebo three times a day via oral inhalation for 2 weeks, followed by a 2 week washout, and then crossed over to the other arm. Study participants, investigators, study staff, and the sponsor were masked to group assignment until all participants had completed the study. The primary efficacy endpoint was change from baseline in objective daytime cough frequency (from 24 h acoustic recording, Leicester Cough Monitor). The primary efficacy analysis included all participants who received at least one dose of study drug and had at least one post-baseline efficacy measurement. Safety analysis included all those who took at least one dose of study drug. In the second cohort, participants with CIC were randomly assigned in a study across four centres with similar design and endpoints. The study was registered with ClinicalTrials.gov (NCT02412020) and the EU Clinical Trials Register (EudraCT Number 2014-004025-40) and both cohorts are closed to new participants. Findings Between Feb 13, 2015, and Feb 2, 2016, 24 participants with IPF were randomly assigned to treatment groups. 28 participants with CIC were enrolled during the same period and 27 received study treatment. In patients with IPF, PA101 reduced daytime cough frequency by 31·1% at day 14 compared with placebo; daytime cough frequency decreased from a mean 55 (SD 55) coughs per h at baseline to 39 (29) coughs per h at day 14 following treatment with PA101, versus 51 (37) coughs per h at baseline to 52 (40) cough per h following placebo treatment (ratio of least-squares [LS] means 0·67, 95% CI 0·48–0·94, p=0·0241). By contrast, no treatment benefit for PA101 was observed in the CIC cohort; mean reduction of daytime cough frequency at day 14 for PA101 adjusted for placebo was 6·2% (ratio of LS means 1·27, 0·78–2·06, p=0·31). PA101 was well tolerated in both cohorts. The incidence of adverse events was similar between PA101 and placebo treatments, most adverse events were mild in severity, and no severe adverse events or serious adverse events were reported. Interpretation This study suggests that the mechanism of cough in IPF might be disease specific. Inhaled PA101 could be a treatment option for chronic cough in patients with IPF and warrants further investigation

    Risk profiles and one-year outcomes of patients with newly diagnosed atrial fibrillation in India: Insights from the GARFIELD-AF Registry.

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    BACKGROUND: The Global Anticoagulant Registry in the FIELD-Atrial Fibrillation (GARFIELD-AF) is an ongoing prospective noninterventional registry, which is providing important information on the baseline characteristics, treatment patterns, and 1-year outcomes in patients with newly diagnosed non-valvular atrial fibrillation (NVAF). This report describes data from Indian patients recruited in this registry. METHODS AND RESULTS: A total of 52,014 patients with newly diagnosed AF were enrolled globally; of these, 1388 patients were recruited from 26 sites within India (2012-2016). In India, the mean age was 65.8 years at diagnosis of NVAF. Hypertension was the most prevalent risk factor for AF, present in 68.5% of patients from India and in 76.3% of patients globally (P < 0.001). Diabetes and coronary artery disease (CAD) were prevalent in 36.2% and 28.1% of patients as compared with global prevalence of 22.2% and 21.6%, respectively (P < 0.001 for both). Antiplatelet therapy was the most common antithrombotic treatment in India. With increasing stroke risk, however, patients were more likely to receive oral anticoagulant therapy [mainly vitamin K antagonist (VKA)], but average international normalized ratio (INR) was lower among Indian patients [median INR value 1.6 (interquartile range {IQR}: 1.3-2.3) versus 2.3 (IQR 1.8-2.8) (P < 0.001)]. Compared with other countries, patients from India had markedly higher rates of all-cause mortality [7.68 per 100 person-years (95% confidence interval 6.32-9.35) vs 4.34 (4.16-4.53), P < 0.0001], while rates of stroke/systemic embolism and major bleeding were lower after 1 year of follow-up. CONCLUSION: Compared to previously published registries from India, the GARFIELD-AF registry describes clinical profiles and outcomes in Indian patients with AF of a different etiology. The registry data show that compared to the rest of the world, Indian AF patients are younger in age and have more diabetes and CAD. Patients with a higher stroke risk are more likely to receive anticoagulation therapy with VKA but are underdosed compared with the global average in the GARFIELD-AF. CLINICAL TRIAL REGISTRATION-URL: http://www.clinicaltrials.gov. Unique identifier: NCT01090362
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