384 research outputs found

    Living beyond placenta accreta spectrum: parent's experience of the postnatal journey and recommendations for an integrated care pathway.

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    Placenta Accreta Spectrum is associated with significant clinical maternal morbidity and mortality, which has been extensively described in the literature. However, there is a dearth of research on the lived experiences of pregnant people and their support partners. The aim of this study is to describe living beyond a pregnancy and birth complicated by PAS for up to four years postpartum. Participants experiences inform the development of an integrated care pathway of family centered support interventions. An Interpretative Phenomenological Analysis approach was applied to collect data through virtual interviews over a 3-month period from February to April 2021. Twenty-nine participants shared their stories; six people with a history of PAS and their support partners were interviewed together (n = 12 participants), six were interviewed separately (n = 12 participants), and five were interviewed without their partner. Pregnant people were eligible for inclusion if they had a diagnosis of PAS within the previous 5 years. This paper focuses on the postnatal period, with data from the antenatal and intrapartum periods described separately. One superordinate theme "Living beyond PAS" emerged from interviews, with 6 subordinate themes as follows; "Living with a different body", "The impact on relationships", "Coping strategies", "Post-traumatic growth", "Challenges with normal care" and recommendations for "What needs to change". These themes informed the development of an integrated care pathway for pregnant people and their support partners to support them from diagnosis up to one year following the birth. Parents described the challenges of the postnatal period in terms of the physical and emotional impact, and how some were able to make positive life changes in the aftermath of a traumatic event. An integrated care pathway of simple supportive interventions, based on participant recommendations, delivered as part of specialist multidisciplinary team care may assist pregnant people and their support partners in alleviating some of these challenges

    The energy dependence of the hard exclusive diffractive processes in pQCD as the function of momentum transfer

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    We predict the dependence on energy of photo(electro) production processes: γ(γ)+pV+X\gamma(\gamma^*)+p\to V+ X with large rapidity gap at small x and large momentum t-t transferred to VV in pQCD. Here V is a heavy quarkonium (J/ψ,ΥJ/\psi, \Upsilon) or longitudinally polarized light vector meson (in the electroproduction processes), etc. In the kinematics of HERA we calculate the dependence on energy of cross sections of these processes as the function of momentum transfer tt, photon virtuality Q2Q^2 and/or quarkonium mass. In the kinematical region Q02tQ2+MV2Q_0^2\le -t\ll Q^2+M^2_V the nontrivial energy dependence of the cross section for the vector meson production due to the photon scattering off a parton follows within QCD from the summing of the double logarithmic terms. In the second regime tQ2+MV2-t\ge Q^2+M^2_V within DGLAP approximation in all orders of perturbation theory the qqˉpartonq\bar q - {\rm parton} elastic cross section is energy independent. We show that the correct account of the double logarithmic terms and of the gluon radiation including kinematical constraints removes the disagreement between pQCD calculations and recent HERA experimental data. The explicit formula for the dependence of the differential cross sectiond2σdtdxJ\displaystyle{\frac{d^2\sigma}{dtdx_J}} of these processes on sγNs_{\gamma^*N} is obtained. We show that perturbative Pomeron type behavior may reveal itself only at energies significantly larger than those available at HERA. In addition we evaluate the energy dependence of DCVS processes.Comment: 22 pages, 4 figure

    Critical Correlations of Wilson Lines in SU(3) and the High Energy γp\gamma^*p Cross Section

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    We discuss deep inelastic scattering at high energies as a critical phenomenon in 2+1 space - time dimensions. In the limit of Bjorken x0x \to 0, QCDQCD SU(3) with quark fields becomes a critical theory with a diverging correlation length ξ(x)x12λ2\xi(x) \propto x^{-\frac{1}{2 \lambda_2}} where the exponent λ2=2.52\lambda_2=2.52 is obtained from the center group Z(3) of SU(3). We conjecture that the dipole wave function of the virtual photon for transverse sizes 1/Q<x<ξ1/Q<x_{\bot}<\xi obeys correlation scaling Ψ(x)(1+n)\Psi \propto (x_{\bot})^{-(1+n)} before exponentially decaying for distances larger than the correlation length. Using this behavior combined with different xx -independent dipole proton cross sections we calculate the proton structure function and compare with the experimental data. We take the good agreement with the measured proton structure function F2(x,Q2)_2(x,Q^2) as an indication that at high energies dimensional reduction to an effective three dimensional theory with a critical point occurs.Comment: 21 pages, 3 figure

    E-retailing ethics in Egypt and its effect on customer repurchase intention

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    The theoretical understanding of online shopping behaviour has received much attention. Less focus has been given to the formation of the ethical issues that result from online shopper interactions with e-retailers. The vast majority of earlier research on this area is conceptual in nature and limited in scope by focusing on consumers’ privacy issues. Therefore, the purpose of this paper is to propose a theoretical model explaining what factors contribute to online retailing ethics and its effect on customer repurchase intention. The data were analysed using variance-based structural equation modelling, employing partial least squares regression. Findings indicate that the five factors of the online retailing ethics (security, privacy, non- deception, fulfilment/reliability, and corporate social responsibility) are strongly predictive of online consumers’ repurchase intention. The results offer important implications for e-retailers and are likely to stimulate further research in the area of e-ethics from the consumers’ perspective

    Machine learning algorithms performed no better than regression models for prognostication in traumatic brain injury

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    Objective: We aimed to explore the added value of common machine learning (ML) algorithms for prediction of outcome for moderate and severe traumatic brain injury. Study Design and Setting: We performed logistic regression (LR), lasso regression, and ridge regression with key baseline predictors in the IMPACT-II database (15 studies, n = 11,022). ML algorithms included support vector machines, random forests, gradient boosting machines, and artificial neural networks and were trained using the same predictors. To assess generalizability of predictions, we performed internal, internal-external, and external validation on the recent CENTER-TBI study (patients with Glasgow Coma Scale <13, n = 1,554). Both calibration (calibration slope/intercept) and discrimination (area under the curve) was quantified. Results: In the IMPACT-II database, 3,332/11,022 (30%) died and 5,233(48%) had unfavorable outcome (Glasgow Outcome Scale less than 4). In the CENTER-TBI study, 348/1,554(29%) died and 651(54%) had unfavorable outcome. Discrimination and calibration varied widely between the studies and less so between the studied algorithms. The mean area under the curve was 0.82 for mortality and 0.77 for unfavorable outcomes in the CENTER-TBI study. Conclusion: ML algorithms may not outperform traditional regression approaches in a low-dimensional setting for outcome prediction after moderate or severe traumatic brain injury. Similar to regression-based prediction models, ML algorithms should be rigorously validated to ensure applicability to new populations

    Multiplicity dependence of inclusive J/psi production at midrapidity in pp collisions at root s=13 TeV

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    Measurements of the inclusive J/psi yield as a function of charged-particle pseudorapidity density dN(ch)/d eta in pp collisions at root s = 13 TeV with ALICE at the LHC are reported. The J/psi meson yield is measured at midrapidity (vertical bar y vertical bar <0.9) in the dielectron channel, for events selected based on the charged-particle multiplicity at midrapidity (vertical bar eta vertical bar <1) and at forward rapidity (-3.7 <eta <-1.7 and 2.8 <eta <5.1); both observables are normalized to their corresponding averages in minimum bias events. The increase of the normalized J/psi yield with normalized dN(ch)/d eta is significantly stronger than linear and dependent on the transverse momentum. The data are compared to theoretical predictions, which describe the observed trends well, albeit not always quantitatively. (C) 2020 European Organization for Nuclear Research. Published by Elsevier B.V.Peer reviewe

    Influence of Conversion and Anastomotic Leakage on Survival in Rectal Cancer Surgery; Retrospective Cross-sectional Study

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    Whole-genome sequencing reveals host factors underlying critical COVID-19

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    Critical COVID-19 is caused by immune-mediated inflammatory lung injury. Host genetic variation influences the development of illness requiring critical care1 or hospitalization2,3,4 after infection with SARS-CoV-2. The GenOMICC (Genetics of Mortality in Critical Care) study enables the comparison of genomes from individuals who are critically ill with those of population controls to find underlying disease mechanisms. Here we use whole-genome sequencing in 7,491 critically ill individuals compared with 48,400 controls to discover and replicate 23 independent variants that significantly predispose to critical COVID-19. We identify 16 new independent associations, including variants within genes that are involved in interferon signalling (IL10RB and PLSCR1), leucocyte differentiation (BCL11A) and blood-type antigen secretor status (FUT2). Using transcriptome-wide association and colocalization to infer the effect of gene expression on disease severity, we find evidence that implicates multiple genes—including reduced expression of a membrane flippase (ATP11A), and increased expression of a mucin (MUC1)—in critical disease. Mendelian randomization provides evidence in support of causal roles for myeloid cell adhesion molecules (SELE, ICAM5 and CD209) and the coagulation factor F8, all of which are potentially druggable targets. Our results are broadly consistent with a multi-component model of COVID-19 pathophysiology, in which at least two distinct mechanisms can predispose to life-threatening disease: failure to control viral replication; or an enhanced tendency towards pulmonary inflammation and intravascular coagulation. We show that comparison between cases of critical illness and population controls is highly efficient for the detection of therapeutically relevant mechanisms of disease
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